Survey
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Indexed in MEDLINE, PubMed, and PubMed Central National Library of Medicine PRSRT STD US POSTAGE PAID PORTLAND OR PERMIT NO 1452 Volume 19 No. 3 — Summer 2015 500 NE Multnomah St, Suite 100 Portland, Oregon 97232 Change Service Requested Summer 2015 Volume 19 No. 3 A peer-reviewed journal of medical science, social science in medicine, and medical humanities Original Research & Contributions 4 Characteristics of Newly Enrolled Members of an Integrated Delivery System after the Affordable Care Act 11 A Metrics Taxonomy and Reporting Strategy for Rule-Based Alerts 21 “Getting off the Bus Closer to Your Destination”: Patients’ Views about Pharmacogenetic Testing 29 A Community-Based Hip Fracture Registry: Population, Methods, and Outcomes THE PERMANENTE JOURNAL Follow @PermanenteJ Printed on acid free paper. The Permanente Journal Summer 2015 Volume 19 No. 3 ISSN 1552-5767 37 Utility of the Multinational Association for Supportive Care in Cancer (MASCC) Risk Index Score as a Criterion for Nonadmission in Febrile Neutropenic Patients with Solid Tumors 48 Evidence-Based Referral: Effects of the Revised “Youth Fit 4 Life” Protocol on Physical Activity Outputs 54 Relationship between Participation in Patient- and Family-Centered Care Training and Communication Adaptability among Medical Students: Changing Hearts, Changing Minds 59 A Ten-Year Case-Control Study of Passive Smoke Exposure as a Risk Factor for Pertussis in Children Special Report 64 2014 Hypertension Guideline: Recommendation for a Change in Goal Systolic Blood Pressure Commentary 81 Does Consuming Sugar and Artificial Sweeteners Change Taste Preferences? Special Report 85 New Kid on the Block Turns Ten! The Brief, Remarkable History of the National Physicians Alliance Narrative Medicine 90 Suicide is a Baobab Tree: A Narrative Medicine Case Study NOW AVAILABLE: Our CME mobile Web application— earn your credits at www.tpjcme.org. See inside for additional content as well as articles found only online www.thepermanentejournal.org BOOKS PUBLISHED BY PERMANENTE AUTHORS: Summer 2015/ Volume 19 No. 3 PermanenteJournal The Mission: The Permanente Journal advances knowledge in scientific research, clinical medicine, and innovative health care delivery. Circulation: 25,000 print readers per quarter, 6900 eTOC readers, and in 2014, TPJ content had 1 million page views—760,000 of those on TPJ articles on PubMed. Viewers visited from 187 countries/territories. ON THE COVER: Rocky Perspective by David L Shenson, MD This photograph was taken at Ruby Beach, on the Olympic Peninsula in Washington. The contrast in depth of field creates an interesting perspective of these stones ground smooth by the elements and the passage of time. Dr Shenson is an Internist at the Mt Scott Medical Office in Clackamas, OR. More of his photography may be viewed at: www.davidshenson.com. ORIGINAL RESEARCH & CONTRIBUTIONS 4 Characteristics of Newly Enrolled Members of an Integrated Delivery System after the Affordable Care Act. Elizabeth A Bayliss, MD, MSPH; Jennifer L Ellis, MSPH; Mary Jo Strobel, RN, MBA; Deanna B McQuillan, MA; Irena B Petsche, PhD; Jennifer C Barrow, MSPH; Arne Beck, PhD Of 89,289 newly enrolled non-Medicare members, 25.3% completed the Brief Health Questionnaire between 1/1/2014, and 8/31/2014. Of these, 3593 respondents were insured through Medicaid, 9434 through the individual health exchange, and 9521 through primarily commercial plans. Of Medicaid, exchange, and commercial members, 19.5%, 7.1%, and 5.3%, respectively, self-reported fair or poor health; 12.9%, 2.0%, and 3.3% of each group self-reported 2 or more Emergency Department visits during the previous year; and 8.1%, 4.3%, and 4.4% self-reported an inpatient admission during the previous year. 11 A Metrics Taxonomy and Reporting Strategy for Rule-Based Alerts. Michael Krall, MD, MS; Alexander Gerace An action-oriented alerts taxonomy according to structure, actions, and implicit intended process outcomes using a set of 333 rule-based alerts at Kaiser Permanente Northwest (KPNW) was developed. The authors identified 9 major and 17 overall classes of alerts and developed a specific metric approach for 5 of these classes, including the 3 most numerous ones in KPNW, accounting for 224 (67%) of the alerts. 21 “Getting off the Bus Closer to Your Destination”: Patients’ Views about Pharmacogenetic Testing. Susan Brown Trinidad, MA; Tara B Coffin, MEd; Stephanie M Fullerton, DPhil; James Ralston, MD, MPH; Gail P Jarvik, MD, PhD; Eric B Larson, MD, MPH 96 CME EVALUATION FORM The Permanente Journal 500 NE Multnomah St, Suite 100 Portland, Oregon 97232 www.thepermanentejournal.org The authors conducted focus groups with patients prescribed antidepressants (pilot session plus 2 focus groups, n = 27); patients prescribed carbamazepine (2 focus groups, n = 17); and healthy patients (2 focus groups, n = 17). Although participants understood the potential advantages of pharmacogenetic testing, many felt that the risks (discrimination, stigmatization, physician overreliance on genomic results, and denial of certain medications) may outweigh the benefits. These concerns were shared across groups but were more strongly expressed among participants with chronic mental health diagnoses. 29 A Community-Based Hip Fracture Registry: Population, Methods, and Outcomes. Maria C S Inacio, PhD; Jennifer M Weiss, MD; Alex Miric, MD; Jessica J Hunt, MA; Gary L Zohman, MD; Elizabeth W Paxton, MA Cases of hip fracture recorded from 1/2009 to 12/2011 were ascertained using the Kaiser Permanente Hip Fracture Registry. The registry collects information on patient, procedure, surgeon, facility, and surgical outcomes. The population (N = 12,562) was predominantly white, women, and older (≥ 75 years), and 32% had at least 5 comorbidities. The average length of follow-up was 1.1 years. Hemiarthroplasty was the most common procedure (33.1%). Most fractures were treated by medium-volume surgeons at high-volume facilities. The 90-day readmission rate was 22.1%, and the mortality rate was 12.3%. 37 Utility of the Multinational Association for Supportive Care in Cancer (MASCC) Risk Index Score as a Criterion for Nonadmission in Febrile Neutropenic Patients with Solid Tumors. Roger A Bitar, MD, MPH Febrile neutropenic episodes in patients with solid tumors were identified electronically from 10/1/2008 to 11/15/2010. Inclusion criteria were met in 198 episodes. Sensitivity, specificity, and positive and negative predictive values of the MASCC risk index score vs complications were, respectively, 94%, 29.6%, 57.7%, and 82.9%. An MASCC risk index score of 21 or greater could not be used as a criterion for “no complication/ do not admit.” Inability to eat should be an admission criterion. 48 Evidence-Based Referral: Effects of the Revised “Youth Fit 4 Life” Protocol on Physical Activity Outputs. James J Annesi, PhD, FAAHB, FTOS, FAPA; Linda L Vaughn, MS, MBA The authors contrasted 2 physical activity/ nutrition treatments on the basis of social cognitive and self-efficacy theory, and a comparison condition, on time in moderateto-vigorous physical activity (MVPA) during the 45-min/day physical activity segment of elementary after-school care. The Revised Youth Fit 4 Life protocol that sought to maximize participants’ cardiovascular physical activity appeared to improve upon the Original Youth Fit For Life treatment on time in MVPA. Thus, pediatricians might have confidence in referring their patients to such evidence-based approaches. Instant Work-Ups: A Clinical Guide to Obstetric and Gynecologic Care Theodore X O’Connell, Kathleen Dor ISBN-10: 1416054618 ISBN-13: 978-1416054610 Philadelphia, PA; Saunders: 2008 Paperback: 268 pages $31.95 Glimpses in Time Nicholas Morell ISBN-10: 1483690202 ISBN-13: 978-1483690209 Bloomington, IN: Xlibris; 2013 Paperback: 228 pages $19.99 If you are a Permanente author and would like your book cited here, send an e-mail to [email protected]. NOW AVAILABLE! The new Web mobile CME application from The Permanente Journal. - Read articles. - Take quizzes. - Earn credit. - Get your CME certificate immediately. www.tpjcme.org ISSN 1552-5767 Follow @PermanenteJ The Permanente Journal/ Summer 2015/ Volume 19 No. 3 For information and/or rates for placing an announcement here, please contact [email protected]. CME credits are available online at www.tpjcme.org. The mail-in CME form can be found on page 96. 54 Relationship between Participation in Patient- and Family-Centered Care Training and Communication Adaptability among Medical Students: Changing Hearts, Changing Minds. Lisa Rossignol, MA A census of 43 third-year medical students at the University of New Mexico School of Medicine participated in Parents Reaching Out: Families as Faculty program during their pediatric rotation. Analysis of variance revealed statistical significance for the factor “appropriate disclosure” (meaning students have become more sensitive to the level of intimacy that the other person is seeking and the student is willing to offer more information). There was a positive correlation between pretest and posttests in social experience, wit, and social confirmation. 59 A Ten-Year Case-Control Study of Passive Smoke Exposure as a Risk Factor for Pertussis in Children. Mark A Schmidt, PhD, MPH; Samantha K Kurosky, MS; John P Mullooly, PhD; Colleen Chun, MD; Sheila Weinmann, PhD The authors conducted a matched casecontrol study of laboratory-confirmed pertussis cases, occurring from 1/1/1996 to 12/31/2005, in children up to 12 years of age who were members of a large managed care organization. Sixty-five laboratoryconfirmed cases of pertussis were identified. Using multivariable conditional logistic regression analysis, the authors did not detect a statistically significant association between pertussis and household passive exposure to cigarette smoking. Special Report 64 2014 Hypertension Guideline: Recommendation for a Change in Goal Systolic Blood Pressure. Joel Handler, MD The 2014 Kaiser Permanente Care Management Institute National Hypertension Guideline was developed to assist primary care physicians and other health care professionals in the outpatient treatment of uncomplicated hypertension in adult men and nonpregnant women aged 18 years and older. A major practice change is the recommendation for goal systolic blood pressure less than 150 mmHg in patients aged 60 years and older who are treated for hypertension in the absence of diabetes or chronic kidney disease. This article describes the reasons for, evidence for, and consequences of the change, and includes the guideline. SOUL OF THE HEALER 20 Pinnacle Brad Christian McDowell, MD 28Seville Samuel H Glassner, MD CASE REPORTS 74 Beer Potomania—An Unusual Cause of Hyponatremia. Dean A Kujubu, MD; Ardeshir Khosraviani, MD The first case of severe hyponatremia, since referred to as beer potomania, in a heavy beer drinker patient was reported in 1972. Excessive consumption of beer in particular, which has a low solute content, may result in severe hyponatremia. We report a case of severe hyponatremia that occurred in a patient who, owing to his underlying colon cancer, was drinking beer and ingesting little food. CLINICAL MEDICINE 77 Dermatologic Diagnosis: Leukocytoclastic Vasculitis. Joseph Einhorn, MD; Joel T Levis, MD, PhD, FACEP, FAAEM Leukocytoclastic vasculitis (LCV), also termed hypersensitivity vasculitis, is a small-vessel vasculitis. The skin is the organ most commonly involved in LCV. Typical presentation is a painful, burning rash predominantly in the lower extremities. The most common skin manifestation is palpable purpura. Other skin manifestations include maculopapular rash, bullae, papules, plaques, nodules, ulcers, and livedo reticularis. 79 ECG Diagnosis: Hyperacute T Waves. Joel T Levis, MD, PhD, FACEP, FAAEM After QT prolongation, hyperacute T waves are the earliest-described electrocardiographic sign of acute ischemia, preceding ST-segment elevation. The principle entity to exclude is hyperkalemia—this T-wave morphology may be confused with the hyperacute T wave of early transmural myocardial infarction. COMMENTARY 81 Does Consuming Sugar and Artificial Sweeteners Change Taste Preferences? Carole Bartolotto, MA, RD Americans consume 22.3 teaspoons of added caloric sweeteners a day. Sweeteners range from 180 to 13,000 times sweeter than sugar. In summer 2014, 20 people from Kaiser Permanente California facilities cut out all added sugars and artificial sweeteners for 2 weeks: 95% of participants found that sweet foods and drinks tasted sweeter or too sweet, 75% found that other foods tasted sweeter, and 95% said moving forward they would use less or even no sugar. Additionally, 86.6% of participants stopped craving sugar after 6 days. Special Report 85 New Kid on the Block Turns Ten! The Brief, Remarkable History of the National Physicians Alliance. Jean Silver-Isenstadt, MD, PhD Founded in 2005 by General Surgeon Lydia J Vaias, MD, MPH, the National Physicians Alliance is a 501c3 public charity with a mission to create research and education programs that promote health and foster active engagement of physicians with their communities to achieve high-quality, affordable health care for all. The National Physicians Alliance offers a professional home to physicians across medical specialties who share a commitment to professional integrity and health justice. As the organization celebrates its tenth birthday, the history and scope of this mission-aligned group is described. NARRATIVE MEDICINE 90 Suicide is a Baobab Tree: A Narrative Medicine Case Study. Adriano Machado Facioli, PhD; Fábio Ferreira Amorim, MD, PhD; Karlo Jozefo Quadros de Almeida, MD; Eliana Mendonça Vilar Trindade, PhD Like the baobab, when suicide or a suicide attempt occurs, suicidal ideations are well cultivated and have often already been repeatedly planted. Consequently, suicide is often difficult to prevent: once the death seed is planted; it is difficult to recreate life. Every year, more than 800,000 people die by suicide worldwide. 95 Why a Hanging Man Dances. Gurpreet Kaur Padam, MD “Do you know why a hanging man dances?” asked Mr B. He was once an intensely independent man, now 80 years old and afflicted with end-stage lung disease. He appeared tired, repositioning himself with great effort to sitting at the edge of the bed, tightly holding onto the bed sheets as if clenching to a life that was slowly escaping him. “No. I don’t want anything that will make me live longer.” ONLINE ONLY See page 2 for additional content from The Permanente Journal available online only. 73Dorothy’s View Bridget Bourgon, PA-C 80 So Much Sky Sharon Lee Hostler, MD The Permanente Journal/ Summer 2015/ Volume 19 No. 3 1 ONLINE ONLY Available at: www.thepermanentejournal.org/Issues/2015/Summer.html CASE REPORTS CLINICAL MEDICINE Pneumomediastinum Diagnosed on Ultrasound in the Emergency Department: A Case Report. Hilary FH Beason, MD; Joshua E Markowitz, MD, RDMS, FACEP Image Diagnosis: Inferior Mesenteric Vein Thrombosis. Avin Aggarwal, MBBS; Shashank Garg, MBBS An emergency ultrasound performed at bedside helped to confirm and to expedite the diagnosis of esophageal perforation in a 23-year-old man. To our knowledge, this is the first published report of using ultrasound as an aid in the diagnosis of Boerhaave syndrome by diagnosing pneumomediastinum in an adult male. Case Report: Pulmonary Papillomatosis in a Patient Presenting with Cough and Hemoptysis. Zhou Zhang, MD; Melisa Chang, MD; Luis M Moreta-Sainz, MD A previously healthy patient was seen in the Emergency Department for evaluation of a one-month history of cough and one-day history of hemoptysis. This case report, from a pulmonologist’s perspective, includes a comprehensive review of the patient’s clinical presentation and outcome, as well as a discussion of recurrent respiratory papillomatosis. A 59-year-old man presented to the gastroenterology clinic with 2 weeks of worsening lower back pain. There was associated poor appetite, fatigue, night sweats, and chills. The patient’s medical history was significant for well-controlled hypertension and sigmoid diverticulosis. The thrombosis probably resulted from inflammation in the adjacent diverticulum. BOOK REVIEW The Body Keeps the Score: Brain, Mind, and Body in the Healing of Trauma. Review by Albert Ray, MD This book explores the ways that patients and healers can develop the skills to appropriately evaluate historic traumatic events and how to successfully begin treating them. From the scientifically oriented physician, the biochemical, physiologic, and anatomic effects of trauma on the body are well explored in this detailed exposé. What is more important though is the invisible mark that is embedded permanently on the mind and body by past traumatic events EDITORIAL & PUBLISHING OFFICE The Permanente Journal, 500 NE Multnomah St, Suite 100, Portland, Oregon, 97232, USA; phone: 503-813-3286; fax: 503-813-2348; E-mail: [email protected]. THE PERMANENTE JOURNAL ONLINE The Permanente Journal is available online at www.thepermanentejournal.org. INSTRUCTIONS FOR AUTHORS Instructions for Authors and Manuscript Submission Instructions are available along with a link to our manuscript submission center at www.thepermanentejournal.org/authors.html. ARTWORK SUBMISSIONS Instructions for Artists and Artwork Submission Instructions are available along with a link to our submission center at www.thepermanentejournal.org/ authors/artwork.html. LETTERS TO THE EDITOR Send your comments to: The Permanente Journal, Letters to the Editor, 500 NE Multnomah St, Suite 100, Portland, Oregon, 97232, Fax: 503-813-2348, E-mail: [email protected]. PERMISSIONS AND REPRINTS To obtain permission to republish, reprint, or adapt material published in The Permanente Journal, please access and complete the Reprint Permission Form available at: www.thepermanentejournal.org/aboutus/5818-reprint-permissions.html. If you have questions, please contact Max McMillen, ELS, by e-mail: [email protected]. ADVERTISING/ANNOUNCEMENTS For rates and information about advertising in The Permanente Journal, contact Amy Eakin, 500 NE Multnomah St, Suite 100, Portland, Oregon, 97232; phone: 503-813-2623; E-mail: [email protected]. SUBSCRIPTION RATES AND SERVICE Subscription rates are shown in the table below. Subscriptions are entered for the calendar year. Advance payment in US dollars is required. For information about subscriptions, missing issues, billing, subscription renewal, and back issues, E-mail: [email protected]. USA Other Countries Institutional $70.00$85.00 Individual $40.00$55.00 ADDRESS CHANGES Send all address changes to The Permanente Journal, 500 NE Multnomah St, Suite 100, Portland, Oregon, 97232; E-mail: [email protected]. Please include both old and new addresses. ANNOUNCEMENT: CME Credits Now Available for Reviewers The Permanente Journal is happy to announce the availability of Continuing Medical Education credits for completing manuscript reviews for The Permanente Journal. Physicians are now eligible to receive up to 15 AMA PRA Category 1 Credits per year (3 AMA PRA Category 1 Credits per manuscript). With this change, we have launched our new For Reviewers home page on our Web site: www.thepermanentejournal.org/reviewers.html. The Permanente Journal (ISSN 1552-5767) is published quarterly by The Permanente Press. The Permanente Journal is available online (ISSN 15525775) at www.thepermanentejournal.org. Periodicals postage paid at Portland and at additional mailing offices. POSTMASTER, send all address changes to The Permanente Journal, 500 NE Multnomah Street, Suite 100, Portland, Oregon, 97232. The Editorial Staff have disclosed that they have no personal, professional, or financial involvement in any of the manuscripts they might judge. Should a conflict arise in the future, the Editorial Staff have agreed to recuse themselves regarding any specific manuscripts. The Editorial Staff also will not use the information gained through working with manuscripts for private gain. Copyright © 2015 The Permanente Journal 2 The Permanente Journal/ Summer 2015/ Volume 19 No. 3 PermanenteJournal The EDITOR-IN-CHIEF: Tom Janisse, MD, MBA ASSOCIATE EDITOR-IN-CHIEF: Lee Jacobs, MD SENIOR EDITORS Vincent Felitti, MD Preventive Medicine, Book Reviews Gus M Garmel, MD, FACEP, FAAEM Clinical Medicine Arthur Klatsky, MD Original Articles Eric Macy, MD Research Scott Rasgon, MD Corridor Consult ASSOCIATE EDITORS Mikel Aickin, PhD Biostatistics James J Annesi, PhD, FAAHB, FTOS, FAPA Health Behavior Research Marthie Baker, MS, MA, RN Nursing Research and Practice Ricky Chen, MD Medicine in Society Gary W Chien, MD Surgery Carrie Davino-Ramaya, MD National Practice Guidelines Charles Elder, MD Integrative Medicine Philip I Haigh, MD, MSc, FRCSC, FACS Surgery Robert Hogan, MD Family Medicine, Health Information Technology David Riley, MD Case Reports Ruth Shaber, MD Women’s Health John Stull, MD, MPH Spirit of Medicine Dialogues KM Tan, MD Continuing Medical Education Calvin Weisberger, MD Cognitive Clinical Medicine Winston F Wong, MD, MS Community Benefit, Disparities Improvement and Quality Initiatives Scott S Young, MD Care Management Institute EDITORIAL & PUBLISHING OFFICE Merry Parker Managing Editor & Publisher Lynette Leisure Creative Director Amy Eakin Business & Publishing Operations Manager Max McMillen, ELS Senior Editor & Staff Writer Christopher Dauterman, MBA Web Developer & Analyst Ian Kimmich, ELS Copy Editor & Publishing Coordinator The Permanente Press EDITORIAL BOARD Maher A Abbas, MD, FACS, FASCRS Chief, Digestive Disease Institute, Cleveland Clinic, Abu Dhabi, UAE; Professor of Surgery, Cleveland Clinic Lerner College of Medicine of Case Western Reserve University, Cleveland, Ohio Richard Abrohams, MD Internal Medicine and Geriatrics, The Southeast Permanente Medical Group, Atlanta, Georgia Fábio Ferreira Amorim, MD, PhD Professor of Medicine, Escola Superior de Ciências da Saúde in the Department of Research and Scientific Communication, Brasilia, Brazil Stanley W Ashley, MD Chief Medical Officer, Brigham and Women’s Hospital; Frank Sawyer Professor of Surgery, Harvard Medical School; Attending Surgeon, Gastrointestinal Cancer Center, Dana Farber Cancer Institute; Chief, General Surgery, Harvard Vanguard Medical Associates, Boston, Massachusetts Thomas Bodenheimer, MD Professor, Dept of Family and Community Medicine, University of California, San Francisco Brian Budenholzer, MD Associate Clinical Professor in the Department of Family Medicine at the Brody School of Medicine at East Carolina University, Greenville, North Carolina Ellen Cosgrove, MD Vice Dean, Academic Affairs and Education, University of Nevada, Las Vegas School of Medicine, Las Vegas, Nevada Quentin Eichbaum, MD, PhD, MPH, MFA, MMCH, FCAP Assistant Dean for Program Development; Associate Director of Transfusion Medicine; Associate Professor of Pathology; Associate Professor of Medical Education and Administration; Director, Fellowship Program in Transfusion Medicine; Member, Vanderbilt Institute for Global Health; Vanderbilt University School of Medicine, Nashville, Tennessee Linda Fahey, RN, NP, MSN Regional Manager, Quality and Patient Safety, Patient Care Services, Kaiser Permanente, Southern California, Pasadena Adrianne Feldstein, MD, MS Associate Medical Director, Quality Services, Kaiser Permanente Northwest; Investigator, Center for Health Research, Portland, Oregon Richard Frankel, PhD Professor of Medicine and Psychiatry, University of Indiana School of Medicine, Indianapolis Carol Havens, MD Family Practice and Addiction Medicine, Director of Clinical Education, The Permanente Medical Group, Oakland, California Alexander M Carson, RN, PhD Associate Dean of Research and Enterprise at the Institute of Health, Medical Sciences and Society at Glyndwr University in Wrexham, Wales, United Kingdom James T Hardee, MD Rita Charon, MD, PhD Professor of Medicine, Founder and Executive Director of the Program in Narrative Medicine at Columbia University Medical Center, New York, New York Arthur Hayward, MD Internal Medicine and Geriatrics, CMI Clinical Lead for Elder Care; Assistant Clinical Professor, Division of General Medicine, Dept of Internal Medicine, Oregon Health Sciences University, Portland Dan Cherkin, PhD Senior Research Investigator, Group Health Cooperative, and Affiliate Professor, Dept of Family Medicine and School of Public Health—Health Services, University of Washington, Seattle Marilyn Chow, RN, DNSc, FAAN Vice President, Patient Care Services, Kaiser Foundation Health Plan; Associate Clinical Professor, Dept of Community Health Systems, School of Nursing, University of California, San Francisco Robert R Cima, MD, FACS, FASCRS Associate Professor of Surgery, Division of Colon and Rectal Surgery; Vice Chairman, Department of Surgery, Mayo Clinic, Rochester, Minnesota Internal Medicine, Colorado Permanente Medical Group; Associate Clinical Professor of Medicine, University of Colorado School of Medicine, Westminster Catherine Hickie, MBBS Director of Clinical Training, Bloomfield Hospital, Greater Western Area Health Service; Conjoint Senior Lecturer in Psychiatry, University of New South Wales, Australia Thomas E Kottke, MD Medical Director for Population Health, HealthPartners; Consulting Cardiologist, HealthPartners Medical Group; Senior Clinical Investigator, HealthPartners Institute for Education and Research; Professor of Medicine, University of Minnesota, Minneapolis Tieraona Low Dog, MD Director of Education, Program in Integrative Medicine, University of Arizona; Clinical Assistant Professor, Department of Medicine, Clinical Lecturer, University of Arizona College of Pharmacy, Tucson Lewis Mehl-Madrona, MD, PhD, MPhil Director of Geriatric Education, Maine Dartmouth Family Medicine Residency; Director of Education and Training, Coyote Institute, Augusta, Maine Michel M Murr, MD, FACS Professor of Surgery, Director of Bariatric Surgery, University of South Florida Health Science Center, Tampa, Florida Sylvestre Quevedo, MD Department of Medicine and Global Health Sciences, University of California, San Francisco Ilan Rubinfeld, MD, MBA, FACS, FCCP Director, Surgical Intensive Care; Associate Program Director, General Surgery Residency; Henry Ford Hospital, Detroit, Michigan; Assistant Professor of Surgery, Wayne State University School of Medicine, Detroit, Michigan Marilyn Schlitz, PhD Ambassador for Creative Projects and Global Affairs, and Senior Scientist, Institute of Noetic Sciences, Petaluma, California Audrey Shafer, MD Associate Professor, Dept of Anesthesia, Co-Director, Biomedical Ethics & Medical Humanities Scholarly Concentration, Stanford University School of Medicine, Palo Alto, California Mark Snyder, MD Specialist Leader, Electronic Medical Record Implementation and Physician Adoption; Deloitte Consulting, LLP, McLean, Virginia Swee Yaw Tan, MBchB (Edin), MRCP (UK), ACSM, FAMS Senior Consultant Cardiologist, National Heart Centre, Adjunct Assistant Professor Duke National University of Singapore Graduate Medical School, Singapore William L Toffler, MD Professor of Family Medicine; Director of Predoctoral Education, Oregon Health and Sciences University, Portland Paul Wallace, MD Senior Vice President and Director, Center for Comparative Effectiveness Research, The Lewin Group, Falls Church, Virginia Tom Janisse, MD, MBA, Publisher The Permanente Journal is published by The Permanente Press The Permanente Journal/ Summer 2015/ Volume 19 No. 3 3 ORIGINAL RESEARCH & CONTRIBUTIONS Characteristics of Newly Enrolled Members of an Integrated Delivery System after the Affordable Care Act Elizabeth A Bayliss, MD, MSPH; Jennifer L Ellis, MSPH; Mary Jo Strobel, RN, MBA; Deanna B McQuillan, MA; Irena B Petsche, PhD; Jennifer C Barrow, MSPH; Arne Beck, PhD Perm J 2015 Summer;19(3):4-10 http://dx.doi.org/10.7812/TPP/14-193 ABSTRACT Context: Little is known about the health status and care needs of new enrollees in health plans since implementation of the Affordable Care Act. Objective: To describe characteristics of new members of an integrated delivery system during early phases of implementation of the act. Design: Descriptive analysis of ongoing collection of operational data. Main Outcome Measures: The 11-question Brief Health Questionnaire, which was administered to new members of Kaiser Permanente Colorado who had benefits effective on or after January 1, 2014. Bivariate analyses compared characteristics of new enrollees by benefit. Results: Of 89,289 newly enrolled non-Medicare members, 22,548 (25.3%) completed the Brief Health Questionnaire between January 1, 2014, and August 31, 2014. Of these, 3593 respondents were insured through Medicaid, 9434 through the individual health exchange, and 9521 through primarily commercial plans. Of Medicaid, exchange, and commercial members, 19.5%, 7.1%, and 5.3%, respectively, self-reported fair or poor health; 12.9%, 2.0%, and 3.3% of each group self-reported 2 or more Emergency Department visits during the previous year; and 8.1%, 4.3%, and 4.4% self-reported an inpatient admission during the previous year. During the preceding year, 31.5% of Medicaid, 30.8% of exchange, and 12.6% of commercial members were uninsured longer than 8 months. Conclusion: Systematic collection of patients’ self-reported information can enhance traditional approaches to initiating care, inform operational planning, and describe newly enrolled populations. Newly enrolled Medicaid beneficiaries may have more initial health care needs than new exchange or commercial members; however, health differences between the latter two groups are subtle. INTRODUCTION The first open enrollment period under the Affordable Care Act (ACA)1 resulted in an estimated eight million individuals gaining insurance coverage through exchanges and an additional six million through Medicaid expansions nationally.2-5 Published estimates of health status for those likely to gain new coverage under the ACA vary widely and are based on limited data.6-8 Accurate and timely information on the care needs of individuals who are either newly insured or transitioning between care plans under the ACA are important because these needs will affect demand for a range of primary and specialty care services.6,8 Most methods for predicting health care resource needs rely on models that incorporate measures of previous service use, morbidity burden, and socioeconomic factors. These factors are strong predictors of future service needs, as are self-reported health and functional status.9-17 However, morbidity and utilization data are unavailable before engagement with the health care system. In the absence of preexisting information on newly enrolled individuals, realtime data collection on health-related characteristics can inform care delivery and resource planning. Operations leaders and researchers in Kaiser Permanente Colorado (KPCO) collaborated to develop a brief health screening questionnaire to anticipate the potential health care needs of newly enrolled members. The goal of the Brief Health Questionnaire (BHQ) is twofold: 1) to identify care needs that can be met before traditional primary care appointments and 2) to characterize the newly enrolled member population. This brief report describes characteristics of new KPCO members during early phases of the ACA implementation. METHODS A not-for-profit, integrated health care delivery system, KPCO provides services in Denver and other metropolitan areas along the Colorado “Front Range” to the north and south of Denver. New members were defined as individuals who had no previous enrollment in KPCO and had new benefits effective on or after January 1, 2014. For families with more than one new enrollee, each individual was eligible to respond to the BHQ. We defined insurance type as Medicaid, individual exchange, and all other (composed primarily of large- and small-group commercial members). New Medicare members were excluded. The 11-question BHQ addresses the following domains: general health status, specific chronic illnesses, prescription Elizabeth A Bayliss, MD, MSPH, is the Director of Scientific Development at the Institute for Health Research in Denver, CO. E-mail: [email protected]. Jennifer L Ellis, MSPH, is a Biostatistician at the Institute for Health Research in Denver, CO. E-mail: [email protected]. Mary Jo Strobel, RN, MBA, is a Regional Administrator of Population Health of Population and Prevention Services for Kaiser Permanente in Denver, CO. E-mail: [email protected]. Deanna B McQuillan, MA, is a Project Manager for the Institute for Health Research in Denver, CO. E-mail: [email protected]. Irena B Petsche, PhD, is a Senior Strategy Consultant in Strategy Management for Kaiser Permanente in Denver, CO. E-mail: [email protected]. Jennifer C Barrow, MSPH, is a Portfolio Manager at the Institute for Health Research in Denver, CO. E-mail: [email protected]. Arne Beck, PhD, is the Director for Quality Improvement and Strategic Research at the Institute for Health Research in Denver, CO. E-mail: [email protected]. 4 The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS Characteristics of Newly Enrolled Members of an Integrated Delivery System after the Affordable Care Act medications, depression screening, pregnancy, financial constraints, prioryear hospitalizations, Emergency Department (ED) use, and insurance coverage.10,18-26 The BHQ is provided in the Appendix: Brief Health Questionnaire (available online at: www.thepermanentejournal.org/files/Summer2015/ Questionnaire.pdf ). Before administration, the questionnaire was pilot tested on 35 new members to assess comprehension and completion time. Starting in late 2013, the BHQ was offered to any new non-Medicare member calling for an appointment and was accessible on the KPCO Web site. After scheduling of an appointment, new members were asked for permission to “route the call to a New Member Specialist for assistance with ‘onboarding.’” This specialist then asked the BHQ questions and entered responses into the member’s electronic health record (EHR). Data collection is ongoing and evolving for this operational project. For example, Community Specialists still reach out to new Medicaid members to assess health and community resource needs. Additionally, new members are now directed (via a welcome telephone call and mailed identification card insert) to a 1-stop shop for all their onboarding needs, which include selecting a primary care physician, understanding benefits and care delivery options, registering on the KPCO Web site, and administration of the BHQ. This New Member Team is also responsible for outreach to new members within their first 90 days of coverage. Table 1. Characteristics of new members responding to the Brief Health Questionnaire between January 1, 2014, and August 31, 2014 (N = 22,548)a New member Medicaid characteristic (n = 3593), No. (%) Sex Female 2097 (58.4) Male 1496 (41.6) Unknown 0 Age group, years 0-9 553 (15.4) 10-19 353 (9.8) 20-29 567 (15.8) 30-39 580 (16.1) 40-49 547 (15.2) 50-59 694 (19.3) ≥ 60 299 (8.3) Response format Web portal 111 (3.1) completion Telephone 3482 (96.9) completion Benefit start month January 179 (5.0) February 365 (10.2) March 495 (13.8) April 592 (16.5) May 586 (16.3) June 513 (14.3) July 406 (11.3) August 457 (12.7) Individual on exchange (n = 9434), No. (%) Other (n = 9521), No. (%) 5511 (58.4) 3923 (41.6) 0 5406 (56.8) 4112 (43.2) 3 (0) 0.0414b 683 (7.2) 547 (5.8) 1477 (15.7) 1715 (18.2) 1477 (15.7) 2160 (22.9) 1375 (14.6) 1865 (19.6) 1104 (11.6) 1832 (19.2) 1699 (17.8) 1310 (13.8) 1251 (13.1) 460 (4.8) < 0.0001 98 (10.5) 918 (9.6) < 0.0001c 8447 (89.5) 8603 (90.4) 3094 (32.8) 710 (7.5) 1104 (11.7) 1357 (14.4) 2293 (24.3) 422 (4.5) 305 (3.2) 149 (1.6) 3324 (34.9) 986 (10.4) 910 (9.6) 985 (10.4) 979 (10.3) 746 (7.8) 1098 (11.5) 493 (5.2) p value RESULTS < 0.0001 Some percentages may not total to 100% because of rounding. Nonsignificant differences between Medicaid and exchange: sex (p = 0.9564). Nonsignificant differences between Medicaid and other: sex (p = 0.1537). c Nonsignificant differences between exchange and other: response format (p = 0.0604). a b The Permanente Journal/ Summer 2015/ Volume 19 No. 3 If new members responded “yes” to any BHQ question, New Member Specialists made telephone appointments for follow-up encounters on the basis of prespecified rules. All BHQs completed on the KPCO Web site were automatically routed to appropriate EHR in-baskets for follow-up. Pharmacists contacted new members regarding refills on prescription medications; Nurse Care Managers assessed those reporting fair or poor health status, specific chronic conditions, a “positive” depression screen (a Patient Health Questionnaire-2 score of 3 or greater27), or potential high morbidity as indicated by hospitalization and emergency service use. Social workers and Community Specialists evaluated reports of financial and social needs. The Obstetrics Department arranged for necessary prenatal care. Documentation of follow-up encounters was entered in the EHR for use at the point of care. Use of the questionnaire is ongoing. We compared demographic characteristics and BHQ responses across groups of new members (Medicaid, exchange, and other) using χ2 tests. We also conducted two descriptive subanalyses comparing 1) individuals who reported having no insurance for more than eight months during the previous year with those insured for that entire year and 2) BHQ respondents and nonrespondents. The KPCO institutional review board reviewed the protocol for the BHQ program and analyses, and determined that it met criteria for an operations intervention with intent to publish, rather than human subjects research. A total of 89,289 members were newly enrolled between January 1, 2014, and August 31, 2014. Of these, 22,548 (25.3%) completed a BHQ by August 31, 2014. By insurance type, 3593 respondents were insured through Medicaid, 9434 through the individual health exchange, and 9521 through other mechanisms, primarily large and small group commercial plans. These responses represented 43.2% (3593/8318) of new Medicaid enrollees, 26.8% (9434/35,113) of new exchange enrollees, and 20.8% (9521/45,858) of 5 ORIGINAL RESEARCH & CONTRIBUTIONS Characteristics of Newly Enrolled Members of an Integrated Delivery System after the Affordable Care Act Table 2. Responses to Brief Health Questionnaire between January 1, 2014, and August 31, 2014, by insurance category (N = 22,548)a Response General health Medicaid (n = 3593), No. (%) Excellent 703 (19.6) Very good 974 (27.1) Good 1118 (31.1) Fair 517 (14.4) Poor 184 (5.1) Missing/no answer 97 (2.7) Self-reported chronic conditions Asthma 301 (8.4) Diabetes 207 (5.8) Heart disease 95 (2.6) High blood pressure 494 (13.8) Positive depression screen 424 (11.8) Other health considerations Pregnant 48 (1.3) Current prescription 1347 (37.5) medications Health conditions interfere 1102 (30.7) with daily activity Emergency Department visits in past year None 2322 (64.6) 1 time 705 (19.6) 2+ times 462 (12.9) Missing data 104 (2.9) Inpatient admissions in past year None 3199 (89.0) 1 time 231 (6.4) 2+ times 59 (1.6) Missing data 104 (2.9) Insurance during past year Had insurance for whole year 1132 (31.5) No insurance for 1-4 months 230 (6.4) No insurance for 5-8 months 167 (4.7) No insurance for > 8 months 1132 (31.5) Prefer not to answer 12 (0.3) Missing data 920 (25.6) Reported financial constraint Health affected by difficulty 823 (22.9) paying for food, medicine, rent, utilities Any positive BHQ response 2185 (60.8) Individual on exchange (n = 9434), No. (%) Other (n = 9521), No. (%) 2893 (30.7) 3370 (35.7) 2421 (25.7) 565 (6.0) 106 (1.1) 79 (0.8) 3381 (35.5) 3377 (35.5) 2209 (23.2) 426 (4.5) 75 (0.8) 53 (0.6) < 0.0001 648 (6.9) 439 (4.7) 213 (2.3) 1239 (13.1) 441 (4.7) 609 (6.4) 290 (3.1) 149 (1.6) 778 (8.2) 325 (3.4) 0.0003 < 0.0001 < 0.0001 < 0.0001 < 0.0001 80 (0.9) 3847 (40.8) 124 (1.3) 3342 (35.1) 0.0048 < 0.0001 1506 (16.0) 1280 (13.4) < 0.0001 8150 (86.4) 1007 (10.7) 191 (2.0) 86 (0.9) 7927 (83.3) 1212 (12.7) 316 (3.3) 66 (0.7) < 0.0001 8938 (94.7) 343 (3.6) 60 (0.6) 93 (1.0) 9035 (94.9) 360 (3.8) 60 (0.6) 66 (0.7) < 0.0001 3893 (41.3) 877 (9.3) 484 (5.1) 2906 (30.8) 40 (0.4) 1234 (13.1) 4499 (47.3) 660 (6.9) 274 (2.9) 1199 (12.6) 20 (0.2) 2869 (30.1) < 0.0001 867 (9.2) 512 (5.4) < 0.0001 5264 (55.8) 4630 (48.6) < 0.0001 p valueb Some percentages may not total to 100% because of rounding. b Nonsignificant differences between Medicaid and exchange: heart disease (p = 0.1947); high blood pressure (p = 0.3551). Nonsignificant differences between Medicaid and other: pregnancy (p = 0.8803). Nonsignificant differences between exchange and other: asthma (p = 0.1913); prior-year inpatient admissions (p = 0.1632). BHQ = Brief Health Questionnaire. a 6 other new enrollees. Most (91.0%) of the BHQ data were collected through telephone calls, with the remainder collected through the KPCO patient portal into the EHR. Responses for new members under age 18 years were provided by parents or guardians. Table 1 lists demographic characteristics of new members by insurance category. New Medicaid and exchange members were older than other/commercial members (mean ages for Medicaid, exchange, and other were 33.8, 40.0, and 29.5 years, respectively). Approximately 58% of respondents were female. Table 2 summarizes responses to the BHQ questions across insurance groups. Fair or poor health was selfreported by 19.5%, 7.1%, and 5.3% of Medicaid, exchange, and other groups, respectively. A greater proportion of Medicaid enrollees (30.7%) reported physical functioning interfering with health, and a greater proportion of exchange enrollees (40.8%) reported prescription medication use. Of BHQ respondents, 11.8% of Medicaid, 4.7% of exchange, and 3.4% of other/ commercial enrollees screened positive for possible depression. During the preceding year there was a greater difference in self-reported ED utilization across groups than in self-reported inpatient hospital admissions, with 12.9% of Medicaid enrollees reporting 2 or more ED visits (compared with 2.0% of exchange and 3.3% of other new members), but less than 2% of all groups reporting 2 or more inpatient admissions. Comparable percentages of Medicaid and exchange enrollees (just over 30%) reported no insurance during more than 8 months during the previous year, compared with 12.6% of other beneficiaries. All variable differences across groups of enrollees were significant at p < 0.001 except for sex, which was significant at p < 0.05. Of new Medicaid enrollees, 60.8% were referred for any additional services on the basis of BHQ responses, compared with 55.8% of new exchange enrollees and 48.6% of other enrollees (p < 0.001). The highest percentage of referrals across insurance groups was because of prescription medication use. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS Characteristics of Newly Enrolled Members of an Integrated Delivery System after the Affordable Care Act Table 3. Brief Health Questionnaire characteristics and responses (N = 14,761) by prior-year insurance: insured for entire year versus no insurance for more than 8 monthsa Characteristic or response Medicaid (n = 2264) Insured Not insured (n = 1132), No. (%) (n = 1132), No. (%) Sex Female 768 (67.8) Male 364 (32.2) Unknown 0 Age group, years 0-9 1 (0.1) 10-19 48 (4.2) 20-29 262 (23.1) 30-39 260 (23.0) 40-49 200 (17.7) 50-59 233 (20.6) ≥ 60 128 (11.3) General health Excellent 151 (13.3) Very good 323 (28.5) Good 406 (35.9) Fair 174 (15.4) Poor 77 (6.8) Missing/no answer 1 (0.1) Self-reported chronic condition Asthma 124 (11.0) Diabetes 95 (8.4) Heart disease 35 (3.1) High blood pressure 211 (18.6) Other health considerations Current prescription 592 (52.3) medication Positive depression 132 (11.7) screen Pregnant 22 (1.9) Health condition 417 (36.8) interferes with daily activity Emergency Department visits in past year None 716 (63.3) 1 time 240 (21.2) 2+ times 176 (15.6) Missing data 0 Inpatient admissions in past year None 1008 (89.1) 1 time 99 (8.8) 2+ times 24 (2.1) Missing data 1 (0.1) Self-reported financial constraints Health affected by 218 (19.3) difficulty paying for food, medicine, rent, utilities Individual on exchange (n = 6799) Insured Not insured (n = 3893), No. (%) (n = 2906), No. (%) Other (n = 5698) Insured Not insured (n = 4499), No. (%) (n = 1199), No. (%) 638 (56.4) 494 (43.6) 0 2310 (59.3) 1583 (40.7) 0 1731 (59.6) 1175 (40.4) 0 2792 (62.1) 1706 (37.9) 1 (0) 630 (52.5) 569 (47.5) 0 0 8 (0.7) 208 (18.4) 202 (17.8) 246 (21.7) 340 (30.0) 128 (11.3) 3 (0.1) 43 (1.1) 624 (16.0) 737 (18.9) 676 (17.4) 1076 (27.6) 734 (18.9) 0 21 (0.7) 455 (15.7) 612 (21.1) 562 (19.3) 794 (27.3) 462 (15.9) 4 (0.1) 95 (2.1) 1119 (24.9) 1094 (24.3) 876 (19.5) 942 (20.9) 369 (8.2) 0 29 (2.4) 391 (32.6) 310 (25.9) 247 (20.6) 171 (14.3) 51 (4.3) 119 (10.5) 282 (24.9) 436 (38.5) 218 (19.3) 75 (6.6) 2 (0.2) 1151 (29.6) 1537 (39.5) 974 (25.0) 201 (5.2) 24 (0.6) 6 (0.2) 581 (20.0) 1022 (35.2) 968 (33.3) 277 (9.5) 54 (1.9) 4 (0.1) 1190 (26.5) 1848 (41.1) 1227 (27.3) 197 (4.4) 31 (0.7) 6 (0.1) 204 (17.0) 418 (34.9) 415 (34.6) 133 (11.1) 28 (2.3) 1 (0.1) 126 (11.1) 79 (7.0) 45 (4.0) 203 (17.9) 319 (8.2) 184 (4.7) 103 (2.7) 565 (14.5) 218 (7.5) 176 (6.1) 73 (2.5) 483 (16.6) 411 (9.1) 193 (4.3) 105 (2.3) 547 (12.2) 87 (7.3) 48 (4.0) 27 (2.3) 128 (10.7) 442 (39.1) 1957 (50.3) 1130 (38.9) 2209 (49.1) 349 (29.1) 209 (18.5) 155 (4.0) 195 (6.7) 166 (3.7) 104 (8.7) 13 (1.2) 458 (40.5) 36 (0.9) 603 (15.5) 25 (0.9) 576 (19.8) 82 (1.8) 696 (15.5) 22 (1.8) 251 (20.9) 742 (65.6) 249 (22.0) 139 (12.3) 2 (0.2) 3430 (88.1) 396 (10.2) 65 (1.7) 2 (0.1) 2496 (85.9) 343 (11.8) 65 (2.2) 2 (0.1) 3851 (85.6) 521 (11.6) 124 (2.8) 3 (0.1) 975 (81.3) 159 (13.3) 65 (5.4) 0 1041 (92.0) 77 (6.8) 3697 (95.0) 165 (4.2) 2793 (96.1) 93 (3.2) 4292 (95.4) 171 (3.8) 1138 (94.9) 49 (4.1) 13 (1.2) 1 (0.1) 28 (0.7) 3 (0.1) 15 (0.5) 5 (0.2) 33 (0.7) 3 (0.1) 11 (0.9) 1 (0.1) 452 (39.9) 196 (5.0) 499 (17.2) 176 (3.9) 204 (17.0) Insured is defined as reporting being insured for entire previous year; uninsured is defined as being uninsured for more than 8 months during the previous year. Sample for this subanalysis does not include respondents reporting either 1 to 4 months or 5 to 8 months without insurance during the previous year. Some percentages may not total to 100% because of rounding. a The Permanente Journal/ Summer 2015/ Volume 19 No. 3 7 ORIGINAL RESEARCH & CONTRIBUTIONS Characteristics of Newly Enrolled Members of an Integrated Delivery System after the Affordable Care Act Rates of chronic disease are notoriously difficult to predict because individuals who are unable to access care may be unaware of diagnoses. The pattern of new Medicaid enrollees having greater morbidity than new exchange or other new enrollees was also evident in proportions of self-reported chronic conditions. Asthma was reported by 8.4% of new Medicaid enrollees, 6.9% of new exchange enrollees, and 6.4% of new other enrollees (p = 0.003). Diabetes was reported by 5.8%, 4.7%, and 3.1% of each group, respectively; heart disease by 2.6%, 2.3%, and 1.6%; and high blood pressure by 13.8%, 13.1%, and 8.2% (p < 0.001 for all). Descriptive subanalyses of new members previously uninsured for more than 8 months vs those insured for the entire year are listed in Table 3. In each benefit group, the previously uninsured individuals report slightly higher rates of fair or poor health, and of health interfering with daily activity, but they do not report greater rates of specific chronic conditions. A higher proportion of individuals in the previously uninsured subpopulations had a positive depression screen, and a higher proportion reported financial constraints. Table 4 compares BHQ respondents vs nonrespondents. Compared with nonrespondents, respondents were significantly more likely to be female, to be older, and to carry Medicaid or exchange insurance (p < 0.001). DISCUSSION Accurate information on the health status and care needs of individuals enrolling in insurance plans during the early phases of the ACA implementation can help optimize care delivery for newly insured and transitioning populations. This snapshot of new members in an integrated delivery system in the Denver Front Range area suggests that new Medicaid enrollees are less healthy than new exchange and new commercial members are; however, differences between new exchange enrollees and new commercial members are more subtle. We found that 19.5% of new Medicaid members and 7.1% of new exchange members overall had fair or poor health. In the smaller subsample of individuals without previous insurance, 25.9% of new Medicaid members and 11.4% of new exchange members reported fair or poor health. Our Medicaid findings are consistent with previous estimates6,7,28 that proportions of the ACA target population with fair or poor health would range from 10% to 25%, with the greater burden falling on individuals below 200% of the Federal Poverty Level. However, the general health status in new exchange enrollees in this population is somewhat better than these predictions.6,7,28 It is also Table 4. Brief Health Questionnaire (BHQ) new member respondents versus nonrespondents (N = 89,289)a Characteristic Sex Female Male Unknown Age group, years 0-9 10-19 20-29 30-39 40-49 50-59 ≥ 60 Insurance Medicaid Individual on exchange Other a 8 No BHQ (n = 66,741), No. (%) BHQ (n = 22,548), No. (%) 31,743 (47.6) 34,976 (52.4) 22 (0) 13,014 (57.7) 9531 (42.3) 3 (0) < 0.0001 11,031 (16.5) 6739 (10.1) 13,312 (20.0) 12,029 (18.0) 9202 (13.8) 9749 (14.6) 4679 (7.0) 3101 (13.8) 2004 (8.9) 3876 (17.2) 3994 (17.7) 3334 (14.8) 4105 (18.2) 2134 (9.5) < 0.0001 4725 (7.1) 25,679 (38.5) 36,337 (54.4) 3593 (15.9) 9434 (41.8) 9521 (42.2) < 0.0001 Some percentages may not total to 100% because of rounding. p value somewhat better than a national population of nongroup enrollees (individuals who purchased their own insurance) surveyed after ACA implementation in Spring 2014, in which 14% reported fair or poor health.29 It is possible that our results reflect characteristics of Colorado residents—which may differ from a nationally representative sample—or that individuals enrolling in Year 1 of the ACA may have better health status than those who remain uninsured. Ongoing surveillance of health status among the newly insured will help clarify their health status and care needs and should inform service requirements for integrated and other delivery systems. Rates of chronic disease are notoriously difficult to predict because individuals who are unable to access care may be unaware of diagnoses. Estimates of heart disease in our Medicaid and exchange sample to date (2% to 3%) are comparable to literature-based predictions, whereas the rate of asthma in BHQ respondents (6.4% to 8.4%) is comparable to rates in previously uninsured populations, but half of asthma rates in Medicaid populations.7,30 Published estimates suggest depression rates in the range of 2% to 17% for Medicaid and exchange enrollees.7,30 Although BHQ respondents had positive depression screens within this range, their diagnoses of depression require further evaluation.27 In 2011, the Kaiser Family Foundation predicted that 65% of exchange purchasers would have been previously uninsured.30 We found that previous insurance coverage was not comprehensive for any of the 3 groups, and that just over 30% of new Medicaid and exchange enrollees reported being uninsured for more than 8 months during the previous year. These proportions may be slightly skewed by missing data, but they are lower than the 57% national figure reported in a 2014 Kaiser Family Foundation survey.29 They may also reflect the insurance marketplace in Colorado and uptake of exchange plans by both insured and uninsured individuals. (Our sample does not include the small-business exchange.) New Medicaid members reported greater past utilization of the ED than The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS Characteristics of Newly Enrolled Members of an Integrated Delivery System after the Affordable Care Act did other respondents. Studies of Medicaid expansions suggest that this pattern may continue after obtaining insurance, although it may be modified by effective primary care relationships.23,31 In the longer term, gaining insurance benefits increases utilization of health care resources, improves mental and physical health, increases the use of preventive services, and decreases mortality for both Medicaid and non-Medicaid populations.28,32-34 Optimizing long-term health outcomes will require maximizing both informational and interpersonal continuity of care for patients who may move between Medicaid and exchange benefit categories and between being insured and uninsured. Although patient-reported data on health status, physical function, emotional well-being, and other constructs are predictive of mortality and utilization, and can guide interventions to improve the quality of care, such measures have previously been used almost exclusively in the context of research rather than care delivery.10,35-38 Recently, health assessments have been incorporated into care delivery for defined populations such as seniors, employees, and Health Plan members.39 The BHQ assessment exemplifies how patient-reported data can be systematically collected to inform care delivery, especially in light of 2014 net growth of approximately 15%, compared with previous annual net growth rates in the range of 2% to 3% for the delivery system. To date, approximately 54% of all BHQ respondents have been referred for either care management or pharmacy services. Future retrospective analyses will determine whether referrals for early medication and care management affect more distal health outcomes such as hospitalization and disease-specific adverse events. Our study has several limitations. Medicaid enrollees enrolling in KPCO were a relatively small subset of all Colorado Medicaid beneficiaries. New KPCO exchange enrollees reflect an approximate 38% share of the Colorado exchange marketplace and only represent those who selected a single integrated delivery system. Newly enrolled patients in other delivery systems and settings will have different The Permanente Journal/ Summer 2015/ Volume 19 No. 3 characteristics. This sample primarily reflects a subset of members who contacted the delivery system during the first 6 months of enrollment, and data collection was limited by the capacity of the call center’s service associates. As illustrated in Table 4, there were a number of demographic differences between BHQ respondents and nonrespondents. Respondents to the BHQ are also more likely to have used health care services. These comparisons support (but do not confirm) a hypothesis that new enrollees with higher morbidity were initial users of the delivery system and more likely to complete a BHQ. Finally, most of the responses were obtained via telephone; although responses obtained through the Web portal may be systematically different, Web-based responses represent a very small proportion of the total and are unlikely to bias the results. Our preliminary cross-sectional description must be supplemented with longitudinal assessments that link patient-reported BHQ responses with subsequent utilization patterns and that link all of these factors with robust health outcomes. CONCLUSION This description suggests that newly enrolled Medicaid beneficiaries may have more initial health care needs than either new exchange or commercial members; however, health differences between the latter 2 groups in this population sample are more subtle. The Congressional Budget Office estimates that by 2023, insurance will be obtained by 13 million individuals through Medicaid expansions and by 24 million through exchange-based plans.40 There is likely to be increasing movement of individuals across benefit categories, as well as increasing inclusion of previously insured populations in Medicaid and exchange insurance plans. Adequately informing care delivery for this changing landscape will require an understanding of which subpopulations are likely to transition between benefit categories and between delivery systems and settings, and which subpopulations risk adverse health outcomes as a function of these transitions. Further evaluation of needs assessments, such as the BHQ process, will inform the development of systematic interventions to optimize health outcomes in newly enrolled populations. v Disclosure Statement The author(s) have no conflicts of interest to disclose. Acknowledgments This project was supported by a grant from the Kaiser Permanente Garfield Memorial Fund. Kathleen Louden, ELS, of Louden Health Communications provided editorial assistance. References 1. The Patient Protection and Affordable Care Act of 2010. Public Law 111-148, 111th Congress, 124 Stat 119, HR 3590, enacted 2010 Mar 23. 2. Health insurance marketplace: summary enrollment report for the initial annual open enrollment period [Internet]. Washington, DC: Department of Health and Human Services, Office of the Assistant Secretary for Planning and Evaluation; 2014 May 1 [cited 2015 Mar 9]. Available from: http://aspe.hhs.gov/health/ reports/2014/MarketPlaceEnrollment/Apr2014/ ib_2014Apr_enrollment.pdf. 3. Medicaid & CHIP: March 2014 monthly applications, eligibility determinations, and enrollment report [Internet]. Baltimore, MD: Centers for Medicare and Medicaid Services, Department of Health and Human Services; 2014 May 1 [cited 2015 Mar 9]. Available from: www. medicaid.gov/medicaid-chip-program-information/ program-information/downloads/march-2014enrollment-report.pdf. 4. Claxton G, Levitt L, Brodie M, Garfield R, Damico A. Measuring change in insurance coverage under the Affordable Care Act [Internet]. Menlo Park, CA: The Henry J Kaiser Family Foundation; 2014 Apr 30 [cited 2015 Mar 9]. Available from: http://kff.org/health-reform/issuebrief/measuring-changes-in-insurance-coverageunder-the-affordable-care-act/. 5. Grob R, Schlesinger M, Pollitz K, Grubstein L. Taking stock and taking steps: a report from the field after the first year of marketplace consumer assistance under the ACA [Internet]. Menlo Park, CA: The Henry J Kaiser Family Foundation; 2014 Oct 1 [cited 2015 Mar 9]. Available from: http://kff. org/health-reform/report/taking-stock-and-takingsteps-a-report-from-the-field-after-the-first-year-ofmarketplace-consumer-assistance-under-the-aca/. 6. Abraham JM. How might the Affordable Care Act’s coverage expansion provisions influence demand for medical care? Milbank Q 2014 Mar;92(1):63-87. DOI: http://dx.doi. org/10.1111/1468-0009.12041. Erratum in: Milbank Q 2014 Jun;92(2):404-5. DOI: http:// dx.doi.org/10.1111/1468-0009.12063. 7. Decker SL, Kostova D, Kenney GM, Long SK. Health status, risk factors, and medical conditions among persons enrolled in Medicaid vs uninsured low-income adults potentially eligible for Medicaid under the Affordable Care Act. JAMA 2013 Jun 26;309(24):2579-86. DOI: http://dx.doi. org/10.1001/jama.2013.7106. 8. Sommers BD, Rosenbaum S. Issues in health reform: how changes in eligibility may move millions back and forth between Medicaid and insurance exchanges. Health Aff (Millwood) 2011 9 ORIGINAL RESEARCH & CONTRIBUTIONS Characteristics of Newly Enrolled Members of an Integrated Delivery System after the Affordable Care Act 9. 10. 11. 12. 13. 14. 15. 16. 17. 18. 19. Feb;30(2):228-36. DOI: http://dx.doi.org/10.1377/ hlthaff.2010.1000. DeSalvo KB, Jones TM, Peabody J, et al. Health care expenditure prediction with a single item, self-rated health measure. Med Care 2009 Apr;47(4):440-7. DOI: http://dx.doi.org/10.1097/ MLR.0b013e318190b716. DeSalvo KB, Fan VS, McDonell MB, Fihn SD. Predicting mortality and healthcare utilization with a single question. Health Serv Res 2005 Aug;40(4):1234-46. DOI: http://dx.doi.org/10.1111/ j.1475-6773.2005.00404.x. Machlin SR, Soni A. Health care expenditures for adults with multiple treated chronic conditions: estimates from the Medical Expenditure Panel Survey, 2009. Prev Chronic Dis 2013 Apr 25; 10:E63. DOI: http://dx.doi.org/10.5888/ pcd10.120172. Naessens JM, Baird MA, Van Houten HK, Vanness DJ, Campbell CR. Predicting persistently high primary care use. Ann Fam Med 2005 JulAug;3(4):324-30. DOI: http://dx.doi.org/10.1370/ afm.352. Parkerson GR Jr, Harrell FE Jr, Hammond WE, Wang XQ. Characteristics of adult primary care patients as predictors of future health services charges. Med Care 2001 Nov;39(11):1170-81. Hoffman C, Rice D, Sung HY. Persons with chronic conditions. Their prevalence and costs. JAMA 1996 Nov 13;276(18):1473-9. DOI: http:// dx.doi.org/10.1001/jama.1996.03540180029029. Boyd C, Leff B, Weiss C, Wolff J, Hamblin A, Martin L. Faces of Medicaid: clarifying multimorbidity patterns to improve targeting and delivery of clinical services for Medicaid populations [Internet]. Hamilton, NJ: Center for Health Care Strategies; 2010 Dec [cited 2015 Mar 9]. Available from: www.chcs.org/resource/ faces-of-medicaid-clarifying-multimorbiditypatterns-to-improve-targeting-and-delivery-ofclinical-services-for-medicaid-populations/. Gao J, Moran E, Li YF, Almenoff PL. Predicting potentially avoidable hospitalizations. Med Care 2014 Feb;52(2):164-71. DOI: http://dx.doi. org/10.1097/MLR.0000000000000041. Nagasako EM, Reidhead M, Waterman B, Dunagan WC. Adding socioeconomic data to hospital readmissions calculations may produce more useful results. Health Aff (Millwood) 2014 May;33(5):786-91. DOI: http://dx.doi.org/10.1377/ hlthaff.2013.1148. Dorr DA, Jones SS, Burns L, et al. Use of healthrelated, quality-of-life metrics to predict mortality and hospitalizations in community-dwelling seniors. J Am Geriatr Soc 2006 Apr;54(4): 667-73. DOI: http://dx.doi.org/10.1111/j.15325415.2006.00681.x. de Boer AG, Wijker W, de Haes HC. Predictors of health care utilization in the chronically ill: 20. 21. 22. 23. 24. 25. 26. 27. 28. 29. 30. a review of the literature. Health Policy 1997 Nov;42(2):101-15. DOI: http://dx.doi.org/10.1016/ S0168-8510(97)00062-6. Donnan PT, Dorward DW, Mutch B, Morris AD. Development and validation of a model for predicting emergency admissions over the next year (PEONY): a UK historical cohort study. Arch Intern Med 2008 Jul 14;168(13):1416-22. DOI: http://dx.doi.org/10.1001/archinte.168.13.1416. McCusker J, Karp I, Cardin S, Durand P, Morin J. Determinants of emergency department visits by older adults: a systematic review. Acad Emerg Med 2003 Dec;10(12):1362-70. DOI: http://dx.doi. org/10.1197/S1069-6563(03)00539-6. Halfon N, Newacheck PW, Wood DL, St Peter RF. Routine emergency department use for sick care by children in the United States. Pediatrics 1996 Jul;98(1):28-34. Ginde AA, Lowe RA, Wiler JL. Health insurance status change and emergency department use among US adults. Arch Intern Med 2012 Apr 23;172(8):642-7. DOI: http://dx.doi.org/10.1001/ archinternmed.2012.34. Li AK, Covinsky KE, Sands LP, Fortinsky RH, Counsell SR, Landefeld CS. Reports of financial disability predict functional decline and death in older patients discharged from the hospital. J Gen Intern Med 2005 Feb;20(2):168-74. DOI: http:// dx.doi.org/10.1111/j.1525-1497.2005.30315.x. Bindman AB, Chattopadhyay A, Auerback GM. Interruptions in Medicaid coverage and risk for hospitalization for ambulatory caresensitive conditions. Ann Intern Med 2008 Dec 16;149(12):854-60. DOI: http://dx.doi. org/10.7326/0003-4819-149-12-200812160-00004. Sudano JJ Jr, Baker DW. Intermittent lack of health insurance coverage and use of preventive services. Am J Public Health 2003 Jan;93(1):130-7. DOI: http://dx.doi.org/10.2105/AJPH.93.1.130. Kroenke K, Spitzer RL, Williams JB. The Patient Health Questionnaire-2: validity of a two-item depression screener. Med Care 2003 Nov;41(11):1284-92. Sommers BD, Baicker K, Epstein AM. Mortality and access to care among adults after state Medicaid expansions. N Engl J Med 2012 Sep 13;367(11):1025-34. DOI: http://dx.doi. org/10.1056/NEJMsa1202099. Hamel L, Norton M, Levitt L, et al. Survey of nongroup health insurance enrollees [Internet]. Menlo Park, CA: The Henry J Kaiser Family Foundation; 2014 Jun 19 [cited 2015 Mar 9]. Available from: http://kff.org/health-reform/report/survey-of-nongroup-health-insurance-enrollees/. A profile of health insurance exchange enrollees [Internet]. Menlo Park, CA: The Henry J Kaiser Family Foundation; 2011 Mar 1 [cited 2015 Mar 9]. Available from: http://kaiserfamilyfoundation. files.wordpress.com/2013/01/8147.pdf. 31. Taubman SL, Allen HL, Wright BJ, Baicker K, Finkelstein AN. Medicaid increases emergencydepartment use: evidence from Oregon’s health insurance experiment. Science 2014 Jan 17;343(6168):263-8. DOI: http://dx.doi. org/10.1126/science.1246183. 32. Michalopoulos C, Wittenburg D, Israel DA, Warren A. The effects of health care benefits on health care use and health: a randomized trial for disability insurance beneficiaries. Med Care 2012 Sep;50(9):764-71. DOI: http://dx.doi.org/10.1097/ MLR.0b013e31825a8bfc. 33. Freeman JD, Kadiyala S, Bell JF, Martin DP. The causal effect of health insurance on utilization and outcomes in adults: a systematic review of US studies. Med Care 2008 Oct;46(10):1023-32. DOI: http://dx.doi.org/10.1097/ MLR.0b013e318185c913. 34. Baicker K, Taubman SL, Allen HL, et al. The Oregon experiment—effects of Medicaid on clinical outcomes. N Engl J Med 2013 May 2;368(18):1713-22. DOI: http://dx.doi. org/10.1056/NEJMsa1212321. 35. Perrin NA, Stiefel M, Mosen DM, Bauck A, Shuster E, Dirks EM. Self-reported health and functional status information improves prediction of inpatient admissions and costs. Am J Manag Care 2011 Dec 1;17(12):e472-8. 36. Diehr P, Williamson J, Patrick DL, Bild DE, Burke GL. Patterns of self-rated health in older adults before and after sentinel health events. J Am Geriatr Soc 2001 Jan;49(1):36-44. DOI: http://dx.doi.org/10.1046/j.15325415.2001.49007.x. 37. Wagner EH, LaCroix AZ, Grothaus LC, Hecht JA. Responsiveness of health status measures to change among older adults. J Am Geriatr Soc 1993 Mar;41(3):241-8. 38. Min L, Ubhayakar N, Saliba D, et al. The vulnerable elders survey-13 predicts hospital complications and mortality in older adults with traumatic injury: a pilot study. J Am Geriatr Soc 2011 Aug;59(8):1471-6. DOI: http://dx.doi. org/10.1111/j.1532-5415.2011.03493.x. 39. Stiefel M, Nolan K. A guide to measuring the triple aim: population health, experience of care, and per capita cost. IHI innovation series white paper. Cambridge, MA: Institute for Healthcare Improvement; 2012. 40. CBO’s May 2013 estimate of the effects of the Affordable Care Act on health insurance coverage: Table 1 [Internet]. Washington, DC: Congressional Budget Office; 2014 May [cited 2015 Mar 9]. Available from: www.cbo.gov/sites/ default/files/cbofiles/attachments/43900-2013-05ACA.pdf. Change Then Changing doctors is with some people a far less serious matter than a change of shirts. — G Frank Lydston, MD, 1858-1923, American urologist and transplant surgeon 10 The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS A Metrics Taxonomy and Reporting Strategy for Rule-Based Alerts Michael Krall, MD, MS; Alexander Gerace Perm J 2015 Summer;19(3):11-19 http://dx.doi.org/10.7812/TPP/14-227 ABSTRACT Context: Because institutions rely on rule-based alerts as an important component of their safety and quality strategies, they should determine whether the alerts achieve the expected benefit. Objective: To develop and to test a method of reporting outcome metrics for rule-based electronic health record alerts on a large scale. Methods: We empirically developed an action-oriented alerts taxonomy according to structure, actions, and implicit intended process outcomes using a set of 333 rule-based alerts at Kaiser Permanente Northwest. Next we developed a method for producing metrics reports for alert classes. Finally, we applied this method to alert taxa. Main Outcome Measures: Outcome measures were the successful development of a rule-based alerts taxonomy and the demonstration of its application in a reporting strategy. Results: We identified 9 major and 17 overall classes of alerts. We developed a specific metric approach for 5 of these classes, including the 3 most numerous ones in our institution, accounting for 224 (67%) of our alerts. Some alert classes do not readily lend themselves to this approach. Conclusions: We developed a taxonomy for rule-based alerts and demonstrated its application in developing outcome metrics reports on a large scale. This information allows tuning or retiring alerts and may inform the need to develop complementary or alternative approaches to address organizational imperatives. A method that assigns alerts to classes each amenable to a particular reporting strategy could reduce the difficulty of producing metrics reports. INTRODUCTION Rule-based alerting within electronic health records (EHRs) is a common approach to addressing safety, quality, and workflow issues in health care. Most mature EHR installations have alerts of this type and some, including ours, have hundreds. Stage 2 of the Center for Medicare and Medicaid Services Meaningful Use incentive program requires that eligible providers and hospitals implement at least five clinical decision-support interventions, most of which will be rule-based alerts. Because institutions look to clinical decision support and rule-based alerts as an important component of their return-on-investment strategy for their EHR investment, it is imperative to know whether the alerts are not only “working” (firing as designed) but are achieving intended benefits.1 This understanding is fundamental to improving clinical decision support and may suggest the necessity for considering additional or alternative strategies to achieve strategic goals. A recent publication of the American Health Lawyers Association on minimizing EHR-related safety events specifically called out alert metrics beyond simply override rate as an important determinant of safety in these systems.2 Knowledge engineers and builders of alerts typically believe, often with limited or no data, that the ones they deploy are functioning well, are well received by their target audience, and are achieving their intended goals. Tools within EHRs to evaluate these beliefs are generally very limited. Alert structures can be complex, and achieving an understanding of their performance characteristics and effectiveness can prove difficult. To develop a detailed understanding of the functioning and outcomes of an alert usually requires creating an individualized report. There are few reports of systematic approaches to monitoring alerts.3 We set out to develop one. Objective Our goal was to develop and test a framework for reporting performance metrics for rule-based EHR alerts at scale. Our intention was to achieve alert outcome reports that extend beyond basic metrics and include process outcomes. As a preliminary step we set out to develop a new action-oriented classification system or taxonomy of alerts on the basis of their structure, especially intended and optimized to facilitate outcomes metrics. Existing taxonomies would not suffice because they do not readily map to a measurement framework.4-8 We sought to generate metrics in sets rather than one by one to reduce the time and expense of developing and maintaining performance metrics for alerts. Background In a proposed five-level evaluation hierarchy of rule-based alert performance, “firing rates” are at the lowest and most commonly reported level. Rates by role such as nurse or physician, specialty such as family medicine or general surgery, site of care such as inpatient or ambulatory, department or unit such as intensive care or urgent care, time of day Michael A Krall, MD, MS, is a part-time Physician Lead for Clinical Decision Support for The Permanente Federation. He retired from Northwest Permanente in 2014 after 30 years practicing Family Medicine and after 20 years engaged in clinical informatics. Dr Krall was the Director of Clinical Decision Support and Knowledge Management for Northwest Permanente. E-mail: [email protected]. Alexander Gerace is an Information Analyst for Care Delivery Analytics for Northwest Permanente. E-mail: [email protected]. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 11 ORIGINAL RESEARCH & CONTRIBUTIONS A Metrics Taxonomy and Reporting Strategy for Rule-Based Alerts or week, and similar factors can extend this metric. The second level is “acceptance” and “override” rates. Proximate “action taken” by users in response to the alert is the next highest level. The fourth level is a measure of intermediate process goals or outcomes achievement. Finally, the highest level is a measure of patient health goals or outcomes or clinician goals or outcomes achievement. Each successive level in the evaluation hierarchy is more difficult to create. In this report we chose to focus on the fourth level, process goals and outcomes. For most alerts, knowing that they fire frequently or infrequently and have a high or low acceptance rate yields only a limited understanding of whether their explicit recommendations were followed or if they were effective in achieving their intended goals. Was the safe practice followed or the unsafe practice averted? Was the evidencebased treatment prescribed? Was the cost-effective choice made, the recommended documentation performed, the dose modified, the procedure ordered or performed? These are “level 4” questions in the hierarchy introduced above. Ultimately, was care improved and the desired health or clinician outcome achieved? These are “level 5” questions. For most alerts, firing, override, and proximate action-taken rates do not answer these higher-order questions because action on the alert may not be the same as action on the triggering event. In EHRs, alerts may be built with a number of available user actions. In the Epic 2012 and earlier versions (Madison, WI) EHR, for example, standard controls include “accept” and “cancel” buttons that take these actions on the alert. However, there may be additional actions such as “open an order set,” “create an order,” or “navigate” to the Problem, Allergy, or Medication List activities to perform an operation, and such actions are intended to address the triggering condition. It is possible for users to “cancel” an alert yet still perform the recommended operation, such as order a laboratory procedure. Alternatively it is possible to “accept” the alert but fail to perform the operation. For example, the user can open an order set attached to an alert and choose 12 not to sign the recommended order, or can navigate to an allergy or medication list and decide not to perform the recommended update. Thus reports that simply count these actions may generate inaccurate and misleading information about alert effectiveness and desired outcomes. In the end, what we want to know is whether the recommended operation was performed, regardless of whether it was done as a direct result of the alert. A reporting strategy that disengages the outcome from a direct action of the alert creates the additional complexity of determining the optimal time frame for measurement. The measurement interval could be defined as immediately proximate to the alert firing (or viewing, in the case of alerts that do not pop up), as the less stringent “any time within the encounter” definition, or as another predefined interval (such as within eight hours of firing). In the first instance, “credit” is assigned to the alert only if the recommended action occurred as a direct result of or immediately following the alert. An order or action fulfilling the recommendation that was placed later in the same encounter would not count as alert “success.” In the second instance, any fulfilling order or action that was taken within the same encounter would count, even though it is not certain that the action taken was directly caused by the alert. In the inpatient setting, where the entire stay might be considered the encounter, this definition could cause difficulty in interpretation. Here the third approach, crediting actions that occurred within a specified time window, such as within an eight-hour shift, might be more meaningful. Conceptually, this requires an approach to metrics similar to an intention-to-treat analysis of a randomized control study. Complete assessment of the appropriateness of a specific alert, the user’s response to that alert, or level five patient or clinician outcomes requires a broader analysis to include patient, user, and environmental factors. Because an automated batch processing of alerts cannot achieve that level of investigation, a more realistic goal is to develop a report that would allow categorizing alerts into those appearing to be “high,” “low,” and “intermediate” in performance. An institution might then, for example, choose to direct its efforts at improving, eliminating, or better understanding those alerts with “low” performance. To do so might require a more in-depth assessment, possibly including medical chart reviews. McCoy et al9 published a framework for evaluating alert appropriateness. To develop a detailed model of alert metrics, it is necessary to have a common understanding of the structure or “anatomy” of an alert. There have been a number of clinical decision support and alert taxonomies developed for different purposes.4-8 In 2007, Wright et al7 at Partners Healthcare System developed a taxonomy for rule-based decision support. They included four functional components they termed triggers, input data, interventions, and offered choices. Later, the National Quality Forum Clinical Decision Support Expert Panel8 proposed a modification of this classification. They replaced “offered choices” with “action steps.” Triggers are the user actions that can invoke an alert. These actions might include, for example, entering or signing an order, opening a chart or a specific screen, or entering documentation. Input data are the elements in the record that might modify the alert performance. Input data might be information about the patient (eg, age, gender, diagnoses, preferences), National Quality Forum Taxonomy: Selected EpicCare Examples Triggers Open chart, open order entry Enter order, enter diagnosis File flow sheet Input data Age, gender, comorbidities Provider type, role Encounter type Interventions Display message in Navigator Send in-basket message Add modifier Pop-up message Action steps Accept or Cancel alert Enter order Open order set The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS A Metrics Taxonomy and Reporting Strategy for Rule-Based Alerts Figure 1. Distribution of alerts at Kaiser Permanente Northwest by class, 2013. about the user (eg, specialty, role, experience, preferences), or about the environment (eg, time of day or week, unit, department, or setting). Interventions refer to computer-human interface actions and the manner in which the alert is displayed, such as via a pop-up message. In some cases the intervention might happen without user awareness, such as if the alert action is to set a modifier or to trigger an asynchronous alert (occurring at a remote time or place). Finally, action steps are recommended or permitted actions that a user can take as a direct result of the alert. Accepting, canceling, and overriding (with or without providing a reason) are the most common actions. Many more actions may also be available in alerts, including opening order sets, accepting an order, and navigating to another activity such as the medication, allergy, or problem list. The Sidebar: National Quality Forum Taxonomy: Selected EpicCare Examples illustrates these structural elements with a few examples from the EpicCare EHR. Most other EHR alerts have similar structure and comparable examples. Combining available triggers, inputs, interventions, and action steps yields a very large number of possible alert forms, particularly since an alert may incorporate more than one element for each functional component. For example, one alert could have an enter-diagnosis and enter-order trigger, multiple data The Permanente Journal/ Summer 2015/ Volume 19 No. 3 inputs, and both a pop-up display and an in-basket notification. Alerts may also have more than one permissible or recommended action step. This complexity is a major reason why it is difficult to create generalized alert outcome reports. For each alert it is necessary both to define its structure and to declare which actions constitute a desired outcome or “success.” Previous taxonomies are not classified by actions taken (such as create or modify an order) and do not attempt to address alert outcomes. METHODS This work was developed at Kaiser Permanente Northwest (KPNW), a Region of the Kaiser Permanente Health Care program located in Oregon and Southwest Washington. The Region employs approximately 1000 physicians and cares for approximately 500,000 Health Plan members. KPNW began implementation of EpicCare in 1994, and it was fully implemented in ambulatory clinics by 1997. The inpatient system was implemented in 2008. KPNW owns and operates 2 hospitals and about 40 outpatient clinic sites, most of which are large and multispecialty. We took an empirical approach to developing the alert metrics taxonomy. Each of 333 active, production rulebased alerts in our system was assigned to a class on the basis of its structure and intended outcome. If an existing class did not adequately encompass the alert in question, a new class was added or an existing class was modified. This process was iteratively repeated until all alerts were assigned and the remaining classes were coherent. Where alerts had characteristics of more than one class, they were assigned on the basis of their apparent primary intention. For example, an alert that recommended substitution of a particular medication for another (a substitution action) but also facilitated documentation of allergy to the recommended choice via a link to the allergy activity (a documentation action) was classified according to the primary intention of substitution. In order to limit project scope, standard, vendor-supplied drug-drug and drugallergy alerts were excluded from this analysis. This was deemed appropriate for several reasons. In the Epic EHR such alerts are presented with a different utility. Although they do conform to the same four-element National Quality Forum functional taxonomy, they have a different data and reporting structure and are very numerous. Moreover, for these alerts “acceptance” and “override” rates are more useful metrics because the valid action steps are fewer and more straightforward—the user either accepts or overrides the recommendation to avoid the drug-drug, drug-allergy, or drug-condition combination. Admittedly, that analysis would necessarily 13 ORIGINAL RESEARCH & CONTRIBUTIONS A Metrics Taxonomy and Reporting Strategy for Rule-Based Alerts “Y” “X” Recommended # Recommended % TSH WITH REFLEX T4 ORDER ALERT 3171 TSH ONLY ALERT 2373 Total/Average 5544 Alert_Description “X+Y” Trigger # Trigger % Trigger+Recommended # Trigger+Recommended % None # None % Total # 59.8% 931 17.5% 868 16.4% 337 6.4% 5307 49.3% 1363 28.3% 953 19.8% 128 2.7% 4817 54.8% 2294 22.7% 1821 18.0% 465 4.6% 10124 Figure 2. Substitute Order Alert with example report: “X” is the procedure that triggered the best-practice alert, “Y” the recommended substitute order, “X+Y” represents encounters in which both tests were ordered and “none” in which neither test was ordered. 2014 Epic Systems Corporation. Used with permission. FT4 = free thyroid; T4 = thyroid hormone; TSH = thyroid stimulating hormone; W = with. be more complex if one considered the possible override reasons that may be required or optionally provided or the alternative actions such as updating medication or allergy lists. Following development of an initial taxonomy, we turned attention to designing a report creation methodology. Starting with the classes with the largest number of members, we examined a representative alert from each class. For each, we developed a formulaic description of the triggering event and recommended outcome. Then we used the data model and data in Clarity, Epic’s analytical database, to create a report comparing initial with final conditions to determine alert outcome. We started with the appropriate trigger table in the reporting data warehouse. For example, we used one table for procedure triggers and another for generic medications. Next, we created a subquery that defines the recommended result, such as a substituted or additional procedure or medication, for each alert in the given class. This recommended result might have been contained, for example, in an order set or in an order attached directly to the alert. We joined this table to the triggered alert by its identifier, the alert locator ID. Next we created a subquery to determine whether the alert trigger and/or the recommended result was ordered or created in a valid time interval, as discussed above. For ambulatory alerts we defined this interval as within the particular patient encounter, usually an office visit or telephone call. Finally, we created a summary report. RESULTS Each alert is unique, owing to its complex structure and specific clinical or operational intention. Nevertheless, through empirical analysis, it appears that there are a manageable number of major structural classes for alert metrics, and these constitute the proposed taxonomy (see Sidebar: Alert Metrics Taxonomy). Each of these classes has a generalized structure that can be expressed in narrative. Substitution alerts, for example, are those in which a clinician orders a test, procedure, or treatment, or enters a diagnosis or finding and the alert recommends a second test, procedure, or finding instead, such as “Replace the order for ‘Chest X-ray AP/LAT’ with an order for ‘Chest X-ray two-views.’” The substitutions are usually of the same type (eg, test for test or diagnosis for diagnosis) but could be of mixed type (eg, medication for procedure). In this case, a trigger “X” causes the alert to recommend substituting an item or action “Y.” Corollary-type alerts are similar.10 In these cases, however, a trigger “X” generates a recommendation of an additional “Y.” For example, “In addition to the order for digoxin, please order a serum potassium and creatinine.” Corollary recommendations may be single or multiple (“Y” and “Y1” and “Yn”), and like substitution alerts, the recommendations may be of the same or mixed type. Alert Metrics Taxonomy Substitution Substitute-Order Substitute-Medication Substitute-Documentation Corollary Corollary-Order Corollary-Medication Corollary-Documentation Modify Modify-Order Modify-Medication Modify-Documentation Create Create-Order Create-Medication Create-Documentation Create-Communication Remove Remove-Order Remove-Medication Perform Perform-Procedure Perform-Documentation Informational only Send communication Other 14 The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS A Metrics Taxonomy and Reporting Strategy for Rule-Based Alerts The other alert classes follow similar patterns. Modify-type alerts recommend changes to new or existing orders or documentation—for example, “Decrease the dosage of digoxin on the basis of the patient’s serum creatinine.” Create alerts recommend new orders or documentation, such as “The patient is due for a mammogram. Please sign the attached mammogram order.” Remove alerts recommend that existing orders or documentation are canceled—for example, “It appears that the patient no longer requires a follow-up CT [computed tomography] scan. If this is correct, please cancel this order.” Perform alerts recommend the execution of specific actions, such as “Because of the elevated initial blood pressure, please repeat a blood pressure in 5 minutes and document in the chart.” Informational Only alerts provide a message without the expectation of a particular action that is captured within the system—for example, “There is a regionwide shortage of influenza vaccine.” Alerts might “Y” “X” send communication through a variety of means including in-basket messages or messages to pagers, faxes, phones, or Internet-enabled devices. Because this taxonomy is not exhaustive, there is necessarily an Other category. In our analysis, the alerts that fell into this category were “one-offs” and did not lend themselves to additional characterization at this time. An example of such an alert is a single one that automatically adds a modifier or marker to the patient’s chart if he is a man older “X+Y” Recommended # Recommended % Trigger # Trigger % Trigger+Recommended # Trigger+Recommended % None # None % Total # CONTRAST IMAGING AND NO PRIOR CREATININE 99 3.3% 938 30.9% 1790 59.0% 206 6.8% 3033 REF EKG 50 5.2% 133 13.7% 723 74.7% 62 6.4% 968 REF EKG WITHIN 30 DAYS 67 8.2% 112 13.7% 589 71.8% 52 6.3% 820 REF PODIATRY OTHER 14 0.8% 732 42.9% 853 50.0% 107 6.3% 1706 LACTATE WITH BLOOD CULTURES ED 3 0.2% 125 8.5% 1337 91.0% 5 0..3% 1470 REF TSH NOT ON MEDS 10 1.5% 109 15.9% 551 80.2% 17 2.5% 687 REF TSH NOT ON MEDS WITHIN 2 YEARS 8 1.2% 72 10.8% 561 84.0% 27 4.0% 668 REF CBC 4 WEEKS 13 1.0% 138 10.2% 1166 86.4% 32 2.4% 1349 REF URIC ACID 22 5.4% 98 23.9% 240 58.5% 50 12.2% 410 REF URIC ACID WITHIN 6 WEEKS 25 7.1% 73 20.9% 207 59.1% 45 12.9% 350 REF PHOSPHOROUS 21 5.3% 92 23.1% 234 58.7% 52 13.0% 399 Total/Average 332 2.8% 2622 22.1% 8251 69.6% 655 5.5% 11860 Alert_Description Figure 3. Corollary-type alerts and report. A referral to nephrology for evaluation of acid-base disturbance generated these alerts for tests recommended before the referral that have not been performed. In the report, “X” is the procedure that triggered the best-practice alert, “Y” the recommended additional order(s); “X+Y” represents encounters in which both tests were ordered: the desired result in this case. 2014 Epic Systems Corporation. Used with permission. BUN = blood urea nitrogen; CA = calcium; CBC = complete blood count; CL = chloride; CO2 = carbon dioxide; CR = creatinine; ED = Emergency Department; EKG = electrocardiogram; GLU = glucose; K = potassium; KPNW = Kaiser Permanente Northwest; NA = sodium; REF = referral; TSH = thyroid stimulating hormone; UA = urinalysis. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 15 ORIGINAL RESEARCH & CONTRIBUTIONS A Metrics Taxonomy and Reporting Strategy for Rule-Based Alerts than age 65 years who has documentation that he is a current or ever-smoker. This marker, in turn, is used by a second alert that recommends screening for abdominal aortic aneurysm. We elected not to create new classes with only single members in our data set. The Sidebar: Alert Metrics Taxonomy also contains subcategories. More granular specification is important because the reporting logic differs for procedures, medications, and documentation. We assigned each of 333 KPNW active, in-production, rule-based alerts to a class. Some alerts recommend or allow more than one action, such as substitute an order and perform documentation. As noted, for the purposes of report creation, simplification, and this initial stage of development, each was assigned to one class only on the basis of their primary or most impactful recommendation. In our system at this time, 3 of 18 categories accounted for more than 60% of all alerts, with Corollary Order, Substitute Medication, and Create Order contributing 106, 58, and 46 alerts, respectively (Figure 1). Categorizing alerts by class allowed us to develop a reporting strategy that works for all members of that class, or at least for those members who do not deviate too much from a prototypical class representative. The Substitution Order class offers an example of our approach. In this case, a user orders test or procedure “X” and the alert recommends substituting test or procedure “Y” (Figure 2). Regardless of whether the user accepted or canceled the alert, or opened or did not open an attached order set if present, what we want to know is, at the end of Figure 4. Substitute Medication Alert and attached ambulatory order set. A benzodiazepine drug was ordered in a patient older than age 64, and a substitution is recommended and facilitated via the attached ambulatory order set containing condition-specific recommended alternatives. Note that there are both pharmacologic and nonpharmacologic alternatives. The anxiety treatment options are in an expandable group. Each of these choices is contained in a separate group or item within the database. 2014 Epic Systems Corporation. Used with permission. AVS = after-visit summary; Disp-30 = dispense 30; Hx=history of; HEDIS = Healthcare Effectiveness Data and Information Set; OTC = over the counter; PO = by mouth; PRN = when necessary; R-5 = refill 5 (ie, 5 refills). 16 The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS A Metrics Taxonomy and Reporting Strategy for Rule-Based Alerts the measurement period (eg, encounter), which was ordered, “X” or “Y”? (Ordering both is also possible, which would usually not be a desired result, as is ordering neither, which might or might not be desirable depending on the situation.) What we need is a program that can determine for all alerts of this type, which order(s) were present in the “result set” at the end of the encounter. Figure 2 also shows an example of a report created for 2 alerts of the Substitution class. In these 2 alerts, the recommended result occurred 54.8% of the time on average. Corollary Order alerts provide a second example. In these situations, a user orders test or procedure “X” and the alert recommends one or more additional test or procedure “Y” (Figure 3). In these cases, regardless of whether the user accepted or canceled the alert or performed other actions as a direct result of the alert, we want to know at the end of the encounter what was ordered, “X,” “Y,” both, or neither? Fortunately, the same approach and logic can be used to generate reports for these alerts. The structure is the same and what differs is the definition of success. In this case, what is desired is “X + Y” and not “X” or “Y” alone. Using this logic, a report for this class of alerts can be generated (Figure 3). In this example, the recommended result occurred in an average of 69.6% of cases. The approach to medication-related alerts is similar but often more complex. It is unusual for there to be a oneto-one recommendation in medication substitutions. Usually a class of medications is contraindicated in a population defined by an age range, laboratory findings such as renal insufficiency, a specific genetic marker, or a diagnosis. The recommended substitution might depend on other factors including the initial reason for prescribing the triggering medication. Thus the recommended substitution values might be organized and contained in two or more groups. Furthermore, the valid medication alternatives themselves usually constitute a class rather than a single entity. The reporting program must be able to detect all the valid substitution values. Figure 4 illustrates a Substitute Medication alert. In this case a class of medications is relatively contraindicated in the elderly because of risks of insomnia, delirium, sedation, and cognitive impairment. Members of this medication class are prescribed for a variety of indications, and recommended alternatives depend on these reasons. Such condition-dependent Alert Description alternatives can be offered within an order set. Despite these complexities, it was possible to develop a program that can automatically detect the triggers and recommended substitutions for medication-related alerts, and produce a report (Figure 5). Using pharmaceutical classes and generic drugs facilitates this. We are also able to take advantage of naming conventions in our order set development where, for example, all groups that contain medications begin with the prefix MED. For the 15 alerts in this example, the average rate of prescribing the preferred medication is just 10% (range, 1.5%-54.3%). Because nonpharmacologic therapies may be very appropriate, prescribing “none” (neither the trigger nor the recommended alternative medications) might be considered a positive outcome. Taking the “none” and “Y” results together yields an overall average success rate of 24.8% (range, 9.4%-75.5%) for these alerts. DISCUSSION It is difficult to understand or to improve what isn’t measured or at least examined. To comprehend which alerts achieve their intended goals, one needs more than only rates of firing, Order Type None “X” “Y” “X+Y” Total ELDERLY AND BENZODIAZEPINES SmartSet 9.7% 36.9% 6.5% 46.9% 6989 ELDERLY AND SKELETAL MUSCLE RELAXANTS SmartSet 19.9% 59.4% 8.2% 12.4% 1723 ELDERLY AND Z DRUG SLEEP AGENTS SmartSet 9.6% 71.5% 11.6% 7.3% 1545 ELDERLY AND ANTIHISTAMINES/ANTICHOLINERGICS SmartSet 21.8% 51.5% 14.6% 12.1% 1540 ELDERLY FALL RISK AND ANTIPSYCHOTICS/SLEEP MEDICATIONS SmartSet 11.6% 63.5% 4.5% 20.5% 978 ELDERLY AND LORAZEPAM OR OXAZEPAM SmartSet 7.7% 83.0% 1.7% 7.7% 951 DRUG INTRCTN CLOPIDOGREL+PO ESOMEPRAZOLE OR OMEPRAZOLE SingOrd 5.6% 25.9% 20.2% 48.3% 752 ELDERLY FALL RISK OR DEMENTIA+TCA/PROCHLORPERAZINE SmartSet 29.7% 49.6% 6.6% 14.1% 708 ELDERLY TERTIARY TRICYCLIC ANTIDEPRESSANTS SmartSet 45.0% 43.9% 4.2% 6.9% 642 ELDERLY AND PROMETHAZINE SmartSet 20.0% 49.2% 21.1% 9.8% 551 DRUG INTERACTION WARFARIN+SULFA SmartSet 21.3% 17.7% 54.3% 6.8% 503 DRUG INTERACTION STATIN+GEMFIBROZIL SmartSet 36.8% 36.2% 22.7% 4.3% 163 ELDERLY AND BUTALBITAL SmartSet 25.8% 60.6% 8.3% 5.3% 132 ELDERLY AND DESICCATED THYROID SmartSet 11.1% 86.1% 2.8% 0.0% 72 ELDERLY AND INDOMETHAZINE SmartSet 18.5% 76.9% 1.5% 3.1% 65 14.8% 48.2% 10.0% 27.0% 17314 Total Figure 5. Substitute Medication Alerts with results. “X” is the medication that triggered the alert, “Y” is the recommended substitution medication. “X+Y” represents encounters in which both medications were ordered. This report also indicated whether the medication was ordered via an ambulatory order set or via an attached single order (SingOrd). PO = by mouth; TCA = tricyclic antidepressant. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 17 ORIGINAL RESEARCH & CONTRIBUTIONS A Metrics Taxonomy and Reporting Strategy for Rule-Based Alerts acceptance, and override. First, one needs an explicit understanding and articulation of the goal. Next, one needs to determine whether that goal was achieved. To make this a realistic endeavor on a large scale, one needs a systematic approach. We developed a classification system that allows development of batch reports on alert process outcomes or goals. Our initial approach was empiric and influenced heavily by the existing alerts in our system. We simplified the classification system by assigning alerts to only a single class, even though some alerts have features of more than one class. For these Alert success reasons, this taxonomy is results … may certainly not exhaustive. seem low and Other classes of alerts no disappointing doubt exist in other systems … but likely today and will exist within will not our system in the future. We next created batch reports surprise those for some classes of alerts. experienced To date, we have dewith alert veloped reports for the acceptance and Corollary-Order, Coroloverride rates. lary-Medication, CreateOrder, Substitute-Order, and Substitute-Medication classes of alerts. These represent the top three plus two less-frequent classes of alerts at KPNW, accounting for fully twothirds of our current alerts. The fourth most common class, Informational Only, is not amenable to reporting of this nature because there is no measurable outcome event. Creating outcomes reports for several other classes, including those related to documentation, may also prove difficult and require special techniques, structured data entry, Concept Unique Identifiers, or natural language processing. In some systems, certain alerts are designed to allow overrides with rationales, usually selected from a list, with or without the ability to add free text comments. We have very few of these in our system, except in the standard drug-drug and drug-allergy alerting activity. A challenging metrics issue is how to handle such alerts. Examples of overrides include “patient refused,” “benefit outweighs risk,” “no good alternative,” “postponed for medical 18 indications,” or “doubtful allergy.” When a valid override or postpone reason is selected, this might be counted as alert success or at least not failure, but this assumes that only valid reasons are available for the given alert and that the reasons are selected with fidelity. In practice, some alerts are overridden, often at a very high rate, because the alert is a “false positive” based on incomplete or faulty data, incorrect alert logic, or inaccurate knowledge synthesis. A complete evaluation of the effectiveness of such an alert could thus require examining the selected override or postpone reasons in light of the actual clinical data to determine whether the reasons were applied appropriately. We provided examples of metrics for three classes of alerts. For the Substitution-Order, Corollary-Order, and Substitution-Medication alerts we measured in this way, the desired outcome was achieved on average 54.8%, 69.6%, and 24.8% of the time, respectively. Running the same report with different alerts, or perhaps even the same alerts after the alert or the alerting environment was modified, would probably yield different numbers. An alert might be modified, for example, by developing a clearer message, making it more specific by incorporating exceptions in the logic, or adding a more useful action step. Examples of modifying the alerting environment would be decreasing the overall number of alerts, providing user education, or changing incentives. Alert success results such as in our Substitute-Medication report (Figure 5) may seem low and disappointing to some people but likely will not surprise those experienced with alert acceptance and override rates. The value in having such data is first that it allows identification and examination of alerts that appear to be underperforming. Viewing this data also allows a better understanding of actual alert performance more generally and might encourage quality and safety officers, decision-support developers, and leaders to plan more realistic and comprehensive safety and quality strategies, rather than blithely assuming success from alerts alone. Findings such as these suggest that alerts may be part of such a strategy but often will not be sufficient. The main outcomes of this study were the successful development of a rule-based alerts taxonomy and the demonstration of its application in a reporting strategy. The full-scale application of this strategy with detailed outcomes to a corpus of alerts was out of the scope for this article and could itself justify a report. However, even preliminary and partial review of our alerts using this approach resulted in the elimination of several poorly performing alerts and the modification of others. Our approach decreases the time and effort to produce alert process performance metrics reports, making it more feasible to run them regularly, and this in turn results in a more complete and dynamic representation of alert functioning. Because increased complexity makes measurement more difficult and costly, alert developers may want to add complexity and to use extra options and actions more thoughtfully and only where they add significant value. This study has some limitations. A single author developed and determined the taxonomy and assigned alerts to the taxa. Although the primary intention and contribution of this work was to develop a reporting framework and approach rather than a broadly applicable and validated taxonomy, it would be useful to do this in the future. Two or more individuals making assignments with a reported interrater agreement would add confidence. We examined alerts in only a single institution using a single EHR, and we know we have not exploited all potential alert actions. There are no doubt alert classes that we did not identify, and we chose not to create an alert class containing only a single member in our data set. Furthermore, we assigned alerts to a single class, although some have actions that might place them in more than one. Alerts assigned to the Other category underline that the current taxonomy is not exhaustive. Further study with additional alerts and at different institutions should result in more classes. The specifics of our reporting approach will be generalizable only to a certain extent because each EHR has its own structure The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS A Metrics Taxonomy and Reporting Strategy for Rule-Based Alerts and data model, although most EHRs will have similar components. Finally, this report did not attempt to address the highest level in the evaluation hierarchy of rule-based alerts performance, whether patient or clinician goals or outcomes were achieved. CONCLUSION We developed a taxonomy for rulebased alerts and demonstrated its application in developing outcome metrics reports on a large scale. CLINICAL RELEVANCE STATEMENT Understanding whether clinical decision alerts achieve their intended function is fundamental to developing effective alerts and realizing the safety, quality, and resource benefits of EHRs. To reach this understanding, individuals and groups charged with developing and maintaining alerts need enhanced tools and reports. The approach presented here allows nuanced effectiveness reports on a large scale. v Disclosure Statement The author(s) have no conflicts of interest to disclose. Acknowledgments We acknowledge Wiley Chan, MD; Dean Sittig, PhD; Sunshine Sommers, MS, RPh; and Adam Wright, PhD, for review of the manuscript and for suggestions. The screenshots of Epic alerts in Figures 2, 3, and 4 are © 2014 Epic Systems Corporation. Used with permission. Mary Corrado, ELS, provided editorial assistance. References 1. Kuperman GJ, Bobb A, Payne TH, et al. Medication-related clinical decision support in computerized provider order entry systems: a review. J Am Med Inform Assoc 2007 JanFeb;14(1):29-40. DOI: http://dx.doi.org/10.1197/ jamia.M2170. 2. Belmont E, Chao S, Chestler AL, et al. EHRrelated metrics to promote quality of care and patient safety. In: Minimizing EHR-related serious safety events. Washington, DC: American Health Lawyers Association; 2013 May 31. p 3. 3. van der Sijs H, Bouamar R, van Gelder T, Aarts J, Berg M, Vulto A. Functionality test for drug safety alerting in computerized physician order entry systems. Int J Med Inform 2010 Apr;79(4):243-51. DOI: http://dx.doi.org/10.1016/j. ijmedinf.2010.01.005. 4. Wang JK, Shabot MM, Duncan RG, Polaschek JX, Jones DT. A clinical rules taxonomy for the implementation of a computerized physician order entry (CPOE) system. Proc AMIA Symp 2002:860-3. 5. Berlin A, Sorani M, Sim I. A taxonomic description of computer-based clinical decision support systems. J Biomed Inform 2006 Dec;39(6):656-67. DOI: http://dx.doi.org/10.1016/j.jbi.2005.12.003. 6. Wright A, Sittig DF, Ash JS, et al. Development and evaluation of a comprehensive clinical decision support taxonomy: comparison of frontend tools in commercial and internally developed electronic health record systems. J Am Med Inform Assoc 2011 May 1;18(3):232-42. DOI: http://dx.doi.org/10.1136/amiajnl-2011-000113. 7. Wright A, Goldberg H, Hongsermeier T, Middleton B. A description and functional taxonomy of rule-based decision support at a large integrated delivery network. J Am Med Inform Assoc 2007 Jul-Aug;14(4):489-96. DOI: http://dx.doi.org/10.1197/jamia.M2364. 8. National Quality Forum. Driving quality and performance measurement—a foundation for clinical decision support: a consensus report [Internet]. Washington, DC: National Quality Forum; 2010 Dec [cited 2013 Nov 29]. Available from: www.qualityforum.org/ Publications/2010/12/Driving_Quality_and_ Performance_Measurement_-_A_Foundation_ for_Clinical_Decision_Support.aspx. 9. McCoy AB, Waitman LR, Lewis JB, et al. A framework for evaluating the appropriateness of clinical decision support alerts and responses. J Am Med Inform Assoc 2012 MayJun;19(3):346-52. DOI: http://dx.doi.org/10.1136/ amiajnl-2011-000185. 10. Overhage JM, Tierney WM, Zhou XH, McDonald CJ. A randomized trial of “corollary orders” to prevent errors of omission. J Am Med Inform Assoc 1997 Sep-Oct;4(5):364-75. DOI: http://dx.doi.org/10.1136/jamia.1997.0040364. Our Wit Languisheth Yet when we content ourselves with their discoveries [ie, those of ancient Greece], and calmly believe (which is mere sleepiness) that there is now no more place for new inventions, the spritely edge of our own wit languisheth, and we extinguish the lamp which they lighted to our hands. — William Harvey, MD, 1578-1657, English physician, first to describe the circulatory system The Permanente Journal/ Summer 2015/ Volume 19 No. 3 19 SOUL OF THE HEALER Pinnacle photograph Brad Christian McDowell, MD This image was captured outside the Denver Art Museum. The sun was aligned behind the building, and the photograph was later processed in Photoshop to give the final result. The Denver Art Museum is a must-visit location in Denver, CO. Dr McDowell is a Plastic Surgeon at the Denver Medical Office in CO. More of his photography can be viewed online at: www.diversityofvision.com. 20 The Permanente Journal/ Summer 2015/ Volume 19 No. 3 credits available for this article — see page 96. ORIGINAL RESEARCH & CONTRIBUTIONS “Getting off the Bus Closer to Your Destination”: Patients’ Views about Pharmacogenetic Testing Susan Brown Trinidad, MA; Tara B Coffin, MEd; Stephanie M Fullerton, DPhil; James Ralston, MD, MPH; Gail P Jarvik, MD, PhD; Eric B Larson, MD, MPH Perm J 2015 Summer;19(3):21-27 http://dx.doi.org/10.7812/TPP/15-046 ABSTRACT Context: Pharmacogenetic testing, a form of precision medicine, has the potential to optimize medication choice and dosing. Yet, relatively little is known about the views of patients—particularly those with chronic psychiatric conditions—with respect to such testing. Objective: To explore patients’ beliefs and attitudes regarding pharmacogenetic testing, with the goal of informing policy development and implementation. Design: Qualitative study design using semistructured focus groups with adults enrolled in Group Health Cooperative, a large health maintenance organization in the Pacific Northwest. We conducted focus groups with patients prescribed antidepressants (pilot session plus 2 focus groups, n = 27); patients prescribed carbamazepine (2 focus groups, n = 17); and healthy patients (2 focus groups, n = 17). Results: Although participants understood the potential advantages of pharmacogenetic testing, many felt that the risks (discrimination, stigmatization, physician overreliance on genomic results, and denial of certain medications) may outweigh the benefits. These concerns were shared across groups but were more strongly expressed among participants with chronic mental health diagnoses. Conclusion: Clinical implementation of pharmacogenetic testing must address patient concerns about privacy, discrimination, quality of care, and erosion of the physician-patient relationship. INTRODUCTION The existence of interindividual differences in medication response is well known: variability exists among patients in terms of drug efficacy, dosage requirements, and susceptibility to adverse drug reactions. Pharmacogenetics, the study of how genetic factors influence pharmacokinetics and drug clearance first envisioned by Motulsky1 in 1957, has a growing role in providing clinically useful prescribing guidance.2 The US Food and Drug Administration currently lists 139 approved drugs with pharmacogenomic information in their labeling, with categories ranging from information about clinical pharmacology to contraindications, information for patient counseling, and dosing considerations.3 Boxed warnings, indicating the potential for serious injury or death for individuals with specific genotypes, are in place for select drugs in anesthesiology (codeine), cardiology (clopidogrel), hematology (lenalidomide), infectious disease (abacavir), oncology (arsenic trioxide, everolimus, rasburicase), and neurology (carbamazepine, valproic acid).3 The hope is that appropriate clinical use of pharmacogenetic testing will contribute to the “triple aim” of improving population health, enhancing patient care, and controlling medical costs.4 Pharmacogenomics, along with related advances in cancer genomic testing, has received new attention with the launch by President Obama of a new Precision Medicine Initiative.5 The value of pharmacogenetic testing will depend in part on its acceptability to physicians and patients. The literature contains some data regarding physicians’ views of pharmacogenetic testing,6-10 and others have explored the views of the general public,11 but less is known about patients’ perceptions.12 The objective of this study was to explore the views of patients with and without chronic conditions regarding pharmacogenetic testing. METHODS Setting and Study Design This study is part of the Electronic Medical Records and Genomics Network, a consortium funded by the National Human Genome Research Institute to develop approaches to and investigate the utility of the clinical integration of genomic information.13,14 Our project is a collaboration between investigators at the Group Health Research Institute and the University of Washington, with study participants at Group Health Cooperative, an integrated health care delivery system that serves more than 600,000 enrollees in Washington and Idaho. We selected a focus group method because interactive discussions are optimal for exploring questions of acceptability, particularly for topics about which participants may feel underqualified to opine15-17; participants may feel more comfortable sharing potentially negative views because the group format can provide a feeling of “safety in numbers” for Susan Brown Trinidad, MA, is a Research Scientist in Bioethics and Humanities at the University of Washington in Seattle. E-mail: [email protected]. Tara B Coffin, MEd, is a Doctoral Candidate in the Institute for Public Health Genetics at the University of Washington in Seattle. E-mail: [email protected]. Stephanie M Fullerton, DPhil, is an Associate Professor in Bioethics and Humanities at the University of Washington in Seattle. E-mail: [email protected]. James Ralston, MD, MPH, is an Associate Investigator at the Group Health Research Institute in Seattle, WA. E-mail: [email protected]. Gail P Jarvik, MD, PhD, is a Professor and Head of the Division of Medical Genetics at the University of Washington in Seattle. E-mail: [email protected]. Eric B Larson, MD, MPH, is the Executive Director and Senior Investigator at the Group Health Research Institute in Seattle, WA. E-mail: [email protected]. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 21 ORIGINAL RESEARCH & CONTRIBUTIONS “Getting off the Bus Closer to Your Destination”: Patients’ Views about Pharmacogenetic Testing participants.18 The study was reviewed and approved by the Group Health Research Institute Human Subjects Review Committee, and written informed consent was obtained from all participants. Sampling Strategy and Recruitment Prospective participants were English-speaking adults age 18 years and older identified through Group Health administrative records. To learn about the perspectives of different “types” of patients, we defined 3 patient cohorts (Table 1). As a proxy for patients who were likely to have had personal experiences with trial and error in medication selection, we selected Group Health enrollees who had been (sequentially) prescribed multiple antidepressant medications.19 To elicit the views of patients for whom pharmacogenetic testing could possibly help to avoid adverse drug events, we identified individuals who had been prescribed carbamazepine. Carbamazepine has been associated with Stevens-Johnson syndrome (toxic epidermal necrolysis) in patients with the HLA-B*1502 allelic variant of the HLA-B gene, which is more common in people of Southeast Asian ancestry3; for this reason, we oversampled for Asian ancestry in this group. For comparison purposes, we identified a third cohort of patients with no particular pharmaceutical concerns or chronic conditions. We mailed 4303 letters to prospective participants describing the study and inviting them to call to enroll; 61 did so, for a total response rate of 1.4%. Data Collection In May 2012, we held a pilot session and 2 semistructured focus groups with the antidepressant cohort and 2 focus groups with patients prescribed carbamazepine. In July 2012, we conducted 2 focus groups with patients without chronic illnesses. The investigators used a written discussion guide in all sessions (Table 2). Each discussion was cofacilitated by 2 members of the study team (SBT and SMF, who introduced themselves as researchers from the University of Washington) and lasted 2 hours. A court transcriptionist attended each session. We provided an informal buffet dinner and paid parking, and each participant was given $50 in cash at the end of each session. Data Analysis Our analytic goal was to produce a qualitative description of participants’ perceptions of pharmacogenetic testing.20 We used thematic analysis and a constant comparison approach to coding.21 Two members of the study team performed several close readings Table 1. Focus group composition Variable Eligibility criteria Sex Male Female Age, years Range Mean Race and ethnicity White Black American Indian Asian Pacific Islander Hispanic Other Educational attainment Some high school High school or GED Some college Associate degree Bachelor’s degree Master’s degree PhD Other advanced degree Antidepressant cohort Prescribed ≥ 2 antidepressants in previous 2 years; new antidepressant prescription within past 3 months, n = 27, No. (%) Carbamazepine cohort Currently prescribed carbamazepine; oversampled for Asian ethnicity, n = 17, No. (%) Healthy cohort GHC enrollees for at least 2 years; ≤ 2 current prescriptions; exclusions: mental health diagnoses, current antidepressant or carbamazepine prescription, n = 17, No. (%) Total n = 61, No. (%) 10 (37) 17 (63) 5 (29) 12 (71) 7 (41) 10 (59) 22 (36) 39 (64) 22-78 54 21-73 50 21-78 50 21-78 51 23 (85) 1 (4) 1 (4) 1 (4) 0 0 1 (4) 11 (65) 1 (6) 0 2 (12) 0 0 3 (18) 15 (88) 0 0 0 0 2 (12) 2 (12) 49 (80) 2 (3) 1 (2) 3 (5) 0 2 (3) 6 (10) 0 2 (7) 6 (22) 1 (4) 9 (33) 8 (30) 1 (4) 0 0 3 (18) 2 (12) 2 (12) 5 (29) 4 (24) 0 1 (6) 1 (6) 0 0 0 8 (47) 7 (41) 0 1 (6) 1 (2) 5 (8) 8 (13) 3 (5) 22 (36) 19 (31) 1 (2) 2 (3) GED = general equivalency diploma; GHC = Group Health Cooperative. 22 The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS “Getting off the Bus Closer to Your Destination”: Patients’ Views about Pharmacogenetic Testing of the de-identified transcripts. The lead analyst drafted a codebook of the major themes, which was revised over several meetings of the analytic team. Transcripts and codes were uploaded into Dedoose (www.dedoose.com), an online software application for qualitative analysis. The codebook went through two substantive revisions before final coding, including independent coding of four transcripts by two team members. The lead analyst performed final coding, with review by a second member of the team. RESULTS Participants were aware of interindividual differences in medication response. Many shared stories about medications that did not work, caused side effects, or were “too strong” or not strong enough. Several related having felt like “guinea pigs” or, in one case, “a test-tube baby” during a process of therapeutic trial and error. A participant in one of the antidepressant groups said, “Sometimes I’ve been prescribed a medication and then find out it’s not maybe doing the job. So we go to the next medication down the list, whereas, for some people, that first one works just fine.” The idea that genetics could make a difference in drug response was less familiar, but some participants believed that medication response could be inherited or shared within families. Participants Believed Pharmacogenetic Testing Could Be Beneficial Upon introduction to the topic, participants understood the potential of pharmacogenetic testing to optimize prescribing decisions, and they could imagine clear benefits from its use. As one participant put it, “I think it’s a great idea. Who wouldn’t want more information about the proper medication to take?” Another compared pharmacogenetic testing to riding a bus: “You could jump off anywhere downtown and get to a store, but you want to get off closer to the store you’re going to.” The value of the test could be even greater in high-stakes situations: a participant who reported that her child is currently awaiting a liver transplant said, “You get the liver, and you’re on medication for a long time. If there was a test that would show us which medications are going to work for him, we’d be on that so fast! Because that’s a huge life-or-death deal.” Participants in the antidepressant and carbamazepine groups seemed particularly sensitized to the challenges patients can face in finding the right medication and avoiding side effects; many related stories of trial-and-error in the therapeutic odyssey. One person, a participant in one of the depression groups, shared her frustration with prior medication experiences and emphasized the value of identifying the optimal drug more quickly: Even if it takes six months [to get pharmacogenetic test results], I have had—looking back, it’s like, you know, gee, do you think that that particular drug was what took like four years out of my life? Yeah. If somebody could go in there and figure it out in four months, yeah, that would be better. A participant in one of the carbamazepine discussions said, “The idea that a genetic test—I know there’s some controversy there—but that it could help limit, or define, [the best] medication, that’s very appealing. I mean, I have had bad years on the wrong thing.” Another participant in the same session commented, “If I were taking lithium, or Depakote, or some medicine with a lot of side effects, and this test could say, well, those aren’t going to help me, I would want to be taken off of those. So I think there could be a benefit to having a complete workup of the information.” Table 2. Focus group discussion topics Step Warm-up and orientation Goals/subtopics - Establish rapport within the group - Introduce pharmacogenetics in a relatable way Directed pharmacogenetic testing (for specific medication or class) - Informed consent - Pros and cons - Factors influencing decision making - Information desired about results Whole-genome sequencing (including pharmacogenomic indication) - Informed consent - Pros and cons - Factors influencing decision making - Data security - Information desired about results The Permanente Journal/ Summer 2015/ Volume 19 No. 3 Sample questions Different people respond differently to medications. For example, codeine—a commonly prescribed pain medication— just doesn’t work for some people. And some people may have severe reactions to medications that work just fine for others. Have you ever heard of anything like this before? Have you ever heard that genes might play a role in such differences? Would you want to know if your doctor planned to order a genetic test before prescribing medication? Would you want this kind of test if you could find out the drug might not work for you? Would you want information suggesting that you may react similarly to related drugs (in addition to the one the doctor wished to prescribe for your current condition)? Would you be willing to undergo sequencing before being prescribed a specific medication (eg, at your annual physical examination)? What would you want to know about the way(s) in which your additional genetic test information might be stored? Eventually such comprehensive genetic testing might include all genes in the genome, not just those most relevant to drug prescribing. This might mean that other information relevant to your current or future health status would also be generated. What are your impressions about this possibility? 23 ORIGINAL RESEARCH & CONTRIBUTIONS “Getting off the Bus Closer to Your Destination”: Patients’ Views about Pharmacogenetic Testing Potential Negative Effects on Quality of Care and the PhysicianPatient Relationship Some participants felt that physicians might rely too heavily on genetic results and fail to give due consideration to all possible factors; others worried that physicians might not understand how to use this new information appropriately. A participant in one of the sessions with healthy patients said, “I can see this testing as a protection for doctors, kind of a cop-out. They won’t have to work quite as hard to dig and find out, ‘What shall I prescribe this person and how much?’ Because they will have this [test result]—‘Oh, okay, we’ll use that.’ So it’s kind of a protection for doctors.” The belief that physicians might regard genetic information as more important than other data, possibly to the patient’s detriment, was a strong motif. Of greatest concern to participants across all sesOf greatest concern sions was the possibility that to participants physicians might rely excluacross all sessions sively on pharmacogenetic was the possibility test results and disregard that physicians patients’ reports about how might rely a medication is working (or failing to work). A number exclusively on of patients in the antidepharmacogenetic pressant and carbamazepine test results and cohorts related incidents in disregard patients’ which they felt that their reports about how reports of medication proba medication is lems had not been taken working (or failing seriously or were actually to work). contradicted. The following exchange, which took place in one of the antidepressant groups, illustrates several participants’ views: PARTICIPANT 4: I want to say that again, what really bothers me the most: you have something static, which is your genome, and the way medication reacts is all different. And all other kinds of physical situations that may affect that medication. And because [the genome is] static, would the doctor be more inclined to say … “I’m sorry, that’s what the test says”? PARTICIPANT 1: And look at you very authoritatively and say, “This must be in your mind. For all the other patients, it works fantastically.” 24 PARTICIPANT 6: It’s not the only piece of information. If you have had [gastrointestinal] surgery, for example, and you can’t absorb a medication, that’s not something that’s going to show up on your genetic profile. PARTICIPANT 7: If you have multiple illnesses, and you take multiple medications, that’s not going to necessarily show up there either. Participants voiced concern about the potential for genetic information to curtail interaction and reduce trust between physicians and patients. In addition to wanting physicians to listen to their concerns and take them into consideration in decision making, participants sought assurance that, in delivering genetic results, the physician would assess the patient’s need for support: Doctors have all this [genetic] information, and you have to look at a person’s mental state. Can they handle certain information, or does that send them off to suicide? Or what’s it going to do? I was told one time I was getting tested for cancer, and then the doctor walked out of the room. I’m like, “What? What? Who?” I’m sitting there all by myself. “You’re testing for cancer?!” So how can you deal with this information? How is that going to be handled? In contrast, a single participant in the antidepressant group envisioned pharmacogenetic testing as an important step toward what he considered the ideal: “the doctor robot,” which would make all clinical decisions on the basis of objective data. Some participants viewed the use of pharmacogenetic information to deny a particular “good” medication as a form of unfair discrimination, as in this example: “The only thing I don’t like about [pharmacogenetic testing is], because of certain percentages, you might not be good on a certain drug, maybe, and they make this whole list of all these good drugs you can’t have. So they would refuse certain medicines to you, your whole life.” Another participant stated that if there were only one medication available to treat a particular, serious condition, and a pharmacogenetic test indicated that the medication could cause harm, it should be up to the patient—not the physician—to decide whether to take the risk. Concerns about Access to Genetic Information Notwithstanding their belief in the value of pharmacogenetic testing, participants identified potential drawbacks to its implementation in the clinic. Concerns about the potential for genetic information to be accessed and (mis)used by unauthorized persons were expressed in all groups. Breach of confidentiality; discrimination in eligibility and coverage for health insurance, long-term care insurance, and disability insurance; employment discrimination; being targeted for pharmaceutical marketing campaigns; and possible misuse by law enforcement agencies were of concern to participants. Discrimination risks were more readily and more strongly expressed in the antidepressant and carbamazepine groups, together with concerns about social stigma associated with mental health diagnoses, as in this example from the carbamazepine group: I already have concerns just about electronic keeping of my records, compared to the way it used to be [when] it was on all on paper. I have already experienced the lack of privacy with my primary doctor … I have mental health issues, so sometimes without even asking—they are supposed to be kept separate—my regular doctor, … just access[es] the mental health thing, and start[s] reading this. And they have already abused it … . That’s why I have a lot of privacy issues, because I have seen how it’s easily taken advantage of. Participants were uncomfortable with the potential for genetic information to be shared legally beyond the health care system, such as with law enforcement agencies or in legal proceedings (eg, for disability determinations). A participant in the antidepressant cohort said: I wouldn’t mind it so much as part of my medical record, if my medical record didn’t go to other people. Like applying for disability insurance, they go through medical records, and what they decide and they define it and interpret it in their own way. So I would be concerned about if they got ahold of genetic The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS “Getting off the Bus Closer to Your Destination”: Patients’ Views about Pharmacogenetic Testing information and what they would do to you this time. Participants across all three cohorts also expressed concern about access to pharmacogenetic information within the health care system. Participants suggested that genetic information should be restricted to clinicians with a clear need to know, and that access should be limited to data relevant to a current clinical concern, as in this comment: “If I could have it on a microchip somewhere and say, okay, ‘If I’m unconscious, you know, I give medical permission to read this.’ Yeah, I probably would go for that. But at the same time, I might say, ‘Well, I don’t necessarily want it in the chart where the person who’s making my appointment can look at it.’” Several other participants suggested that genetic information be given directly to the patient, who would be responsible for determining when it should be shared. One participant commented, “It’s us having power over the information. We still want to be a very important part of the equation. And that we get to make some decisions about how it’s used.” Patients’ Understanding of “Genetic Testing” Is Discordant with Clinicians’ Definition As designed, the focus group guide progressed from discussion of a narrow, single-indication pharmacogenetic test—looking at a small portion of the genome specific to a particular medication—to discussion of wholegenome sequencing, which would include pharmacogenetic results. In each of the sessions, however, we had substantial difficulty focusing participants’ conversation on the less comprehensive test scenario. In other words, participants considered “genetic testing” to refer to examination of the entire genome, and most understood the purpose of genetic testing to be predicting one’s susceptibility to heritable illness. For example, one participant in the healthy cohort said, “I came in with the idea that this is a testing of your genes, your genetic makeup, to find out if you are more predestined for a certain disease …. Life-threatening things, that’s what The Permanente Journal/ Summer 2015/ Volume 19 No. 3 I thought it was all about.” Overall, participants evinced little understanding of the distinction between singlegene tests, panels, and whole-genome sequencing. Participants felt that payers (and to a lesser extent, physicians) would prefer more comprehensive testing approaches for reasons of efficiency and cost-effectiveness. Whole-Genome Sequencing Was Viewed Differently from Narrower Tests Once we had explained the differences among single-indication testing, pharmacogenomic panels, and wholegenome sequencing, many participants told us that they regarded whole-genome sequencing as a riskier undertaking than a more narrowly focused test, even if pharmacogenetic information were the primary goal of sequencing. With the generation of additional information, participants believed, the potential for misuse and discrimination would increase as well. One participant stated: I kind of want to know how much information they can get from that blood sample. And will they then be able to go back and use other pieces of that test in an unrelated way that [doesn’t] have anything to do with the specific treatment I need at that moment? And I also want to know, after it’s been utilized for something specific, if it can be taken out of my medical record, or once it’s there, is it there forever? If I’m using it for something very, very specific, that sort of works, but they are also getting information about my IQ, my willingness to work Monday through Friday, or my need to call in for a vacation day every three weeks, or three days? I don’t want that in there. Several participants pointed to the 1997 science-fiction film GATTACA,22 in which the government constrains individuals’ life choices on the basis of their genomes, as a depiction of what could go wrong if laws and social standards fail to provide appropriate privacy protections. Some participants said that comprehensive sequencing would also be more likely to generate information they might not want, particularly for serious health risks they “couldn’t do anything about.” The potential risks to other family members, given that genetic information about one person says something about their first-degree relatives, were also of concern. On the other hand, whole-genome sequencing was very attractive to a few participants who reported many seemingly unrelated health problems in themselves and in their families. One such participant said: For me, I would find it beneficial, because I suffer from a lot of different ailments. I would definitely be like, “Yeah, give me that test,” because it could show that they are treating symptoms of a different ailment. So it doesn’t add up unless you come in with a sheet this long [gestures], by the way, all of this happens. So I think a test like that could rule out what you are treating and actually show what you have … . I would find this would be something very important to have in my records for my family to see, simply because of my family history. My daughter is autistic. And then on my mom’s side, we have tremors, don’t know what causes those. So it’s definitely something I’m very interested in. These individuals expressed great interest in comprehensive testing, which they thought could provide a coherent explanation for the multitude of challenges they face. DISCUSSION Prior studies on patient views of pharmacogenetic testing have focused on the general public and have generally presented hypothetical scenarios with limited personal relevance to participants.23,24 Others have explored the perceptions and values of patients undergoing treatment of life-threatening conditions, who generally express strong support for treatment-focused genetic testing and markedly less concern about the potential risks of discrimination and breach of privacy.25-27 This study adds to the perspectives of individuals diagnosed with chronic mental-health conditions. In speaking with participants in the carbamazepine cohort, we learned that many had been prescribed carbamazepine for bipolar disorder rather than seizure disorders (a common indication for this 25 ORIGINAL RESEARCH & CONTRIBUTIONS “Getting off the Bus Closer to Your Destination”: Patients’ Views about Pharmacogenetic Testing medication). Our study thus included a majority of individuals with mental health diagnoses. Concerns about privacy, discrimination, and unauthorized access to genetic information are a theme throughout the existing literature.28,29 In this study, participants in the antidepressant and carbamazepine groups voiced especially strong concerns about the potential for stigmatization, discrimination, and mistreatment resulting from pharmacogenetic testing and unauthorized access to results. Although these findings may not generalize across entire populations, they highlight an underrepresented perspective that is of particular relevance to ongoing pharmacogenetic research in neuropsychiatry.2,30,31 Our passive recruitment strategy may have generated a greater than usual selection bias. Pharmacogenetics has often been described as among the most straightforward and near-term applications of genetic information in personalized medicine.5,31-34 An important finding of this study is that some patients who could potentially benefit from pharmacogenetic testing have substantial, deeply held concerns about the tradeoffs involved in allowing genetic information to be generated about them and maintained outside their control. Our participants were not naïve patients; they were very interested in reducing the time to optimal treatment, and many told us they had personally experienced negative effects from current pharmaceutical therapies. Even so, they did not consider pharmacogenetic testing of clear benefit. Our findings are consistent with the results of an Australian study in which chronically ill patients endorsed the potential value of pharmacogenetic testing but emphasized the need for antidiscrimination measures and a holistic approach to diagnosis and prescribing. 35 Avoiding a life-threatening drug reaction is obviously a good thing, but when the benefits are less compelling, patients with chronic illnesses—and perhaps especially those with potentially stigmatizing diagnoses—may decide that the risks of pharmacogenetic testing outweigh the benefits. 26 We were struck by the strength and prevalence of participants’ worries that physicians might overvalue genetic results to the exclusion of patient reports and the detriment of the therapeutic alliance. Although patients understood that such information could be useful in achieving optimal treatment outcomes, they nonetheless expressed misgivings about the possibility that physicians would privilege genetic results over patients’ lived experience. This message represents an important counterpoint to the enthusiastic discourse surrounding next-generation sequencing and personalized medicine. If personalized medicine is to be fully embraced by patients, it will be important to ensure that physicians’ enactment of “personalization” includes responding to the patient as an individual and not merely a collection of genomic data.36 Despite the proposed central role of genetics in the coming era of data-driven health care, some patients see pharmacogenetic testing as a potential threat to communication, health care quality, and the physician-patient relationship. Participants in this study wanted pharmacogenetic testing and whole-genome sequencing to complement, not replace, other information about medication response. CONCLUSIONS The success of precision medicine, or the provision of “the right drug at the right dose to the right patient,” will rely on the broad acceptability of genomic testing by diverse patient cohorts.5 Our findings suggest that pharmacogenetic solutions designed around the needs and preferences of patients who are basically well may fail to meet the needs of patients with mental health diagnoses or other chronic conditions that may carry social stigma. Health systems and physician practices considering implementation of pharmacogenetic testing must address patient concerns about privacy, discrimination, overreliance on genomic results, and erosion of the physician-patient relationship through public outreach, physician education, and accountable oversight procedures and governance. v Disclosure Statement Funding: This project was supported by the National Human Genome Research Institute (1U01HG006375-01). The study sponsor did not play a role in study design; data collection, analysis, or interpretation; writing the report; or the decision to submit for publication. The author(s) have no conflicts of interest to disclose. Acknowledgments The authors wish to thank Wylie Burke, MD, PhD for helpful advice in the development of this manuscript. We also thank Kevin Filocamo and Kelly Hansen for assistance in coordinating the focus groups and Aaron Scrol for his help in preparing Table 1 and obtaining documentation of IRB review. Mary Corrado, ELS, provided editorial assistance. References 1 Motulsky AG. Drug reactions, enzymes, and biochemical genetics. J Am Med Assoc 1957 Oct 19;165(7):835-7. DOI: http://dx.doi.org/10.1001/ jama.1957.72980250010016. 2. Drozda K, Müller DJ, Bishop JR. Pharmacogenomic testing for neuropsychiatric drugs: current status of drug labeling, guidelines for using genetic information, and test options. Pharmacotherapy 2014 Feb;34(2):166-84. DOI: http://dx.doi.org/10.1002/phar.1398. 3. Table of pharmacogenomic biomarkers in drug labeling [Internet]. Silver Spring, MD: US Food and Drug Administration; 2014 Aug 18 [updated 2015 Mar 27; cited 2015 Feb 9]. Available from: www.fda.gov/drugs/scienceresearch/ researchareas/pharmacogenetics/ucm083378.htm. 4. Berwick DM, Nolan TW, Whittington J. The triple aim: care, health, and cost. Health Aff (Millwood) 2008 May-Jun;27(3):759-69. DOI: http://dx.doi. org/10.1377/hlthaff.27.3.759. 5. Collins FS, Varmus H. A new initiative on precision medicine. N Engl J Med 2015 Feb 26;372(9):793-5. DOI: http://dx.doi.org/10.1056/ NEJMp1500523. 6. Haga SB, Burke W, Ginsburg GS, Mills R, Agans R. Primary care physicians’ knowledge of and experience with pharmacogenetic testing. Clin Genet 2012 Oct;82(4):388-94. DOI: http:// dx.doi.org/10.1111/j.1399-0004.2012.01908.x. 7. Haga SB, O’Daniel JM, Tindall GM, Mills R, Lipkus IM, Agans R. Survey of genetic counselors and clinical geneticists’ use and attitudes toward pharmacogenetic testing. Clin Genet 2012 Aug; 82(2):115-20. DOI: http://dx.doi.org/10.1111/ j.1399-0004.2012.01848.x. 8. Hoop JG, Lapid MI, Paulson RM, Roberts LW. Clinical and ethical considerations in pharmacogenetic testing: views of physicians in 3 “early adopting” departments of psychiatry. J Clin Psychiatry 2010 Jun;71(6):745-53. DOI: http://dx.doi. org/10.4088/JCP.08m04695whi. 9. Stanek EJ, Sanders CL, Taber KA, et al. Adoption of pharmacogenetic testing by US physicians: results of a nationwide survey. Clin Pharmacol Ther 2012 Mar;91(3):450-8. DOI: http://dx.doi. org/10.1038/clpt.2011.306. 10. Dorfman EH, Brown Trinidad S, Morales CT, Howlett K, Burke W, Woodahl EL. Pharmacogenomics in diverse practice settings: implementation beyond major metropolitan areas. Pharmacoge- The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS “Getting off the Bus Closer to Your Destination”: Patients’ Views about Pharmacogenetic Testing 11. 12. 13. 14. 15. 16. 17. 18. nomics 2015 Mar;16(3):227-37. DOI: http://dx.doi. org/10.2217/pgs.14.174. Patel HN, Ursan ID, Zueger PM, Cavallari LH, Pickard AS. Stakeholder views on pharmacogenomic testing. Pharmacotherapy 2014 Feb;34(2):151-65. DOI: http://dx.doi.org/10.1002/ phar.1364. Shaw JL, Robinson R, Starks H, Burke W, Dillard DA. Risk, reward, and the double-edged sword: perspectives on pharmaogenetic research and clinical testing among Alaska Native people. Am J Public Health 2013 Dec;103(12):2220-5. DOI: http://dx.doi.org/10.2105/AJPH.2013.301596. Gottesman O, Kuivaniemi H, Tromp G, et al; eMERGE Network. The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future. Genet Med 2013 Oct;15(10):761-71. DOI: http://dx.doi.org/ 10.1038/gim.2013.72. McCarty CA, Chisholm RL, Chute CG, et al; eMERGE Team. The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies. BMC Med Genomics 2011 Jan 26;4:13. DOI: http://dx.doi.org/10.1186/1755-8794-4-13. Kahan JP. Focus groups as a tool for policy analysis. Analyses of Social Issues and Public Policy 2001 Dec;1(1):129-46. DOI: http://dx.doi. org/10.1111/1530-2415.00007. Morse JM, Barrett M, Mayan M, Olson K, Spiers J. Verification strategies for establishing reliability and validity in qualitative research. Int J Qual Methods 2002;1(2):13-22. Powell RA, Single HM. Focus groups. Int J Qual Health Care 1996 Oct;8(5):499-504. DOI: http:// dx.doi.org/10.1093/intqhc/8.5.499. Kitzinger J. Qualitative research. Introducing focus groups. BMJ 1995 Jul 29;311(7000): 299-302. DOI: http://dx.doi.org/10.1136/ bmj.311.7000.299. 19. Simon G. Choosing a first-line antidepressant: equal on average does not mean equal for everyone. JAMA 2001 Dec 19;286(23):3003-4. DOI: http://dx.doi.org/10.1001/jama.286.23.3003. 20. Sandelowski M. Whatever happened to qualitative description? Res Nurs Health 2000 Aug;23(4): 334-40. DOI: http://dx.doi.org/10.1002/1098240X(200008)23:4%3C334::AID-NUR9% 3E3.0.CO;2-G. 21. Glaser B, Strauss A. The discovery of grounded theory: strategies for qualitative research. Hawthorne, NY: Aldine Publishing Company; 1967. 22. Niccol A. Gattaca. Los Angeles, CA: Sony Pictures; 1997. 23. Haga SB, O’Daniel JM, Tindall GM, Lipkus IR, Agans R. Survey of US public attitudes toward pharmacogenetic testing. Pharmacogenomics J 2012 Jun;12(3):197-204. DOI: http://dx.doi. org/10.1038/tpj/2011.1. 24. O’Daniel J, Lucas J, Deverka P, et al. Factors influencing uptake of pharmacogenetic testing in a diverse patient population. Public Health Genomics 2010;13(1):48-54. DOI: http://dx.doi. org/10.1159/000217795. 25. Fargher EA, Eddy C, Newman W, et al. Patients’ and healthcare professionals’ views on pharmacogenetic testing and its future delivery in the NHS. Pharmacogenomics 2007 Nov;8(11):1511-9. DOI: http://dx.doi.org/10.2217/14622416.8.11.1511. 26. Meiser B, Gleeson M, Kasparian N, et al. There is no decision to make: experiences and attitudes toward treatment-focused genetic testing among women diagnosed with ovarian cancer. Gynecol Oncol 2012 Jan;124(1):153-7. DOI: http://dx.doi. org/10.1016/j.ygyno.2011.09.040. 27. Rogith D, Yusuf RA, Hovick SR, et al. Attitudes regarding privacy of genomic information in personalized cancer therapy. J Am Med Inform Assoc 2014 Oct;21(e2):e320-5. DOI: http://dx.doi. org/10.1136/amiajnl-2013-002579. 28. Hazin R, Brothers KB, Malin BA, et al. Ethical, legal, and social implications of incorporating genomic information into electronic health records. Genet Med 2013 Oct;15(10):810-6. DOI: http://dx.doi.org/10.1038/gim.2013.117. 29. McEwen JE, Boyer JT, Sun KY. Evolving approaches to the ethical management of genomic data. Trends Genet 2013 Jun;29(6): 375-82. DOI: http://dx.doi.org/10.1016/j. tig.2013.02.001. 30. Malhotra AK, Zhang JP, Lencz T. Pharmacogenetics in psychiatry: translating research into clinical practice. Mol Psychiatry 2012 Jul;17(8):760-9. DOI: http://dx.doi. org/10.1038/mp.2011.146. 31. Zhang JP, Malhotra AK. Pharmacogenetics and antipsychotics: therapeutic efficacy and side effects prediction. Expert Opin Drug Metab Toxicol 2011 Jan;7(1):9-37. DOI: http://dx.doi.org/ 10.1517/17425255.2011.532787. 32. Hamburg MA, Collins FS. The path to personalized medicine. N Engl J Med 2010 Jul 22;363(4):301-4. DOI: http://dx.doi.org/10.1056/ NEJMp1006304. Erratum in: N Engl J Med 2010 Sep 9;363(11):1092. DOI: http://dx.doi. org/10.1056/NEJMx100055. 33. Manolio TA, Chisholm RL, Ozenberger B, et al. Implementing genomic medicine in the clinic: the future is here. Genet Med 2013 Apr;15(4):258-67. DOI: http://dx.doi.org/10.1038/gim.2012.157. 34. Roses AD. Pharmacogenetics and the practice of medicine. Nature 2000 Jun 15;405(6788):857-65. DOI: http://dx.doi.org/10.1038/35015728. 35. Haddy CA, Ward HM, Angley MT, McKinnon RA. Consumers’ views of pharmacogenetics—a qualitative study. Res Social Adm Pharm 2010 Sep;6(3):221-31. DOI: http://dx.doi.org/10.1016/j. sapharm.2009.08.002. 36. Burke W, Brown Trinidad S, Press NA. Essential elements of personalized medicine. Urol Oncol 2014 Feb;32(2):193-7. DOI: http://dx.doi. org/10.1016/j.urolonc.2013.09.002. Life-Histories We would wish that … life-histories were found in every family, showing the health and diseases of its different members. We might thus in time find evidences of pathological connections and morbid liabilities not now suspected. — Sir William Withey Gull, MD, 1st Baronet of Brook Street, 1816-1890, English physician, Fullerian Professor of Physiology, and President of the Clinical Society The Permanente Journal/ Summer 2015/ Volume 19 No. 3 27 SOUL OF THE HEALER Seville photograph Samuel H Glassner, MD This photograph was taken in Seville, Andalusia, Spain in November 2012. Founded in the 8th century, Seville has been governed by Roman, Muslim, and Christian sovereigns. The city served as a major economic hub during the centuries of Spanish imperialism, and it remains an important European center for culture and the arts. Dr Glassner is an Emergency Physician at the Walnut Creek Medical Center in CA. 28 The Permanente Journal/ Summer 2015/ Volume 19 No. 3 credits available for this article — see page 96. ORIGINAL RESEARCH & CONTRIBUTIONS A Community-Based Hip Fracture Registry: Population, Methods, and Outcomes Maria C S Inacio, PhD; Jennifer M Weiss, MD; Alex Miric, MD; Jessica J Hunt, MA; Gary L Zohman, MD; Elizabeth W Paxton, MA Perm J 2015 Summer;19(3):29-36 http://dx.doi.org/10.7812/TPP/14-231 ABSTRACT Introduction: Hip fracture is associated with substantial morbidity and mortality. A large integrated health care system developed a registry to characterize its current patient population with hip fractures. This report describes the population, methods used, and outcomes of patients registered during the initial three years (2009-2011). Methods: Cases of hip fracture recorded from January 2009 through December 2011 were ascertained using the Kaiser Permanente Hip Fracture Registry. The registry collects information on patient, procedure, surgeon, facility, and surgical outcomes. Outcomes monitored included length of stay, readmissions, mortality, revisions, surgical site infections, deep vein thrombosis, pulmonary embolism, pneumonia, pressure ulcers, dislocations, and myocardial infarction. Results: The population (N = 12,562) was predominantly white (77.8%), women (68.6%), and older (71.6% aged ≥ 75 years), and 32% had at least 5 comorbidities. The average length of follow-up was 1.1 years (standard deviation = 0.9). The most prevalent comorbidities were hypertension (70.8%) and anemia (29.4%). Femoral neck fractures (54.6%) were the most common fracture type. Hemiarthroplasty was the most common procedure (33.1%). Most fractures were treated by medium-volume (10 to 29 cases per year) surgeons (68.4%) at high-volume (≥ 130 cases per year) facilities (63.0%). The 90-day readmission rate was 22.1%, and the mortality rate was 12.3%. The most common postoperative complications were pneumonia (11.4%) and pressure ulcers (2.9%). There were 2.2 revisions per 100 observation years. Conclusion: A hip fracture registry provides important information regarding patient characteristics, intraoperative practices, and postoperative outcomes, which can be analyzed, interpreted, and used to reduce morbidity and mortality. INTRODUCTION In the US, 306,000 hip fractures occurred in 2010.1 By 2040, it is estimated there will be 500,000 hip fractures per year.2 Most hip fractures occur among the elderly for whom complications are common and often life threatening. The morbidity and mortality associated with hip fractures is substantial, with reported mortality rates of 16% to 23% within 1 year after injury.3-5 Although the incidence of hip fractures may be on the decline, the cost associated with the treatment of hip fractures, which is among the most costly orthopedic procedures,6 continues to grow.7,8 The high morbidity, mortality, and cost associated2-6 with hip fractures emphasizes the need to monitor the outcomes of these patients, identify risk factors associated with adverse events, and evaluate the comparative effectiveness of techniques and implants for this high-risk population. These opportunities for care improvement can significantly reduce morbidity and mortality associated with these events and can reduce cost. Patient registries are one potential tool for monitoring outcomes in a real-world setting. In orthopedic surgery, arthroplasty registries introduced in the 1970s have led to a reduction in revision rates by providing feedback to surgeons on specific implants and techniques.9,10 National arthroplasty registries have also been critical in early identification of defective implants,11-13 including one of the most costly orthopedic recalls to date, the DePuy ASR hip system recall.14 Although the US does not yet have a fully functional national arthroplasty registry, institutional and regional registries have contributed to increased patient safety, quality improvement, identification of clinical best practices, and cost reduction.15,16 Hip fractures are captured by arthroplasty registries in some European countries,17-19 Australia,12 New Zealand,20 and Canada.21 In countries such as Norway,22 Sweden,23 and the United Kingdom (UK),24 dedicated hip fracture registries exist. These hip fracture registries monitor all procedures used to treat these events.22-24 In the US, singleinstitution studies and large-scale administrative databases have provided data for evaluation of hip fracture outcomes.25 Although these databases and claims data provide important information, some gaps in knowledge remain because these data sources contain limited detail, inaccurate codes, and unvalidated outcomes. To help fill this gap, Kaiser Permanente (KP), the largest US integrated health care system, developed the Hip Fracture Registry. The registry is intended to serve as a quality surveillance tool, and to monitor patients who undergo a surgical procedure because of a hip fracture. Maria C S Inacio, PhD, is an Epidemiologist in the Surgical Outcomes and Analysis Department at Kaiser Permanente in San Diego, CA. E-mail: [email protected]. Jennifer M Weiss, MD, is an Orthopedic Surgeon at the Sunset Medical Center in Los Angeles, CA. E-mail: [email protected]. Alex Miric, MD, is an Orthopedic Surgeon at the Sunset Medical Center in Los Angeles, CA. E-mail: [email protected]. Jessica J Hunt, MA, is a Clinical Project Manager in the Surgical Outcomes and Analysis Department at Kaiser Permanente in San Diego, CA. E-mail: [email protected]. Gary L Zohman, MD, is an Orthopedic Surgeon at the Orange County Medical Center in CA. E-mail: [email protected]. Elizabeth W Paxton, MA, is the Director of the Surgical Outcomes and Analysis Department at Kaiser Permanente in San Diego, CA. E-mail: [email protected]. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 29 ORIGINAL RESEARCH & CONTRIBUTIONS A Community-Based Hip Fracture Registry: Population, Methods, and Outcomes It includes information on patient characteristics, surgical procedures, morbidity and mortality, and characteristics of both the surgeon and the hospital. The purpose of this report is to provide an overview of the methods used by the KP Hip Fracture Registry and to describe the population and outcomes of patients registered during the first three years (2009-2011). if they performed 10 to 29 cases per year, and high volume if they performed 30 or more cases per year. The average annual hospital volume was also captured by the Hip Fracture Registry. Hospitals were considered low volume if they treated fewer than 60 cases per year, medium volume if 60 to 129 cases per year, and high volume if 130 or more cases per year. METHODS Setting and Population Outcomes KP is an integrated health care system that covers more than 9.5 million individuals throughout 7 US geographic Regions. This integrated health care system provides medical services, owns hospitals, employs its clinicians, and provides patients with health insurance, ensuring a captured and stable population. Additionally, a comprehensive integrated electronic medical record (EMR) is used by the system (with full implementation in 2008), allowing monitoring of patients’ activities using unique identifiers. The KP membership has been shown to be mostly demographically and socioeconomically representative of the largest geographic areas it covers.26,27 The registry’s target population is patients with fractures of the femoral neck, intertrochanteric region, or subtrochanteric region, which comprise nearly all operative, low-energy, fragility-type fractures in the elderly population. Pelvic, acetabular, distal femur, and shaft fractures are not included in the Hip Fracture Registry. This report describes patient information ascertained between January 2009 and December 2011. Data Collection Procedures The Hip Fracture Registry identifies relevant hip fracture cases using International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM), diagnostic and procedure codes recorded into KP’s EMR and administrative claims. All data are extracted electronically on a quarterly schedule and sent to a data repository for data management, validation, and reporting. The Hip Fracture Registry captures data collected from the 7 geographic Regions of the integrated health care system. The patients included in this report are from the 2 largest Regions covered by the Hip Fracture Registry—Northern and Southern California—with 33 Medical Centers and 474 participating surgeons. Variables Characterizing Patients, Surgeries, Surgeons, and Hospitals The Hip Fracture Registry has information related to the patient, procedure, surgeon, and hospital where the hip fracture was treated. Patient variables include age, sex, race, American Society of Anesthesiologists (ASA) score,28 comorbidities,29 and body mass index. Procedure variables include laterality and stipulate whether an open or closed reduction with internal fixation, internal fixation of bone without fracture reduction, hemiarthroplasty (partial hip replacement), or total hip arthroplasty was used to treat the hip fracture. Surgeon variables include information about total joint arthroplasty fellowship training as well as average annual volume of hip fracture surgical cases. Surgeons were classified as low volume if they performed fewer than 10 cases per year, medium volume 30 The Hip Fracture Registry monitors 10 outcomes associated with hip fractures. These outcomes are length of stay (LOS), any readmissions within 30 and 90 days, pneumonia, pressure ulcers, dislocations, myocardial infarction, surgical site infections (deep and superficial), thromboembolic events (deep vein thrombosis [DVT] and pulmonary embolism [PE]), revisions, and mortality. Except for LOS and mortality, the outcomes were captured using ICD-9-CM diagnosis and procedure codes recorded into the EMR and administrative claims.30,31 The outcomes of revisions, surgical site infections, DVTs, and PEs were adjudicated by clinical content experts who reviewed the patient charts. The other outcomes were ascertained using only administrative and EMR data. Table 1. Characteristics of primary hip fracture cohort (N = 12,562) Characteristic Age, yearsa < 65 65-74 75-84 ≥ 85 Sex Female Male Unknown ASA category 1 and 2 ≥3 Unknown Diabetes Race/ethnicityb White Hispanic Asian Black Unknown Multiracial Other Native American Continous variables Median age, years Median BMI,c kg/m2 No. (%) 1645 (13.1) 1922 (15.3) 4354 (34.7) 4639 (36.9) 8611 (68.6) 3947 (31.4) 4 (< 0.1) 3143 (25.0) 828 (65.9) 113 (9.1) 3392 (27.0) 9772 (77.8) 1241 (9.9) 719 (5.7) 624 (5.0) 70 (0.6) 63 (0.5) 49 (0.4) 24 (0.2) 82 (73-87) 23.7 (20.8-27.2) Missing data in < 0.1% (n = 1). Percentages total to more than 100% because of rounding. Missing data in 0.7% (n = 92). ASA = American Society of Anesthesiologists; BMI = body mass index. a b c The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS A Community-Based Hip Fracture Registry: Population, Methods, and Outcomes Revisions are defined as an operation that required any implant exchange after the primary hip fracture procedure. Revisions are tracked for the lifetime of the patient. Surgical site infections are adjudicated using the guidelines of the Centers for Disease Control and Prevention’s National Healthcare Safety Network; they include superficial infections that occur within 30 days and deep infections that occur within 1 year after an implant procedure.32 Death information was available for all patients (with possible delayed reporting) using data from the Social Security Administration updated with information recorded into the EMR. Statistical Analysis Descriptive statistics, including frequencies, proportions, means, standard deviations (SDs), medians, and interquartile ranges (IQRs), were computed using the software program SAS 9.2 (SAS Institute Inc, Cary, NC). Crude complication rates for all outcomes captured by the registry were provided as proportions of events, with the entire hip fracture population being included in the denominator. Revision density, which is the rate of revision per 100 years of observation, was also provided. Patients were considered lost to follow-up if they disenrolled from the integrated health care system or died during the study period. RESULTS Characteristics of Patients Between 2009 and 2011, a total of 12,562 primary hip fractures were registered in the Hip Fracture Registry. The median age of the population was 82 (IQR = 73-87) years old, 68.6% were women, and 77.8% were white. See Table 1 for detailed population characteristics. Only 5.7% of the population had no comorbidities at the time of hip fracture, and most had multiple comorbidities (Table 2). The most common comorbidities were hypertension (70.8%), deficiency anemia (29.4%), renal failure (25.2%), fluid and electrolyte disorders (22.0%), chronic pulmonary disease (21.4%), and peripheral vascular disease (20.0%). Table 3 presents the detailed fracture type and procedures for the population. The most prevalent fracture types were femoral neck fractures (43%) followed by closed intertrochanteric femoral neck fractures (36.0%). The most common procedures for hip fracture treatment were hemiarthroplasty (33.1%), open reduction of fracture with internal fixation (29.7%), and closed reduction of fracture with internal fixation (23.8%). Outcomes after Hip Fractures The median LOS at hospitals for patients with a hip fracture was 4 days (IQR = 3-6 days). Within 90 days of the primary hip fracture, 22.1% of patients were readmitted to the hospital and 12.3% died. The most common complication in this population was pneumonia (11.4%), followed by pressure ulcers (2.9%), and DVT (1.4%). Revisions occurred in 2.4% of patients (or 2.2 revisions/100 years of observation). The average follow-up duration for patients was 1.1 years (SD = 0.9), and 2.6% were lost to follow-up (Table 4). The Permanente Journal/ Summer 2015/ Volume 19 No. 3 Participating Hospitals and Surgeons Of the 12,562 hip fractures, 13.7% were treated by surgeons with joint arthroplasty fellowship training. The median number of hip fracture cases a surgeon treated yearly was 18 (IQR = 13-24), and most surgeons were considered medium volume (10 to 29 cases per year; 68.4%; Table 5). The median number of cases per hospital treated yearly was 167 (IQR = 114-219), and most of the cases were treated in high-volume hospitals (63.0%; Table 5). Table 2. Comorbidity profile of primary hip fracture cohort Comorbidity parameter Total number in cohort Comorbidities (at least 1) Number of comorbiditiesa 0 1 2 3 4 ≥5 Specific conditionsb AIDS Alcohol abuse Chronic blood loss anemia Chronic pulmonary disease Coagulopathy Congestive heart failure Deficiency anemias Depression Drug abuse Fluid and electrolyte disorders Hypertension Hypothyroidism Liver disease Lymphoma Metastatic cancer Other neurologic disorders Paralysis Peptic ulcer disease, bleeding Peripheral vascular disease Psychoses Pulmonary circulation disease Renal failure Rheumatoid arthritis/collagen vascular disease Solid tumor without metastasis Valvular disease Weight loss No. (%) 12,562 (100.0) 11,648 (92.7) 716 (5.7) 1395 (11.1) 1976 (15.7) 2242 (17.9) 2068 (16.5) 3967 (31.6) 25 (0.2) 498 (4.0) 485 (3.9) 2685 (21.4) 961 (7.7) 1943 (15.5) 3696 (29.4) 1063 (8.5) 114 (0.9) 2769 (22.0) 8887 (70.8) 2462 (19.6) 331 (2.6) 165 (1.3) 461 (3.7) 2201 (17.5) 629 (5.0) 7 (0.1) 2515 (20.0) 1513 (12.0) 593 (4.7) 3162 (25.2) 529 (4.2) 381 (3.0) 1381 (11.0) 1598 (12.7) Missing data in 1.6% (n = 198). Elixhauser comorbidity measures. Diabetes and obesity are omitted from this list because they are obtained from different sources. Diabetes data are obtained from regional diabetic registries, and obesity data are obtained from body mass index measurements. Both comorbidities are included in Table 1. AIDS = acquired immunodeficiency syndrome. a b 31 ORIGINAL RESEARCH & CONTRIBUTIONS A Community-Based Hip Fracture Registry: Population, Methods, and Outcomes DISCUSSION A Hip Fracture Registry was established to capture detailed information on hip fractures treated surgically in the KP integrated health care system. The current registered cohort was treated by 474 surgeons across 33 hospitals. The population identified by this registry is similar to the populations captured in other hip fracture registries, but some important differences were identified. Operative practices and outcomes associated with procedures differ in certain instances from those previously reported in the literature. Patients included in the registry were mostly women, elderly, white, and had multiple comorbid conditions. Women constituted 68.6% of the population, which is similar to the 70% figure reported by other registries12,18,22-24 and agrees Table 3. Patient-specific diagnosis and procedure type in primary hip fracture cohorta Diagnostic codes Total Fracture type Intracapsular (733.14, 820.00, 820.01, 820.02, 820.03, 820.09) Extracapsular (820.20, 820.21, 820.22, 821.00) Other/cannot be determined (820.8, other) ICD-9 code specific 733.14: Pathologic fracture neck of femur 820.00: Fracture, femur neck; closed; intracapsular section, unspecified 820.01: Fracture, femur neck; closed; epiphysis (separation) (upper), transepiphyseal 820.02: Fracture, femur neck; closed; midcervical section, transcervical NOS 820.03: Fracture, femur neck; closed; base of neck, cervicotrochanteric section 820.09: Fracture, femur neck; closed; other, head of femur, subcapital 820.20: Fracture, femur neck; pertrochanteric, closed; trochanteric section, unspecified, trochanter: NOS, greater, lesser 820.21: Fracture, femur neck; pertrochanteric, closed; intertrochanteric section 820.22: Fracture, femur neck; pertrochanteric, closed; subtrochanteric section 820.8: Fracture; unspecified part of neck of femur, closed, hip NOS, neck of femur NOS 821.00: Fracture; closed; unspecified part of femur, thigh, upper leg Other diagnosis Total, No. (%) 12,562 (100.0) Hemiarthroplasty (code 81.52), No. (%) 4163 (33.1) Internal fixation, with open reduction of fracture (code 79.35), No. (%) 3731 (29.7) Internal fixation, with closed reduction of fracture (code 79.15), No. (%) 2989 (23.8) Internal fixation, without fracture reduction (code 78.55), No. (%) 1127 (9.0) Total hip arthroplasty (code 81.51), No. (%) 270 (2.1) Other, No. (%) 282 (2.2) 2603 (20.7) 1317 (31.6) 347 (9.3) 510 (17.1) 285 (25.3) 82 (30.4) 62 (22.0) 5671 (45.2) 147 (3.5) 2995 (80.3) 1880 (62.9) 543 (48.2) 21 (7.8) 85 (30.1) 4288 (34.1) 2699 (64.8) 389 (10.4) 599 (20.0) 299 (26.5) 167 (61.9) 135 (47.9) 665 (5.3) 248 (6.0) 151 (4.1) 114 (3.8) 117 (10.4) 15 (5.6) 20 (7.1) 78 (0.6) 50 (1.2) 3 (0.1) 16 (0.5) 4 (0.4) 2 (0.7) 3 (1.1) 50 (0.4) 0 (0.0) 4 (0.1) 1 (0.0) 21 (1.9) 0 (0.0) 24 (8.5) 118 (0.9) 81 (2.0) 5 (0.1) 26 (0.9) 3 (0.3) 3 (1.1) 0 (0.0) 260 (2.1) 112 (2.7) 73 (2.0) 38 (1.3) 24 (2.1) 11 (4.1) 2 (0.7) 1432 (11.4) 826 (19.8) 111 (3.0) 315 (10.5) 116 (10.3) 51 (18.9) 13 (4.6) 286 (2.3) 17 (0.4) 164 (4.4) 66 (2.2) 26 (2.3) 2 (0.7) 11 (3.9) 4517 (36.0) 123 (3.0) 2338 (62.7) 1602 (53.6) 411 (36.5) 16 (5.9) 27 (9.6) 706 (5.6) 6 (0.1) 414 (11.1) 205 (6.9) 68 (6.0) 2 (0.7) 11 (3.9) 3964 (31.6) 2550 (61.3) 343 (9.2) 568 (19.0) 264 (23.4) 162 (60.0) 77 (27.3) 162 (1.3) 1 (0.0) 79 (2.1) 7 (0.2) 38 (3.4) 1 (0.4) 36 (12.8) 324 (2.6) 149 (3.6) 46 (1.2) 31 (1.0) 35 (3.1) 5 (1.9) 58 (20.6) Some percentages may not total to 100 because of rounding. ICD-9 = International Classification of Diseases, Ninth Revision; NOS = not otherwise specified. a 32 The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS A Community-Based Hip Fracture Registry: Population, Methods, and Outcomes with the higher incidence of hip fractures in women around the world.25 Of the registered patients, nearly 72% were age 75 years or older. This higher age is consistent with that of the population of hip fracture registries in Norway and the UK,22,24 but it is slightly younger than reported by arthroplasty registries. The Australian arthroplasty registry reported that in its bipolar hemiarthroplasty cohort at least 76% were age 75 years or older and 92% of its monoblock cohort was older than 75 years. This elderly population is consistent with the higher risk of hip fractures in older patients.25 Racial and ethnicity data, which are available in our patient population (21.7% of the population is nonwhite), were not available in other hip fracture registries and are most likely not captured data elements because of their countries’ homogenous populations. This adds value to future findings from the presented registry, which can contribute information regarding minority groups. Finally, 65.9% of the patients had an ASA score greater than 3, indicating substantial systemic disease, which is similar to the rate reported by the UK registry between 2011 and 2013 (approximately 60%).24 The proportion of patients with higher ASA score, however, was higher than reported by the Norwegian Hip Fracture Register (47%),22 which could be because of their inclusion of younger patients in their registry. We also found a high number of comorbid conditions in our patient population; 92.7% had at least 1 comorbid condition, and conditions such as hypertension, deficiency anemias, renal failure, and fluid and Racial and electrolyte disorders were common at the time of ethnicity data, the hip fracture hospitalization. Other registries … available did not report on specific comorbid conditions, in our patient but a high prevalence of comorbid conditions has population (21.7% been reported by studies using administrative data are nonwhite), in the US.2,33 were not available The most common type of fractures in our population was intertrochanteric femoral neck in other hip fracture (36%, ICD-9-CM 820.21) and unspecifracture registries fied femoral neck fractures (31.6%, ICD-9-CM and … adds value 820.8). Because the registry relies on ICD-9-CM … regarding codes for identifying type of fracture, it cannot minority groups. determine with certainty whether cases with unspecified location fracture codes are intracapsular vs extracapsular, or displaced vs undisplaced fractures. It can, however, determine the main treatment groups from the combination of ICD-9-CM procedure codes and diagnoses. Table 4. Postoperative outcomes of primary hip fracture cohort by procedure typea Hemiarthroplasty (code 81.52), Postoperative outcome Total, No. (%) No. (%) Total 12,562 (100.0) 4163 (33.1) Mortality, utilization, and outcomes identified with administrative/EMR data Death within 30 days 783 (6.2) 291 (7.0) Death within 90 days 1546 (12.3) 563 (13.5) Death (ever) 3278 (26.1) 1160 (27.9) Readmission within 30 days 1532 (12.2) 568 (13.6) Readmission within 90 days 2775 (22.1) 978 (23.5) Pneumonia 1427 (11.4) 496 (11.9) Pressure ulcers 365 (2.9) 141 (3.4) Dislocation 114 (0.9) 89 (2.1) Myocardial infarction 110 (0.9) 27 (0.7) Median length of stay, days (IQR)b 4 (3-6) 4 (4-6) Validated outcomesc Revision (all cause) 305 (2.4) 102 (2.5) Septic revision 32 (0.3) 23 (0.6) Revision rate per 100 years 1342 (2.2) 4506 (2.3) of observation Deep vein thrombosis 173 (1.4) 65 (1.6) Pulmonary embolism 156 (1.2) 59 (1.4) Surgical site infection (any) 136 (1.1) 77 (1.9) Surgical site infection (deep) 75 (0.6) 47 (1.1) Surgical site infection (superficial) 61 (0.5) 30 (0.7) Internal fixation, with open reduction of fracture (code 79.35), No. (%) 3731 (29.7) Internal fixation, with closed reduction of fracture (code 79.15), No. (%) 2989 (23.8) Internal fixation, without fracture reduction (code 78.55), No. (%) 1127 (9.0) Total hip arthroplasty (code 81.51), No. (%) 270 (2.1) Other, No. (%) 282 (2.2) 240 (6.4) 481 (12.9) 1002 (26.9) 459 (12.3) 840 (22.5) 441 (11.8) 117 (3.1) 3 (0.1) 29 (0.8) 4 (3-6) 171 (5.7) 340 (11.4) 744 (24.9) 328 (11.0) 630 (21.1) 333 (11.1) 67 (2.2) 1 (0.0) 35 (1.2) 4 (3-5) 61 (5.4) 127 (11.3) 293 (26.0) 145 (12.9) 261 (23.2) 117 (10.4) 25 (2.2) 5 (0.4) 16 (1.4) 4 (3-5) 5 (1.9) 13 (4.8) 35 (13.0) 18 (6.7) 43 (15.9) 24 (8.9) 9 (3.3) 9 (3.3) 3 (1.1) 4 (3-6) 15 (5.3) 22 (7.8) 44 (15.6) 14 (5.0) 23 (8.2) 16 (5.7) 6 (2.1) 7 (2.5) 0 (0.0) 3 (1-5) 81 (2.2) 3 (0.1) 4173 (1.9) 78 (2.6) 1 (0.0) 3216 (2.4) 29 (2.6) 1 (0.1) 1208 (2.4) 7 (2.6) 1 (0.4) 288 (2.4) 8 (2.8) 3 (1.1) 360 (2.2) 57 (1.5) 43 (1.2) 27 (0.7) 12 (0.3) 15 (0.4) 25 (0.8) 33 (1.1) 15 (0.5) 7 (0.2) 8 (0.3) 12 (1.1) 13 (1.2) 6 (0.5) 1 (0.1) 5 (0.4) 8 (3.0) 5 (1.9) 5 (1.9) 3 (1.1) 2 (0.7) 6 (2.1) 3 (1.1) 6 (2.1) 5 (1.8) 1 (0.4) Some percentages do not total to 100 because of rounding. Codes are from the International Classification of Diseases, Ninth Revision, Clinical Modification. Missing data in 1.3% (n = 164). c Only crude estimates of incidence are presented. No adjustments for confounders, loss to follow-up, or follow-up time are included (with the exception of the revision rate per 100 years of observation). EMR = electronic medical record; IQR = interquartile range. a b The Permanente Journal/ Summer 2015/ Volume 19 No. 3 33 ORIGINAL RESEARCH & CONTRIBUTIONS A Community-Based Hip Fracture Registry: Population, Methods, and Outcomes Table 5. Surgeon and hospital characteristics in primary hip fracture cohort (N = 12,562) Characteristic Joint arthroplasty fellowship training Yes No Unknown Surgeon volume category, average per yeara Low (< 10) Medium (10-29) High (≥ 30) Surgeon yearly volume, median (IQR)a Hospital volume category, average per year Low (< 60) Medium (60-129) High (≥ 30) Hospital yearly volume, median (IQR) No. of surgeries (%) 1728 (13.7) 5284 (42.1) 5550 (44.2) 1520 (12.1) 8590 (68.4) 2450 (19.5) 18 (13-24) 207 (1.7) 4439 (35.3) 7916 (63.0) 167 (114-219) Missing data in < 0.1% (n = 2). IQR = Interquartile range. a By our estimates, at least 43% (n = 5315) of our registered fractures are intracapsular fractures (2603 from diagnostic codes only and 2712 from the procedures and diagnoses combined), making this the most common type of fracture in our registry, which is in agreement with other registries where a traditional fracture classification is used. In Sweden, the UK, and Norway the reported prevalence of intracapsular fractures is 54%, 58%, and 63%, respectively. The most common procedures used to treat fractures were internal fixation and hemiarthroplasty, in agreement with other registries’ populations. Overall, 33.1% of the cases in our population were treated with hemiarthroplasty, which is slightly higher than the overall numbers of 25% reported by Sweden and 21% by Norway (no overall numbers available for the UK).22-24 Hemiarthroplasty is the most common procedure used for treatment of intracapsular fractures in our population (93% had a hemiarthroplasty), and it is also the most commonly used procedure to address intracapsular fractures in other registries, although only for displaced intracapsular fractures (53% Norway, 63% Sweden, and 77.5% UK).22-24 For the second most common fracture in our population, intertrochanteric femur neck fractures (36%), 96% were treated with internal fixation: 9% without fracture reduction, 35% with closed reduction, and 52% with open reduction. This again agrees with the reported internal fixation rate for these types of fracture in the UK, Sweden, and Norway (all > 95%).22-24 Finally, the use of total hip arthroplasty for addressing hip fractures is infrequent (2.1%), and this rate agrees with the small proportions seen by other registries (range = 1.1%-5%). Medium- and high-volume surgeons (89.7%) and hospitals (98.3%) treat the majority of the hip fractures in our population. This information is not available in the reports of other dedicated hip fracture registries. The proportion of patients treated in high volume (63%) hospitals is, however, 34 similar to those reported by studies using Medicare data (approximately 60% consistently from 1991 to 2008).5 Previous studies evaluating the outcomes of hip fracture treatment by hospital and surgeon volume suggest surgeon volume is an important factor when evaluating hip fracture outcomes, but hospital volume may not be as important.5 Ten postoperative outcomes were available in the KP Hip Fracture Registry. Mortality, LOS, pressure ulcers, and repeated operations (“reoperations”) are the common outcomes monitored by the dedicated fracture registries. The incidence of mortality in our population within 30 days was 6.2%; this is comparable to mortality in the Norwegian registry (only a 4-month estimate is available and is 14%)22 and is slightly lower than in the UK registry (8%).24 This is also consistent with contemporary estimates from the US Medicare population of 5% to 6%.2,34 The LOS in our cohort was much shorter (median = 4 days) than that reported by other registries (range = 11-16 days)23,24 but was similar to the LOS in the US Medicare hip fracture cohort.2,34 Differences in LOS are probably because of the overall health care system structure and hip fracture care practices in the various countries. Pressure ulcers occurred in 2.9% of our population, which is comparable to the 3.7% reported by the UK hip fracture registry.24 Finally, the only reoperations monitored by our registry are subsequent revision procedures (defined as a surgery where one component is either removed and/or replaced for any reason) of the original hip fracture components, which we found occur at a rate of 2.2/100 years of observation (2.4% crude overall revision incidence). This rate is significantly lower than the 18% reoperation rate reported by the Norwegian Hip Fracture Register, probably because they track all subsequent reoperations and not just revisions.22 Complications related to the hip fractures such as pneumonia, myocardial infarction, DVT, PE, dislocations, and surgical site infections also are monitored by this registry but not by others. These complications, except for pneumonia, were infrequent (< 1.4%), an incidence that is mostly consistent with reports from other large hip fracture cohorts.33,35-39 Pneumonia was the most common complication in our population (11.4%) and was higher than the 5% reported by a meta-analysis of clinical trials by Lawrence et al.35 This higher incidence in our cohort could be caused by our use of administrative data to ascertain the cases without validating them with other records, which was probably done by the clinical trials included in the meta-analysis study. This report’s main limitation is the reliance of its data source, the KP Hip Fracture Registry, on ICD-9-CM diagnostic and procedure codes to determine fracture location and procedures performed to address these fractures. Information on whether the fractures were displaced or nondisplaced was not available. Additionally, confirmation of whether they were located in the intracapsular or extracapsular area was not possible in all cases. The Hip Fracture Registry leverages the existing system’s EMR and administrative data sources to capture all hip fractures in the system. This is done instead of relying on the surgeon to report, which would not achieve full capture of this population. The tradeoff for full case capture means the Hip Fracture Registry has limited fracture location The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS A Community-Based Hip Fracture Registry: Population, Methods, and Outcomes information. In addition, procedure codes do not offer information on specific types of hemiarthroplasty procedures (bipolar or unipolar) or internal fixation (whether screws only, screws and plates, or intramedullary rods were used). However, this limitation is currently being addressed by the Hip Fracture Registry by implementing procedure classification on the basis of the collected implant information from the procedure. This work is under development, but we hope to include it in future reports on the registry’s cohort. Other limitations were a lack of certain comorbidity information, such as osteoporosis and intestinal disorders, which were not captured by the validated comorbidity algorithm used by the registry. Additionally, this report was descriptive and did not evaluate relationships between specific variables and outcomes associated with hip fracture procedures. No inferences can be made regarding the outcomes and specific treatments presented in this report. Our report strengths include the description of a fully captured hip fracture population in a large and diverse integrated health care system in the US. Using unique identifiers and the EMR, the Hip Fracture Registry captured the full spectrum of care delivered to these patients after surgery and prospectively monitored several outcomes associated with these events in addition to the traditional outcomes tracked by other studies and registries. Some of the outcomes monitored (ie, surgical site infection, DVT, PE, reoperation, and revision surgery) are also adjudicated using additional sources, which guarantees a high internal validity for these data elements. Additionally, because data for the Hip Fracture Registry are captured electronically, possible response bias introduced by relying on clinicians to report events and complete the required registry information was nonexistent. Finally, the population captured included cases from a large number of hospitals and surgeons with a wide variety of surgical experience, which is representative of the larger orthopedic community. CONCLUSION A community-based registry of hip fractures was used to identify a contemporaneous cohort of patients with hip fractures who were mostly women, elderly, and white, with substantial multimorbidity. The KP Hip Fracture Registry population was treated predominantly with internal fixations or hemiarthroplasty procedures, which were performed primarily in high-volume hospitals by medium-volume surgeons. The incidence of 30-day mortality, readmission, and pneumonia was high in this patient population, and the incidence of other monitored complications was relatively low. Using a hip fracture registry to understand patients and procedures performed to treat hip fractures, as well as the possible complications and outcomes associated with these events, can give orthopedic clinicians a major advantage in planning for the care of these patients. v Disclosure Statement The author(s) have no conflicts of interest to disclose. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 Acknowledgment We acknowledge all the Kaiser Permanente orthopedic surgeons who contribute to the National Implant Registries and the Surgical Outcomes and Analysis Department, which coordinates Registry operations. Kathleen Louden, ELS, of Louden Health Communications provided editorial assistance. References 1. National hospital discharge survey [Internet]. Atlanta, GA: Centers for Disease Control and Prevention, National Center for Health Statistics; 2013 [updated 2015 Feb 12; cited 2014 Jan 23]. Available from: www.cdc.gov/nchs/data/ nhds/2average/2010ave2_firstlist.pdf. 2. Brauer CA, Coca-Perraillon M, Cutler DM, Rosen AB. Incidence and mortality of hip fractures in the United States. JAMA 2009 Oct 14;302(14):1573-9. DOI: http://dx.doi.org/10.1001/jama.2009.1462. 3. Blomfeldt R, Törnkvist H, Ponzer S, Söderqvist A, Tidermark J. Comparison of internal fixation with total hip replacement for displaced femoral neck fractures. Randomized, controlled trial performed at four years. J Bone Joint Surg Am 2005 Aug;87(8):1680-8. DOI: http://dx.doi.org/10.2106/JBJS.D.02655. 4. Blomfeldt R, Törnkvist H, Ponzer S, Söderqvist A, Tidermark J. Displaced femoral neck fracture: comparison of primary total hip replacement with secondary replacement after failed internal fixation: a 2-year follow-up of 84 patients. Acta Orthop 2006 Aug;77(4):638-43. DOI: http://dx.doi. org/10.1080/17453670610012728. 5. Miller BJ, Lu X, Cram P. The trends in treatment of femoral neck fractures in the Medicare population from 1991 to 2008. J Bone Joint Surg Am 2013 Sep 18;95(18):e132. DOI: http://dx.doi.org/10.2106/JBJS.L.01163. 6. Elixhauser A, Andrews RM. Profile of inpatient operating room procedures in US hospitals in 2007. Arch Surg 2010 Dec;145(12):1201-8. DOI: http://dx.doi. org/10.1001/archsurg.2010.269. 7. Adams AL, Shi J, Takayanagi M, Dell RM, Funahashi TT, Jacobsen SJ. Ten-year hip fracture incidence rate trends in a large California population, 1997-2006. Osteoporos Int 2013 Jan;24(1):373-6. DOI: http://dx.doi.org/10.1007/s00198012-1938-5. 8. Crisp A, Dixon T, Jones G, et al. Declining incidence of osteoporotic hip fracture in Australia. Arch Osteoporos 2012;7(1-2):179-85. DOI: http://dx.doi. org/10.1007/s11657-012-0095-y. 9. Herberts P, Malchau H. Long-term registration has improved the quality of hip replacement: a review of the Swedish THR Register comparing 160,000 cases. Acta Orthop Scand 2000 Apr;71(2):111-21. DOI: http://dx.doi. org/10.1080/000164700317413067. 10. Labek G, Janda W, Agreiter M, Schuh R, Böhler N. Organisation, data evaluation, interpretation and effect of arthroplasty register data on the outcome in terms of revision rate in total hip arthroplasty. Int Orthop 2011 Feb;35(2): 157-63. DOI: http://dx.doi.org/10.1007/s00264-010-1131-4. 11. Konan S, Haddad FS. Joint registries: a Ptolemaic model of data interpretation? Bone Joint J 2013 Dec;95-B(12):1585-6. DOI: http://dx.doi.org/10.1302/0301620X.95B12.33353. 12. Australian Orthopedic Association national joint replacement registry. Hip and knee arthroplasty: 2014 annual report [Internet]. Adelaide, South Australia, Australia: Australian Orthopaedic Association; 2014 [cited 2014 Nov 3]. Available from: https://aoanjrr.dmac.adelaide.edu.au/documents/10180/172286/ Annual%20Report%202014. 13. Smith AJ, Dieppe P, Vernon K, et al. Failure rates of stemmed metal-on-metal hip replacements: analysis of data from the National Joint Registry of England and Wales. Lancet 2012 Mar 31;379(9822):1199-204. DOI: http://dx.doi. org/10.1016/S0140-6736(12)60353-5. 14. Cohen D. Out of joint: the story of the ASR. BMJ 2011 May 13;342:d2905. DOI: http://dx.doi.org/10.1136/bmj.d2905. 15. Gioe TJ, Killeen KK, Mehle S, Grimm K. Implementation and application of a community total joint registry: a twelve-year history. J Bone Joint Surg Am 2006 Jun;88(6):1399-404. DOI: http://dx.doi.org/10.2106/JBJS.E.01198. 16. Paxton EW, Inacio MC, Kiley ML. The Kaiser Permanente implant registries: effect on patient safety, quality improvement, cost effectiveness, and research opportunities. Perm J 2012 Spring;16(2):36-44. DOI: http://dx.doi.org/10.7812/ TPP/12-008. 17. Garellick G, Rogmark C, Kärrholm J, Rolfson O. Swedish hip arthroplasty register: annual report 2012 [Internet]. Gothenburg, Sweden: Swedish Hip Arthroplasty Register; 2012 [cited 2014 Oct 31]. Available from: www.shpr.se/ Libraries/Documents/AnnualReport_2012_Eng_WEB.sflb.ashx. 18. Stea S, Bordini B, De Clerico M, Petropulacos K, Toni A. First hip arthroplasty register in Italy: 55,000 cases and 7 year follow-up. Int Orthop 2009 Apr;33(2):339-46. DOI: http://dx.doi.org/10.1007/s00264-007-0465-z. 35 ORIGINAL RESEARCH & CONTRIBUTIONS A Community-Based Hip Fracture Registry: Population, Methods, and Outcomes 19. National joint registry for England and Wales: 7th annual report 2010 [Internet]. Hemel Hempstead, England: National Joint Registry; 2010 [cited 2011 Jul 6]. Available from: www.njrcentre.org.uk/NjrCentre/LinkClick.aspx?fileticket=QkPI7k k6B2E%3d&tabid=86&mid=523. 20. The New Zealand joint registry. Fourteen year report: January 1999 to December 2012 [Internet]. Wellington, New Zealand: New Zealand Orthopaedic Association; 2013 Nov [cited 2014 Oct 31. Available from: www.nzoa.org.nz/ system/files/NJR%2014%20Year%20Report.pdf. 21. Sayana MK, Lakshmanan P, Peehal JP, Wynn-Jones C, Maffulli N. Total hip replacement for acute femoral neck fracture: a survey of National Joint Registries. Acta Orthop Belg 2008 Feb;74(1):54-8. Erratum in: Acta Orthop Belg 2008 Dec;74(6):890. 22. Gjertsen JE, Engesaeter LB, Furnes O, et al. The Norwegian Hip Fracture Register: experiences after the first 2 years and 15,576 reported operations. Acta Orthop 2008 Oct;79(5):583-93. DOI: http://dx.doi. org/10.1080/17453670810016588. 23. Thorngren KG. National registration of hip fractures in Sweden. In: Bentley G, editor. European instructional lectures: volume 9, 2009; 10th EFORT Congress, Vienna, Austria. New York, NY: Springer Science & Business Media, LLC; 2009. DOI: http://dx.doi.org/10.1007/978-3-642-00966-2_2. 24. Falls and Fragility Fracture Audit Programme (FFFAP). National Hip Fracture Database (NHFD) annual report 2014 [Internet]. London, England: Royal College of Physicians; 2014 Sep [cited 2014 Oct 31]. Available from: www.nhfd.co.uk/20/hipfractureR.nsf/vwcontent/2014reportPDFs/$file/ NHFD2014SummaryReport.pdf?OpenElement. 25. Cooper C, Cole ZA, Holroyd CR, et al; IOF CSA Working Group on Fracture Epidemiology. Secular trends in the incidence of hip and other osteoporotic fractures. Osteoporos Int 2011 May;22(5):1277-88. DOI: http://dx.doi. org/10.1007/s00198-011-1601-6. 26. Karter AJ, Ferrara A, Liu JY, Moffet HH, Ackerson LM, Selby JV. Ethnic disparities in diabetic complications in an insured population. JAMA 2002 May 15;287(19):2519-27. DOI: http://dx.doi.org/10.1001/jama.287.19.2519. 27. Koebnick C, Langer-Gould AM, Gould MK, et al. Sociodemographic characteristics of members of a large, integrated health care system: comparison with US Census Bureau data. Perm J 2012 Summer;16(3):37-41. DOI: http://dx.doi.org/10.7812/TPP/12-031. 28. Owens WD, Felts JA, Spitznagel EL Jr. ASA physical status classifications: a study of consistency of ratings. Anesthesiology 1978 Oct;49(4):239-43. DOI: http://dx.doi.org/10.1097/00000542-197810000-00003 [password protected]. 29. Elixhauser A, Steiner C, Harris DR, Coffey RM. Comorbidity measures for use with administrative data. Med Care 1998 Jan;36(1):8-27. DOI: http://dx.doi. org/10.1097/00005650-199801000-00004. 30. Postoperative pulmonary embolism or deep vein thrombosis rate. Patient safety indicators #12: technical specifications [Internet]. Rockville, MD: Agency for Healthcare Research and Quality; 2012 Mar [cited 2012 Aug 31]. Available from: www.qualityindicators.ahrq.gov/Downloads/Modules/PSI/V44/TechSpecs/ PSI%2012%20Postoperative%20PE%20or%20DVT%20Rate.pdf. 31. Inacio MC, Paxton EW, Chen Y, et al. Leveraging electronic medical records for surveillance of surgical site infection in a total joint replacement population. Infect Control Hosp Epidemiol 2011 Apr;32(4):351-9. DOI: http://dx.doi. org/10.1086/658942. 32. Horan TC, Andrus M, Dudeck MA. CDC/NHSN surveillance definition of health care-associated infection and criteria for specific types of infections in the acute care setting. Am J Infect Control 2008 Jun;36(5):309-32. DOI: http:// dx.doi.org/10.1016/j.ajic.2008.03.002. Erratum in: Am J Infect Control 2008 Nov;36(9):655. DOI: http://dx.doi.org/10.1016/j.ajic.2008.10.001. 33. Lawrence VA, Hilsenbeck SG, Noveck H, Poses RM, Carson JL. Medical complications and outcomes after hip fracture repair. Arch Intern Med 2002 Oct 14;162(18):2053-7. DOI: http://dx.doi.org/10.1001/archinte.162.18.2053. 34. Neuman MD, Rosenbaum PR, Ludwig JM, Zubizarreta JR, Silber JH. Anesthesia technique, mortality, and length of stay after hip fracture surgery. JAMA 2014 Jun 25;311(24):2508-17. DOI: http://dx.doi.org/10.1001/ jama.2014.6499. 35. Lawrence VA, Cornell JE, Smetana GW; American College of Physicians. Strategies to reduce postoperative pulmonary complications after noncardiothoracic surgery: systematic review for the American College of Physicians. Ann Intern Med 2006 Apr 18;144(8):596-608. DOI: http://dx.doi. org/10.7326/0003-4819-144-8-200604180-00011. 36. Roche JJ, Wenn RT, Sahota O, Moran CG. Effect of comorbidities and postoperative complications on mortality after hip fracture in elderly people: prospective observational cohort study. BMJ 2005 Dec 10;331(7529):1374. DOI: http://dx.doi.org/10.1136/bmj.38643.663843.55. 37. Rosencher N, Vielpeau C, Emmerich J, Fagnani F, Samama CM; ESCORTE group. Venous thromboembolism and mortality after hip fracture surgery: the ESCORTE study. J Thromb Haemost 2005 Sep;3(9):2006-14. DOI: http://dx.doi. org/10.1111/j.1538-7836.2005.01545.x. 38. Edwards C, Counsell A, Boulton C, Moran CG. Early infection after hip fracture surgery: risk factors, costs and outcome. J Bone Joint Surg Br 2008 Jun;90(6):770-7. DOI: http://dx.doi.org/10.1302/0301-620X.90B6.20194. 39. Duckworth AD, Phillips SA, Stone O, Moran M, Breusch SJ, Biant LC. Deep infection after hip fracture surgery: predictors of early mortality. Injury 2012 Jul;43(7):1182-6. DOI: http://dx.doi.org/10.1016/j.injury.2012.03.029. Fixation I assert that a fractured thigh, if treated by extension only, would be accompanied with vastly more muscular irritability than if the same case was placed in a modern appliance, in which the limb was immoveable in the strict meaning of the term fixation. — Disease of the Hip, Knee and Ankle Joints, Hugh Owens Thomas, MD, 1834-1891, Welsh surgeon who is considered to be the father of orthopaedic surgery in Britain 36 The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS Utility of the Multinational Association for Supportive Care in Cancer (MASCC) Risk Index Score as a Criterion for Nonadmission in Febrile Neutropenic Patients with Solid Tumors Roger A Bitar, MD, MPH Perm J 2015 Summer;19(3):37-47 http://dx.doi.org/10.7812/TPP/14-188 ABSTRACT Objectives: This retrospective study was initiated in febrile neutropenic inpatients with solid tumors in 4 community hospitals, to discover how the Multinational Association for Supportive Care in Cancer (MASCC) risk index score (RIS) of 21 or greater correlated with complications occurring in 198 episodes: whether it could help determine which patients not to admit, the savings of not admitting patients without complications, and whether an algorithm could facilitate management of those not admitted. Methods: Febrile neutropenic episodes in patients with solid tumors were identified electronically between October 1, 2008, and November 15, 2010. Electronic charts were reviewed manually for inclusion criteria and data extraction. Episodes were stratified by an MASCC RIS below 21 or 21 or greater. Complications were correlated with the index. Results: Inclusion criteria were met in 198 episodes. Sensitivity, specificity, and positive and negative predictive values of the MASCC RIS vs complications were 94%, 29.6%, 57.7%, and 82.9%, respectively. In episodes with an RIS 21 or greater, 42.3% had complications, misclassifying to low risk 69 episodes with complications. “Unable to eat” correlated with complications in 84% of episodes. In 3 patients stratified to no complication, a complication developed 24 hours after admission. Conclusions: An MASCC RIS of 21 or greater could not be used as a criterion for “no complication/do not admit.” Inability to eat should be an admission criterion. Savings of approximately $1 million per 100 uncomplicated admissions could be realized if appropriate criteria for nonadmission could be devised. An algorithm to facilitate outpatient management is suggested. INTRODUCTION Treatment of malignancies is routine in community hospitals. Chemotherapy, one of the common forms of treatment, frequently results in neutropenic fever. Guidelines for the management of febrile neutropenia include antimicrobial therapy and, for patients with solid tumors, antecedent granulocyte colony-stimulating factor.1,2 Before these guidelines, virtually all febrile neutropenic patients were hospitalized. However, the depth and duration of neutropenia in patients receiving chemotherapy for hematologic and lymphoproliferative neoplasms is more profound than that occurring following chemotherapy for patients with solid tumors; thus, complications following chemotherapy for solid tumors are less frequent. Some investigators postulated that patients not experiencing complications would not need hospitalization, and thus, they have striven to identify these noncomplicated cases prospectively and manage them on an outpatient basis, resulting in substantial savings. To this end, a stratification tool, the Multinational Association for Supportive Care in Cancer (MASCC) risk index score (RIS) was developed to predict the risk of serious complications. These risk criteria are listed in the Sidebar: Klastersky Criteria.3 There are 2 important features to note. First, only 2 of the 10 Klastersky criteria are objective, which introduces a problem in the methods. There is no objective definition of these criteria: confusion or altered mental state, such as the Glasgow Coma Scale; congestive heart failure requiring treatment, such as pulmonary edema with a Pao2 below 60 mmHg; bleeding severe enough to require transfusion, such as a hemoglobin level below 7 g/dL; arrhythmia or electrocardiographic changes requiring treatment, such as systolic blood pressure (BP) below 90 mmHg; or renal failure requiring treatment, such as a creatinine level above 4 mg/dL. Furthermore, the last criterion is completely subjective: “other complications judged serious and clinically significant by the investigator.” Second, an exclusion to this criterion was included as a footnote: “Viral or fungal, microbiologically documented primary infection during the febrile episode, without any described complication and resolving under therapy, was considered a part of the infectious process and was not considered a serious complication.”3p3040 Table 1 lists the components of the MASCC RIS.3 (Note that only 4 of the 7 criteria are objective. Burden of illness, chronic obstructive pulmonary disease (COPD), and “no dehydration” are not objective criteria.) An MASCC RIS of 21 or above equals a low risk of complications; an MASCC RIS below 21 equals a high risk of complications. Using an MASCC RIS of 21 or greater as low risk, only 6% of a validation group (n = 551) experienced serious complications compared with 39% who had a score below 21. Validation of this index Roger A Bitar, MD, MPH, is a Consultant with Mission Infectious Disease and Infusion Consultants, Inc, in Poway, CA, and a former Infectious Disease Specialist at the San Diego Medical Center. E-mail: [email protected]. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 37 ORIGINAL RESEARCH & CONTRIBUTIONS Utility of the MultinationalAssociation for Supportive Care in Cancer (MASCC) RiskofIndex as a Criterion for Nonadmission in FebrileCare Neutropenic Patients with Solid Utility the Score Multinational Association for Supportive in Cancer (MASCC) RiskTumors Index Score as a Criterion for Nonadmission in Febrile Neutropenic Patients with Solid Tumors METHODS Patient Selection Table 1. Components of the Multinational Association for Supportive Care in Cancer Indexa Clinical characteristic Burden of illness (1 of the 3 options only): No or mild symptoms Moderate symptoms Scoreb 5 3 Severe symptoms 0 No hypotension (systolic BP > 90 mmHg) No chronic obstructive pulmonary disease Solid tumor or no prior fungal infection in patient with hematologic neoplasm 5 4 4 No dehydration (hydration with IV fluids not required) Outpatient at onset of fever Age < 60 years 3 3 2 Burden of illness, no chronic obstructive pulmonary disease, and no dehydration are not objective criteria. Maximum score: 26 (5 + 5 + 4 + 4 + 3 + 3 + 2). Low risk for complication = score ≥ 21; high risk for complication = score < 21. BP = blood pressure; IV = intravenous. a b has been declared in publications from academic (university) medical centers. However, the definitions in all these studies (eg, burden of illness, COPD, or dehydration) were not consistently provided, and the mix of patients with solid vs hematologic and lymphoproliferative neoplasms was not the same, raising the question of whether the results are comparable.4-8 The current retrospective study of inpatients from 4 community hospitals Klastersky criteria1 Systolic blood pressure (BP) < 90 mmHg or need for [vaso]pressor support to maintain BP Arterial oxygen pressure (Pao2) ≤ 60 mmHg while breathing room air or need for mechanical ventilation Intensive care unit admission Disseminated intravascular coagulation Confusion or altered mental state Congestive cardiac failure seen on chest x-ray and requiring treatment Bleeding severe enough to require transfusion Arrhythmia or ECG [electrocardiographic] changes requiring treatment Renal failure requiring investigation and/or treatment with IV [intravenous] fluids, dialysis, or any other intervention Other complications judged serious and clinically significant by the investigator 1. Klastersky J, Paesmans M, Rubenstein EB, et al. The Multinational Association for Supportive Care in Cancer risk index: a multinational scoring system for identifying low-risk febrile neutropenic cancer patients. J Clin Oncol 2000 Aug;18(16):3038-51. 38 was devised to answer the following questions. 1.How many times were the named items in the Klastersky criteria used as reasons for admission to the hospital by the general internists admitting patients? (As noted earlier, when a febrile neutropenic patient with an infection makes initial contact with a health care practitioner for that febrile episode, the Klastersky criteria do not consider that infection a complication, and, in addition, there are unnamed complications in the Klastersky criteria.) 2.Are there additional complications, not listed by name in the Klastersky criteria, that a physician might consider important in the nonadmission decision? 3.Would the course of patients stratified to the low-risk category (MASCC RIS ≥ 21) be without serious complications and, thus, be able to be managed as outpatients (ie, stratified to “Do not admit”)? 4.If inpatients with an MASCC RIS of 21 or higher did experience complications, what were they and on what day of hospitalization did they occur? 5.If the patients with an MASCC RIS of 21 or above were not admitted and experienced complications, what management algorithm could be proposed to identify these complications early? 6.What savings would be realized if all the patients without serious complications were not admitted to the hospital? Management of febrile neutropenic patients, at the time of this study and at the medical centers listed, was admission to the hospital, evaluation in the usual manner with appropriate laboratory tests and imaging studies, administration of granulocyte colony-stimulating factor (89%), and antimicrobial agents. All but 10 patients received acceptable antimicrobial regimens. Charts were retrospectively reviewed for the following inclusion criteria: adult inpatients with solid tumors who became neutropenic (absolute neutrophil count < 500/μL, except for 2 that were 600/uL) after chemotherapy, who were given an admission or discharge diagnosis of neutropenic fever, who had documented fever by self-report or on admission, and who received antimicrobial therapy for neutropenic fever. Patients younger than 18 years and those whose admissions lasted less than 24 hours were excluded. All inpatient electronic medical records of patients admitted to 4 Kaiser Permanente (KP) hospitals in California were searched for drug-induced neutropenia (International Classification of Diseases, Ninth Revision, code 288.0) and feverpresenting conditions classified elsewhere (code 780.61). The hospitals were San Diego Medical Center (admissions from October 1, 2008, to November 15, 2010); Irvine Medical Center and Anaheim Medical Center (Orange County; admissions from October 1, 2008, to April 30, 2010); and Woodland Hills Medical Center (admissions from October 1, 2008, to April 30, 2010). The charts of these patient episodes were sequentially and manually screened for inclusion criteria and reviewed in detail. If inclusion criteria were met, data were extracted. Data included: age, sex, admission date, discharge date, death date, the type of solid tumor, whether it was metastatic beyond local nodes, admitting physician’s reason for admission, length of stay (LOS), reason for extended hospital stay, intensive care unit care, comfort care, other diagnoses in the problem list which might be considered immunocompromising, The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS Utilityofofthethe Multinational Association forSupportive CareinCancer (MASCC) IndexScore aCriterionforNonadmissioninFebrileNeutropenicPatientswithSolidTumors Utility Multinational Association for Supportive Care in CancerRisk (MASCC) RiskasIndex Score as a Criterion for Nonadmission in Febrile Neutropenic Patients with Solid Tumors smoking status, diagnosis of COPD, occurrence of fever associated with neutropenia, days to temperature ≤ 37.5 and ≤ 38 C, an ANC < 500 cells/uL, return of ANC to greater than 500 cells/uL, duration of neutropenia, death, reception of filgrastim before and subsequently after admission, gastrointestinal symptoms (nausea, vomiting, diarrhea, abdominal pain, “unable to eat,”), serum biochemical tests (creatinine > 2 mg/dL, potassium < 3 mEq/L, sodium of < 130 mEq/L, phosphorus of < 2.7 mg/dL), density/ intensity of chemotherapy, types of infections, positive bacterial cultures, microorganisms isolated, antimicrobial agents prescribed when outpatient and inpatient, results of pertinent imaging studies, MASCC RIS components, and medical complications listed in the Klastersky criteria. All febrile neutropenic patient episodes meeting inclusion criteria were divided into 2 groups on the basis of complications: Group 1, no complication (equivalent to “do not admit”), or Group 2, complication (equivalent to “admit”). Group 1 (n = 100) had only fever and neutropenia, had none of the medical complications (Table 2) on admission or within 24 hours of admission, and were able to eat. Group 2 (n = 98) had 1 or more of the complications listed in Table 2 at admission or within 24 hours of admission. There were 3 patients in Group 1 in whom complications developed 24 hours after admission, which if they had been present on presentation would have classified each patient into Group 2 initially. Each patient episode was assigned to an MASCC RIS of 21 or greater or below 21, and these scores were correlated with the no complication and complication groups (Figure 1). The KP Southern California institutional review board approved the study. Medical Centers In 2012, beds and discharges per month were as follows: San Diego, 392 beds and 32,491 discharges; Orange County, 350 beds (2 hospitals), 28,564 discharges; and Woodland Hills, 262 beds and 13,741 discharges. All 4 hospitals fall into the tertiary care category, providing a full range of basic and sophisticated diagnostic and treatment services, including many specialized services. Statistical Analysis A sample size of 200 episodes was chosen as the basis for another study, not yet published, from which this analysis was done. Two episodes did not meet criteria, leaving 198 episodes. Standard methods of calculating sensitivity, specificity, positive predictive value, and negative predictive value were used. The Wilcoxon rank sum test was used to compare for those who were unable to eat and for those who were able to eat. RESULTS Patient characteristics are shown in Table 3. Klastersky Criteria versus Complications Table 2 lists the components of the Klastersky criteria; complications, which includes the reasons for admission and subsequent complications; the MASCC RIS; and LOS. There are 69 patients in Table 2 who had an MASCC RIS of 21 or above and had reasons for admission and/or complications. Only 20 patients of the 69 had complications named in the Klastersky criteria as a reason for admission. If the Klastersky criteria were to be applied, the other 49 reasons for admission would have to be assumed to fall into the last Klastersky category, “other complications judged serious or clinically significant by the investigator.” Thirty-eight patients were unable to eat, 22 had identified infections, 21 could be considered to have mucositis, and 5 were found to have typhlitis. Risk Index Score versus Complications The sensitivity of the MASCC RIS was 94% (94 of 100 episodes) with a 95% confidence interval (CI) of 87.4% to 97.8%, and specificity was 29.6% (29/98; 95% CI = 20.8% to 39.7%). The positive predictive valve was 57.67% (94/163; 95% CI = 49.7% to 65.4%), and the negative predictive valve was 82.9% (29/35; 95% CI = 66.34% to 93.4%). Figure 1. Assignment of episodes of febrile neutropenia to Multinational Association for Supportive Care in Cancer (MASCC) risk index score (RIS) and complications.a a Three complications occurred after admission to the hospital in patients stratified to “no complication” and would have occurred on an outpatient basis if the patients had not been admitted. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 39 ORIGINAL RESEARCH & CONTRIBUTIONS Utility of the MultinationalAssociation for Supportive Care in Cancer (MASCC) RiskofIndex as a Criterion for Nonadmission in FebrileCare Neutropenic Patients with Solid Utility the Score Multinational Association for Supportive in Cancer (MASCC) RiskTumors Index Score as a Criterion for Nonadmission in Febrile Neutropenic Patients with Solid Tumors Table 2. Klastersky criteria and complications in 69 patients with an MASCC RIS > 21 Patient episode number Klastersky criteria (named) Klastersky criteria (Presumed to be in ”Other complications judged serious and clinically significant by the investigator”) Reason for admission Complication after admission MASCC RIS Length of stay, days 1 None None Cellulitis None 21 3 2 SBP < 90 mmHg/need for vasopressors Nausea, vomiting SBP < 98 mmHg in a 90 year old None 21 5 3 None Unable to eat Unable to eat, mucositis None 21 5 4 None Unable to eat, K 2.9 mEq/L Unable to eat, K 2.9 mEq/L Day 3: K 3 mEq/L 21 5 5 None Unable to eat, nausea, diarrhea, abdominal pain Unable to eat, nausea, diarrhea, abdominal pain None 21 5 6 None Unable to eat, nausea, vomiting, abdominal pain Unable to eat, nausea, vomiting, abdominal pain None 21 5 7 SBP < 90 mmHg/need for vasopressors Diarrhea Diarrhea/SBP < 90 mmHg None 21 6 8 Arrhythmia, ECG changes Unable to eat, nausea, vomiting Unable to eat, nausea, vomiting, atrial flutter None 21 6 9 None Unable to eat, difficulty swallowing Unable to eat, difficulty swallowing None 21 6 10 None Nausea, vomiting Nausea, vomiting, bacteremia None 21 7 11 None Nausea, abdominal pain, K < 3 mEq/L Nausea, abdominal pain, Typhlitis, K < 3 mEq/L None 21 7 12 None Unable to eat, diarrhea Unable to eat, diarrhea Stomatitis 21 7 13 None Nausea, vomiting, Nausea, Vomiting, positive blood culture None 21 7 14 SBP < 90 mmHg/need for vasopressors, arrhythmia, ECG changes Nausea, vomiting Nausea, vomiting, Low SBP within first 24 hours, SVT 3 days 21 8 15 SBP < 90 mmHg/need for vasopressors, bleeding requiring transfusion Penile bleeding Penile bleeding Day 3: Na 124 mEq/L, Day 4: SBP < 90 mmHg, Day 7: fluid overload 21 9 16 Confusion, altered mental state Unable to eat Unable to eat, confusion, brain metastases None 21 9 17 None Unable to eat, nausea, diarrhea Unable to eat, nausea, diarrhea, C diff Day 2: K 2.6 mEq/L, Day 5: atrial fibrillation 21 11 18 None Unable to eat, nausea, abdominal pain Unable to eat, nausea, abdominal pain, mucositis Day 5: K 2.3 mEq/L, required TPN, fever 21 13 19 None Unable to eat, nausea, vomiting, diarrhea, lower GI bleeding, K 2.8 mEq/L, Mg 0.8 mEq/L Unable to eat, nausea, vomiting, diarrhea, lower GI bleeding, K 2.8 mEq/L, Mg 0.8 mEq/L None 21 15 20 SBP < 90 mmHg/need for vasopressors, ICU admission Unable to eat, diarrhea, K 2.2 mEq/L Unable to eat, diarrhea, mucositis, K 2.2 mEq/L Day 4: hypotension, ICU, pneumonia, C diff, MI 21 18 21 None Unable to eat, nausea, vomiting, diarrhea Unable to eat, nausea, vomiting, diarrhea, C diff None 21 19 22 Renal failure Nausea, vomiting, abdominal pain Nausea, vomiting, abdominal pain, ARF, bilateral hydronephrosis Day 10: K 2.9 mEq/L, Day 14: colostomy 21 20 23 Confusion, altered mental state Unable to eat Unable to eat, cellulitis, mucositis Day 4: confusion, carcinomatous meningitis 21 29 24 None Unable to eat, abdominal pain, inpatient chemotherapy required, Unable to eat, abdominal pain, SBO Inpatient chemotherapy required, neutropenia, fever, bacteremia 21 31 25 None Nausea, diarrhea, abdominal pain Nausea, diarrhea, abdominal pain, typhlitis None 22 4 26 None None Pleural effusion None 22 6 27 None K 2.2 mEq/L, Hb 6.6 g/dL Bacteremia, K 2.2 mEq/L, decubitus débridement Day 2: Hb 6.6 g/dL 22 6 28 None Nausea, K 2.6 mEq/L Nausea, K 2.6 mEq/L None 22 6 29 SBP < 90 mmHg/need for vasopressors, confusion, altered mental state, or seizure Nausea, vomiting, diarrhea, abdominal pain, K 2 mEq/L, Nausea, vomiting, diarrhea, abdominal pain, altered mental state Day 2: K 2 mEq/L, Day 3 SBP < 90 mmHg 22 8 30 SBP < 90 mmHg/need for vasopressors, Pao2 < 60 mmHg/need for ventilation Impending hip fracture Impending hip fracture Day 3: hypotension, Day 5: hypoxia, ARDS 22 8 31 None Unable to eat, difficulty swallowing, Day 4: K 5.6 mEq/L, Day 9: K 6.1 mEq/L Unable to eat, difficulty swallowing, mucositis Day 4: K 5.6 mEq/L, Day 9: K 6.1 mEq/L 22 10 32 Pao2 < 60 mmHg/need for ventilation, Nausea, diarrhea Nausea, diarrhea, dehydration, Cr 2.7 mg/dL Day 3: hypoxia: Day 4: Cr 5.3 mg/dL, Day 6: colitis, hemodialysis 22 11 33 None Na 126 mEq/L Pneumonia, Na 126 mEq/L None 23 3 34 None Nausea, diarrhea, abdominal pain, Na 118 Nausea, diarrhea, abdominal pain, hypotension, Na 118 mEq/L None 23 3 (Continued on next page.) 40 The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS Utilityofofthethe Multinational Association forSupportive CareinCancer (MASCC) IndexScore aCriterionforNonadmissioninFebrileNeutropenicPatientswithSolidTumors Utility Multinational Association for Supportive Care in CancerRisk (MASCC) RiskasIndex Score as a Criterion for Nonadmission in Febrile Neutropenic Patients with Solid Tumors (Continued from previous page.) Patient episode number Klastersky criteria (named) Klastersky criteria (Presumed to be in ”Other complications judged serious and clinically significant by the investigator”) Reason for admission Complication after admission MASCC RIS Length of stay, days 35 None Unable to eat, nausea, vomiting, diarrhea, difficulty swallowing, Hb 6.6 g/dL Unable to eat, nausea, vomiting, diarrhea, difficulty swallowing Day 2: Hb 6.6 g/dL 23 6 36 None None Pneumonia None 23 7 37 None Unable to eat, nausea, vomiting, diarrhea Unable to eat, nausea, vomiting, diarrhea, abdominal pain, mucositis, colitis None 23 8 38 None Unable to eat, nausea, vomiting, abdominal pain, intestinal perforation Unable to eat, nausea, vomiting, abdominal pain, intestinal perforation None 23 8 39 None Unable to eat, nausea, vomiting, abdominal pain, SBO Unable to eat, nausea, vomiting, abdominal pain SBO None 23 10 40 None Unable to eat Unable to eat, mucositis None 24 3 41 None Cellulitis None 24 5 42 None Unable to eat, nausea Unable to eat, nausea, difficulty swallowing, mucositis None 24 5 43 None Unable to eat Unable to eat, mucositis None 24 5 44 None Nausea, vomiting, diarrhea, abdominal pain Nausea, vomiting, diarrhea, abdominal pain, typhlitis None 24 6 45 None None Abscess None 24 6 46 SBP < 90 mmHg/need for vasopressors None Perirectal abscess Day 1: hypotension 24 6 47 None Unable to eat, nausea, vomiting Unable to eat, nausea, vomiting, mucositis None 24 6 48 SBP < 90 mmHg/need for vasopressors Unable to eat Unable to eat Day 3: hypotension 24 7 49 Pao2 < 60 mmHg/need for ventilation, arrhythmia, ECG changes None Syncope, K 2.1 mEq/L Day 2: SVT, hypoxia 24 8 50 None Nausea, vomiting, abdominal pain Nausea, vomiting, abdominal pain, colitis None 24 8 51 None Unable to eat, diarrhea, K 2.5 mEq/L Unable to eat, diarrhea, difficulty swallowing, mucositis, K 2.5 mEq/L None 24 8 52 None Unable to eat, nausea, vomiting, diarrhea, K 2.7 mEq/L Unable to eat, nausea, vomiting, diarrhea, difficulty swallowing, K 2.7 mEq/L None 24 8 53 None None Bacteremia ARF 24 12 54 None None, chest pain Chest pain None 24 13 55 None Unable to eat, nausea, vomiting, intractable hiccups Unable to eat, nausea, vomiting, esophagitis Day 1: intractable hiccups 24 20 56 None Unable to eat, nausea, vomiting Unable to eat, nausea, vomiting None 26 3 57 None None Cellulitis None 26 4 58 None Nausea, vomiting, diarrhea, abdominal pain Nausea, vomiting, diarrhea, abdominal pain, typhlitis None 26 4 59 None Nausea, vomiting, abdominal pain Nausea, vomiting, abdominal pain, typhlitis None 26 5 60 None Unable to eat, abdominal pain Unable to eat, abdominal pain, typhlitis None 26 5 61 None Unable to eat, nausea, vomiting Unable to eat, nausea, vomiting Day 1: perianal herpes simplex virus 26 5 62 None Nausea, diarrhea, K 2.6 mEq/L Nausea, diarrhea, K 2.6 mEq/L Enterovaginal fistula 26 6 63 None Unable to eat, vomiting, abdominal pain Unable to eat, vomiting, abdominal pain, mucositis None 26 7 64 None Unable to eat, nausea, vomiting, diarrhea, abdominal pain, hypokalemia Unable to eat, nausea, vomiting, diarrhea, abdominal pain, enteritis Low K 26 7 65 None Unable to eat, nausea, vomiting, rectal pain Unable to eat, nausea, vomiting, rectal pain None 26 9 66 None Hb < 6 g/dL, unable to eat, abdominal pain, K 2.9 mEq/L Unable to eat, abdominal pain, Hb 5.4 g/dL, K 2.9 mEq/L None 26 9 67 None Unable to eat, nausea, difficulty swallowing Unable to eat, nausea, mucositis, difficulty swallowing None 26 10 68 None Unable to eat, nausea Unable to eat, nausea, mucositis Day 2: fever, Day 6: ARF 26 11 69 None Unable to eat, nausea, vomiting, diarrhea, abdominal pain Unable to eat, nausea, vomiting, diarrhea, abdominal pain, esophagitis, colitis Day 6: ARF 26 13 ARDS = acute respiratory distress syndrome; ARF = acute renal failure; C diff = Clostridium difficile; Cr = creatinine; ECG = electrocardiogram; GI = gastrointestinal tract; Hb = hemoglobin; ICU = intensive care unit admission; K = potassium; MASCC = Multinational Association for Supportive Care in Cancer; Mg = magnesium; MI = myocardial infarction; Na = sodium; Pao2 = partial pressure of oxygen; RIS = risk index score; SBO = small-bowel obstruction; SBP = systolic blood pressure; SVT = supraventricular tachycardia; TPN = total parenteral nutrition. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 41 ORIGINAL RESEARCH & CONTRIBUTIONS Utility of the MultinationalAssociation for Supportive Care in Cancer (MASCC) RiskofIndex as a Criterion for Nonadmission in FebrileCare Neutropenic Patients with Solid Utility the Score Multinational Association for Supportive in Cancer (MASCC) RiskTumors Index Score as a Criterion for Nonadmission in Febrile Neutropenic Patients with Solid Tumors Table 3. Characteristics of 198 patient episodes of solid tumors,a Characteristic Age, years Median Range Sex Male Female Neoplasms Breast Gastrointestinal Lung Sarcoma Head and neck Ovary Prostate Bladder Testis PNET Unknown Melanoma Uterus Total neoplasms Comorbidities Diabetes mellitus CKD stage ≥ 3 Cirrhosis Rheumatoid arthritis Systemic lupus CREST Polymyalgia rheumatica Transplant Anti-TNF Hepatitis B Hepatitis C HIV infection Hypogammaglobulinemia Hemochromatosis Ulcerative colitis Other Unable to eat GCSF, inpatient after admission GCSF, outpatient before admission Chemotherapy density and intensity meeting GCSF criteria Documented infection Antimicrobials before admission Adequate antimicrobial regimen on admission No. of patients (%) MASCC RIS score < 21 (n = 35), no. (%) MASCC RIS score ≥ 21 (n = 163), no. (%) 61 18-86 67.5 35-81 59 18-86 57 (29) 141 (71) 17 18 40 123 93 (47.0) 39 (19.7) 18 (9.1) 12 (6.1) 9 (4.5) 8 (4.0) 7 (3.5) 4 (2.0) 2 (1.0) 2 (1.0) 2 (1.0) 1 (0.5) 1 (0.5) 198 (100) 7 (20.0) 6 (17.1) 7 (20.0) 5 (14.3) 2 (5.7) 3 (8.6) 2 (5.7) 2 (5.7) 0 (0) 1 (2.9) 0 (0) 0 (0) 0 (0) 35 (100) 86 (52.8) 33 (20.3) 11 (6.8) 7 (4.3) 7 (4.3) 5 (3.1) 5 (3.1) 2 (1.2) 2 (1.2) 1 (0.6) 2 (1.2) 1 (0.6) 1 (0.6) 163 (100) 16 (8.1) 18 (9.1) 2 (1.0) 2 (1.0) 0 (0) 0 (0) 2 (1.0) 1 (0.5) 1 (0.5) 4 (11.4) 6 (17.1) 1 (2.9) 1 (2.9) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 15 (9.2) 12 (7.4) 1 (0.6) 1 (0.6) 0 (0) 1 (0.6) 2 (1.2) 1 (0.6) 1 (0.6) 1 (0.5) 5 (2.5) 1 (0.5) 2 (1.0) 2 (1.0) 1 (0.5) 0 (0) 0 (0) 0 (0) 0 (0) 1 (2.9) 0 (0) 1 (0.6) 5 (3.1) 1 (0.6) 2 (1.2) 1 (0.6) 1 (0.6) 54 (27.3) 177 (89.4) 33 (16.7) 51 (25.8) 16 (45.7) 31 (88.6) 6 (17.1) 5 (14.3) 38 (23.3) 146 (89.6) 27 (16.6) 46 (28.2) 38 (19.2) 18 (9.1) 187 (94.4) 12 (34.3) 4 (11.4) 34 (97.1) 26 (16) 14 (8.6) 153 (93.9) Some percentages may not total to 100 because of rounding. CKD = chronic kidney disease; CREST = calcinosis, Raynaud syndrome, esophageal dysmotility, sclerodactyly, and telangiectasia; GCSF = granulocyte colony-stimulating factor; HIV = human immunodeficiency virus; MASCC = Multinational Association for Supportive Care in Cancer; PNET = primitive neuroectodermal tumor; RIS = risk index score; TNF = tumor necrosis factor. a 42 There were 163 inpatient episodes with an MASCC RIS of 21 or higher. Sixty-nine of these had complications and/or reasons for admission on presentation. Thirty-eight of the 69 were unable to eat; 32 of the 38 had reasons for admission and/or complications. The other 31 of the 69 patients, those who were able to eat, required admission for various other reasons. See Table 2 for the reasons for admission and subsequent complications of the 32 episodes. There were 35 episodes with an MASCC RIS below 21 (high risk for complication). Six of these patient episodes were misclassified by the MASCC RIS because no complication occurred that required hospitalization. The mean LOS for these 6 patients was 4.7 days (5, 3, 5, 5, 4, and 6 days, the last with a urinary tract infection that could have been treated orally with ciprofloxacin) compared with a mean LOS of 4.6 days for Group 1 and 7.6 days for Group 2. Inability to Eat Inability to eat was considered a serious complication and reason for admission; thus, it placed a patient episode in Group 2: complication. There were 54 episodes of 198 in which patients were unable to eat, 38 of whom had an MASCC RIS of 21 or above and 16 of whom had a score below 21. These 38 patient episodes were a subset of the 69 discordant patient episodes with an MASCC RIS of 21 or greater and a complication (Table 2). Inability to eat was associated with other serious complications in 32 of 38 episodes (84%). The 38 patients who were unable to eat had a mean LOS of 9.66 days compared with the mean LOS of the 31 patients who could eat, 7.0 days (p = 0.08 by Wilcoxon rank sum test). The mean MASCC RIS of those unable to eat and those able to eat was 23.1 and 22.8, respectively. Correlation of Index with Other Outcomes There was no useful correlation between the MASCC RIS and either the days to a body temperature at or below 37.5°C or the LOS (data not shown). Table 4 shows a correlation with deaths and the potential cost savings of preventing hospital admission (Table 5). The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS Utilityofofthethe Multinational Association forSupportive CareinCancer (MASCC) IndexScore aCriterionforNonadmissioninFebrileNeutropenicPatientswithSolidTumors Utility Multinational Association for Supportive Care in CancerRisk (MASCC) RiskasIndex Score as a Criterion for Nonadmission in Febrile Neutropenic Patients with Solid Tumors DISCUSSION If patients with identified infections; intractable vomiting and diarrhea, either of the latter caused by mucositis or another complication; and inability to eat are included in the patients to whom the MASCC RIS is applied, the sensitivity of an MASCC RIS of 21 or greater to identify patients as a criterion for nonadmission was high (94%), but the positive predictive value was only 57.7% and the specificity only 29.6%. The range of the specificity of the MASCC RIS in some published studies (Table 6) varied from 40% to 95% (mean = 67.5%) in prospective studies and from 52% to 63.7% (mean = 60.9%) in retrospective studies. The variance of the specificity in these studies and the present study has not been explained, and a detailed analysis is beyond the scope of this article; however, a more detailed analysis is available in the guideline from the American Society of Clinical Oncology (ASCO).9 In most of these publications, it is not clear if patients, presenting with identifiable infections; intractable vomiting and diarrhea, either of the latter caused by mucositis or another complication; and the inability to eat and swallow medications were excluded before the calculation of the MASCC RIS because these clinical features were considered aspects of the febrile neutropenic syndrome and not complications. Thus, study design is a possible factor accounting for the variance. Another factor might be that the median age of the patients in the studies listed in the references was about 51 years compared with 61 years in the present study. In the MASCC RIS, 2 points are awarded for age younger than 60 years, indicating that those patients aged 60 years or older are at increased risk of complications. As noted earlier, in 69 of 163 inpatient episodes with an MASCC RIS of 21 or more, admission was necessary because of complications present on admission or which occurred during hospitalization (Table 2). The patients with these 69 misclassified inpatient episodes would not have been admitted if an MASCC RIS of 21 or greater was used as the criterion for nonadmission. If these patients were not admitted, the complications that occurred during hospitalization would have occurred outside the hospital, resulting in either reevaluation in a health care setting or death. There were also 3 inpatient episodes with an MASCC RIS of 21 or above (Group 1), in which a complication occurred 24 hours after admission, a complication that would have been Table 4. Patient deaths MASCC RIS 13 19 19 19 Circumstances and causes leading to death Bacteremia, Staphylococcus aureus Readmitted with intestinal perforation, died same day Unable to eat, became obtunded on TPN Pneumonia Death related to initial infection Yes No Comfort care Yes No No Yes Yes Yes Clostridium difficile, low BP, ICU, HAP, AMI SBO, died 31 days after admission Encephalopathy No Yes No No Yes Yes No No Yes 22 Multiple intraabdominal, extraintestinal air-fluid levels ARDS, progressive hypoxemia, hypotension Diarrhea, colitis, ARF, hypotension Yes Planned for next day Yes 23 Sepsis, then acute hypotension Yes Yes 23 Admitted with SBO and discharged; readmitted following week with intestinal perforation, intraabdominal abscess (declined abcess drainage) Fluid overload, failed to respond to diuresis Readmitted obtunded, ARF, hypotensive New SVT, hypoxemia No No No Yes No No 21 21 21 22 22 24 24 24 Neoplasm Sarcoma Advanced lung cancer Advanced ovarian cancer Lung cancer Advanced esophageal cancer Colon cancer Advanced breast cancer Advanced endometrial cancer Advanced prostate cancer Advanced lung cancer Advanced breast cancer Ovarian cancer Death after discharge, within 28 days of admissiona No No Duration of neutropenia/ length of stay, days 7/7 3/8 Days to temperature ≤ 38°C/days to temperature ≤ 37.5°C 6/6 8/8 No 2 / 18 1/2 No 1/4 1/1 No 9 / 18 3/3 No No 6 / 31 1 / 29 1/1 7/9 Yes 5/6 2/4 No 2/8 8/8 No 4/8 4/4 No 2/3 1/3 Yes 3/4 3/3 No 6/9 6/9 No Metastatic; primary cancer not known Breast cancer Yes 3 / 14 3/8 Yes Gastric cancer No 8/8 4/7 “No” = died in hospital. AMI = acute myocardial infarction; ARDS = acute respiratory distress syndrome; ARF = acute renal failure; BP = blood pressure; HAP = hospital-acquired pneumonia; ICU = intensive care unit admission; MASCC = Multinational Association for Supportive Care in Cancer; RIS = risk index score; SBO = small-bowel obstruction; SVT = supraventricular tachycardia; TPN = total parenteral nutrition. a The Permanente Journal/ Summer 2015/ Volume 19 No. 3 43 ORIGINAL RESEARCH & CONTRIBUTIONS Utility of the MultinationalAssociation for Supportive Care in Cancer (MASCC) RiskofIndex as a Criterion for Nonadmission in FebrileCare Neutropenic Patients with Solid Utility the Score Multinational Association for Supportive in Cancer (MASCC) RiskTumors Index Score as a Criterion for Nonadmission in Febrile Neutropenic Patients with Solid Tumors Table 5. Savings of preventing hospital admission Savings Approximate cost of 1 day of hospitalization (2012 US dollars) Number of patient episodes Number of patient episode days x number of patient episodes Estimated cost of hospitalization (2012 US dollars) best managed in the hospital. If the patients had not been admitted, or had been admitted and discharged after 24 hours of observation, they would have experienced these complications as outpatients. Those complications were hypokalemia (serum potassium concentration of 2.9 mEq/L) on Day 2, hypophosphatemia (phosphorus level of 2.2 mg/dL) on Day 3, and recurrent fever on Day 4. An additional 52-yearold woman, not identified as feeling or appearing sick or being dehydrated, had a temperature of 38.7°C, a BP of 81/54 mmHg, and a pulse of 130/min (3 criteria for systemic inflammatory response syndrome10) in urgent care. She was referred to the Emergency Department, where she was hydrated and placed on an intravenous antimicrobial regimen. She was intermittently hypotensive until the BP finally stabilized 25 hours and 37 minutes later. Her MASCC RIS was 21 at the time of admission, but the RIS would have been different depending on when, in the If the MASCC course of this patient episode, index were it was calculated. to be used to Because many complicadetermine tions, such as hypokalemia, hypophosphatemia, and recur“do not admit,” rent fever, cannot be predicted it would have with an MASCC RIS of 21 to be employed or higher, use of a protocol, after determining algorithm, or guideline seems whether a person appropriate to help clinicians was or was not decide on the proper manable to eat or agement. One is the ASCO swallow … guideline from 2012, 9 and another is the National Comprehensive Cancer Network (NCCN) guideline. 11 The recommended initial observation period in the ASCO guideline is 4 hours, and in the NCCN guideline it is 2 to 12 hours. The hypotensive patient described could have been considered stable at 2 to 4 hours and possibly discharged to home. 44 No complication $2124 100 455 $966,420 However, the physician, simply using clinical judgment, decided this patient needed admission. This decision was consistent with the ASCO guideline, which clearly states that a patient with criteria for systemic inflammatory response syndrome should be admitted. Therefore, following the ASCO guideline would have ensured admission for this last patient, but using an MASCC RIS of 21 or higher would not. The limitataion of the MASCC RIS is evident by consulting Table 4 of the ASCO guideline (available at: http://jco.ascopubs. org/content/31/6/794/T4.expansion. html).9 The table lists 41 exclusions (42 if the footnote regarding systemic inflammatory response syndrome is included) to using an MASCC RIS of 21 or greater as a criterion for treating a febrile neutropenic patient as an outpatient.9 Furthermore, neither the NCCN guideline for the management of nonadmitted patients nor the ASCO guideline specify frequency of laboratory testing for these potential outpatients. Rubenstein et al12 suggested obtaining a complete blood cell count every other day and biochemical panels on Day 7 or the last day of observation. If the biochemical panels for the patients with hypokalemia and hypophosphatemia had been drawn on Day 7, a delay in detection would have occurred. The protocol for patients discharged from the hospital on a regimen of oral antimicrobial therapy in the article by Klastersky et al13 included temperature recorded every 6 hours, laboratory tests every other day for 5 days, and phone contact with the patient every other day. The ASCO guideline recommends daily telephone contact and “frequent evaluation for at least 3 days in clinic or at home.” Data in the present study support the ASCO guideline for management of these patients. Although the ASCO guideline recognizes the lack of data supporting multiple aspects of outpatient management, modifications to the guideline, following discharge to an outpatient setting, could include recording the patient’s vital signs approximately every 6 to 8 hours, establishing phone contact with the patient or caregiver within 8 to 12 hours following discharge, and serum biochemical tests (electrolytes, creatinine, calcium, phosphorus, and magnesium) daily or every other day for 3 times, or until results are normal. Importance of Inability to Eat This study chose inability to eat, as an admission criterion, vs inability to swallow oral medications because “unable to eat” was recorded in the progress notes. In my view, neither is adequate or objective because outpatients need both adequate nutrition and appropriate medications. Some patients who are unable to eat can swallow oral medications, and some patients who are unable (or unwilling) to swallow oral medications are able and willing to swallow nutritional liquid drinks. Inability to swallow oral medications is considered by the ASCO guideline to be an exclusion for outpatient management. It is not named as one of the complications in the Klastersky criteria. In the study by Klastersky et al,13 which identified patients who were stable and ready for discharge from the hospital after 24 hours of observation, the equivalent of “unable to eat”— “able to swallow”—was employed after stratification by the MASCC index and was not incorporated into the MASCC index. Those unable to swallow were excluded from early discharge despite an MASCC RIS of 21 or higher. If the MASCC RIS were to be used to determine “do not admit,” it would have to be employed after determining whether a person was or was not able to eat or swallow, or the criterion “unable to eat/ unable to swallow oral medications” would have to be incorporated into the MASCC RIS. As noted earlier, inability to eat was associated with other serious complications, and all physicians admitting patients in this study considered it a criterion for admission. However, because The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS Utilityofofthethe Multinational Association forSupportive CareinCancer (MASCC) IndexScore aCriterionforNonadmissioninFebrileNeutropenicPatientswithSolidTumors Utility Multinational Association for Supportive Care in CancerRisk (MASCC) RiskasIndex Score as a Criterion for Nonadmission in Febrile Neutropenic Patients with Solid Tumors there are 42 exclusions in the ASCO guideline9 for managing a patient as an outpatient, as mentioned earlier, there is questionable utility to modifying the MASCC RIS to include “unable to eat/ unable to swallow oral medications.” That inability to eat is important has been highlighted in a study by Escalante et al,14 who noted that 80% of patients with Grade 3 or higher mucositis required admission. The NCCN guideline also includes Grades 3 to 4 mucositis as a criterion for high risk. Until patients who are unable to eat or to swallow oral medications, yet who have no other complications, can be managed as outpatients, they will require admission. are objective; 2) the majority, 49 of the 69, of the complications experienced by the patients in this study with an MASCC RIS of 21 or higher were not among the named complications; and 3) inability to eat and inability to swallow are not named. The MASCC RIS of 21 or above is inadequate for the nonadmission decision for these reasons: 1) only 4 of the 7 components of the MASCC RIS are objective; 2) it misclassified to low risk 42.3% of patient episodes with complications; 3) it has to be checked against 42 other exclusions based on the ASCO guideline9; and 4) “unable to eat/unable to swallow” are not incorporated. Limitations of Klastersky Criteria and Index Alternative to Index The Klastersky criteria are inadequate as nonadmission criteria for these reasons: 1) only 2 of the 10 complications The alternative to the MASCC RIS is clinical judgment or a more reliable index. Although the MASCC RIS has been incorporated into both Infectious Diseases Society of America1 and ASCO guidelines,9 I believe a fair question is: Is this index really superior to clinical judgment? Furthermore, I believe it would be beneficial to conduct a study in which a physician assigns an MASCC RIS at the point of entry to health care and again at the point when an admitting physician, blinded to the MASCC RIS, evaluates the patient regarding admission. The admitting physician would decide, on the basis of clinical acumen and the ASCO guideline, whether the patient should be admitted. The patient would be observed in the hospital for 24 hours. Complications would be correlated with the MASCC RIS and the clinical decision. Savings The cost of intensive outpatient management would probably be less than the cost of inpatient management Table 6. Sensitivity and specificity of the MASCC RIS in various studies Source, year Uys,8 2004 Type of study Prospective Total Baskaran,5 2008 Retrospective Total Innes,6 2008 Prospective Total André,18 2010 Prospective Solid tumor, lymphoma, % 70 34.5 100 No serious medical complication 57 3 60 68 5 73 87 8 95 Not SS/SSh 70 38 108 308 15 323 1349 410 1759 137 Serious medical complication 1 19 20 14 29 43 3 2 5 SS/SSh 22 67 89 35 38 73 139 244 383 23 < 21 32 169 Don’t admit 35 58 Admit 67 227 > 21 < 21 94 6 100 69 29 98 163 35 198 MASCC RIS > 21 < 21 > 21 < 21 > 21 < 21 56 > 21 < 20 Total Ahn,19 2011 Retrospective Total Paesmans,20 2011 Retrospective Total Hui,4 2011 Prospective Total Bitar, 2013a Retrospective 71.5 57 79.7 > 21 < 21 > 21 < 21 > 21 100 Total Total 58 22 80 82 34 116 90 10 100 92 105 197 343 53 396 1488 654 2142 160 Sensitivity, % 95 Specificity, % 95 Deaths, % 0 36.4 67 7 29 93 91.6 40 70 75 NA NA 52 1.5 18.9 63.7 1 14.2 95 77 81 1.9 60 9 29.6 4.9 11.4 94 Results of the current study. MASCC = Multinational Association for Supportive Care in Cancer; NA = not available; RIS = risk index score; SS/SSh = severe sepsis or septic shock. a The Permanente Journal/ Summer 2015/ Volume 19 No. 3 45 ORIGINAL RESEARCH & CONTRIBUTIONS Utility of the MultinationalAssociation for Supportive Care in Cancer (MASCC) RiskofIndex as a Criterion for Nonadmission in FebrileCare Neutropenic Patients with Solid Utility the Score Multinational Association for Supportive in Cancer (MASCC) RiskTumors Index Score as a Criterion for Nonadmission in Febrile Neutropenic Patients with Solid Tumors (approximately $10,000 per uncomplicated admission12). In 1993, Rubenstein and colleagues12 estimated the medication cost of outpatient management as $2302 for oral therapy and $7336 for intravenous therapy, but the total cost of managing the patients was not provided. Elting et al15 calculated the costs of outpatient vs inpatient management in 2008 and found the total cost of inpatient management to be about twice that of outpatients. Study Limitations There are some limitations to this study. First, as noted earlier, the MASCC RIS lists only 4 actual objective criteria. The burden of illness category is purely subjective, dependent on the recorder (Table 1). The burden of illness was assigned following a detailed review of the chart by the physician author and not by the admitting physician. The physician reviewing the charts for this study did review the publication by Pompei and associates,16 which originally proposed the burden of illness designation. Although a retrospective chart review has some element of subjectivity, it is no less objective than the criteria used to evaluate charts in the original publication by Klastersky et al.3 Second, this study accepted designations such as COPD, dehydration, and other terms such as vomiting, diarrhea, unable to eat, and so on, without requiring an objective definition. (The ASCO guideline, Table 2, [available at: http://jco.ascopubs.org/ content/31/6/794/T2.expansion.html] attempts to address this problem, but does not resolve it.9) Third, this was a retrospective review of the charts by a single physician. However, his experience included more than 37 years as a physician and 23 years as an infectious disease physician. Fourth, the definition of febrile neutropenia was based on the admitting physician’s acceptance of the self-report of fever or the documentation of fever in the clinic or Emergency Department and not a documented temperature of above 38.3°C on one occasion or above 38°C on 2 or more occasions during a 12-hour period.17 Fifth, this was a study of only febrile neutropenic patients with solid tumors, so the sensitivity and specificity of the MASCC RIS in this study should be compared only with similar studies of febrile neutropenic patients with solid tumors. (Table 6 shows data extracted from 7 studies with the percentage of patients with solid tumors or lymphoma and the sensitivity and specificity of the MASCC RIS for each.4-6,8,18-20) CONCLUSIONS Figure 2. Proposed outpatient management algorithm.b Modified from the American Society of Clinical Oncology (ASCO) guideline, to include the following: Patient agrees to outpatient treatment while neutropenic, including potential frequent visits to clinic/hospital. Residence ≤ 1 hour or ≤ 30 miles (48 km) from clinic or hospital, even in inclement weather. Patient’s primary care physician and infectious disease physician, or oncologist agrees to outpatient management. Attendant or attendants who agree to outpatient treatment and are competent at observation and communication, and at home 24 hours a day until neutropenia and other clinical problems resolve. Telephone and transportation available 24 hours a day. Either an oncology or infectious disease nurse practitioner or physician’s assistant or a clinically trained home infusion pharmacist or clinically trained oncology nurse or infectious disease nurse able to communicate with patient daily. b High risk indicates usual clinical criteria for admission (criteria on which a general internist bases a decision to admit or to not admit) using the 2013 clinical practice guideline from the ASCO, which includes all patients unable to eat. Low risk indicates absence of usual admission criteria/ASCO guideline. Ca = calcium; CBC = complete blood count; Cr = creatinine; h = hours; Mg = magnesium; VS = vital signs. a 46 This study answered the 6 questions presented in the Introduction. First, of 69 misclassified patients with complications and an MASCC RIS of 21 or greater, only 20 had serious complications named in the Klastersky criteria, meaning that the other 49 patients had complications not named and which had to be assumed to be included in the last component, “other complications judged serious and clinically significant by the investigator.” Second, there were additional complications, not named in the Klastersky criteria, which were important in the nonadmission decision, such as inability to eat (Table 2). Third, the MASCC RIS of 21 or greater could not be used to make the nonadmission decision for a febrile neutropenic patient with a solid tumor because, in this study, a score of 21 or higher misclassified 42.3% of patients with complications to low risk. Fourth, 3 patients with an MASCC RIS of 21 or greater experienced complications 24 hours after admission; the The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS Utilityofofthethe Multinational Association forSupportive CareinCancer (MASCC) IndexScore aCriterionforNonadmissioninFebrileNeutropenicPatientswithSolidTumors Utility Multinational Association for Supportive Care in CancerRisk (MASCC) RiskasIndex Score as a Criterion for Nonadmission in Febrile Neutropenic Patients with Solid Tumors complication and the day of occurrence were noted. Because 2 of the 3 complications that occurred were biochemical and the additional one was recurrent fever, the index is unlikely to be able to predict their occurrence. Fifth, therefore, an algorithm or protocol for the management of outpatients is advisable. An algorithm has been constructed from the implications of the data in this study and the ASCO guideline (Figure 2). Sixth, substantial savings could be realized if uncomplicated patients could be managed as outpatients (approximately $1 million per 100 uncomplicated admissions in 2012 dollars). The possibility of creating an MASCClike RIS from truly objective data, which could be used to predict complications and the safety of not admitting a febrile neutropenic patient, requires further investigation. v 3. 4. 5. 6. 7. Disclosure Statement The author(s) have no conflicts of interest to disclose. Acknowledgment The author thanks Elizabeth Le for data extraction and formulation, without which this study would not have been possible. Kathleen Louden, ELS, of Louden Health Communications provided editorial assistance. 8. 9. References 1. Freifeld AG, Bow EJ, Sepkowitz KA, et al; Infectious Diseases Society of America. Clinical practice guideline for the use of antimicrobial agents in neutropenic patients with cancer: 2010 update by the Infectious Diseases Society of America. Clin Infect Dis 2011 Feb 15;52(4):e56-93. DOI: http://dx.doi.org/10.1093/cid/cir073. 2. Smith TJ, Khatcheressian J, Lyman GH, et al. 2006 update of recommendations for the use of white blood cell growth factors: an evidencebased clinical practice guideline. J Clin Oncol 10. 2006 Jul 1;24(19):3187-205. DOI: http://dx.doi. org/10.1200/JCO.2006.06.4451. Klastersky J, Paesmans M, Rubenstein EB, et al. The Multinational Association for Supportive Care in Cancer risk index: a multinational scoring system for identifying low-risk febrile neutropenic cancer patients. J Clin Oncol 2000 Aug;18(16):3038-51. Hui EP, Leung LK, Poon TC, et al. Prediction of outcome in cancer patients with febrile neutropenia: a prospective validation of the Multinational Association for Supportive Care in Cancer risk index in a Chinese population and comparison with the Talcott model and artificial neural network. Support Care Cancer 2011 Oct;19(10):1625-35. DOI: http://dx.doi. org/10.1007/s00520-010-0993-8. Baskaran ND, Gan GG, Adeeba K. Applying the Multinational Association for Supportive Care in Cancer risk scoring in predicting outcome of febrile neutropenia patients in a cohort of patients. Ann Hematol 2008 Jul;87(7):563-9. DOI: http://dx.doi.org/10.1007/s00277-008-0487-7. Innes H, Lim SL, Hall A, Chan SY, Bhalla N, Marshall E. Management of febrile neutropenia in solid tumours and lymphomas using the Multinational Association for Supportive Care in Cancer (MASCC) risk index: feasibility and safety in routine clinical practice. Support Care Cancer 2008 May;16(5):485-91. DOI: http://dx.doi. org/10.1007/s00520-007-0334-8. Carmona-Bayonas A, Gómez J, GonzálezBillalabeitia E, et al. Prognostic evaluation of febrile neutropenia in apparently stable adult cancer patients. Br J Cancer 2011 Aug 23; 105(5):612-7. DOI: http://dx.doi.org/10.1038/ bjc.2011.284. Uys A, Rapoport BL, Anderson R. Febrile neutropenia: a prospective study to validate the Multinational Association of Supportive Care of Cancer (MASCC) risk-index score. Support Care Cancer 2004 Aug;12(8):555-60. DOI: http://dx.doi. org/10.1007/s00520-004-0614-5. Flowers CR, Seidenfeld J, Bow EJ, et al. Antimicrobial prophylaxis and outpatient management of fever and neutropenia in adults treated for malignancy: American Society of Clinical Oncology clinical practice guideline. J Clin Oncol 2013 Feb 20;31(6):794-810. DOI: http:// dx.doi.org/10.1200/JCO.2012.45.8661. Bone RC, Balk RA, Cerra FB, et al. Definitions for sepsis and organ failure and guidelines for the use of innovative therapies in sepsis. The ACCP/SCCM Consensus Conference Committee. American College of Chest Physicians/ Society of Critical Care Medicine. Chest 1992 Jun;101(6):1644-55. DOI: http://dx.doi. org/10.1378/chest.101.6.1644. 11. NCCN guidelines: prevention and treatment of cancer-related infections [Internet]. Fort Washington, PA: National Comprehensive Cancer Network; 2013 [cited 2015 Apr 2]. Available from: www.nccn.org/professionals/physician_gls/f_ guidelines.asp#infections. 12. Rubenstein EB, Rolston K, Benjamin RS, et al. Outpatient treatment of febrile episodes in low-risk neutropenic patients with cancer. Cancer 1993 Jun 1;71(11):3640-6. DOI: http://dx.doi.org/ 10.1002/1097-0142(19930601)71:11%3C3640:: AID-CNCR2820711128%3E3.0.CO;2-H. 13. Klastersky J, Paesmans M, Georgala A, et al. Outpatient oral antibiotics for febrile neutropenic cancer patients using a score predictive for complications. J Clin Oncol 2006 Sep 1;24(25): 4129-34. DOI: http://dx.doi.org/10.1200/ JCO.2005.03.9909. 14. Escalante CP, Weiser MA, Manzullo E, et al. Outcomes of treatment pathways in outpatient treatment of low risk febrile neutropenic cancer patients. Support Care Cancer 2004 Sep;12(9):657-62. DOI: http://dx.doi.org/10.1007/ s00520-004-0613-6. 15. Elting LS, Lu C, Escalante CP, et al. Outcomes and cost of outpatient or inpatient management of 712 patients with febrile neutropenia. J Clin Oncol 2008 Feb 1;26(4):606-11. DOI: http://dx.doi. org/10.1200/JCO.2007.13.8222. 16. Pompei P, Charlson ME, Ales K, MacKenzie CR, Norton M. Relating patient characteristics at the time of admission to outcomes of hospitalization. J Clin Epidemiol 1991;44(10):1063-9. DOI: http:// dx.doi.org/10.1016/0895-4356(91)90008-W. 17. Hughes WT, Pizzo PA, Wade JC, Armstrong D, Webb CD, Young LS. Evaluation of new antiinfective drugs for the treatment of febrile episodes in neutropenic patients. Infectious Diseases Society of America and the Food and Drug Administration. Clin Infect Dis 1992 Nov;15 Suppl 1:S206-15. DOI: http://dx.doi.org/10.1093/ clind/15.Supplement_1.S206. 18. André S, Taboulet P, Elie C, et al. Febrile neutropenia in French emergency departments: results of a prospective multicentre survey. Crit Care 2010;14(2):R68. DOI: http://dx.doi. org/10.1186/cc8972. 19. Ahn S, Lee YS, Chun YH, et al. Predictive factors of poor prognosis in cancer patients with chemotherapy-induced febrile neutropenia. Support Care Cancer 2011 Aug;19(8):1151-8. DOI: http://dx.doi.org/10.1007/s00520-010-0928-4. 20. Paesmans M, Klastersky J, Maertens J, et al. Predicting febrile neutropenic patients at low risk using the MASCC score: does bacteremia matter? Support Care Cancer 2011 Jul;19(7): 1001-8. DOI: http://dx.doi.org/10.1007/s00520010-0925-7. State of Mind A cancer is not only a physical disease, it is a state of mind. — Michael Baden, MD, b 1934, physician and forensic pathologist The Permanente Journal/ Summer 2015/ Volume 19 No. 3 47 ORIGINAL RESEARCH & CONTRIBUTIONS Evidence-Based Referral: Effects of the Revised “Youth Fit 4 Life” Protocol on Physical Activity Outputs James J Annesi, PhD, FAAHB, FTOS, FAPA; Linda L Vaughn, MS, MBA Perm J 2015 Summer;19(3):48-53 http://dx.doi.org/10.7812/TPP/14-228 ABSTRACT Background: Lack of physical activity is prevalent in youths. Pediatricians seek referrals to reliably increase outputs, especially in their overweight and underactive patients. Objective: Within a randomized controlled trial, we contrasted 2 physical activity/nutrition treatments on the basis of social cognitive and self-efficacy theory, and a comparison condition, on time in moderate-to-vigorous physical activity (MVPA) during the 45-min/day physical activity segment of elementary afterschool care. Methods: In youths ranging in age from 9 to 12 years (9.7 ± 0.8 years, overall), the Original Youth Fit For Life treatment (Original YFFL; n = 49), the Revised Youth Fit 4 Life treatment (Revised YF4L, n = 43), and a comparison condition of typical care (Comparison, n = 46) were contrasted using a 3 (groups) × 2 (sexes) analysis of variance incorporating means of 3 accelerometer measurements over 12 weeks. Results: There was a significantly greater amount of time in MVPA in the Revised YF4L group than either the Original YFFL or Comparison groups (F2, 132 = 281.20, p < 0.001). Boys completed significantly more time in MVPA than girls (F2, 132 = 16.43, p < 0.001); however, there was not a significant group × sex interaction. Supplementary analyses indicated sedentary time was significantly less by 29% in the Revised YF4L when contrasted with the Comparison group. Conclusion: The Revised YF4L protocol that sought to maximize participants’ cardiovascular physical activity appeared to improve upon the Original YFFL treatment on time in MVPA. Thus, pediatricians might have confidence in referring their patients to such evidence-based approaches. Future research should also evaluate the effects of YF4L on psychosocial predictors of physical activity and change in body mass index. INTRODUCTION In the US, more than one-third of youths are presently overweight or obese.1 Comorbidities include increased risk for type 2 diabetes, heart disease, orthopedic injuries, cardiorespiratory problems, and self-esteem issues.2,3 Physical activity among children of all ages has decreased,4 and this decrease is associated with an inappropriately high weight.5 The Centers for Disease Control and Prevention’s recommendation for physical activity in children is at least 60 minutes per day of moderateto-vigorous physical activity (MVPA).6 However, a recent population-based study using accelerometry found that only 42% of US children ages 9-11 years attained this volume.7 Consistent with other research,8 the percentage of boys attaining the recommended amount of physical activity (49%) was considerably greater than that of girls (35%). Notably, the percentages fall to an even more dismal 8% completing the recommended minimum starting at age 12 (3% for girls).7 Because physical activity is the strongest predictor of controlling weight as one ages,9 these patterns of low activity suggest a continuation of the obesity epidemic unless substantial changes occur. Pediatricians take seriously the need for children to obtain enough physical activity to prevent or improve inappropriately high weight, as well as for promoting cardiovascular fitness. Because pediatricians are not likely to be in a position to directly provide physical activity to patients, they often seek community-based resources as referrals. However, the effectiveness of these resources may vary greatly. For example, although local sports and recreation programs are widely available, overweight, deconditioned, and nonathletic children might feel threatened around more fit and athletic peers. This might lead to even less desire for physical activity for them in the future. Also, many popular sports (eg, baseball, softball, bowling) might not provide much MVPA. Although physical education (PE) class during the school day provides an obvious venue for physical activity in elementary school students, recent research found that only 27% of a typical class period of 45 minutes (~12 min) is spent in MVPA.10 This is consistent with earlier findings, 11-13 and falls significantly short of the Centers for Disease Control and Prevention’s recommendations of at least 50% of the PE class period being in MVPA.14 Fewer than 4% of elementary schools provide daily PE, and walking or bicycling to school and recess time have decreased.4 Although physical activity is associated with favorable academic performance,15 school administrators have been unwilling to increase or improve PE. Thus, the highly utilized after-school care setting has been suggested as important for facilitating physical activity.16 Although the provision of dedicated time and space for physical activity during after-school care is common, James J Annesi, PhD, FAAHB, FTOS, FAPA, is the Director of Wellness Advancement, YMCA of Metropolitan Atlanta and Professor in the Department of Health Promotion at Kennesaw State University in GA. E-mail: [email protected]. Linda L Vaughn, MS, MBA, is Director of Wellness Initiatives at the YMCA of Metropolitan Atlanta, GA. E-mail: [email protected]. 48 The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS Evidence-Based Referral: Effects of the Revised “Youth Fit 4 Life” Protocol on Physical Activity Outputs treatments or protocols have varied widely in terms of their supervision, structure, and physical outputs. 16,17 They have ranged from supervised “free play” (participation optional), to highly structured protocols based on accepted theoretical models of health behavior change. Youth Fit For Life (YFFL), first evaluated in 2005,18 was one such structured program; it is based on tenets of social cognitive theory19 and self-efficacy theory20 such as building self-regulatory skills and feelings of ability and mastery, and utilizing social supports. It included components of cardiovascular exercise, resistance exercise, self-regulation skills building (eg, goal setting, controlled self-talk), and nutrition education. Although elementary after-school care treatments have often been atheoretical and lacking in significant health outcomes, numerous studies suggested the positive impact of YFFL on physical activity (both within and outside of structured settings),21-23 body mass index (BMI), 24 psychological wellbeing,25-27 and psychosocial predictors of health behaviors.18,22,23,28 After its validation, YFFL was made available nationally as a program certified by the Research-Tested Intervention Program of the National Institutes of Health and the National Cancer Institute (http:// rtips.cancer.gov/rtips/programDetails.do?programId = 293932), usable within a number of community-based venues serving elementary school-age youths. In an effort to better tailor the treatment processes of the Original YFFL to specific age ranges, enhance self-regulatory skills training, improve participants’ nutrition behaviors, better address overweight/obesity, and further increase time in MVPA, a revision of the YFFL protocol (entitled Youth Fit 4 Life [YF4L]) was recently developed. The present preliminary study aimed to contrast the Revised YF4L with typical care and the Original YFFL on time in MVPA during elementary after-school care, while also considering the sex of participants. This is the first investigation on the effects of YF4L, which sought to extend and improve upon YFFL by maximizing participants’ time in cardiovascular exercise, making The Permanente Journal/ Summer 2015/ Volume 19 No. 3 self-regulation skills more palatable, and better supporting consistent nutrition themes. Ages 9-12 were selected for this investigation because there was a somewhat different YF4L curriculum for ages 5-8 and 9-12 (suggesting the need for separate study). It was expected that the Revised YF4L treatment would be associated with a significantly greater duration of time in MVPA, and significantly less time in sedentary and light physical activities, than both the Original YFFL treatment and typical after-school care processes. Boys were expected to demonstrate greater time in MVPA, regardless of group. It was hoped that this initial validation study would inform revisions of the YF4L treatment in regard to its effects on physical activity outputs. Also, results might provide data for pediatricians to assess the usefulness of YF4L for referral of their patients. METHODS Participants Participants included youths, ages 9-12 years, enrolled in randomly selected elementary after-school care programs operated by YMCA facilities in the greater Atlanta, GA, area. Parents/ legal guardians signed written consent forms, and participants provided verbal assent to study staff. Institutional review board approval was received, and processes conformed to the provisions of the Declaration of Helsinki. An inclusion requirement was attendance in at least 2 of the 3 monthly measurement sessions. Data were excluded if a youth arrived late or left early, demonstrated inappropriate behavior, or reported an injury. Thus, the final sample sizes for the 1) typical after-school care processes (Comparison, n = 46), 2) Original YFFL protocol (n = 49), and 3) Revised YF4L protocol (n = 43) reflected those adjustments. The sample size adjustments did not significantly differ by group (χ2(df = 2) = 1.09, p = 0.579), with a mean removal of 26.9% of youths, overall, caused by the above conditions. There was also no significant group difference in age (F2, 135 = 0.90, p = 0.410; overall mean ± SD = 9.7 ± 0.8 years), sex (χ2(df = 2) = 2.37, p = 0.305; 51.4% girls, overall), or ethnic grouping (χ2(df = 8) = 14.10, p = 0.079; 31.9% white, 43.5% African American, 14.5% Hispanic, 6.5% Asian, and 3.6% of other ethnicities, overall). On the basis of postal zip codes of participants’ residences, almost all were in the middle class. Measures Physical activity intensity category and time were quantified using the Actigraph GT3X accelerometer (ActiGraph, Pensacola, FL). Consistent with previous research,29 the monitor was attached at the left side of the waist with a belt, over participants’ clothing. A 30-s sampling interval (epoch) was used to best capture activity patterns found in youths of ages 9 to 12 years.30 The accelerometer recorded 45 minutes (± 1 min) of physical activity during each of the 3 monthly measurements. No measurements were made in the initial week of after-school care because the learning of new physical activity tasks associated with the present protocols might have affected outputs most during this time. The ActiGraph ActiLife data analysis software, version 5.10.0 (ActiGraph, Pensacola, FL), converted accelerometer counts into time in sedentary, light, moderate, and vigorous physical activity on the basis of cut points established by Evenson,30 which were subsequently determined to be the most accurate estimations available for ages 5 to 15 years.31 MVPA was derived by summing the times in moderate and vigorous physical activity. Several previous studies reported strong interinstrument reliability of the ActiGraph accelerometer (r = 0.84-0.92).32-34 There were also significant correspondences between scores derived from the ActiGraph accelerometer and VO2 treadmill testing (r = 0.82-0.87)34 and doubly labeled water measurements (r = 0.39-0.54)35 in children within the age range of this research. It was suggested that the ActiGraph accelerometer had the largest body of research supporting its use.36 Procedure YMCA-based after-school care was administered in the same elementary school that participants attended during 49 ORIGINAL RESEARCH & CONTRIBUTIONS Evidence-Based Referral: Effects of the Revised “Youth Fit 4 Life” Protocol on Physical Activity Outputs the school day by the existing afterschool care counselors. Regardless of group, the school gymnasium was used for the standard session of 45 min/day reserved for physical activity. Study staff secured the accelerometers to each participant’s waist. Although it was obvious that the accelerometer assessed physical activity, there was no coaching given to participants or counselors by study staff to either maximize or minimize intensities. As far as possible, all were kept blind to the purposes of the study. After-school care Competition with counselors were generally unoneself, rather familiar with PE instruction than with other methods before the trainparticipants, was ing provided on the present emphasized. protocols. No counselor was involved with more than 1 group. The number of participants per group ranged from 10 to 18, although not all youths present were included in this research (owing mostly to an inability of study staff to secure written consent from parents/guardians). For the Comparison group, there was no training provided to afterschool care counselors beyond information needed for supervision of physical activity in a safe environment. This was provided during the job orientation. For this study, counselors were asked to administer the physical activity component of after-school care in the manner that was typical for them. Some participants ran, some played skill-games in small groupings, and some engaged in primarily sedentary pursuits. It was also an option for participants to use the sport or physical activity equipment (eg, balls and jump ropes) that were stored in the gymnasium. For the Original YFFL group, afterschool care counselors were provided 5 hours of training in the protocol’s 4 components: cardiovascular exercise, strength exercise (via rubber resistance bands), behavioral skills, and nutrition. This was supported by an instructor manual and participant workbook that guided program processes37 and the required apparatus (eg, balls, bean bags, resistance bands). In addition to the behavioral skills (eg, short- and longterm goal setting, obtaining progress feedback, thought stopping and use of 50 productive self-talk, recruiting social supports) and nutrition-education components, 30 to 35 minutes was to be dedicated to physical activity via noncompetitive games or tasks that were designated as either high or moderate intensity. Every attempt was to be made to keep participants 1) active, 2) challenging themselves, and 3) fostering feelings of mastery and self-efficacy regarding their fitness and physical abilities. The treatment was intended for ages 5 to 12 years. For the Revised YF4L group, afterschool care counselors were provided a newly designed training of approximately 5 hours, a supporting manual, and apparatus similar to the Original YFFL.38 There was a separate training manual for ages 5 to 8 years; however, only the 9- to 12-year-old version applied here.38 Although application of behavioral skills training and nutrition education remained in the Revised YF4L (in an enhanced form), the separate strength training component was omitted. Rather, participants’ own body weight now replaced use of the resistance bands in an effort to minimize time being nearly stationary. Also, both behavior and nutrition topics were reinforced through the use of a new array of cardiovascular activities (ie, “content reinforcement activities”), and new moderate- and high-intensity tasks were incorporated. Competition with oneself, rather than with other participants, was emphasized. On the basis of earlier research on the Original YFFL,21,23 behavioral skills and their associated graphics (eg, posters, hand-outs) were intended to better improve participants’ physical self-concept, fitness goal progress, and self-efficacy. As with the Original YFFL, 30 to 35 min/session was to be dedicated to physical activities, and a goal of attaining a mean of 25 to 30 minutes in MVPA was set. Although the physical activity component of after-school care was five days/week, and the Original YFFL and Revised YF4L protocols met three days/ week and four days/week, respectively, analyses were based on single sessions to facilitate statistical contrasts. All personal identifiers were removed before data analyses. Fidelity checks for physical activity programming were completed once every two weeks by YMCA wellness staff using a structured observation form. Any problems were quickly resolved in association with the after-school counselor’s supervisor. Data Analyses To detect the moderate effect size found in related analyses and pilot research39 at the statistical power of 0.80, an overall minimum sample size of 117 was required.40 The significance level was set at α = 0.05 (2-tailed). It was previously suggested that 3 accelerometer measurements foster accuracy in assessing physical activity outputs in youth.41 Thus, after using the expectation-maximization algorithm for imputation of missing data of no more than 1 of the 3 monthly measurements,42 the mean number of minutes in each physical activity category (ie, sedentary, light, moderate, and vigorous) was calculated. There was no significant difference in scores based on date of measurement for any of the physical activity categories. For the primary analysis, a 2-way between-subjects analysis of variance of 3 (groups) × 2 (sexes) was used to contrast the Comparison, Original YFFL, and Revised YF4L groups; boys and girls; and their interaction on mean number of minutes in MVPA. Post hoc followup tests using the Least Significant Difference method were incorporated for pairwise contrasts. Supplementary analyses were also completed on each of the 4 separately measured physical activity intensity categories (ie, sedentary, light, moderate, and vigorous) in the same manner. Effect sizes were expressed as partial eta-square (η2p) where 0.01, 0.06, and 0.14 denote small, moderate, and large effects, respectively. RESULTS Primary Analysis For MVPA, the main effect for treatment group was significant (F2, 132 = 281.20, p < 0.001, η2p = 0.17). The main effect for sex was also significant (F2, 132 = 16.43, p < 0.001, η2p = 0.11). There was not a significant group × sex interaction (F2, 132 = 0.54, p = 0.582, η2p = 0.01). Descriptive statistics and The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS Evidence-Based Referral: Effects of the Revised “Youth Fit 4 Life” Protocol on Physical Activity Outputs results of all pairwise post hoc analyses are given in Table 1. Supplementary Analyses For sedentary time, the main effect for treatment group was significant (F2, 132 = 5.57, p = 0.005, η2p = 0.08). The main effect for sex was not significant (F2, 132 = 1.91, p = 0.169, η2p = 0.01). There was not a significant group × sex interaction (F2, 132 = 0.21, p = 0.813, η2p = 0.003). For light physical activity, the main effect for treatment group was not significant (F2, 132 = 2.08, p = 0.130, η2p = 0.03). The main effect for sex was significant (F2, 132 = 4.81, p = 0.030, η2p = 0.04). There was not a significant group × sex interaction (F2, 132 = 0.29, p = 0.748, η2p = 0.004). For moderate physical activity, the main effect for treatment group was not significant (F2, 132 = 2.52, p = 0.085, η2p = 0.04). The main effect for sex was significant (F2, 132 = 12.01, p = 0.001, η2p = 0.08). There was not a significant group × sex interaction (F2, 132 = 1.05, p = 0.354, η2p = 0.02). For vigorous physical activity, the main effect for treatment group was significant (F2, 132 = 24.13, p < 0.001, η2p = 0.27). The main effect for sex was also significant (F2, 132 = 10.04, p = 0.002, η2p = 0.07). There was not a significant group × sex interaction (F2, 132 = 0.37, p = 0.692, η2p = 0.01). Table 1. Minutes in physical activity intensity categories, by group and participants’ sex Boys Mean ± SD (n) Group Moderate-to-vigorous physical activity Comparison 13.51 ± 5.57 (21) Original YFFL 14.70 ± 3.46 (28) Revised YF4L 17.48 ± 4.76 (18) Overall 15.07* ± 4.75 (67) Sedentary time Comparison 11.23 ± 6.69 (21) Original YFFL 10.12 ± 5.19 (28) Revised YF4L 7.80 ± 3.05 (18) Overall 9.84 ± 5.36 (67) Light physical activity Comparison 20.26 ± 6.66 (21) Original YFFL 21.01 ± 2.84 (28) Revised YF4L 19.67 ± 4.95 (18) Overall 20.42 ± 4.83 (67) Moderate physical activity Comparison 9.54 ± 4.23 (21) Original YFFL 8.76 ± 2.00 (28) Revised YF4L 9.98 ± 2.68 (18) Overall 9.33* ± 3.03 (67) Vigorous physical activity Comparison 3.97 ± 2.33 (21) Original YFFL 5.94 ± 2.42 (28) Revised YF4L 7.50* ± 3.17 (18) Overall 5.74 ± 2.91 (67) Girls Mean ± SD (n) Overall Mean ± SD (n) 9.25 ± 6.32 (25) 11.43 ± 3.69 (21) 15.29 ± 3.43 (25) 12.02 ± 5.32 (71) 11.19a ± 6.30 (46) 13.30a ± 3.88 (49) 16.20b ± 4.14 (43) 13.50 ± 5.26 (138) 12.99 ± 6.69 (25) 10.60 ± 4.23 (21) 9.19 ± 2.69 (25) 10.94 ± 5.06 (71) 12.19a ± 6.68 (46) 10.32 ± 4.76 (49) 8.61b ± 2.90 (43) 10.41 ± 5.22 (138) 22.49 ± 3.42 (25) 22.93 ± 4.50 (21) 20.52 ± 3.91 (25) 21.93*± 4.02 (71) 21.47 ± 5.22 (46) 21.83a ± 3.73 (49) 20.16b ± 4.34 (43) 21.19 ± 4.48 (138) 6.54 ± 4.54 (25) 7.33 ± 2.69 (21) 8.75 ± 2.03 (25) 7.55 ± 3.38 (71) 7.91a ± 4.61 (46) 8.15a ± 2.40 (49) 9.26b ± 2.38 (43) 8.42 ± 3.33 (138) 2.71 ± 1.99 (25) 4.10 ± 1.88 (21) 6.54 ± 2.93 (25) 4.47 ± 2.83 (71) 3.28a ± 2.22 (46) 5.15b ± 2.37 (49) 6.94c ± 3.03 (43) 5.09 ± 2.93 (138) A different letter superscript adjacent to the mean score (a, b, or c) within the same measure denotes a statistically significant difference within the post hoc test among the 3 groups (Comparison, Original Youth Fit For Life [YFFL], Revised Youth Fit 4 Life [YF4L]). For example, in the moderate-to-vigorous physical activity measure, the Comparison and Original YFFL groups did not significantly differ from each other, but the Revised YF4L group did significantly differ from both. An asterisk (*) within the same measure denotes a significantly greater score, by sex. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 DISCUSSION The Revised YF4L treatment was associated with a significantly greater duration of time in accelerometermeasured MVPA when contrasted with typical after-school care and the Original YFFL protocol. This is an important finding because numerous studies suggested the positive effects of the original theory-based protocol on various health behaviors and their psychosocial predictors.18,22-28 For the Revised YF4L, sedentary time was also significantly less than with typical after-school care processes. Consistent with other research,7 boys were more active than girls. Although there was no treatment × sex interaction found, future research should integrate and evaluate intervention components that might increase MVPA specifically for girls (possibly by incorporating modes of activity that might be especially appealing to them). Although it was above the typical proportion of MVPA/overall time in PE class previously reported for elementary school ages,10-13 the goal of 25 to 30 minutes/day in MVPA was not attained. Approximately one-third of the treatment time presently spent in light physical activity and sedentary time (~9 min/day) would need to be converted to moderate and/or vigorous activity to attain that goal. Although an attempt was made to reinforce the learning of behavioral skills and nutrition information through physical activities, such activities might also be extended to the time during the learning process itself to increase total time in MVPA in the future. Limitations Although various ethnicities were represented, future research should evaluate the benefit of YF4L specifically in underrepresented and minority groups, who also tend to have the greatest health risks.1 Replication should also be completed on the YF4L version for ages 5 to 8 years. Although limitations included a lack of data on 1) psychosocial mediators of MVPA; 2) effects on BMI, nutrition, and changes in MVPA outside of the programs, and 3) expectation effects (eg, Hawthorne effect; 51 ORIGINAL RESEARCH & CONTRIBUTIONS Evidence-Based Referral: Effects of the Revised “Youth Fit 4 Life” Protocol on Physical Activity Outputs Rosenthal effect),43 these initial findings on the Revised YF4L protocol in elementary after-school care were informative. Additional validation research is now required to evaluate effects of YF4L on BMI and psychosocial factors. Also, because resistance training was omitted in the new YF4L curriculum (except for some body weight resistance incorporated within the increased cardiovascular exercise time), favorable benefits related to muscle mass and muscular strength gains might have been reduced. CONCLUSION It is hoped that, ultimately, widespread dissemination of evidence- and theory-based protocols such as YF4L will allow pediatricians to have confidence in referring patients in need of programs for increasing their MVPA and, possibly, normalizing their BMI. Involvement from physicians in matters of health behavior change is increasingly warranted and could have immense pay-offs for the future health of the nation. v Disclosure Statement The author(s) have no conflicts of interest to disclose. Acknowledgments We acknowledge Sarah Samter and Brittney Greenwood for their expertise provided in the data collection phase of this study. We also acknowledge contributions provided on protocol development by the staff of Children’s Healthcare of Atlanta. Mary Corrado, ELS, provided editorial assistance. References 1. Ogden CL, Carroll MD, Kit BK, Flegal KM. Prevalence of childhood and adult obesity in the United States, 2011-2012. JAMA 2014 Feb 26;311(8):806-14. DOI: http://dx.doi.org/10.1001/ jama.2014.732. 2. Daniels SR, Arnett DK, Eckel RH, et al. Overweight in children and adolescents: pathophysiology, consequences, prevention, and treatment. Circulation 2005 Apr 19;111(15):19992012. DOI: http://dx.doi.org/10.1161/01. CIR.0000161369.71722.10. 3. Dietz WH. Overweight in childhood and adolescence. N Engl J Med 2004 Feb 26;350(9):855-7. DOI: http://dx.doi.org/10.1056/ NEJMp048008. 4. Building evidence to prevent childhood obesity [Internet]. Minneapolis, MN: Healthy Eating Research; [cited 2015 Apr 22]. Available from: http://healthyeatingresearch.org/who-we-are/thechildhood-obesity-epidemic/. 52 5. Must A, Tybor DJ. Physical activity and sedentary behavior: a review of longitudinal studies of weight and adiposity in youth. Int J Obes (Lond) 2005 Sep;29 Suppl 2:S84-96. DOI: http://dx.doi. org/10.1038/sj.ijo.0803064. 6. Childhood obesity facts [Internet]. Atlanta, GA: Centers for Disease Control and Prevention; [updated 2014 Dec 11; cited 2015 Mar 18]. Available from: www.cdc.gov/healthyyouth/ obesity/facts.htm. 7. Troiano RP, Berrigan D, Dodd KW, Mâsse LC, Tilert T, McDowell M. Physical activity in the United States measured by accelerometer. Med Sci Sports Exerc 2008 Jan;40(1):181-8. DOI: http://dx.doi.org/10.1249/ mss.0b013e31815a51b3. 8. Lenhart CM, Hanlon A, Kang Y, Daly BP, Brown MD, Patterson F. Gender disparity in structured physical activity and overall activity level in adolescence: evaluation of youth risk behavior surveillance data. ISRN Public Health [Internet] 2012 [cited 2015 Mar 12];2012:[8 p]. DOI: http:// dx.doi.org/10.5402/2012/674936. Available from: www.hindawi.com/journals/isrn/2012/674936/cta/. 9. Svetkey LP, Stevens VJ, Brantley PJ, et al; Weight Loss Maintenance Collaborative Research Group. Comparison of strategies for sustaining weight loss: the weight loss maintenance randomized controlled trial. JAMA 2008 Mar 12;299(10):1139-48. DOI: http://dx.doi. org/10.1001/jama.299.10.1139. 10. Matthews-Ewald MR, Moore LC, Harris CV, Bradlyn AS, Frost SS. Assessing moderate to vigorous physical activity in rural West Virginia elementary school physical education classes. W V Med J 2013 Jul-Aug;109(4):12-6. 11. McKenzie TL, Feldman H, Woods SE, et al. Student activity levels and lesson context during third-grade physical education. Res Q Exerc Sport 1995 Sep;66(3):184-93. DOI: http://dx.doi. org/10.1080/02701367.1995.10608832. 12. Simons-Morton BG, Taylor WC, Snider SA, Huang IW. The physical activity of fifth-grade students during physical education classes. Am J Public Health 1993 Feb;83(2):262-4. DOI: http:// dx.doi.org/10.2105/AJPH.83.2.262. 13. UCLA Center to Eliminate Health Disparities; Samuels & Associates. Failing fitness: physical activity and physical education in schools [Internet]. Los Angeles, CA: The California Endowment; 2007 Jan [cited 2014 Oct 15]. Available from: www.calendow.org/uploadedFiles/ failing_fitness.pdf. 14. Guidelines for school and community programs to promote lifelong physical activity among young people [Internet]. Atlanta, GA: Centers for Disease Control and Prevention; 1997 Mar 7 [cited 2014 Oct 15]. Available from: http://wonder.cdc.gov/ wonder/Prevguid/m0046823/m0046823.asp. 15. Rasberry CN, Lee SM, Robins L, et al. The association between school-based physical activity, including physical education, and academic performance: a systematic review of the literature. Prev Med 2011 Jun;52 Suppl 1:S10-20. DOI: http://dx.doi.org/10.1016/j. ypmed.2011.01.027. 16. Atkin AJ, Gorely T, Biddle SJ, Cavill N, Foster C. Interventions to promote physical activity in young people conducted in the hours immediately after school: a systematic review. Int J Behav Med 2011 Sep;18(3):176-87. DOI: http://dx.doi. org/10.1007/s12529-010-9111-z. 17. Beets MW, Huberty J, Beighle A; Healthy Afterschool Program Network. Physical activity of children attending afterschool programs: research- and practice-based implications. Am 18. 19. 20. 21. 22. 23. 24. 25. 26. 27. 28. 29. 30. 31. J Prev Med 2012 Feb;42(2):180-4. DOI: http:// dx.doi.org/10.1016/j.amepre.2011.10.007. Annesi JJ, Westcott WL, Faigenbaum AD, Unruh JL. Effects of a 12-week physical activity protocol delivered by YMCA after-school counselors (Youth Fit For Life) on fitness and self-efficacy changes in 5-12-year-old boys and girls. Res Q Exerc Sport 2005 Dec;76(4):468-76. DOI: http://dx.doi.org/10.1080/02701367.2005. 10599320. Bandura A. Health promotion by social cognitive means. Health Educ Behav 2004 Apr;31(2):143-64. DOI: http://dx.doi. org/10.1177/1090198104263660. Bandura A. Self-efficacy: the exercise of control. New York, NY: WH Freeman Publishers; 1997. Annesi JJ. Relations of physical self-concept and self-efficacy with frequency of voluntary physical activity in preadolescents: implications for after-school care programming. J Psychosom Res 2006 Oct;61(4):515-20. DOI: http://dx.doi. org/10.1016/j.jpsychores.2006.04.009. Annesi JJ, Moore JC, Dixon GM. Correlates of changes in voluntary physical activity associated with the Youth Fit For Life intervention during after-school care. Psychol Rep 2008 Jun;102(3):911-9. DOI: http://dx.doi.org/10.2466/ pr0.102.3.911-919. Annesi JJ, Faigenbaum AD, Westcott WL, Smith AE. Relations of self-appraisal and mood changes with voluntary physical activity changes in African American preadolescents in an afterschool care intervention. J Sports Sci Med 2008 Jun 1;7(2):260-8. Annesi JJ, Marti CN, Stice E. A meta-analytic review of the Youth Fit For Life intervention for effects on body mass index in 5- to 12-year-old children. Health Psychol Rev 2010;4(1):6-21. DOI: http://dx.doi.org/10.1080/17437190903168561. Annesi JJ. Relations of age with changes in self-efficacy and physical self-concept in preadolescents participating in a physical activity intervention during afterschool care. Percept Mot Skills 2007 Aug;105(1):221-6. DOI: http://dx.doi. org/10.2466/pms.105.1.221-226. Annesi JJ. Improvements in self-concept associated with reductions in negative mood in preadolescents enrolled in an after-school physical activity program. Psychol Rep 2005 Oct;97(2):400-4. DOI: http://dx.doi.org/10.2466/ pr0.97.2.400-404. Annesi JJ. Correlations of depression and total mood disturbance with physical activity and self-concept in preadolescents enrolled in an after-school exercise program. Psychol Rep 2005 Jun;96(3 Pt 2):891-8. DOI: http://dx.doi. org/10.2466/pr0.96.3c.891-898. Annesi JJ, Faigenbaum AD, Westcott WL. Relations of transtheoretical model stage, selfefficacy, and voluntary physical activity in African American preadolescents. Res Q Exerc Sport 2010 Jun;81(2):239-44. DOI: http://dx.doi.org/10.1 080/02701367.2010.10599671. Pate RR, Almeida MJ, McIver KL, Pfeiffer KA, Dowda M. Validation and calibration of an accelerometer in preschool children. Obesity (Silver Spring) 2006 Nov;14(11):2000-6. DOI: http://dx.doi.org/10.1038/oby.2006.234. Evenson KR, Catellier DJ, Gill K, Ondrak KS, McMurray RG. Calibration of two objective measures of physical activity for children. J Sports Sci 2008 Dec;26(14):1557-65. DOI: http://dx.doi.org/10.1080/02640410802334196. Trost SG, Loprinzi PD, Moore R, Pfeiffer KA. Comparison of accelerometer cut points for predicting activity intensity in youth. Med Sci The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS Evidence-Based Referral: Effects of the Revised “Youth Fit 4 Life” Protocol on Physical Activity Outputs 32. 33. 34. 35. Sports Exerc 2011 Jul;43(7):1360-8. DOI: http:// dx.doi.org/10.1249/MSS.0b013e318206476e. Metcalf BS, Curnow JS, Evans C, Voss LD, Wilkin TJ. Technical reliability of the CSA activity monitor: The EarlyBird Study. Med Sci Sports Exerc 2002 Sep;34(9):1533-7. Puyau MR, Adolph AL, Vohra FA, Butte NF. Validation and calibration of physical activity monitors in children. Obes Res 2002 Mar;10(3):150-7. DOI: http://dx.doi.org/10.1038/ oby.2002.24. Trost SG, Ward DS, Moorehead SM, Watson PD, Riner W, Burke JR. Validity of the computer science and applications (CSA) activity monitor in children. Med Sci Sports Exerc 1998 Apr;30(4):629-33. DOI: http://dx.doi. org/10.1097/00005768-199804000-00023. Ekelund U, Sjöström M, Yngve A, et al. Physical activity assessed by activity monitor and doubly 36. 37. 38. 39. labeled water in children. Med Sci Sports Exerc 2001 Feb;33(2):275-81. DOI: http://dx.doi. org/10.1097/00005768-200102000-00017. de Vries SI, Bakker I, Hopman-Rock M, Hirasing RA, van Mechelen W. Clinimetric review of motion sensors in children and adolescents. J Clin Epidemiol 2006 Jul;59(7):670-80. DOI: http://dx.doi.org/10.1016/j.jclinepi.2005.11.020. Annesi J, Westcott W, Faigenbaum A. Youth Fit For Life training manual. Atlanta, GA: YMCA of Metropolitan Atlanta; 2005. Annesi JJ, Walsh SM, Smith AE, et al. Youth Fit 4 Life program training manual, ages 9-12. Atlanta, GA: Children’s Healthcare of Atlanta; 2014. Annesi JJ, Faigenbaum AD, Westcott WL, Smith AE, Unruh JL, Hamilton FG. Effects of the Youth Fit For Life protocol on physiological, mood, self-appraisal, and voluntary physical activity changes in African American preadolescents: 40. 41. 42. 43. contrasting after-school care and physical education formats. Int J Clin Health Psychol 2007;7(3):641-59. Cohen J. Statistical power analysis for the behavioral sciences. 2nd ed. Mahwah, NJ: Lawrence Erlbaum Associates; 1988. Pate RR, Pfeiffer KA, Trost SG, Ziegler P, Dowda M. Physical activity among children attending preschools. Pediatrics 2004 Nov;114(5):1258-63. DOI: http://dx.doi. org/10.1542/peds.2003-1088-L. Schafer JL, Graham JW. Missing data: our view of the state of the art. Psychol Methods 2002 Jun;7(2):147-77. DOI: http://dx.doi. org/10.1037//1082-989X.7.2.147. Morgan WP. Methodological considerations. In: Morgan WP, editor. Physical activity and mental health. Washington, DC: Taylor & Francis; 1997. p 3-32. Exercise Nothing is to be found that can substitute for exercise in any way … . Exercise will expel the harm done by most of the bad regimens that most men follow. Not all motion is exercise. Exercise is powerful or rapid motion or a combination of both, vigorous motion which alters breathing and increases its rate. — Moses Maimonides, 1138-1204, medieval Sephardic Jewish philosopher, astronomer, Torah scholar, and physician The Permanente Journal/ Summer 2015/ Volume 19 No. 3 53 credits available for this article — see page 96. ORIGINAL RESEARCH & CONTRIBUTIONS Relationship between Participation in Patient- and Family-Centered Care Training and Communication Adaptability among Medical Students: Changing Hearts, Changing Minds Lisa Rossignol, MA Perm J 2015 Summer;19(3):54-58 http://dx.doi.org/10.7812/TPP/14-110 ABSTRACT Background: Patient- and family-centered care (PFCC) training is an important component of many medical school curricula in the US. Purpose: To determine if an existing quantitative measure of communication adaptability can be used to determine skills acquired by medical students after PFCC training. Methods: A census was conducted of 43 third-year medical students at the University of New Mexico School of Medicine, Albuquerque, NM. Students participated in the Families as Faculty program of Parents Reaching Out during their pediatric rotation. A pretest and posttest of Duran’s 1983 Communicative Adaptability Scale was performed. Results: A one-way analysis of variance was conducted and revealed that there was statistical significance for the factor called appropriate disclosure (p = 0.04). When mean plot was conducted, there was a positive correlation between pretest and posttests in social experience, wit, and social confirmation. There was a negative correlation for articulation and social composure, which was not significant. Conclusion: The Communicative Adaptability Scale was an effective way to evaluate communication skills that students acquire from PFCC training. An increase in appropriate disclosure is an important gain because it means students have become more sensitive to the level of intimacy that the other person is seeking and the student is willing to offer more information. Information sharing is one of the core concepts of PFCC. Finally, the negative correlation for articulation and social composure indicate that Families as Faculty may increase anxiety for medical students, so this is an area of the education that may need to be revisited. INTRODUCTION This study seeks to determine if a standardized measurement of communicative adaptability can be used to evaluate skills taught to medical students after patient- and family-centered care (PFCC) training. PFCC care ensures the health and well-being of children and their families through a respectful professional-family partnership. It honors the strengths, cultures, traditions, and expertise that everyone brings to this relationship. According to the US Maternal and Child Health Bureau Division of Services for Children with Special Health Needs, family-centered care is the standard of practice that results in high-quality services.1 The University of New Mexico in Albuquerque, NM, uses the services of these two programs: Families as Faculty (FAF), which is a division of Parents Reaching Out, a statewide nonprofit interested in advocacy for individuals with disabilities, and the New Mexico Leadership Education in Neurodevelopmental and Related Disabilities, located at the university’s Center for Development and Disability. Families that have a child with a disability welcome a medical student from the University of New Mexico into their home for an informal visit, in which the family members talk openly about their collective experience with various practitioners and medical systems. The goal is that medical students gain insight into how families function and how they feel about health care, which leads to the acquisition of communication skills that deliver greater expressions of respect and dignity, information sharing, participation, and collaboration.2 Despite several attempts by other universities to study PFCC training, there has been little success in articulating what students are learning or how they are being professionally transformed. Because PFCC training is delivered through the mode of verbal and nonverbal communication from health care workers, PFCC education would influence how students communicate. This study seeks to determine if an existing construct, the Communicative Adaptability Scale (CAS), is an effective tool to evaluate whether students acquire the ability to communicate more effectively because of PFCC training. LITERATURE REVIEW The purpose of this literature review is to build the theoretical groundwork for evaluating what effect PFCC education has on the communication adaptability that medical students use with patients when they become physicians. This study is an effort to corroborate the expectations of these programs or to produce recommended modifications to the programs or future studies. As knowledge of the concepts of PFCC grow in popularity among hospital administrators, there continues to be very little study about the effectiveness of educational programs on this topic. There has been limited success in capturing any data about PFCC education and the impact it Lisa Rossignol, MA, is the current Fellow at the Georgetown Leadership Academy in Cultural Competence and Cultural and Linguistic Diversity in Santa Fe, NM. She served for two years on the Patient Centered Outcomes Research Initiative Improving Healthcare Systems Advisory Board, and is now serving as Parent Liaison to the American Academy of Pediatrics’ Council on Quality Improvement and Patient Safety. NM. E-mail: [email protected]. 54 The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS Relationshipbetween Participation inPatientandFamily-Centered CareTraining andTraining Communication Relationship between Participation in Patientand Family-Centered Care and AdaptabilityamongMedicalStudents:ChangingHearts,ChangingMinds Communication Adaptability among Medical Students: Changing Hearts, Changing Minds has on professional-family communication. Cegala and Broz3 posit that of the physician training research that has been conducted, “Less than 30% of the studies … had a design adequate for assessing the effects of training interventions … .” If PFCC training is not working in the manner that is expected, it may be necessary to modify education programs or to abandon initiatives altogether. In exploring this question, it is important to look at a study that has examined the population of college students for relationships between communication adaptability and intercultural apprehension. Duran4 defines communication adaptability as “the ability to perceive socio-interpersonal relationships and adapt one’s interaction goals and behaviors accordingly.” Intercultural apprehension is defined as follows: “One’s level of fear or anxiety associated with interacting with people of different cultures and ethnic and/ or racial groups.”5 Long and Anarbaeva6 used the CAS, which has a high interitem reliability (α = 0.948), and the Personal Report of Intercultural Communication Apprehension, which also has a high interitem reliability (Cronbach α = 0.941).7 The questionnaire was completed by 124 graduate and undergraduate students between the ages of 18 and 45 years. A strong relationship between the 2 variables was revealed. Long and Anarbaeva concluded: “As communicative adaptability increased, intercultural communication apprehension decreased.” This study showed that a clear relationship exists between communication adaptability and intercultural apprehension. Next, intercultural communication must be linked to physician-patient relationships. Manderson and Allotey8 defined intercultural or cross-cultural communication as the “conveying of information and the response to the information in an interaction between members from different cultures.” They proposed that “In the clinical interaction, this occurs between individuals from a culture of health professionals and individuals who fall into the category of ‘patient’ or ‘sick client.’” Manderson and Allotey suggested that the greatest deficit of the prevailing participatory decision-making model8,9 is that it lacks an education component for the physician. The participatory decision-making model supposes that the clinician might employ variations of education for the patient but does not factor the demand for a physician to be educated by a patient with a different cultural background and belief system. “These influences affect the development of a sense of the other’s competence, the practitioner’s sense of the patient’s ability to comply with treatment, and the practitioner’s ability to deliver effective treatment.”8 In a study designed to monitor the long-term reproductive health issues of African and Middle Eastern refugees in Australia, researchers studied 150 women by using quantitative instruments, focus groups, and interviews. They wrote, “Twenty percent specifically raised issues of communication difficulties with the health services, which included the lack of availability of interpreters, the practitioner giving them information that they perceived to be inappropriate, and an inability of doctors to ‘hear what they were being told.’”10 Despite the women being from diverse ethnic, economic, The Permanente Journal/ Summer 2015/ Volume 19 No. 3 and religious backgrounds, there was a “strong perception of discrimination, miscommunication and poor quality service provision within health and welfare agencies.” Hamilton11 continued the evaluation of the participatory decision-making model of physician-patient interaction. This model is taught in most Western universities and assumes that patients “both linguistically and culturally are equipped to engage in a discussion with their doctor about diagnosis and treatment, working together to develop a treatment management plan.” As was discussed by Manderson and Allotey, patients represent their own culture, which might not benefit from this traditional model.8 Hamilton proposed that effective communication by practitioners would require “… multiple models to accommodate cultural and other differences in their patients.”11 Franck and Callery12 conducted an extensive, critical literature review of all PFCC literature in an attempt to find operational definitions, themes, constructs, and empirical indicators. The authors found inconsistency in definition of terms and in the practical application of PFCC throughout various systems. The largest deficit cited was that “health professionals’ judgments about the credibility of mothers’ reports sometimes led them to dismiss important assessments.” Franck and Callery were unable to find any evidence that education in PFCC concepts has led to any acquisition of skills and suggested that the construct of partnership “should lead to the concept of shared decision-making and subconcept of participation in decision-making.” Another study looked at cultural competency, intercultural communication, and family-centered care even more specifically by examining the experience of professionals working with children with special health care needs and their parents.13 The professionals studied were participants in the Virginia Leadership Education in Neurodevelopment and Related Disabilities program. Participants completed the program between 1996 and 2006 and had been working in their discipline for at least 1 year. The Measure of Processes of Care for Service Providers was used.14 The device contained 27 questions on a Likert-style scale that represented 4 factors of family-centered care: 1) showing interpersonal sensitivity, 2) providing general information, 3) communicating specific information about the child, and 4) treating people respectfully. Researchers also included a qualitative question: “What have been the greatest barriers to family-centered care in your occupation?” Thirty-three graduates of the Virginia Leadership Education in Neurodevelopment and Related Disabilities program replied to the survey, resulting in the identification of five major qualitative themes: 1) institutional culture, 2) absence of a care coordinator, 3) insufficient training in intercultural/ interpersonal communication skills, 4) policy factors, and 5) family factors. Quantitative results showed that “interdisciplinary professionals were providing care consistent with the principles of PFCC in the areas of treating people respectfully, communicating specific information to families, and showing interpersonal sensitivity.” The study recognized the very small population of respondents and suggested that only those who were actively engaged in PFCC practices responded. Lotze 55 ORIGINAL RESEARCH & CONTRIBUTIONS Relationship between Participation in Patient- and Family-Centered CareTrainingRelationship and Communication Adaptability among Changing Hearts, Changing Minds between Participation in Medical Patient- Students: and Family-Centered Care Training and Communication Adaptability among Medical Students: Changing Hearts, Changing Minds et al13 also recognized that no data from practitioners existed before they attended in-depth PFCC training. Finally, Johnson et al15 addressed the effectiveness of familycentered care education of medical students at the University of Vermont College of Medicine, Burlington, VT. That program was the template for the FAF program, which Parents Reaching Out and the University of New Mexico School of Medicine have used since 1997. When the University of Vermont medical students completed a visit with their family faculty, they were asked to complete and submit a paper on “what they learned from the family and how that might influence their practice in the future.” Three reviewers completed a pilot study that consisted of 45 papers collected from July 2001 to June 2002 in order to establish a set of themes. Then, a fourth, independent reviewer was given the task of reviewing 58 papers that were completed between July 2002 and June 2003 using the categories provided by the pilot study. An early theme that was found concerned the issues the families had with physicians; this theme was broken into 14 categories—all consisting of communication failures. The top 2 most frequent themes were collaboration with families and listening. The authors proposed that an evaluation of the application of communication skills resulting from this program would be an interesting study. Collectively these studies indicate a need for establishing measurements for the skill acquisitions that may result from PFCC training. Although the CAS has been used in very limited studies, the strong relationship it showed to intercultural apprehension7 makes it a desirable device for evaluating PFCC training. The hypothesis of the current research is that PFCC training will result in increased communicative adaptability by medical students. numbers were then entered into a chart that sorted the scores into 6 categories: social experience (the ability to take skills learned from previous encounters to improve future social exchanges and enjoy new and challenging social interactions); wit (skillful, intellectual humor); social composure (a speaker who appears to be calm and composed); articulation (an ability to speak clearly and to choose words appropriately); social confirmation (the ability to appropriately gauge what another person needs from an interaction); and appropriate disclosure (an ability to divulge or withhold appropriate amounts of personal information). Students were not provided with a space for any identifying information or demographic information for this study. After completion of the FAF seminar, the medical students were given the same survey. The posttest was administered, in paper form, at the end of the debriefing session at Parents Reaching Out. Again, subjects were not provided space for any demographic information such as sex, race, or age. METHODS RESULTS After an extensive literature review, I concluded that there was a need to establish measurements for the skill acquisitions that may result from PFCC training for medical students. The CAS has been used in very limited studies, but it has a high reliability and has been used in university students by Long and Anarbaeva,7 making it a strong device for measuring PFCC education programs. Although there are several newer, valid instruments for physicians who practice medicine, there has been little work looking directly at medical school education in PFCC or communication training and skills. A census was conducted of 71 medical students in their third year at the University of New Mexico School of Medicine beginning in August 2011 through August 2012. There was a 100% voluntary participation rate. Students participated in Parents Reaching Out’s FAF program during their pediatric rotation. A pretest was administered, in paper form, to medical students during their orientation into the FAF training at the University of New Mexico Hospital, Albuquerque, NM. The pretest used the CAS, which has a high interitem reliability (α = 0.948). The participants were asked to rate themselves with 30 Likert-style statements, with answers from 1 to 5, with 1 being “least likely” and 5 being “most likely.” The 56 Table 1. Impact of medical students’ training in patientand family-centered care on factors of Communicative Adaptability Scale Factor Social experience Wit Social composure Articulation Social confirmation Appropriate disclosure df 1, 84 1, 84 1, 84 1, 84 1, 84 1, 84 F ratio 1.60 1.48 0.01 0 1.89 4.39 p valuea 0.21 0.23 0.91 0.96 0.64 0.04 One-way between-groups analysis of variance, with significance < 0.05. df = degrees of freedom. a A one-way between-groups analysis of variance was conducted to explore the impact of PFCC training on medical students as measured by the CAS. Questionnaires were divided into pretest and posttests, and means were compared on the 6 factors: social experience, wit, social composure, articulation, social confirmation, and appropriate disclosure. There was statistical significance at the p < 0.04 for appropriate disclosure shown in Table 1. A mean plot was conducted on each of the six factors, which revealed a positive correlation between pretest and posttests for each factor except for social composure and articulation, which illustrated negative slopes (not significant). DISCUSSION The CAS questionnaire is a moderately effective way to evaluate communication skills that students acquire from PFCC training. An increase in appropriate disclosure is an important gain because it means students have likely become more sensitive to the level of intimacy that the other person is seeking and the student is willing to offer more information. Information sharing is one of the core concepts of PFCC, so gains in this factor are important. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS Relationshipbetween Participation inPatientandFamily-Centered CareTraining andTraining Communication Relationship between Participation in Patientand Family-Centered Care and AdaptabilityamongMedicalStudents:ChangingHearts,ChangingMinds Communication Adaptability among Medical Students: Changing Hearts, Changing Minds One possibility is that students learn the importance of articulating their own values about patients and families aloud. During the FAF presentation, the facilitator displayed a value statement that said, “We believe all families care deeply about their children” and continued to discuss the importance of articulating, to families, that physicians share these values. The values expressed by PFCC seem to be commonsense, but patients and families may not believe that physicians hold these ideas. Conversely, FAF may increase anxiety for medical students. Although not statistically significant, the mean plots did show a negative shift of skills relating to comfort with communicating and the ability to express ideas clearly. This area of the education may need to be revisited. One possible explanation for the rise in anxiety levels about communicating could stem from a new understanding that, to be successful, the students will have to become more intimate with some patients who desire interactions that are more intimate. The medical school curriculum does not necessarily provide instruction on ways to communicate with diverse populations of patients and families. Study Limitations The population size of this study was very small because the University of New Mexico only admits 60 to 75 students per year to the School of Medicine, so there is very little opportunity to increase the study population unless other universities that use FAF programs participate. At such a small size, it is difficult to assess outcomes of FAF training, on 6 factors, accurately. It is possible that a larger study could reveal more statistical significance between the pretest and posttest. Also, because this is a census of all medical students at the University of New Mexico’s School of Medicine in their third year and pediatric rotation, this information cannot be generalized to any other population. However, as a steppingstone to more robust, substantial studies into medical school education, this study provides an important contribution to the medical literature. The construction of this specific PFCC training may also be a factor in the outcome of this study. Although the speakers at the one-hour FAF orientation were almost always the same, the host families where students went were diverse in socioeconomic, racial, religious, and ethnic backgrounds. Future studies may need to conduct research into the type of messages that are being delivered via the host families. Perhaps the messages students are receiving are negative or hostile toward physicians, and that accounts for the negative tendency of posttest scores on the articulation and social composure elements. Evaluating the messages of host families may allow future researchers to control and test different styles of messaging or content during family visits to determine whether family stories have an impact on student experience. Possible confounding that may have occurred is additional PFCC training that students received from attending physicians and other residents during their pediatric rotation. Further study would be beneficial into the other types of The Permanente Journal/ Summer 2015/ Volume 19 No. 3 PFCC training the students are receiving during this rotation or other rotations. It is possible that students are receiving negative guidance from other staff that suggests communicating with families is not a high priority and that they will be penalized for spending too much time chatting with patients. Despite the possibility of contrary messages, this study documents that students are experiencing alterations in the way they perceive and adapt to what the other person needs from a communication interaction, which is a strong showing for a training program that is designed to improve how physicians and patients work together. The values expressed by PFCC seem to be commonsense, but patients and families may not believe that physicians hold these ideas. CONCLUSION Future studies may seek to link CAS scores with other measures, such as patient satisfaction scores or safety data. It is important to understand that this study was not intended to study physicians who are already practicing, but it may prove useful to link CAS scores with future performance of physicians once they have set up their own practice. Finally, the ultimate goal of this study was to link existing, highly reliable communication research measures to health care research. In the past few decades, physicians have begun to see the benefit of employing communication scholars in research that involves interaction and messaging. This notion is not to say that physicians are not capable of successful research involving communication, but that their work can only be strengthened by interdisciplinary collaboration with scholars who have the ability to provide new insight into interactions and relational dynamics. v Disclosure Statement The author(s) have no conflicts of interest to disclose. Acknowledgment The author would like to thank Judith White, PhD, Associate Professor at the University of New Mexico Department of Communication and Journalism, for her support and guidance. I would also like to acknowledge Jan Winslow and Cathy Salazar from Parents Reaching Out and Lourdes Vizcarra, MD, from the University Of New Mexico Continuum of Care for allowing me to conduct this study. I would also like to acknowledge Judith Hendry, PhD, Faculty at the University of New Mexico Department of Communication and Journalism, for inspiring this paper. I would like to acknowledge my mentor, Tanya Baker McCue and Bryan Wilcox for reviewing earlier versions of this paper. This paper was presented at The 5th International Conference on Patientand Family-Centered Care, June 5, 2012, in Washington, DC. Kathleen Louden, ELS, of Louden Health Communications provided editorial assistance. References 1. Maternal and Child Health Bureau [Internet]. [cited 2015 Mar 18]. Available from: http://mchb.hrsa.gov/chscn/pages/family.htm. 2. Institute for patient- and family-centered care [Internet]. Bethesda, MD: Institute for Patient- and Family-Centered Care; c2014 [cited 2014 Aug 1]. Available from: www.ipfcc.org/faq.html. 3. Cegala DJ, Broz SL. Provider and patient communication skills training. In: Thompson TL, Dorsey A, Miller KI, Parrott R, editors. Handbook of health communication. Mahwah, NJ: Lawrence Erlbaum Associates, Inc; 2003. p 95-119. 57 ORIGINAL RESEARCH & CONTRIBUTIONS Relationship between Participation in Patient- and Family-Centered CareTrainingRelationship and Communication Adaptability among Changing Hearts, Changing Minds between Participation in Medical Patient- Students: and Family-Centered Care Training and Communication Adaptability among Medical Students: Changing Hearts, Changing Minds 4. Duran RL. Communicative adaptability: a measure of social communicative competence. Commun Q 1983;31(4):320-6. DOI: http://dx.doi. org/10.1080/01463378309369521. 5. Neuliep JW, Ryan DJ. The influence of intercultural communication apprehension and socio-communicative orientation on uncertainty reduction during initial cross-cultural interaction. Commun Q 1998;46(1):88-99. DOI: http:// dx.doi.org/10.1080/01463379809370086. 6. Long B, Anarbaeva S. Communicative adaptability and intercultural communication apprehension: gender and cultural differences in college students [conference paper]. National Communication Association 94th Annual Convention; 2008 Nov 21-24; San Diego, CA. Washington, DC: National Communication Association; 2008 Jan. p 1. 7. Neuliep JW, McCroskey JC. The development of intercultural and interethnic communication apprehension scales. Commun Res Rep 1997;14(2):145-56. DOI: http://dx.doi.org/10.1080/08824099709388656. 8. Manderson L, Allotey P. Cultural politics and clinical competence in Australian health services. Anthropol Med 2003;10(1):71-85. DOI: http://dx.doi. org/10.1080/13648470301266. 9. Kaplan SH, Greenfield S, Gandek B, Rogers WH, Ware JE Jr. Characteristics of physicians with participatory decision-making styles. Ann Intern Med 1996 Mar 1;124(5):497-504. DOI: http://dx.doi.org/10.7326/0003-4819-124-5-19960301000007. 10. Allotey P, Manderson L, Grover S. The politics of female genital surgery in displaced communities. Crit Public Health 2001;11(3):189-201. DOI: http:// dx.doi.org/10.1080/09581590110066649. 11. Hamilton J. The collaborative model of doctor-patient consultation—is it always culturally appropriate? What do doctors and patients need to know to make it work in intercultural contexts? Med Teach 2009 Feb;31(2):163-5. DOI: http:// dx.doi.org/10.1080/01421590802530914. 12. Franck LS, Callery P. Re-thinking family-centred care across the continuum of children’s healthcare. Child Care Health Dev 2004 May;30(3):265-77. DOI: http://dx.doi.org/10.1111/j.1365-2214.2004.00412.x. 13. Lotze GM, Bellin MH, Oswald DP. Family-centered care for children with special health care needs: are we moving forward? J Fam Soc Work 2010;13(2):100-13. DOI: http://dx.doi.org/10.1080/10522150903487099. 14. Woodside JM, Rosenbaum PL, King SM, King GA. Family-centered service: developing and validating a self-assessment tool for pediatric service providers. Child Health Care 2001;30(3):237-52. DOI: http://dx.doi.org/10.1207/ S15326888CHC3003_5. 15. Johnson AM, Yoder J, Richardson-Nassif K. Using families as faculty in teaching medical students family-centered care: what are students learning? Teach Learn Med 2006 Summer;18(3):222-5. DOI: http://dx.doi.org/10.1207/ s15328015tlm1803_6. The Move to Touch A practitioner of experience does not seize the patient’s forearm with his hand as soon as he comes, but first sits down and with a cheerful countenance asks how the patient finds himself; and if the patient has any fear, he calms him with entertaining talk, and only after that moves his hand to touch the patient. — De Medicina, Aulus Aurelius Cornelius Celsus, c 25 BC – c 50 AD, Roman encyclopaedist 58 The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS A Ten-Year Case-Control Study of Passive Smoke Exposure as a Risk Factor for Pertussis in Children Mark A Schmidt, PhD, MPH; Samantha K Kurosky, MS; John P Mullooly, PhD; Colleen Chun, MD; Sheila Weinmann, PhD Perm J 2015 Summer;19(3):59-63 http://dx.doi.org/10.7812/TPP/14-233 ABSTRACT Context: Passive exposure to cigarette smoke in the household as a risk factor for pertussis disease has not been well characterized. Objective: To determine whether pertussis was associated with household secondhand smoke in children. Methods: We conducted a matched case-control study of laboratory-confirmed pertussis cases occurring from January 1, 1996, through December 31, 2005, in children up to 12 years of age who were members of a large managed care organization. Controls were matched one-to-one on age group and type of Health Plan account. Passive cigarette smoking was determined through a retrospective review of the medical records of cases, controls, and their respective household members. Main Outcome Measures: Cases of pertussis infection were identified from a microbiology laboratory database and through diagnostic codes from the International Classification of Diseases, Ninth Revision, with the diagnosis confirmed by culture or polymerase chain reaction. Results: Sixty-five laboratory-confirmed cases of pertussis were identified. Cases and controls were similar in sex (p = 0.73), race (p = 0.57), and receipt of pertussis antigen-containing vaccine (p = 0.24). Using multivariable conditional logistic regression analysis, we did not detect a statistically significant association between pertussis and household passive exposure to cigarette smoking (adjusted odds ratio = 1.2; 95% confidence interval = 0.5-2.9). Conclusion: Although we did not detect an association in this analysis, the possible relationship between passive exposure to smoking and childhood pertussis remains an important research question and should be a priority for future studies. INTRODUCTION Pertussis, or whooping cough, is a respiratory tract infection and a major public health burden because of its high infectivity and severe manifestations among infants. Pertussis is caused by the bacterial species, Bordetella pertussis, which is transmitted from person to person via aerosolized droplets. Rates of childhood immunization against pertussis in the US are high, with more than 83% of children younger than age 3 years having received 4 doses of pertussis antigen-containing vaccine.1 However, children too young to be fully immunized, older underimmunized children, and immunized teenagers and adults with waned immunity are at risk of pertussis infection acquired from symptomatically infected individuals. Whereas adolescents and adults may have a relatively mild illness, pertussis in infants is particularly severe. According to the Centers for Disease Control and Prevention in 2011, infants younger than age 2 months who were too young to be immunized accounted for 57% of all infant hospitalizations and 85% of all infant deaths due to pertussis in the US.2 Passive cigarette smoke exposure (PSE) in the household as a possible risk factor for pertussis infection among children has not been well characterized in the literature. Our prior work investigating the impact of PSE on pneumococcal infection3 prompted us to conduct a case-control study within the population of a large managed care organization to compare household smoking exposure histories recorded in the electronic medical record (EMR) of pediatric pertussis cases with those of matched controls. METHODS We conducted our study among the member population of the Kaiser Permanente Northwest (KPNW) Health Plan, using a similar protocol and the same control group described for our investigation of PSE as a risk factor for invasive pneumococcal disease.3 We selected pertussis cases occurring from January 1, 1996, through December 31, 2005, among KPNW members from birth through age 12 years. Potential cases were identified from either of the following: 1) a microbiology laboratory database as having pertussis confirmed by culture, direct fluorescent-antibody testing, or polymerase chain reaction or 2) the EMR as having a pertussis-related code from the International Classification of Diseases, Ninth Revision (ICD-9; 033, 033.0, 033.8, 033.9, and 484.3). When ICD-9 codes were used for case identification, we manually reviewed the EMR to exclude those without documented laboratory confirmation of pertussis infection. Mark A Schmidt, PhD, MPH, is a Research Associate for the Center for Health Research Northwest in Portland, OR. E-mail: [email protected]. Samantha K Kurosky, MS, is a Research Associate for the Center for Health Research Northwest in Portland, OR. E-mail: [email protected]. John P Mullooly, PhD, is an Emeritus Senior Investigator for the Center for Health Research Northwest in Portland, OR. E-mail: [email protected]. Colleen Chun, MD, is a Pediatric Infectious Disease Specialist for Northwest Permanente and a Professor of Infectious Diseases at Oregon Health and Science University in Portland, OR. E-mail: [email protected]. Sheila Weinmann, PhD, is an Investigator for the Center for Health Research Northwest in Portland, OR. E-mail: [email protected]. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 59 ORIGINAL RESEARCH & CONTRIBUTIONS A Ten-Year Case-Control Study of Passive Smoke Exposure as a Risk Factor for Pertussis in Children Where possible, we used our control population from the study of invasive pneumococcal disease. Among this group, we determined which potential controls were closest in age to our cases on their “reference date,” defined as the collection date of the pertussispositive specimen from the case, and matched 1 control to each pertussis case, by age group (0-2, 3-5, and 6-12 years) and type of Health Plan account. We matched controls and cases on the basis of the reference date to avoid confounding the relationship between smoking exposure and pertussis occurrence by secular changes in pertussis incidence and capture of smoking history within the EMR. Because the study design involved collecting PSE information from the EMR of family members if available to us, we matched group members based on Health Plan account (child plus family members or child alone) to equalize our access to the family member’s EMR between cases and their matched controls. For 11 pertussis cases without a suitable control from this control population, we randomly selected 1 control for each case from the KPNW member population, using the same criteria. We reviewed the health records of all cases and new controls, plus the records of their family members where available, to collect PSE history, using standardized data collection instruments. We categorized each case and control as definitely exposed, probably exposed, probably not exposed, definitely not exposed, or unknown (Table 1). For all cases and controls, we collected information about receipt of pertussis antigen-containing vaccines before the collection date of the pertussis-positive specimen (cases) or equivalent reference date (controls) through electronic abstraction of the Vaccine Safety Datalink vaccine dataset.4,5 We defined vaccine exposure as “vaccinated” if the subject had received Table 1. Categorization of passive household smoking exposure for pertussis cases and matched controls Category of exposure Definitely exposed Probably exposed Probably not exposed Definitely not exposed Unknown 60 Definition One or more persons in the household (including babysitter) smokes, recorded within two years of the reference date (RD). No conflicting information from family members’ charts. No mention in the child’s record that adults smoke outside. Conflicting information on smoking in the household, but at least one record that someone in the household smokes, or Meets criteria for “definitely exposed” but the child’s record mentions that adults smoke outside. Evidence must show that all adults in the household smoke outside for the child to be classified as “probably exposed” rather than “definitely exposed,” or Meets criteria for “definitely exposed” except that the only available information is recorded more than two years before RD. One parent is a nonsmoker. No information on smoking status of the other parent, or One or more adults quit smoking but either quit within the last five years or quit at some unknown date, and the child’s record says household is nonsmoking, or Any notation in any family member’s record that no one in the household smokes, or Both parents are documented nonsmokers or former smokers but information on at least one parent is more than two years old. Unequivocal information from a child’s record within two years of RD that no one in the household smokes, or Information present within two years before RD that both parents are nonsmokers. Former smoker parents quit more than five years before RD. No smoking-related information found in any family member’s medical record. at least one pertussis antigen-containing vaccine before the reference date or “unvaccinated” if they had not. We determined whether cases and controls were up to date with the receipt of pertussis antigen-containing vaccines, as appropriate for age, using Advisory Committee on Immunization Practices recommendations.6 We constructed conditional logistic regression models to investigate the relationship between PSE and pertussis. Our main model included only the matched case-control pairs for whom PSE history was categorized for both members of the pair. Because of the small number of study participants, we considered participants to be “exposed” if they were categorized as “definitely exposed” or “probably exposed.” We considered participants to be “unexposed” if they were categorized as “definitely not exposed” or “probably not exposed.” Variables evaluated for confounding in multivariable models included sex, race, history of being breastfed, daycare attendance, and receipt of pertussis antigencontaining vaccine before the reference date. The latter was retained in the final multivariable model. To account for any possible selection bias related to the exclusion of casecontrol pairs in which at least one of the members had an unknown PSE history, we conducted a sensitivity analysis, including all case-control pairs in two separate models. For Model 1, we compared the combination of unexposed and unknown pairs with exposed pairs; for Model 2, we compared the combination of unexposed pairs with exposed and unknown pairs. We included vaccine history in both models to adjust for potential confounding. This protocol was reviewed and approved by the KPNW institutional review board. RESULTS We identified 65 laboratory-confirmed pertussis cases meeting our criteria, 33 of which occurred in infants younger than 1 year of age. Positive test results for pertussis included 53 cases confirmed by culture, 5 by direct fluorescent-antibody testing, 4 by The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS A Ten-Year Case-Control Study of Passive Smoke Exposure as a Risk Factor for Pertussis in Children culture and direct fluorescent-antibody testing, and 3 by polymerase chain reaction. Table 2 describes demographic and exposure information of pertussis cases and matched controls. Cases and controls were similar with respect to sex (p = 0.73) and white vs nonwhite race (p = 0.57). A similar proportion of Table 2. Demographic and exposure characterization of 65 pertussis cases and matched controls Demographic Sex (male) Race (white) Age < 1 yearb 1-2 yearsb 3-5 years 6-12 years Exposure Vaccinated against pertussis Up-to-date vaccination for age < 1 year 1-2 years 3-5 years 6-12 years Passive smokec Exposed Unexposed Unknown Cases, no. (%)a Controls, no. (%)a Chi squared p value 33 (51) 18/20 (90) 36 (56) 25/26 (96) 0.73 0.57 33 (51) 7 (11) 7 (11) 18 (28) 23 (35) 17 (26) 7 (11) 18 (28) 44 (68) 34/44 (77) 19/21 (90) 2/3 (67) 1/3 (33) 12/17 (71) 51 (78) 40/51 (78) 11/12 (92) 2/3 (67) 11/12 (92) 16/24 (67) 0.24 0.89 24 (37) 36 (55) 5 (8) 18 (27) 35 (54) 12 (18) 0.69 N = 65 unless otherwise noted (eg, 18/20, in which case n = 20). Cases were matched to controls in the 0- to 2-year age group; this group had a total of 40 cases and 40 controls. c “Exposed” includes participants categorized as “definitely exposed” or “probably exposed.” “Unexposed” includes participants categorized as “definitely not exposed” or “probably not exposed.” a b Table 3. Adjusted odds ratios of conditional logistic models assessing the relationship between passive smoke exposure and pertussis, adjusting for receipt of pertussis vaccine Variablea Main analysis Unexposed Exposed Vaccinated Sensitivity analysis, Model 1 Unexposed + unknown Exposed Vaccinated Sensitivity analysis, Model 2 Unexposed Exposed + unknown Vaccinated Odds ratio (95% CI)b p value Reference 1.2 (0.5-2.9) 0.9 (0.5-2.3) Reference 0.67 0.75 Reference 1.7 (0.8-3.8) 0.5 (0.2-1.2) Reference 0.19 0.11 Reference 1.1 (0.5-2.3) 0.5 (0.2-1.3) Reference 0.87 0.15 “Exposed” includes participants categorized as “definitely exposed” or “probably exposed.” “Unexposed” includes participants categorized as “definitely not exposed” or “probably not exposed.” b Conditional adjusted odds ratio for main model included 50 pairs with known passive smoke exposure, 22 of which were discordant. Conditional adjusted odds ratio for sensitivity analysis models included 65 pairs, 35 of which were discordant. CI = confidence interval. a The Permanente Journal/ Summer 2015/ Volume 19 No. 3 cases (68%; n = 44) and controls (78%; n = 51) had received a pertussis antigencontaining vaccine (p = 0.24). Among those vaccinated, a similar proportion of cases (77%; n = 34) and controls (40; 78%) were up to date with pertussis vaccination for their age (p = 0.89). Because cases and controls were similar by up-to-date vaccination status and because our small sample size would potentially limit our ability to consider additional variables in our main model, we decided to consider only whether our subjects were vaccinated or unvaccinated for the remainder of the analysis. A higher proportion of cases than controls was categorized as exposed to PSE (37% vs 27%), but the control group had a higher proportion of subjects with missing data on PSE (18% in controls vs 8% in cases). For 15 (23%) of the case-control pairs, 1 or both members had unknown PSE, and these pairs were excluded from our main-effects analysis. Among the remaining 50 case-control pairs, 28 (56%) had concordant case-control exposure histories (7 in which both members were exposed and 21 in which both members were unexposed). In our conditional logistic regression model, which calculated the odds ratio (OR) using data from the 22 discordant pairs, we found no statistically significant relationship between pertussis and PSE in the household (OR = 1.2; 95% confidence interval [CI] = 0.5-2.8; Table 3). Our results remained similar after adjusting for receipt of pertussis antigencontaining vaccine (adjusted OR = 1.2; 95% CI = 0.5-2.9). We included the 15 case-control pairs with at least 1 member with unknown PSE in our sensitivity analyses. In Model 1, we placed those with missing PSE data in the unexposed category; in Model 2, we placed them in the exposed category. Thus, the range of ORs that could have resulted from this study if there had been no missing data was 1.1 to 1.7. DISCUSSION We did not detect an association between laboratory-confirmed pertussis and PSE in the household in this analysis; however, this remains an important 61 ORIGINAL RESEARCH & CONTRIBUTIONS A Ten-Year Case-Control Study of Passive Smoke Exposure as a Risk Factor for Pertussis in Children research question to study. In an in vitro model, cigarette smoke exposure was associated with an increased number of B pertussis organisms binding to buccal epithelial cells from nonsmokers compared with unexposed cells.7 Among cigarette smokers, studies have described decreased mucociliary clearance,8 decreased levels of circulating immunoglobulins, decreased natural killer cell activity, depressed neutrophil chemotaxis and phagocytic activity, and decreased release of pro-inflammatory cytokines.9 Cigarette smoking also is associated with increased permeability of the respiratory epithelium.10 Further research is needed to investigate whether similar immune alterations occur in children exposed to cigarette smoke. Among children, PSE has been associated with an increased risk of invasive bacterial infections from Streptococcus pneumoniae,11,12 Neisseria meningitidis,13-18 Haemophilus influenzae type b,18,19 pulmonary Mycobacterium tuberculosis infection,20 and viral infections, including respiratory syncytial virus.21 In Among cigarette addition, smokers with smokers, studies have pertussis infection are described decreased more infectious than nonmucociliary clearance, smokers because of greater decreased levels severity and duration of of circulating cough.22 This is especially immunoglobulins, important, as household decreased natural members are the estikiller cell activity, mated source for 60% to 83% of infant cases of depressed neutrophil pertussis, and adults have chemotaxis and been responsible for inphagocytic activity, troducing pertussis into and decreased release the household in 26% of of pro-inflammatory household outbreaks and cytokines. for 42% of all household secondary cases.23-26 Our main study strengths were the use of information from EMR and laboratory records, reducing exposure misclassification and outcome misclassification, and a study period that extended over 10 years. Our main limitation was the small sample size of the study population because of a low incidence of pertussis during the study period.27 Our sample size was further restricted by incomplete household PSE history for some study participants, although 62 we accounted for this through our sensitivity analysis and this limitation did not alter our findings. 3. CONCLUSION Pertussis is now considered a resurgent disease; its incidence has increased overall during the past 3 decades, with more notable increases and multiple outbreaks since the mid- to late 2000s. 28 In 2012, Oregon had an outbreak of pertussis and recorded more than 900 cases (23.3 cases per 100,000)—its highest occurrence since 1953.29 The incidence rate was highest among infants (253/100,000 persons), followed by children aged 10 to 14 years (104/100,000), aged 1 to 4 years (81/100,000), and aged 5 to 9 years (67/100,000). Twenty-six infants had severe disease requiring hospitalization. If PSE is linked to increased risk or severity of pertussis in childhood, this would allow targeted education for parents about eliminating household PSE and would assist clinicians in assessing the child’s risk for pertussis infection. Improved documentation of PSE in the EMR would assist future studies of the relationship between PSE and pertussis risk in children. v Disclosure Statement The author(s) have no conflicts of interest to disclose. Financial support: Centers for Disease Control and Prevention (through agreement 200-200200732 with America’s Health Insurance Plans [AHIP]). The findings and conclusions in this report are those of the authors and do not necessarily represent the views of the funding agency. The findings and conclusions do not necessarily represent the views or policies of the Department of Health and Human Services or AHIP, nor does mention of trade names, commercial products, or organizations imply endorsement by the US Government. Acknowledgment Kathleen Louden, ELS, of Louden Health Communications provided editorial assistance. References 1. Elam-Evans LD, Yankey D, Singleton JA, Kolasa M; Centers for Disease Control and Prevention. National, state, and selected local area vaccination coverage among children aged 19-35 months—United States, 2013. MMWR Morb Mortal Wkly Rep 2014 Aug 29;63(34):741-8. 2. Terranella A, Asay GR, Messonnier ML, Clark TA, Liang JL. Pregnancy dose Tdap 4. 5. 6. 7. 8. 9. 10. 11. 12. 13. 14. 15. 16. and postpartum cocooning to prevent infant pertussis: a decision analysis. Pediatrics 2013 Jun;131(6):e1748-56. DOI: http://dx.doi. org/10.1542/peds.2012-3144. Chun CS, Weinmann S, Riedlinger K, Mullooly JP. Passive cigarette smoke exposure and other risk factors for invasive pneumococcal disease in children: a case-control study. Perm J 2015 Winter;19(1):38-43. DOI: http://dx.doi. org/10.7812/TPP/14-010. Chen RT, Glasser JW, Rhodes PH, et al. Vaccine Safety Datalink project: a new tool for improving vaccine safety monitoring in the United States. The Vaccine Safety Datalink Team. Pediatrics 1997 Jun;99(6):765-73. DOI: http://dx.doi.org/10.1542/peds.99.6.765. Chen RT, DeStefano F, Davis RL, et al. The Vaccine Safety Datalink: immunization research in health maintenance organizations in the USA. Bull World Health Organ 2000;78(2):186-94. Diphtheria, tetanus, and pertussis: recommendations for vaccine use and other preventive measures. Recommendations of the Immunization Practices Advisory committee (ACIP). MMWR Recomm Rep 1991 Aug 8;40(RR-10):1-28. El Ahmer OR, Essery SD, Saadi AT, et al. The effect of cigarette smoke on adherence of respiratory pathogens to buccal epithelial cells. FEMS Immunol Med Microbiol 1999 Jan;23(1):27-36. DOI: http://dx.doi.org/10.1111/ j.1574-695X.1999.tb01713.x. Sherman CB. The health consequences of cigarette smoking. Pulmonary diseases. Med Clin North Am 1992 Mar;76(2):355-75. Arcavi L, Benowitz NL. Cigarette smoking and infection. Arch Intern Med 2004 Nov 8; 164(20):2206-16. DOI: http://dx.doi.org/10.1001/ archinte.164.20.2206. Jones JG, Minty BD, Lawler P, Hulands G, Crawley JC, Veall N. Increased alveolar epithelial permeability in cigarette smokers. Lancet 1980 Jan 12;1(8159):66-8. DOI: http:// dx.doi.org/10.1016/S0140-6736(80)90493-6. Gessner BD, Ussery XT, Parkinson AJ, Breiman RF. Risk factors for invasive disease caused by Streptococcus pneumoniae among Alaska native children younger than two years of age. Pediatr Infect Dis J 1995 Feb;14(2):123-8. DOI: http://dx.doi.org/10.1097/00006454199502000-00008. O’Dempsey TJ, McArdle TF, Morris J, et al. A study of risk factors for pneumococcal disease among children in a rural area of West Africa. Int J Epidemiol 1996 Aug;25(4):885-93. DOI: http:// dx.doi.org/10.1093/ije/25.4.885. Fischer M, Hedberg K, Cardosi P, et al. Tobacco smoke as a risk factor for meningococcal disease. Pediatr Infect Dis J 1997 Oct;16(10):979-83. DOI: http://dx.doi. org/10.1097/00006454-199710000-00015. Haneberg B, Tønjum T, Rodahl K, GeddeDahl TW. Factors preceding the onset of meningococcal disease, with special emphasis on passive smoking, symptoms of ill health. NIPH Ann 1983 Dec;6(2):169-73. Kriz P, Bobak M, Kriz B. Parental smoking, socioeconomic factors, and risk of invasive meningococcal disease in children: a population based case-control study. Arch Dis Child 2000 Aug;83(2):117-21. DOI: http://dx.doi. org/10.1136/adc.83.2.117. Lee CC, Middaugh NA, Howie SR, Ezzati M. Association of secondhand smoke exposure with pediatric invasive bacterial disease and bacterial carriage: a systematic review and meta-analysis. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS A Ten-Year Case-Control Study of Passive Smoke Exposure as a Risk Factor for Pertussis in Children 17. 18. 19. 20. 21. PLoS Med 2010 Dec 7;7(12):e1000374. DOI: http://dx.doi.org/10.1371/journal.pmed.1000374. Murray RL, Britton J, Leonardi-Bee J. Second hand smoke exposure and the risk of invasive meningococcal disease in children: systematic review and meta-analysis. BMC Public Health 2012 Dec 10;12:1062. DOI: http://dx.doi. org/10.1186/1471-2458-12-1062. Pereiró I, Díez-Domingo J, Segarra L, Ballester A, Albert A, Morant A. Risk factors for invasive disease among children in Spain. J Infect 2004 May;48(4):320-9. DOI: http://dx.doi. org/10.1016/j.jinf.2003.10.015. Arnold C, Makintube S, Istre GR. Day care attendance and other risk factors for invasive Haemophilus influenzae type b disease. Am J Epidemiol 1993 Sep 1;138(5):333-40. Altet MN, Alcaide J, Plans P, et al. Passive smoking and risk of pulmonary tuberculosis in children immediately following infection. A case-control study. Tuber Lung Dis 1996 Dec;77(6):537-44. DOI: http://dx.doi. org/10.1016/S0962-8479(96)90052-0. DiFranza JR, Masaquel A, Barrett AM, Colosia AD, Mahadevia PJ. Systematic literature review assessing tobacco smoke exposure as a risk 22. 23. 24. 25. 26. factor for serious respiratory syncytial virus disease among infants and young children. BMC Pediatr 2012 Jun 21;12:81. DOI: http://dx.doi. org/10.1186/1471-2431-12-81. De Serres G, Shadmani R, Duval B, et al. Morbidity of pertussis in adolescents and adults. J Infect Dis 2000 Jul;182(1):174-9. DOI: http:// dx.doi.org/10.1086/315648. Baptista PN, Magalhães VS, Rodrigues LC. The role of adults in household outbreaks of pertussis. Int J Infect Dis 2010 Feb;14(2):e111-4. DOI: http://dx.doi.org/10.1016/j.ijid.2009.03.026. de Greeff SC, Mooi FR, Westerhof A, et al. Pertussis disease burden in the household: how to protect young infants. Clin Infect Dis 2010 May 15;50(10):1339-45. DOI: http://dx.doi. org/10.1086/652281. Bisgard KM, Pascual FB, Ehresmann KR, et al. Infant pertussis: who was the source? Pediatr Infect Dis J 2004 Nov;23(11):985-9. DOI: http:// dx.doi.org/10.1097/01.inf.0000145263.37198.2b. Wendelboe AM, Njamkepo E, Bourillon A, et al; Infant Pertussis Study Group. Transmission of Bordetella pertussis to young infants. Pediatr Infect Dis J 2007 Apr;26(4):293-9. DOI: http:// dx.doi.org/10.1097/01.inf.0000258699.64164.6d. 27. Bancroft J, Byster L. Selected reportable communicable disease summary: 20082009—Pertussis [Internet]. Salem, OR: Oregon Department of Human Services; 2010 Dec [cited 2015 May 13]. Available from: https://public.health.oregon.gov/ DiseasesConditions/CommunicableDisease/ DiseaseSurveillanceData/AnnualReports/ arpt0809/Documents/arpt0809.pdf. 28. Clark TA. Changing pertussis epidemiology: everything old is new again. J Infect Dis 2014 Apr 1;209(7):978-81. DOI: http://dx.doi. org/10.1093/infdis/jiu001. 29. Selected reportable communicable disease summary: 2012 state of Oregon [Internet]. Portland, OR: Oregon Health Authority; 2013 Sep [cited 2014 Apr 3]. Available from: http://public.health.oregon.gov/ DiseasesConditions/CommunicableDisease/ DiseaseSurveillanceData/AnnualReports/ arpt2012/Pages/index.aspx. Pertussis Fevers attacked boys of four months, of ten months and a little older, countless numbers of whom died. Principally that common cough, which is usually called Quinta or Quintana … . Serious are the symptoms of this … . For they are without this troublesome coughing for … four or five hours … then this paroxysm of coughing returns, now so severe that blood is expelled with force through the nose and through the mouth. — Guillaume de Baillou (Ballonius), 1538-1616, French physician and considered founder of modern epidemiology The Permanente Journal/ Summer 2015/ Volume 19 No. 3 63 credits available for this article — see page 96. ORIGINAL RESEARCH & CONTRIBUTIONS Special Report 2014 Hypertension Guideline: Recommendation for a Change in Goal Systolic Blood Pressure Joel Handler, MD Perm J 2015 Summer;19(3):64-72 http://dx.doi.org/10.7812/TPP/14-226 Editor’s note: A copy of the August 2014 Kaiser Permanente Adult Hypertension National Guideline follows this article. ABSTRACT The 2014 Kaiser Permanente Care Management Institute National Hypertension Guideline was developed to assist primary care physicians and other health care professionals in the outpatient treatment of uncomplicated hypertension in adult men and nonpregnant women aged 18 years and older. The new guideline reflects general acceptance, with minor modifications, of the “Evidence-Based Guideline” report by the panel members appointed to the National Heart, Lung, and Blood Institute 8th Joint National Committee. A major practice change is the recommendation for goal systolic blood pressure less than 150 mmHg in patients aged 60 years and older who are treated for hypertension in the absence of diabetes or chronic kidney disease. This article describes the reasons for, evidence for, and consequences of the change, and is followed by the National Guidelines handout. INTRODUCTION The 2014 Kaiser Permanente (KP) Care Management Institute National Hypertension Guideline was developed to assist primary care physicians and other health care professionals in the outpatient treatment of uncomplicated hypertension in adult men and nonpregnant women aged 18 years and older. The new guideline reflects general acceptance of the “Evidence-Based Guideline” report by the panel members appointed to the National Heart, Lung, and Blood Institute (NHLBI) 8th Joint National Committee (JNC 8).1 A major practice change is the recommendation for goal systolic blood pressure less than 150 mmHg in patients aged 60 years and older who are treated for hypertension in the absence of diabetes or chronic kidney disease (CKD) compared with the previous standard less than 140 mmHg. This change has major consequences for the routine primary care management of patients with hypertension. How Large Is the Affected Population and How Strong Is the New Recommendation? Using the results of the National Health and Nutrition Examination Survey between 2005 and 2010, it has been estimated that the US treatment-eligible adult hypertension population would decrease from 20.3% to 19.2% compared with that of the 7th Joint National Committee guideline, and the population with treatment-eligible hypertension who are aged 60 years and older would decline from 68.9% to 61.2%.2 As of October 2014, with an 85% hypertension control rate less than 140/90 mmHg, there are 18,690 patients aged 60 years and older without diabetes or CKD in the KP Southern California hypertension registry who have systolic blood pressures of 140 to 149 mmHg and are affected by the new recommendation. These patients represent 2.5% of the total KP Southern California adult hypertension registry of 740,003 individuals. Evidentiary support for this recommendation was strong, according to the Care Management Institute Grading of Recommendations Assessment, Development and Evaluation standard for grading the quality of evidence scale, and it received a strong rating using principles evaluating the strength of the body of evidence and degree of certainty developed by the NHLBI before it convened the first JNC 8 panel meeting in August 2008. This recommendation was a segue from the relevant Evidence Statements, which evaluated randomized clinical trials passing scrutiny from a 14-category evidence assessment scale used by a trained and independent methodology team collaborating with those experts appointed to the JNC 8 panel. These Evidence Statements are available in the full online Evidence-Based Guideline report.1 What is the Basis of the Supportive Evidence? The age 60 years threshold for the systolic blood pressure target was decided on the basis of the Systolic Hypertension in the Elderly Program (SHEP) trial findings and the Systolic Hypertension in Europe (Syst-Eur) trial results.3,4 In these highly rated randomized controlled trials, stroke, the primary endpoint, was reduced by 36% and 42%, respectively, and major cardiovascular events were reduced by 32% and 31%, respectively. These two large trials containing representative population samples fulfill the NHLBI strong evidence requirement for multiple supportive randomized controlled trials. The JNC 8 Evidence Statements 1 to 3 for Clinical Question 2 describe the evidence, and a strong recommendation is the logical result.1p82-3 There is no evidence from a randomized controlled clinical trial to support the opinion that a systolic blood pressure goal less than 140 mmHg in the elderly hypertensive population is superior to a systolic goal less than 150 mmHg. The absence Joel Handler, MD, was an Expert Panel Member of the Eighth Joint National Committee on High Blood Pressure; Hypertension Clinical Lead, Care Management Institute; and Hypertension Lead for Southern California Kaiser Permanente, Anaheim, CA. E-mail: [email protected]. 64 The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS 2014 Hypertension Guideline: Recommendation for a Change in Goal Systolic Blood Pressure of evidence for a lower blood pressure target does not equal benefit. One opinion properly criticizes the strength of the Japanese Trial to Assess Optimal Systolic Blood Pressure in Elderly Hypertensive Patients5 and Valsartan in Elderly Isolated Hypertension Study6 results demonstrating equivalency of goal systolic pressure less than 140 mmHg compared with goal systolic pressures less than 150 mmHg and less than 160 mmHg, because these were short-term trials.7 However, that critique does not offer additional information to the previously published Evidence-Based Guideline Clinical Question 2: Evidence Statement 6, which attached low-quality evidence to these trials.1p84-5 PROBLEMS WITH USE OF ACHIEVED BLOOD PRESSURE TRIALS Achieved blood pressure trials are those in which the intervention is to introduce antihypertensive medication to examine the effect of medication on cardiovascular risk reduction rather than to examine outcomes achieving a prespecified goal blood pressure. These trial results should not be used to inform blood pressure targets because they ask a different question. Retrospective analyses correlating achieved blood pressures to outcome measures are inherently biased. The NHLBI process followed by the panel appointed to JNC 8 is in agreement with The Cochrane Collaboration methodologists who independently decided the following: The cohort of patients with low blood pressure as identified by achieved blood pressure selects for patients who did not have sustained elevated blood pressure in the first place … , for patients in whom the blood pressure is most easily reduced with low doses of antihypertensive drugs, for patients with the lowest baseline blood pressure, and for patients who are most compliant with drug and non-drug therapy to lower blood pressure … . All of these factors are also most likely associated with a lower risk of having an adverse cardiovascular event. The approach is thus heavily biased for finding [fewer] cardiovascular events in the patients with lower blood pressure, and thus must not be encouraged.8 These limitations of analyses based on post hoc achieved blood pressures were confirmed in an analysis of the African American Study of Kidney Disease and Hypertension, which concluded that the retrospective use of achieved blood pressures would have erroneously led to the opposite conclusion of the intention-to-treat goal blood pressure analysis in this landmark study.9 The Felodipine Event Reduction study,10 the Perindopril Protection against Recurrent Stroke trial,11 and Blood Pressure Trialists’ Collaboration reports12-14 purport to show that additional blood pressure lowering is beneficial. These are examples of clinical trials and meta-analyses representing on-treatment achieved blood pressure results rather than intention-to-treat goal blood pressure outcomes and were rejected by the NHLBI methodology team because of bias. Notably, reference to mean achieved systolic blood pressures in the SHEP and Syst-Eur trials of 142 mmHg and 144 mmHg, The Permanente Journal/ Summer 2015/ Volume 19 No. 3 respectively, fails to mention the mean achieved systolic blood pressure in Syst-Eur, which was 151 mmHg.4 The argument to use “totality of evidence” does not constitute sufficient rationale for inclusion of clinical trials and meta-analyses containing inherent bias. Where Does the Lower-is-Better Blood Pressure Hypothesis Originate, and Has It been Validated? Much of the “lower is better” paradigm is based on strong prospective observational data of more than 1 million patients in 61 prospective studies15 as well as on many retrospective analyses of achieved blood pressures in the clinical trials. However, the retrospective findings are mixed. A more recent population-based retrospective cohort study revealed no difference between systolic intensification thresholds of 130 mmHg to 150 mmHg across a broad spectrum of baseline cardiovascular risk.16 Analyses of large numbers of hypertensive KP patients with hypertension, as well as US military veterans with hypertension and CKD, suggest increased mortality and end-stage kidney disease associated with lower attained blood pressures.17,18 Does the treatment of blood pressure to lower blood pressure targets, as opposed to higher blood pressure targets, reverse cardiovascular risk? Seven randomized clinical trials have investigated this hypothesis in high-risk patients with CKD, diabetes, older age, and a personal history of stroke. None has shown significant benefit for meeting the primary endpoint with more intense antihypertensive therapy that seeks a lower blood pressure goal.5,6,19-23 WHAT IS THE RISK OF REVERSING POPULATION GAINS IN CARDIOVASCULAR BENEFIT? How can we be sure that a higher systolic goal will not reverse gains already made in stroke and cardiovascular disease reduction? Gains in cardiovascular disease reduction have been associated with hypertension control, widespread use of high-potency statins, and improved secondary prevention in patients with known coronary artery disease and stroke.24,25 Because patients are receiving better overall care, power calculations for recent hypertension treatment trials on the basis of adverse rates of cardiovascular events for historic cohorts often fall short of forecasts, leading to underpowering.19,20 Given the success of population care strategies achieving very high rates of blood pressure control and eliminating racial performance gaps in large diverse populations,26-29 we need to ensure that we use the highest evidence base to define blood pressure targets. Implementation difficulties and problems with clinical inertia are independent issues and should not be used to justify inappropriately low blood pressure goals. What are the Risks of Overtreatment? Overtreatment needs to be a concern. In the KP Southern California adult hypertension registry in which nearly 90% of patients attained blood pressure control less than 140/90 mmHg, the mean systolic pressure is 127 mmHg, and almost 10% of patients receiving antihypertensive therapy have a most recent systolic pressure less than 110 mmHg. The 65 ORIGINAL RESEARCH & CONTRIBUTIONS 2014 Hypertension Guideline: Recommendation for a Change in Goal Systolic Blood Pressure disadvantages of overtreatment include: 1) exposure to side effects of unnecessary medications and excessive medication doses; 2) polypharmacy in the elderly30; 3) reduced medication adherence associated with a large number of medications31; 4) a possible increase in falls with serious injury32; 5) possibly a J- or U-curve increase in cardiovascular risk17; and 6) unnecessary use of limited health care resources, including office visits, population care outreach, medication prescriptions, and laboratory testing. A general review of 16 treatment trials indicated the potential for harm with more aggressive antihypertensive therapy in the absence of benefit.33 Is There a Risk of Changing Goal Blood Pressure in the Presence of Uncertainty? How can we be certain that the systolic blood pressure target less than 150 mmHg for patients with hypertension aged 60 years and older is accurate? The purpose of guideline development is to gather evidence with the least chance of bias, and this sort of evidence is best obtained from higher-quality randomized controlled clinical trials. All the panelists appointed to JNC 8 concurred with the NHLBI evidence review process, and, following several straw votes during more than one year, the final recorded vote at a face-to-face meeting conducted in Bethesda, … there is MD, at the National Institutes of Health on Februgreater certainty ary 27-28, 2013, on Recommendation 1 was 15 in defining the age favor and 2 against. The final recorded vote on the 3 group 60 years evidence statements supporting Recommendation 1 and older, rather was unanimously in favor. The SHEP and Syst-Eur than age 80 trial results3,4 provide strong evidence to support the years and older, Evidence-Based Guideline’s recommended goal blood for goal systolic pressure in elderly patients. In contrast, there are no known clinical trials that address goal blood pressure pressure less that have examined the 18- to 59-year age stratum, than 150 mmHg. and therefore recommendation for less than 140/90 mmHg for this population is based on expert opinion. There is a need for additional clinical trials examining the question of goal blood pressure for various populations of hypertensive individuals. Those trials should include examination of important health outcomes at a goal systolic pressure less than 150 mmHg compared with less than 130 mmHg in elderly patients with diabetes and CKD. There is good evidence to justify such a randomized clinical trial in patients with diabetes,3,4,34 including Evidence Statement 18 for Clinical Question 2 in James et al.1 If the ongoing Systolic Blood Pressure Intervention Trial does not find a significant outcome difference treating to goal systolic pressure less than 140 mmHg compared with less than 120 mmHg in patients with CKD, a future trial comparing less than 150 mmHg with less than 130 mmHg would be justified in this population as well. IS THE EVIDENCE-BASED GUIDELINE RECOMMENDATION FOR GOAL SYSTOLIC PRESSURE LESS THAN 150 MMHG FOR AGE 60 AND OLDER AN OUTLIER COMPARED WITH OTHER GUIDELINES? Recommendations from the 2013 European Society of Hypertension/European College of Cardiology for blood 66 pressure goals in the treatment of hypertension in elderly patients include a few “may consider,” “if treatment is well tolerated” recommendations along with a top “solid evidence” recommendation.35 That single, solid-evidence recommendation targets a goal systolic blood pressure 140 mmHg to 150 mmHg “in the elderly.” In the SHEP and Syst-Eur trials, “elderly” enrollment began at age 60 years. In an e-mail from Giuseppe Mancia, MD, co-chair of the European Society of Hypertension/European College of Cardiology guideline, which was circulated to panel members appointed to JNC 8, elderly was defined as beginning at age 65 years (G Mancia, MD; personal communication, 2013 Dec).a In a letter to the European Society of Hypertension/European College of Cardiology guideline authors in the December 2013 issue of the Journal of Hypertension, a writer expressed concern regarding the new blood pressure goal stating that it was “rational” but worried about the impact on clinical inertia. In their letter of reply, Mancia et al36 stated, “Clinical inertia has to be fought … by other means than by recommending inappropriately low [blood pressure] targets.” Therefore, there is fair concordance in the age group targeted for a systolic blood pressure goal target less than 150 mmHg in hypertension guidelines submitted by hypertension experts on both sides of the Atlantic. Why Not Make the Threshold for the less than 150 mmHg Goal Recommendation Age 80 Rather than Age 60? Given the findings of the SHEP and Syst-Eur trials,3,4 there is greater certainty defining the age group 60 years and older, rather than age 80 years and older, for goal systolic pressure less than 150 mmHg. Only a single trial, the Hypertension in the Very Elderly Trial, has established goal systolic blood pressure in the age 80 years and older population less than 150 mmHg, a population described as the “very elderly.”37 A single randomized clinical trial does not constitute sufficient evidence to merit a strong recommendation at this age level in the presence of multiple randomized clinical trials in support of the age 60 threshold. Does the less than 150 mmHg Goal Recommendation Include Higher Risk Groups? Epidemiologic data have defined higher cardiovascular risk strata in the general population, but randomized controlled clinical trials demonstrating statistically significant reversal of risk with lower blood pressure goals in higher-risk groups have been notably absent.5,6,19-23 SHEP and Syst-Eur enrolled patient populations that were representative of a broad spectrum of cardiovascular risk. Increasing age alone is a dominant cardiovascular disease risk factor.15 Additionally, the SHEP trial population included 14% African-American patients compared with 12.6% in the US population. Both SHEP and Syst-Eur also included patients with a history of myocardial infarction and stroke.1,3 Sixty-one percent of patients in SHEP had a baseline electrocardiographic abnormality. Thirty percent of patients in Syst-Eur had a prior “cardiovascular complication.” The The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ORIGINAL RESEARCH & CONTRIBUTIONS 2014 Hypertension Guideline: Recommendation for a Change in Goal Systolic Blood Pressure Hypertension in the Very Elderly Trial included patients with myocardial infarction, stroke, and heart failure.36 Attention has been drawn to the Secondary Prevention of Small Subcortical Strokes trial comparing goal systolic pressure less than 150 mmHg to less than 130 mmHg in patients with a personal history of lacunar stroke.20 Although the primary endpoint of recurrent stroke was nonsignificant ( p = 0.08), c onfidence in tervals (0 .64 to 1. 03) did not preclude benefit o f t he l ower g oal. F urthermore, the subgroup of intracerebral hemorrhage was significantly reduced (p = 0.03).6 However, “there was no heterogeneity in treatment effect o n t he p rimary o utcome i n a ny o f t he demographic or clinical subgroups,” the annual primary stroke rate in the control group was only 2.77% vs 7% predicted, and intracerebral hemorrhage comprised fewer than 10% of total strokes.20 The nonstatistically significant separation of total stroke in the more intensively treated group compared with the less intensively treated group in the Secondary Prevention of Small Subcortical Strokes trial was only 0.5% events per year. Therefore, the evidence favoring a goal systolic pressure other than lower than 150 mmHg in hypertensive individuals aged 60 years and older with a personal history of stroke is speculative. ENDORSEMENTS OF THE EVIDENCE-BASED GUIDELINE The American Academy of Family Physicians, representing more than 100,000 primary care physicians, has endorsed the Evidence-Based Guideline. That approval is important because nearly all hypertensive patients receive hypertension care from primary care physicians. Additionally, the National Quality Committee for Quality Assurance has adopted the new reform, and goal systolic blood pressure less than 150 mmHg in the absence of diabetes is a 2014 performance measure for the Healthcare Effectiveness Data and Information Set. The Veteran’s Administration and Department of Defense patient care systems have adopted goal systolic blood pressure less than 150 mmHg for general population hypertension patients age 60 and over.38 It will be difficult to reproduce the methodologic rigor and independent sponsorship of the Evidence-Based Guideline now that the NHLBI has unfortunately decided to remove itself from stewardship of future hypertension guidelines, and will not approve any guideline. The level of evidence-based medicine used to develop this hypertension guideline, on the basis of Institute of Medicine principles, is unsurpassed. An essential point is that blood pressure goals for patients with hypertension must be based on a high degree of evidence, and bias is best removed by reliance on the randomized controlled clinical trials to make this determination. A common rationale for recommending blood pressure goals lower than those that are evidence based is to combat clinical inertia. However, implementation is a separate issue, and high-performing systems of health care have addressed clinical inertia successfully.26-29,39 v a Cochair, European Society of Hypertension/European College of Cardiology guideline committee, Milano, Italy. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 Disclosure Statement The author(s) have no conflicts of interest to disclose. Acknowledgments This work was developed under the auspices of Kaiser Permanente’s National Guideline Program. We would like to recognize the National Guideline Directors, the Integrated Cardiovascular Health Clinical Leads, and the Hypertension Guideline Development Team. Kathleen Louden, ELS, of Louden Health Communications provided editorial assistance. References 1. James PA, Oparil S, Carter BL, et al. 2014 evidence-based guideline for the management of high blood pressure in adults: report from the panel members appointed to the Eighth Joint National Committee (JNC 8). JAMA 2014 Feb 5;311(5):507-20. DOI: http://dx.doi.org/10.1001/jama.2013.284427. 2. Navar-Boggan AM, Pencina MJ, Williams K, Sniderman AD, Peterson ED. Proportion of US adults potentially affected by the 2014 hypertension guideline. JAMA 2014 Apr 9;311(14):1424-9. DOI: http://dx.doi.org/10.1001/ jama.2014.2531. Erratum in: JAMA 2014 Aug 27;312(8):848. DOI: http://dx.doi. org/10.1001/jama.2014.10343. 3. Prevention of stroke by antihypertensive drug treatment in older persons with isolated systolic hypertension. Final results of the Systolic Hypertension in the Elderly Program (SHEP). SHEP Cooperative Research Group. JAMA 1991 Jun 26;265(24):3255-64. 4. Staessen JA, Fagard R, Thijs L, et al. Randomised double-blind comparison of placebo and active treatment for older patients with isolated systolic hypertension. The Systolic Hypertension in Europe (Syst-Eur) Trial Investigators. Lancet 1997 Sep 13;350(9080):757-64. DOI: http://dx.doi. org/10.1016/S0140-6736(97)05381-6. 5. JATOS Study Group. Principal results of the Japanese trial to assess optimal blood pressure in elderly hypertensive patients (JATOS). Hypertens Res 2008 Dec;31(12):2115-27. DOI: http://dx.doi.org/10.1291/hypres.31.2115. 6. Ogihara T, Saruta T, Rakugi H, et al; Valsartan in Elderly Isolated Systolic Hypertension Study Group. Target blood pressure for treatment of isolated systolic hypertension in the elderly: valsartan in elderly isolated systolic hypertension study. Hypertension 2010 Aug;56(2):196-202. DOI: http://dx.doi. org/10.1161/HYPERTENSIONAHA.109.146035. 7. Wright JT Jr, Fine LJ, Lackland DT, Ogedegbe G, Dennison Himmelfarb CR. Evidence supporting a systolic blood pressure goal of less than 150 mmHg in patients aged 60 years or older: the minority view. Ann Intern Med 2014 Apr 1; 160(7):499-503. DOI: http://dx.doi.org/10.7326/M13-2981. 8. Arguedas JA, Perez MI, Wright JM. Treatment blood pressure targets for hypertension. Cochrane Database Syst Rev 2009 Jul 8;(3):CD004349. DOI: http://dx.doi.org/10.1002/14651858.CD004349.pub2. 9. Davis EM, Appel LJ, Wang X, et al; African American Study of Kidney Disease and Hypertension Research Collaborative Group. Limitations of analyses based on achieved blood pressure: lessons from the African American study of kidney disease and hypertension trial. Hypertension 2011 Jun;57(6):1061-8. DOI: http:// dx.doi.org/10.1161/HYPERTENSIONAHA.111.169367. 10. Liu L, Zhang Y, Liu G, Li W, Zhang X, Zanchetti A; FEVER Study Group. The Felodipine Event Reduction (FEVER) Study: a randomized long-term placebo-controlled trial in Chinese hypertensive patients. J Hypertens 2005 Dec;23(12):2157-72. 11. PROGRESS Collaborative Group. Randomised trial of a perindopril-based blood-pressure-lowering regimen among 6,105 individuals with previous stroke or transient ischaemic attack. Lancet 2001 Sep 29;358(9287):1033-41. DOI: http://dx.doi.org/10.1016/S0140-6736(01)06178-5. Erratum in: Lancet 2002 Jun 15;359(9323):2120. DOI: http://dx.doi.org/10.1016/S0140-6736(02)08935-3. Erratum in: Lancet 2001 Nov 3;358(9292):1556. DOI: http://dx.doi.org/10.1016/ S0140-6736(01)06617-X. 12. Staessen JA, Wang JG, Thijs L. Cardiovascular protection and blood pressure reduction: a meta-analysis. Lancet 2001 Oct 20;358(9290):1305-15. DOI: http:// dx.doi.org/10.1016/S0140-6736(01)06411-X. Erratum in: Lancet 2002 Jan 26;359(9303):360. DOI: http://dx.doi.org/10.1016/S0140-6736(02)07527-X. 13. Turnbull F; Blood Pressure Lowering Treatment Trialists’ Collaboration. Effects of different blood-pressure-lowering regimens on major cardiovascular events: results of prospectively-designed overviews of randomised trials. Lancet 2003 Nov;362(9395):1527-35. DOI: http://dx.doi.org/10.1016/S0140-6736(03)14739-3. 14. Blood Pressure Lowering Treatment Trialists’ Collaboration, Sundström J, Arima H, Woodward M, et al. Blood pressure-lowering treatment based on cardiovascular risk: a meta-analysis of individual patient data. Lancet 2014 Aug 16;384(9943):591-8. DOI: http://dx.doi.org/10.1016/S0140-6736(14)61212-5. 67 ORIGINAL RESEARCH & CONTRIBUTIONS 2014 Hypertension Guideline: Recommendation for a Change in Goal Systolic Blood Pressure 15. Lewington S, Clarke R, Qizilbash N, Peto R, Collins R; Prospective Studies Collaboration. Age-specific relevance of usual blood pressure to vascular mortality: a meta-analysis of individual data for one million adults in 61 prospective studies. Lancet 2002 Dec 14;360(9349):1903-13. DOI: http:// dx.doi.org/10.1016/S0140-6736(02)11911-8. Erratum in: Lancet 2003 Mar 22;361(9362):1060. DOI: http://dx.doi.org/10.1016/S0140-6736(03)12816-4. 16. Xu W, Goldberg SI, Shubina M, Turchin A. Optimal systolic blood pressure target time to intensification, and time to follow-up in treatment of hypertension: population based retrospective cohort study. BMJ 2015 Feb 5;350:h158. DOI: http://dx.doi.org/10.1136/bmj.j148. 17. Sim JJ, Shi J, Kovesdy CP, Kalantar-Zadeh K, Jacobsen SJ. Impact of achieved blood pressures on mortality risk and end-stage renal disease among a large, diverse hypertension population. J Am Coll Cardiol 2014 Aug 12;64(6):588-97. DOI: http://dx.doi.org/10.1016/j.jacc.2014.04.065. 18. Kovesdy CP, Bleyer AJ, Molnar MZ, et al. Blood pressure and mortality in US veterans with chronic kidney disease: a cohort study. Ann Intern Med 2013 Aug 20;159(4):233-42. DOI: http://dx.doi.org/10.7326/0003-4819-159-4201308200-00004. 19. ACCORD Study Group, Cushman WC, Evans GW, Byington RP, et al. Effects of intensive blood-pressure control in type 2 diabetes mellitus. N Engl J Med 2010 Apr 29;362(17):1575-85. DOI: http://dx.doi.org/10.1056/NEJMoa1001286. 20. SPS3 Study Group, Benavente OR, Coffey CS, Conwit R, et al. Blood-pressure targets in patients with recent lacunar stroke: the SPS3 randomised trial. Lancet 2013 Aug 10;382(9891):507-15. DOI: http://dx.doi.org/10.1016/S01406736(13)60852-1. 21. Wright JT Jr, Bakris G, Greene T, et al; African American Study of Kidney Disease and Hypertension Study Group. Effect of blood pressure lowering and antihypertensive drug class on progression of hypertensive kidney disease: results from the AASK trial. JAMA 2002 Nov 20;288(19):2421-31. DOI: http://dx.doi.org/10.1001/jama.288.19.2421. Erratum in: JAMA 2006 Jun 21;295(23):2726. DOI: http://dx.doi.org/10.1001/jama.295.23.2726-c. 22. Klahr S, Levey AS, Beck GJ, et al. The effects of dietary protein restriction and blood-pressure control on the progression of chronic renal disease. Modification of Diet in Renal Disease Study Group. N Engl J Med 1994 Mar 31;330(13): 877-84. DOI: http://dx.doi.org/10.1056/NEJM199403313301301. 23. Ruggenenti P, Perna A, Loriga G, et al; REIN-2 Study Group. Blood pressure control for renoprotection in patients with non-diabetic chronic renal disease (REIN-2): multicentre, randomised controlled trial. Lancet 2005 Mar 12-18; 365(9463):939-46. DOI: http://dx.doi.org/10.1016/S0140-6736(05)71082-5. 24. Ford ES, Ajani UA, Croft JB, et al. Explaining the decrease in US deaths from coronary disease, 1980-2000. N Engl J Med 2007 Jun 7;356(23):2388-98. DOI: http://dx.doi.org/10.1056/NEJMsa053935. 25. Yeh RW, Sidney S, Chandra M, Sorel M, Selby JV, Go AS. Population trends in the incidence and outcomes of acute myocardial infarction. N Engl J Med 2010 Jun 10;362(23):2155-65. DOI: http://dx.doi.org/10.1056/NEJMoa0908610. 26. Jaffe MG, Lee GA, Young JD, Sidney S, Go AS. Improved blood pressure control associated with a large-scale hypertension program. JAMA 2013 Aug 21;310(7):699-705. DOI: http://dx.doi.org/10.1001/jama.2013.108769. 27. Sim JJ, Handler J, Jacobsen SJ, Kanter MH. Systemic implementation strategies to improve hypertension: the Kaiser Permanente Southern California experience. Can J Cardiol 2014 May;30(5):544-52. DOI: http://dx.doi. org/10.1016/j.cjca.2014.01.003. 28. Shaw KM, Handler J, Wall HK, Kanter MH. Improving blood pressure control in a large multiethnic California population through changes in health care delivery, 2004-2012. Prev Chronic Dis 2014 Oct 30;11:E191. DOI: http://dx.doi.org/10.5888/ pcd11.140173. 29. Ayanian JZ, Landon BE, Newhouse JP, Zaslavsky AM. Racial and ethnic disparities among enrollees in Medicare Advantage plans. N Engl J Med 2014 Dec 11;371(24):2288-97. DOI: http://dx.doi.org/10.1056/NEJMsa1407273. 30. Fung V, Huang J, Brand R, Newhouse JP, Hsu J. Hypertension treatment in a medicare population: adherence and systolic blood pressure control. Clin Ther 2007 May;29(5):972-84. DOI: http://dx.doi.org/10.1016/j.clinthera.2007.05.010. 31. Tinetti ME. Clinical practice. Preventing falls in elderly persons. N Engl J Med 2003 Jan 2;348(1):42-9. DOI: http://dx.doi.org/10.1056/NEJMcp020719. 32. Tinetti ME, Han L, Lee DS, et al. Antihypertensive medications and serious fall injuries in a nationally representative sample of older adults. JAMA Intern Med 2014 Apr;174(4):588-95. DOI: http://dx.doi.org/10.1001/ jamainternmed.2013.14764. 33. Filippone EJ, Foy A, Newman E. Goal-directed antihypertensive therapy: lower may not always be better. Cleve Clin J Med 2011 Feb;78(2):123-33. DOI: http:// dx.doi.org/10.3949/ccjm.78a.10101. 34. Tight blood pressure control and risk of macrovascular and microvascular complications in type 2 diabetes: UKPDS 38. UK Prospective Diabetes Study Group. BMJ 1998 Sep 12;317(7160):703-13. DOI: http://dx.doi.org/10.1136/ bmj.317.7160.703. Erratum in: BMJ 1999 Jan 2;318(7175):29. DOI: http://dx.doi. org/10.1136/bmj.318.7175.29p. 35. Mancia G, Fagard R, Narkiewicz K, et al; Task Force Members. 2013 ESH/ESC Guidelines for the management of arterial hypertension: the Task Force for the management of arterial hypertension of the European Society of Hypertension (ESH) and of the European Society of Cardiology (ESC). J Hypertens 2013 Jul;31(7):1281-357. DOI: http://dx.doi.org/10.1097/01.hjh.0000431740.32696.cc. 36. Mancia G, Fagard R. New blood pressure control goals, more rational but facilitating therapeutic inertia?: reply. J Hypertens 2013 Dec;31(12):2462-5. DOI: http://dx.doi.org/10.1097/HJH.0000000000000005. 37. Beckett NS, Peters R, Fletcher AE, et al; HYVET Study Group. Treatment of hypertension in patients 80 years of age or older. N Engl J Med 2008 May 1;358(18):1887-98. DOI: http://dx.doi.org/10.1056/NEJMoa0801369. 38. VA/DoD clinical practice guidelines: management of hypertension (HTN) in primary care (2014) [Internet]. Washington, DC: US Department of Veterans Affairs; 2014 [cited 2015 Apr 6]. Available from: www.healthquality.va.gov/ guidelines/CD/htn. 39. Choma NN, Huang RL, Dittus RS, Burnham KE, Roumie CL. Quality improvement initiatives improve hypertension care among veterans. Circ Cardiovasc Qual Outcomes 2009 Jul;2(4):392-8. DOI: http://dx.doi.org/10.1161/ CIRCOUTCOMES.109.862714. Normal If we possessed instruments delicate enough we might be able to determine what the normal arterial pressure of a given individual was, and to note any variation from it … . We are … driven to depend upon the most treacherous of all methods, the impressions conveyed to our minds through the sensory nerves of the fingers … . By constant practice and study, each physician makes for himself a standard of atrial pressure which he recognizes as normal. — The Study of the Pulse, Sir James Mackenzie, MD, 1853-1925, Scottish cardiologist and pioneer in the study of cardiac arrhythmias 68 The Permanente Journal/ Summer 2015/ Volume 19 No. 3 Kaiser Permanente National Guideline Adult Hypertension CLINICIAN GUIDE AUGUST 2014 Screening for Hypertension TOOL 1. Key Points ff Hypertension is an important and modifiable risk factor for atherosclerotic cardiovascular disease (ASCVD). ff For all adults, encourage a heart-healthy lifestyle to reduce the risk of ASCVD. This includes regular physical activity, weight reduction and maintenance, smoking cessation, and controlling blood pressure, cholesterol, and diabetes. ff For adults aged 60 and older without diabetes or chronic kidney disease (CKD), treat to a goal systolic blood pressure (SBP) <150 mmHg and goal diastolic blood pressure (DBP) <90 mmHg. ff For all adults aged under 60, and those aged 60 and older with diabetes or chronic kidney disease (CKD), treat to a goal SBP <140 mmHg and goal DBP <90 mmHg. Introduction This Clinician Guide is based on the 2014 KP National Hypertension Guideline. It was developed to assist primary care physicians and other health care professionals in the outpatient treatment of hypertension in nonpregnant adults aged 18 and older. The drug treatment algorithm excludes patients with known stage 4-5 chronic kidney disease, coronary artery disease, and heart failure. The KP National Hypertension Guideline has adopted the new recommendations from the 2014 Evidence-Based Guideline for the Management of High Blood Pressure in Adults: Report From the Panel Members Appointed to the Eighth Joint National Committee (JNC 8) with minor modifications. It is not intended or designed as a substitute for the reasonable exercise of independent clinical judgment by practitioners. ff Screen all adults aged 18 and older for hypertension. ff Screen adults with normal blood pressure (<120/<80) every two years. ff Screen adults with pre-hypertension or cardiovascular risk factors annually. Treatment Initiation and BP Targets In addition to lifestyle interventions, the following are recommendations for the general population without diabetes or chronic kidney disease (CKD): TOOL 3. Treatment Initiation Lifestyle modifications: • Consume a diet that is moderately low-sodium, low-fat with a high intake of fruits and vegetables (DASH diet) • Weight reduction - for patients with a BMI ≥25 kg/m2 • Limit alcohol consumption • Exercise - at a moderate pace to achieve 150 min/week (i.e., 30 min/5 days/week) • Stop smoking or use of tobacco products • Assist patients to achieve medication and lifestyle adherence by means of a vigorous step-care approach to therapy and an organized system of regular medical follow-up and review • Prescribe once-daily medication and combination therapy, whenever possible • Address depression/anxiety issues in order to maximize patient adherence • Use patient education in conjunction with other strategies, particularly in the context of team care utilizing nurses and pharmacists • Educate patients about their goal blood pressure Presence of DM or CKD? No _ Age > 60 years? Definitions • Initiate pharmacologic treat- The KP National Hypertension Guideline Team uses the JNC 7 classification of hypertension, which is based on the mean of two or more properly measured seated BP readings on each of two or more office visits. TOOL 2. Definition of Hypertension (JNC 7) The JNC 7 Report defines Systolic Blood Presblood pressure (BP) as: sure (SBP) mmHg Normal Yes Yes § Diastolic Blood Pressure (DBP) mmHg <120 <80 Prehypertension 120 – 139 80 – 89 Stage I Hypertension 140 – 159 90 – 99 Stage II Hypertension ≥160 ≥100 ©2015 Kaiser Permanente Care Management Institute No ment to lower BP when SBP > _150 mmHg or DBP > _90 mmHg • Treat to a goal SBP <150 mmHg and goal DBP <90 mmHg • If pharmacologic treatment for high BP results in lower achieved SBP (e.g., <140 mmHg) and treatment is well-tolerated and without adverse effects on health or quality of life, treatment does not need to be adjusted • Initiate pharmacologic treatment to lower BP when SBP > _140 mmHg or DBP > _ 90 mmHg • Treat to a goal SBP <140 mmHg and goal DBP <90 mmHg • Initiate pharmacologic treatment to lower BP in all adults with CKD*/ diabetes when SBP > _140 mmHg or DBP > _ 90 mmHg • Treat to a goal SBP <140 mmHg and goal DBP <90 mmHg Footnotes § Because elderly patients are at higher risk of side effects of treatment, including risk of postural hypotension, check standing blood pressures to guide treatment decisions. * When weighing the risks and benefits of a lower BP goal for people aged 70 years or older with estimated GFR less than 60 mL/min/ 1.73 m2, antihypertensive treatment should be individualized, taking into consideration factors such as frailty, comorbidities, albuminuria, and estimation of non-age-related eGFR decline (e.g., if eGFR + ½ age is <85). KP National Guideline | Adult Hypertension CLINICIAN GUIDE | AUGUST 2014 GENERAL POPULATION ff Aged ≥60 years without diabetes or chronic kidney disease (CKD): • Initiate pharmacologic treatment to lower blood pressure (BP) when systolic blood pressure (SBP) ≥150 mmHg or diastolic blood pressure (DBP) ≥90 mmHg. • Treat to a goal SBP <150 mmHg and goal DBP <90 mmHg. • If pharmacologic treatment for high BP results in lower achieved SBP (e.g., <140 mmHg) and treatment is well-tolerated and without adverse effects on health or quality of life, treatment does not need to be adjusted. ff Aged <60 years and those aged > 60 with diabetes or chronic kidney disease (CKD): • Initiate pharmacologic treatment to lower BP when SBP ≥140 or DBP ≥90 mmHg. • Treat to a goal SBP <140 mmHg and goal DBP <90 mmHg. CHRONIC KIDNEY DISEASE (CKD) ff N OTE: When weighing the risks and benefits of a lower BP goal for people aged 70 years or older with estimated GFR less than 60 mL/min/ 1.73 m2, antihypertensive treatment should be individualized, taking into consideration factors such as frailty, comorbidities, albuminuria, and estimation of non-age-related eGFR decline (e.g., if eGFR + ½ age is <85). TOOL 4. eGFR Calculator ff eGFR (mL/min/1.73m2) = 186 × SCr -1.154 × age -0.203 (in men) (in women multiply with 0.74; in Afro-American multiply with 1.21) RISK OF POSTURAL HYPOTENSION IN THE ELDERLY ff B ecause elderly patients are at higher risk of side effects of treatment, including risk of postural hypotension, check standing blood pressures to guide treatment decisions. First-Line Drug Treatment for Hypertension* ff I n the general nonblack population, including those with diabetes, initial antihypertensive treatment includes a thiazide-type diuretic, calcium channel blocker (CCB), angiotensin-converting enzyme inhibitor (ACEI), or angiotensin receptor blocker (ARB). ff In the general black population, including those with diabetes, initial antihypertensive treatment includes a thiazide-type diuretic or CCB. ff In the population aged ≥18 years with CKD, initial (or add-on) antihypertensive treatment includes an ACEI or ARB to improve kidney outcomes. This applies to all CKD patients with hypertension, regardless of race or diabetes status. ff Medication up-titrations are recommended at intervals of 2-4 weeks (for most patients) until control is achieved. Consider follow-up labs when up-titrating or adding lisinopril, lisinopril/HCTZ, chlorthalidone, HCTZ, or spironolactone. *TOOL 5. Management of Adult Hypertension (see next page) INITIAL COMBINATION TREATMENT OF HYPERTENSION ff T he main objective of hypertension treatment is to attain and maintain goal BP. ff If goal BP is not reached within 4 weeks of treatment, increase the dose of the initial drug or add a second drug from one of the classes listed for first-line treatment (thiazide-type diuretic, CCB, ACEI, or ARB). ff C ontinue to assess BP and adjust the treatment regimen until goal BP is reached. If goal BP cannot be reached with 2 drugs, add and titrate a third drug from the list provided. Do not use an ACEI and ARB together in the same patient. ff If goal BP cannot be reached using only the drugs listed for first-line treatment due to a contraindication or need to use more than 3 drugs to reach goal BP, use antihypertensive drugs from other classes. ff Consider referral to a hypertension specialist for patients in whom goal BP cannot be attained using the above strategy or for the management of complicated patients for whom additional clinical consultation is needed. STEP-CARE THERAPY Because most people with hypertension will need more than one drug to control their hypertension effectively: ff Initial single-pill combination therapy with lisinopril-hydrochlorothiazide is preferred. ff For three drugs: If blood pressure is not controlled on a thiazidetype diuretic + ACEI, then use a thiazide-type diuretic plus ACEI plus dihydropyridine calcium channel blocker. ff For four drugs: If blood pressure is not controlled on a thiazide-type diuretic plus ACEI plus dihydropyridine calcium channel blocker, then use thiazide-type diuretic plus ACEI plus dihydropyridine calcium channel blocker plus spironolactone or beta-blocker. Lifestyle Modifications ff S upplement treatment of uncomplicated hypertension with lifestyle modifications: • Consume a diet that is moderately low-sodium, low-fat with a high intake of fruits and vegetables (DASH diet), Sodium restriction (≤2.4 gm sodium daily) • Weight reduction for patients with a BMI ≥25 kg/m2 TOOL 6. BMI Calculator BMI = weight (kg) height squared (m ) 2 BMI = weight (pounds) x 703 height squared (inches2) • Limit alcohol consumption - no more than one alcoholic drink (for women) or two alcoholic drinks (for men) daily • Exercise - at a moderate pace to achieve 150 min/week (i.e., 30 min/5 days/week) • Stop smoking or use of tobacco products ff Encourage adherence to medications and lifestyle modifications: • A ssist patients to achieve medication and lifestyle adherence by means of a vigorous step-care approach to therapy and an organized system of regular medical follow-up and review. • Prescribe once-daily medication and combination therapy, whenever possible. • Address depression and anxiety issues in order to maximize patient adherence. See KP National Depression Guideline at: http://cl.kp.org/pkc/national/cmi/programs/depression/guideline/index.html • Use patient education in conjunction with other strategies, particularly in the context of team care utilizing nurses and pharmacists. • Educate patients about their goal blood pressure, because patients who are knowledgeable about their goal BP are more likely to achieve it. ©2015 Kaiser Permanente Care Management Institute KP National Guideline | Adult Hypertension CLINICIAN GUIDE | AUGUST 2014 TOOL 5. Management of Adult Hypertension BLOOD PRESSURE (BP) GOALS • ≤139/89 mmHg: Aged 18-59, and aged 60 and over with Chronic Kidney Disease (CKD)1 or Diabetes • ≤149/89 mmHg: Aged 60 and over in the absence of Chronic Kidney Disease (CKD)1 or Diabetes ACE-Inhibitor 2/ Thiazide Diuretic Lisinopril / HCTZ (advanced as needed) 20/25 mg X ½ daily 20/25 mg X 1 daily 20/25 mg X 2 daily If ACEI intolerant or pregnancy potential Thiazide Diuretic3 HCTZ 25 mg 50 mg OR Chlorthalidone 12.5 mg 25 mg Pregnancy Potential: Avoid ACE-Inhibitors1 If not in control For ACEI intolerance due to cough, use ARB3 Add losartan 25 mg daily 50 mg daily 100 mg daily Pregnancy Potential: Avoid ARBs1 If not in control Calcium Channel Blocker2 Add amlodipine 5 mg X ½ daily 5 mg X 1daily 10 mg daily If not in control Spironolactone OR Beta-Blocker2 If on thiazide AND eGFR > _ 60 mL/min/1.73 m2 AND K <4.5 Add spironolactone 12.5 mg daily 25 mg daily OR Add atenolol 25 mg daily 50 mg daily (keep heart rate >55) If not in control • Consider medication non-adherence. • Consider interfering agents (e.g., NSAIDs, excess alcohol). • Consider white coat effect. Consider BP checks by medical assistant (e.g., two checks with 2 readings each, 1 week apart). • Consider discontinuing lisinopril/HCTZ and changing to chlorthalidone 25 mg plus lisinopril 40 mg daily. Consider additional agents (hydralazine, terazosin, minoxidil). • Consider stopping atenolol and adding diltiazem to amlodipine, keeping heart rate >55. • Avoid using clonidine, verapamil, or diltiazem together with a beta-blocker. These heart rate-slowing drug combinations may cause symptomatic bradycardia over time. • Consider secondary etiologies. • Consider consultation with a hypertension specialist. 1. CKD is defined as albuminuria (>30 mg of albumin/g of creatinine) at any age and any level of GFR, or an estimated GFR or measured GFR <60 mL/min/1.73 m2 in people aged <70 years. When weighing the risks and benefits of a lower BP goal for people aged 70 years or older with estimated GFR < 60 mL/min/1.73 m2, antihypertensive treatment should be individualized, taking into consideration factors such as frailty, comorbidities, albuminuria, and estimation of non-age-related eGFR decline (e.g., if eGFR + ½ age is <85). 2. ACE-inhibitors and ARBs are contraindicated in pregnancy and not recommended in most women of childbearing age. calcium channel blockers and spironolactone (Pregnancy Risk Category C), and beta-blockers (Pregnancy Risk Category D) should only be used in pregnancy when clearly needed and the benefits outweigh the potential hazard to the fetus. In the general black population, including those with diabetes, initial antihypertensive treatment includes a thiazide-type diuretic or CCB. 3. For patients with CKD, age 18-75 and intolerant to ACEI with cough and lacking pregnancy potential, losartan should be started prior to adding thiazide. ©2015 Kaiser Permanente Care Management Institute KP National Guideline | Adult Hypertension CLINICIAN GUIDE | AUGUST 2014 Special Considerations HYPERTENSION TREATMENT FOR WOMEN OF CHILDBEARING POTENTIAL ff B ecause half of all pregnancies are unplanned, unless there is a compelling indication, do not prescribe medications contraindicated in pregnancy, such as ACEIs/ARBs, to women of childbearing potential. ff For women of childbearing potential taking medications contraindicated in pregnancy, such as ACEIs/ARBs: • Discuss the potential risks to the fetus should they become pregnant. • Discuss practicing contraceptive measures with extremely low failure rates (sterilization, implant, or IUD). ff Advise women using ACEIs/ARBs to stop these medications and contact their OB/GYN provider immediately if they become pregnant. ff Advise women using ACEIs/ARBs for heart failure or cardiomyopathy and become pregnant to contact their obstetrician immediately. Their obstetrician, in consultation with cardiology, will substitute a suitable alternative to avoid decompensation. LIPID THERAPY IN PATIENTS TAKING HYPERTENSION MEDICATIONS ff E valuate patients with hypertension for dyslipidemia and initiate or continue statin treatment according to their total cardiovascular risk profile. ff Refer to the KP National Cardiovascular Risk and Dyslipidemia Clinician Guide at: http://cl.kp.org/pkc/national/cmi/programs/dyslipidemia/guideline/index.html ff Determine the need to initiate or continue lipid-lowering therapy based on ASCVD risk assessment using the AHA/ACC Pooled Cohort Equations: http://my.americanheart.org/cvriskcalculator and http://tools.cardiosource.org/ASCVD-Risk-Estimator/ ASPIRIN THERAPY IN PATIENTS TAKING HYPERTENSION MEDICATIONS ff E valuate patients with hypertension for aspirin use and initiate or continue statin treatment according to their total cardiovascular risk profile and risk of adverse events ff Refer to the KP National Aspirin Clinician Guide at: http://cl.kp.org/national/cmi/programs/cvd_risk_reduction/guideline/index.html RECOMMENDATIONS FOR PATIENTS WITH ACEI INTOLERANCE DUE TO COUGH ff H CTZ 25 mg, then 50 mg to achieve BP goal ff Add losartan 25 mg, then 50 mg, then 100 mg to achieve BP goal ff Add amlodipine 2.5 mg, then 5 mg, then 10 mg to achieve BP goal TOOL 7. Dosage Range for Selected Antihypertensive Medications* SELECTED ANTIHYPERTENSIVE MEDICATION Thiazide-type Diuretics Thiazide-type Diuretic Single Pill Combinations ACE Inhibitors (ACEI) Long-Acting Dihydropyridine Calcium Channel Blockers (CCB) Angiotensin II Receptor Blockers (ARB) Aldosterone Receptor Blocker Beta-Blockers (BB) USUAL DOSAGE RANGE Chlorthalidone (Hygroton) 12.5 – 25 mg daily Hydrochlorothiazide (HCTZ) (Esidrix) HCTZ /lisinopril (Prinzide) Spironolactone/HCTZ (Aldactazide) Lisinopril (Zestril, Prinivil) Captopril (Capoten) Amlodipine (Norvasc) Felodipine ER (Plendil) Nifedipine ER (Procardia XL) 25 – 50 mg daily 10/12.5 mg - 20/25 mg BID 25/25 mg daily 10 – 40 mg daily 12.5 – 50 mg BID 2.5 – 10 mg daily 2.5 – 20 mg daily 30 – 90 mg daily Losartan (Cozaar) Spironolactone (Aldactone) Atenolol (Tenormin) Bisoprolol (Zebeta) Carvedilol (Coreg) Metoprolol (Lopressor) Metoprolol ER (Toprol XL) 25 – 100 mg daily 12.5 – 25 mg daily 25 – 100 mg total, daily or BID 5 – 10 mg daily 3.125 – 37.5 mg BID 25 – 100 mg BID 25 – 200 mg daily *Availability of medications may vary depending on regional formularies. DISCLAIMER TOOL Overview TOOL 1. TOOL 2. TOOL 3. TOOL 4. TOOL 5. TOOL 6. TOOL 7. Key Points Definition of Hypertension (JNC 7) Treatment Initiation eGFR Calculator Management of Adult Hypertension BMI Calculator Dosage Range for Seleceted Antihypertensive Medications Page 1 Page 1 Page 1 Page 2 Page 3 Page 2 Page 4 Kaiser Permanente Clinical Practice Guidelines, Clinician Guides, and Clinical Tools/Resources have been developed to assist clinicians by providing an analytical framework for the evaluation and treatment of selected common problems encountered in patients. They are not intended to establish a protocol for all patients with a particular condition. While the guidelines provide one approach to evaluating a problem, clinical conditions may vary significantly from individual to individual. Therefore, the clinician must exercise independent judgment and make decisions based upon the situation presented. While great care has been taken to assure the accuracy of the information presented, the reader is advised that KP cannot be responsible for continued currency of the information, for any errors or omissions in this guideline, or for any consequences arising from its use. These recommendations are not used to make utilization management determinations regarding the medical necessity of a member’s care. ©2015 Kaiser Permanente Care Management Institute SOUL OF THE HEALER Dorothy’s View photograph Bridget Bourgon, PA-C This photograph was taken at sunrise from a hot air balloon above the town of Göreme in the Cappadocia region of Turkey. Cappadocia is known for its natural pillar-like rock formations, which ancient peoples carved into houses, churches, and monasteries. Ms Bourgon is a Physician Assistant in Urgent Care at Kaiser Permanente Orange County in Santa Ana, CA. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 73 CASE REPORTS Beer Potomania—An Unusual Cause of Hyponatremia Dean A Kujubu, MD; Ardeshir Khosraviani, MD Perm J 2015 Summer;19(3):74-76 http://dx.doi.org/10.7812/TPP/14-181 ABSTRACT The first case of severe hyponatremia, since referred to as beer potomania, in a heavy beer drinker patient was reported in 1972. Electrolyte abnormalities are common findings in patients with a history of heavy alcohol use. Excessive consumption of beer in particular, which has a low solute content (sodium concentration, 1.8 mEq/L and potassium concentration, 7.2 mEq/L), to the exclusion of other solute intake may result in severe hyponatremia. We report a case of severe hyponatremia that occurred in a patient who, owing to his underlying colon cancer, was drinking beer and ingesting little other food. His hyponatremia improved with increased solute intake and, upon correction of his serum sodium, he had no subsequent neurologic sequelae. INTRODUCTION The first case of severe hyponatremia in a heavy beer drinker patient was reported in 1972 by Gwinup et al.1 This condition has since been referred to as beer potomania. Electrolyte abnormalities are common findings in patients with a history of heavy alcohol use. In the study by Liamis et al,2 among hospitalized patients with history of chronic alcohol consumption, 17.3% had hyponatremia. The excessive consumption of beer in particular, which has a low solute content (sodium concentration, 1.8 mEq/L; potassium concentration, 7.2 mEq/L), to the exclusion of other solute intake may result in severe hyponatremia. We report a case of severe hyponatremia that occurred in a patient who, owing to his underlying colon cancer, was drinking beer and ingesting little other food. His hyponatremia improved with increased solute intake and, upon correction of his serum sodium, he had no subsequent neurologic sequelae. CASE PRESENTATION A Hispanic man, age 84 years, with history of chronic alcohol abuse and recently diagnosed stage IV sigmoid adenocarcinoma presented to the Emergency Department with nausea, weakness, decreased appetite, and abdominal pain for the past 3 to 4 days. The patient had been ingesting approximately 12 cans of beer daily in addition to his usual diet for the preceding 50 years, but during the week before his presentation, because of worsening abdominal pain, he was drinking his habitual quantities of beer but otherwise eating minimally. On physical examination, his temperature was 37.1°C, blood pressure 142/81 mmHg, pulse rate 78 beats/ min, without orthostatic changes, respiratory rate 18 breaths/ min, and oxygen saturation 97% on room air. He was in no acute distress and did not appear intravascularly volume depleted. His lungs were clear bilaterally, and his heart sounds were normal without murmurs. He had tenderness in the epigastric area without rebound tenderness, with normal bowel sounds and no organomegaly. He was oriented and coherent in conversation. His neurologic exam and deep tendon reflexes were normal. He had no tremors. The patient’s laboratory data showed white blood cells 15.4 × 1000/mcL, hemoglobin 12.7 g/dL, platelets 347 × 1000/mcL, international normalized ratio 1.1, glucose 160 mg/dL, sodium 116 mEq/L, potassium 4.1 mEq/L, chloride 85 mEq/L, CO2 19 mEq/L, blood urea nitrogen 6 mg/dL, creatinine 0.58 mg/dL, serum osmolality 250 mOsm/kg, uric acid 3 mg/dL, phosphorus 2.8 mg/dL, calcium 8.3 mg/dL, magnesium 1.1 mg/dL, alanine transaminase 20 U/L, aspartate transaminase 27 U/L, total bilirubin 0.8 mg/dL, thyroid stimulating hormone 2.19 mcIU/ml, albumin 2.8 g/dL, and cortisol 23.8 mcg/dL. His urinalysis showed specific gravity 1.005, pH 6, negative leukocyte esterase, negative nitrite, white blood cells 0-2, red blood cells 0-3, urine sodium 35 mEq/L, urine chloride 37 mEq/L, urine potassium 11 mEq/L, urine creatinine 26 mg/dL, and urine osmolality 182 mOsm/kg. A computed tomography scan of his abdomen and pelvis with intravenous contrast revealed a new abscess adjacent to the previously seen sigmoid carcinoma with local lymphadenopathy and hepatic metastatic disease. The patient received 1 L of 0.9% sodium chloride intravenously in the Emergency Department and was started on antibiotics for the sigmoid abscess. The surgical consultant did not recommend surgical intervention. He received intravenous thiamine and magnesium supplementation for his history of heavy alcohol drinking and hypomagnesemia. He was encouraged to increase his oral intake with a normal diet as tolerated. He subsequently underwent a brisk diuresis of approximately 1.8 L during the first 8 hours. His intravenous fluid was promptly discontinued and the patient’s serum sodium was checked every 2 to 3 hours to monitor for overly rapid correction. His serum sodium increased by 8 mEq/L in the first 24 hours and 14 mEq/L in the first 48 hours. His serum sodium remained between 130 mEq/L and 133 mEq/L Dean A Kujubu, MD, is the Director of the Nephrology Fellowship program at the Los Angeles Medical Center in CA. E-mail: [email protected]. Ardeshir Khosraviani, MD, is a Nephrology Fellow at the Los Angeles Medical Center in CA. E-mail: [email protected]. 74 The Permanente Journal/ Summer 2015/ Volume 19 No. 3 CASE REPORTS Beer Potomania—An Unusual Cause of Hyponatremia Common Causes of Hyponatremia Hyponatremia with high osmolality • Hyperglycemia, mannitol infusion, advanced renal failure Hyponatremia with normal osmolality • Hyperlipidemia, paraproteinemia Hyponatremia with low osmolality • Hypovolemic hyponatremia – Volume depletion with sodium loss in excess of water • Hypervolemic hyponatremia – Heart failure, cirrhosis, nephrotic syndrome • Euvolemic hyponatremia – Syndrome of inappropriate antidiuretic hormone, reset osmostat – Hypothryoidism, glucocorticoid deficiency, renal failure – Primary polydipsia, beer potomania, low solute intake – Medications, including thiazide diuretics throughout the remainder of his hospitalization. He was closely observed for any change in his neurologic status or signs and symptoms of acute alcohol withdrawal. None appeared. DISCUSSION The most common electrolyte abnormality seen in clinical practice is hyponatremia, which is also found in up to 30% of hospitalized patients.3 In the study by Liamis et al,2 hyponatremia was the third most common electrolyte abnormality detected in 127 hospitalized chronic alcoholic patients, with a prevalence of 17.3%. Traditionally, the evaluation of hyponatremia begins with the determination of serum osmolality followed by a clinical assessment of volume status (see Sidebar: Common Causes of Hyponatremia). Most clinical hyponatremia is associated with a low serum osmolality. In patients with normal renal function, excessive water ingestion does not result in severe hyponatremia because of the kidneys’ ability to excrete large amounts of free water, provided the daily dietary intake of solute is normal. For Management Recommendations for Hyponatremia Caused by Beer Potomania • Nothing by mouth except medications for 24 hours • No intravenous fluids unless symptomatic • Prescribe intravenous fluids in finite amounts if needed • Intensive care status • Check serum sodium every 2 hours • Goals – Serum sodium increase < 10 mEq/L in first 24 hours – Serum sodium increase < 18 mEq/L in first 48 hours • Reduce serum sodium levels if necessary • Give any intravenous medications in sugar solution (5% dextrose in water) • If caloric intake is needed, use intravenous sugar solution (5% dextrose in water) The Permanente Journal/ Summer 2015/ Volume 19 No. 3 example, if the normal daily intake of solute is between 600 mOsm/day and 900 mOsm/day for an individual on a typical Western diet, and if the maximal urinary dilution capacity is 50 mOsm/kg, a person with normal kidney function would be able to excrete between 12 L to 18 L of free water daily without becoming hyponatremic. In contrast, if such a person were to have a daily intake of only 200 mOsm to 300 mOsm solute, his ability to excrete free water becomes limited to 4 L/day to 6 L/day provided he is able to dilute his urine to the same degree.4 The intake of fluid in excess of this amount will result in a dilutional hyponatremia. Moreover, the ingestion of large volumes of fluid in these patients results in the washout of the medullary urea concentration gradient, reducing the kidneys’ ability to produce maximally dilute urine.5 When additional solute is provided, a brisk diuresis ensues, resulting in rapidly increasing serum sodium concentrations, necessitating careful, frequent monitoring as well as the administration of electrolyte-free fluids or even antidiuretic hormone analogues should the serum sodium rise by more than 8 mEq/24 hours to 10 mEq/24 hours. Precipitating the osmotic demyelination syndrome (ODS) in chronically hyponatremic patients by infusing saline load is a real danger.5 Case reports of ODS with rapid sodium correction in patients with beer potomania have been published. In a literature review done by Sanghvi et al,6 of 22 patients with beer potomania, 4 (18%) had ODS. Although infusion of hypertonic saline classically has been associated with development of ODS, Karp and Laureno7 suggest that the rapid correction of hyponatremia may occur even with infusion of normal saline or with fluid restriction alone, resulting in ODS. On the basis of the underlying pathophysiology of beer potomania, Sanghvi et al6 provided clinical recommendations for the management of these patients (see Sidebar: Management Recommendations for Hyponatremia Caused by Beer Potomania). Because of the potential for overly rapid correction of serum sodium resulting in irreversible neurologic consequences in these patients with beer potomania, intensive care and frequent, serial measurements of serum electrolytes are recommended. Our patient’s history, clinical euvolemic state, and prompt diuresis in response to 1 L of intravenous normal saline administered in the Emergency Department led us to suspect that he indeed had beer potomania. Our patient was consuming 12 cans (12 ounces each) of beer daily, which is approximately 4.3 L. According to the published content of beer, our patient’s solute intake was approximately 30 mEq potassium, 7 mEq sodium, 150 g carbohydrate, and 20 g protein per day. If the metabolism of every 10 g of protein results in the generation of 50 mmoles of urea, we estimate that our patient’s daily solute intake was in the range of 200 mOsm/day to 250 mOsm/day. Our patient was older so it was unlikely that he would be able to maximally dilute his urine to 50 mOsm/kg, because with aging the kidneys’ ability to produce dilute urine declines.8 The capacity is further limited by the washout of his medullary concentration gradient owing to excessive fluid intake. If the maximally dilute urine 75 CASE REPORTS Beer Potomania—An Unusual Cause of Hyponatremia our patient could produce was 75 mOsm/kg rather than 50 mOsm/L, with daily solute intake of 200 mOsm/day to 250 mOsm/day he would need to drink only in excess of 2.7 L to 3.3 L of fluid per day before he would become hyponatremic, which was well below the range of his intake. After the initial correction of his hyponatremia during the first 48 hours, his serum sodium remained in the range of 130 mEq/L to 133 mEq/L for the rest of his hospitalization. His persistent hyponatremia was most probably because of an underlying syndrome of inappropriate antidiuretic hormone secretion from metastatic cancer or a reset osmostat owing to his poor nutritional state, malignant tumor, or alcoholism.9,10 His underlying tendency toward hyponatremia prevented his serum sodium from overcorrecting while his solute intake increased and his water intoxication resolved. v Disclosure Statement The author(s) have no conflicts of interest to disclose. Acknowledgment Mary Corrado, ELS, provided editorial assistance. References 1. Gwinup G, Chelvam R, Jabola R, Meister L. Beer drinker’s hyponatremia. Inappropriate concentration of the urine during ingestion of beer. Calif Med 1972 Mar;116(3):78-81. 2. Liamis GL, Milionis HJ, Rizos EC, Siamopoulos KC, Elisaf MS. Mechanisms of hyponatraemia in alcohol patients. Alcohol Alcohol 2000 Nov-Dec;35(6):612-6. DOI: http://dx.doi.org/10.1093/alcalc/35.6.612. 3. Upadhyay A, Jaber BL, Madias NE. Incidence and prevalence of hyponatremia. Am J Med 2006 Jul;119(7 Suppl 1):S30-5. DOI: http://dx.doi. org/10.1016/j.amjmed.2006.05.005. 4. Berl T. Impact of solute intake on urine flow and water excretion. J Am Soc Nephrol 2008 Jun;19(6):1076-8. DOI: http://dx.doi.org/10.1681/ ASN.2007091042. 5. Kelly J, Wassif W, Mitchard J, Gardner WN. Severe hyponatraemia secondary to beer potomania complicated by central pontine myelinolysis. Int J Clin Pract 1998 Nov-Dec;52(8):585-7. 6. Sanghvi SR, Kellerman PS, Nanovic L. Beer potomania: an unusual cause of hyponatremia at high risk of complications from rapid correction. Am J Kidney Dis 2007 Oct;50(4):673-80. DOI: http://dx.doi.org/10.1053/j.ajkd.2007.07.015. 7. Karp BI, Laureno R. Pontine and extrapontine myelinolysis: a neurologic disorder following rapid correction of hyponatremia. Medicine (Baltimore) 1993 Nov;72(6):359-73. DOI: http://dx.doi.org/10.1097/00005792-199311000-00001. 8. Sands JM. Urinary concentration and dilution in the aging kidney. Semin Nephrol 2009 Nov;29(6):579-86. DOI: http://dx.doi.org/10.1016/j. semnephrol.2009.07.004. 9. Kahn T. Reset osmostat and salt and water retention in the course of severe hyponatremia. Medicine 2003 May;82(3):170-6. DOI: http://dx.doi. org/10.1097/01.md.0000076007.64510.15. 10. DeFronzo RA, Goldberg M, Agus ZS. Normal diluting capacity in hyponatremic patients. Reset osmostat or a variant of the syndrome of inappropriate antidiuretic hormone secretion. Ann Intern Med 1976 May;84(5):538-42. DOI: http://dx.doi.org/10.7326/0003-4819-84-5-538. Hard Drinking The effects of hard drinking are flatulence, loss of appetite, morning sickness, wasting of the flesh and strength, tremblings, pains of the stomach, cough, jaundice, dropsy, forgetfulness and inattention, giddiness, diarrhea, broken sleep. — William Heberden, MD, 1710-1801, English physician 76 The Permanente Journal/ Summer 2015/ Volume 19 No. 3 CLINICAL MEDICINE Dermatologic Diagnosis: Leukocytoclastic Vasculitis Joseph Einhorn, MD; Joel T Levis, MD, PhD, FACEP, FAAEM Perm J 2015 Summer;19(3):77-78 http://dx.doi.org/10.7812/TPP/15-001 Leukocytoclastic vasculitis (LCV), also termed hypersensitivity vasculitis, is a small-vessel vasculitis with a reported incidence rate of about 30 cases per million people per year and is thought to affect men and women in equal numbers.1,2 The skin is the organ most commonly involved in LCV. Typical presentation is a painful, burning rash predominantly in the lower extremities (Figure 1), with up to one-third of patients presenting with trunk and upper extremity involvement.3 The most common skin manifestation of LCV is palpable purpura.1-3 Other skin manifestations include maculopapular rash, bullae, papules, plaques, nodules, ulcers, and livedo reticularis.4 Patients with LCV may also present with arthralgias or arthritis involving the knees or ankles.4 The differential diagnosis for LCV includes drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome, amyloidosis, antiphospholipid syndrome, atrial myxoma, Behcet disease, Churg-Strauss syndrome, granulomatosis with polyangiitis, Henoch-Schonlein Purpura, urticarial vasculitis, immune thrombocytopenic purpura, and meningococcemia.5 Multiple etiologic factors including drugs, infections, foods, autoimmune diseases, collagen vascular diseases, and malignancies have been associated with LCV.1 Although the exact pathogenic mechanism remains to be elucidated, circulating immune complexes are believed to be involved.6 In the evaluation of patients with LCV, laboratory tests including a complete blood count, erythrocyte sedimentation rate, biochemistry profile with liver and renal function, and urinalysis are useful in excluding other vasculitides, determining the presence of systemic disease, and identifying an associated disorder, which can provide prognostic information.4 Patients with suspected LCV presenting to the Emergency Department may require parenteral analgesics for pain control, and those patients not requiring hospitalization should be referred to a dermatologist upon discharge. Diagnosis of LCV is confirmed on histologic examination of a biopsy from the affected area that demonstrates perivascular and vascular leukocytic infiltrates along with fibrinoid necrosis.1 Mild, skin-limited LCV does not require treatment apart from rest, elevation of the legs, ice packs to the affected area, and removal or treatment of the inciting cause.7 Presence of arthralgia or arthritis requires use of nonsteroidal antiinflammatory drugs, or a short course of oral steroids (eg, prednisone or methlprednisolone) at a dose of 1 mg/kg/day for 4 weeks Figure 1. Lower extremities of a 31-year-old woman presenting to the Emergency Department. The patient reported several days of arthralgias and a moderately painful, burning rash involving the legs and extending to the lower abdomen, preceded by a viral syndrome. This image demonstrates nonblanching palpable purpura to the lower extremities with some areas coalescing to form plaques. Findings are consistent with leukocytoclastic vasculitis. followed by a steroid taper. Most patients respond to such treatment.8 A single-pulse dose of intravenous corticosteroids (eg, methylprednisolone, 15 mg/kg) may be required, followed by oral corticosteroids in more severe cases. Colchicine has also reportedly been useful in patients with skin and joint symptoms, though success in a small, randomized controlled trial was limited.9 Colchicine should be used with caution in persons with kidney disease and in pregnant women. Most patients with cutaneous leukocytoclastic vasculitis are treated in an outpatient setting. Inpatient care is needed in patients who have severe systemic vasculitic syndromes and severe organ dysfunction. In the absence of internal involvement, the majority of cases of LCV resolve within weeks to months, with approximately 10% of patients experiencing chronic or recurrent disease.10 v Joseph Einhorn, MD, is an Emergency Medicine Resident in the Stanford/Kaiser Emergency Medicine Residency Program in CA. E-mail: [email protected]. Joel T Levis, MD, PhD, FACEP, FAAEM, is a Senior Emergency Physician at the Santa Clara Medical Center, and Clinical Assistant Professor of Emergency Medicine (Surgery) at Stanford University. He is the Medical Director for the Foothill College Paramedic Program in Los Altos, CA. E-mail: [email protected]. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 77 CLINICAL MEDICINE Dermatologic Diagnosis: Leukocytoclastic Vasculitis References 1. Hussain N, Mustafa U, Davis J, et al. Indomethacin-related leukocytoclastic vasculitis: a case report and review of literature. Case Rep Dermatol 2013 Jan;5(1):33-7. DOI: http://dx.doi.org/10.1159/000348240. 2. González-Gay MA, García-Porrúa C. Systemic vasculitis in adults in northwestern Spain, 1988-1997. Clinical and epidemiologic aspects. Medicine (Baltimore) 1999 Sep;78(5):292-308. 3. Brown K, Martin J, Zito S. Severe leukocytoclastic vasculitis secondary to the use of naproxen and requiring amputation: a case report. J Med Case Rep 2010 Jul 1;4:204. DOI: http://dx.doi.org/10.1186/1752-1947-4-204. 4. Martinez-Taboada VM, Blanco R, Garcia-Fuentes M, Rodriguez-Valverde V. Clinical features and outcome of 95 patients with hypersensitivity vasculitis. Am J Med 1997 Feb;102(2):186-91. DOI: http://dx.doi.org/10.1016/S00029343(96)00405-6. 5. Gibson LE. A review of cutaneous vasculitis. Journal of the Egyptian Women’s Dermatologic Society 2004;1(1):1-15. 6. Mackel SE, Jordon RE. Leukocytoclastic vasculitis. A cutaneous expression of immune complex disease. Arch Dermatol 1982 May;118(5):296-301. DOI: http:// dx.doi.org/10.1001/archderm.1982.01650170010012. 7. Binamer Y. Dermacase. Can you identify this condition? Drug-induced leukocytoclastic vasculitis. Can Fam Physician 2013 Jul;59(7):748, 750-1. 8. Fiorentino DF. Cutaneous vasculitis. J Am Acad Dermatol 2003 Mar;48(3): 311-40. DOI: http://dx.doi.org/10.1067/mjd.2003.212. 9. Sais G, Vidaller A, Jucglà A, Gallardo F, Peyrí J. Colchicine in the treatment of cutaneous leukocytoclastic vasculitis. Results of a prospective, randomized controlled trial. Arch Dermatol 1995 Dec;131(12):1399-402. DOI: http://dx.doi. org/10.1001/archderm.1995.01690240061009. 10. Loricera J, Calvo-Río V, Ortiz-Sanjuán F, et al. The spectrum of paraneoplastic cutaneous vasculitis in a defined population: incidence and clinical features. Medicine (Baltimore) 2013 Nov;92(6):331-43. DOI: http://dx.doi.org/10.1097/ MD.0000000000000009. Medicine The critical sense and sceptical attitude of the Hippocratic school laid the foundations of modern medicine on broad lines, and we owe to it: first, the emancipation of medicine from the shackles of priestcraft and of caste; secondly, the conception of medicine as an art based on accurate observation, and as a science, an integral part of the science of man and of nature; thirdly, the high moral ideals, expressed in that most “memorable of human documents” (Gomperz), the Hippocratic oath; and fourthly, the conception and realization of medicine as the profession of a cultivated gentleman. — Sir William Osler, MD, 1st Baronet, 1849-1919, Canadian physician and one of four founding professors of Johns Hopkins Hospital 78 The Permanente Journal/ Summer 2015/ Volume 19 No. 3 CLINICAL MEDICINE ECG Diagnosis: Hyperacute T Waves Joel T Levis, MD, PhD, FACEP, FAAEM Perm J 2015 Summer;19(3):79 http://dx.doi.org/10.7812/TPP/14-243 After QT prolongation, hyperacute T waves are the earliest-described electrocardiographic sign of acute ischemia, preceding ST-segment elevation.1 Hyperacute T waves are broad-based and symmetrical, usually with increased amplitude and often associated with a depressed ST take off.1 Hyperacute T waves are most evident in the anterior chest leads and are more apparent when a previous electrocardiogram is available for comparison.2 Hyperacute T waves are noted early after the onset of coronary occlusion and transmural infarction and tend to be a short-lived structure that evolves rapidly into ST-segment elevation.3 The electrocardiographic differential diagnosis of the hyperacute T wave includes both transmural acute myocardial infarction and hyperkalemia as well as early repolarization, left ventricular hypertrophy, and acute myopericarditis.4 The principle entity to exclude is hyperkalemia—this T-wave morphology may be confused with the hyperacute T wave of early transmural myocardial infarction. In contrast to hyperacute T waves associated with myocardial ischemia or infarction, hyperkalemic T waves tend to be narrow and peaked with a prominent or sharp apex.4 For patients presenting with hyperacute T waves in the setting of suspected myocardial ischemia or infarction, treatment includes symptomatic control with nitroglycerin or morphine, oral antiplatelet agents (aspirin), consideration of anticoagulation with unfractionated heparin, and obtaining frequent serial 12-lead electrocardiograms (every 5 to 10 minutes). Prompt consultation with a cardiologist is indicated in these cases. v References 1. Goldberger AL. Hyperacute T waves revisited. Am Heart J 1982 Oct;104(4 Pt 1):888-90. DOI: http://dx.doi.org/10.1016/00028703(82)90038-2. 2. Nable JV, Brady W. The evolution of electrocardiographic changes in ST-segment elevation myocardial infarction. Am J Emerg Med 2009 Jul;27(6):734-46. DOI: http://dx.doi. org/10.1016/j.ajem.2008.05.025. 3. Morris F, Brady WJ. ABC of clinical electrocardiography: acute myocardial infarction—part I. BMJ 2002;324:831. DOI: http:// dx.doi.org/10.1136/bmj.324.7341.831. 4. Brady W, Morris F. Electrocardiographic abnormalities encountered in acute myocardial infarction. J Accid Emerg Med 2000 Jan;17(1):40-45. DOI: http://dx.doi.org/10.1136/emj.17.1.40. Figure 1. 12-lead electrocardiogram from a 47-year-old man presenting to the Emergency Department with left-sided chest discomfort, now resolved following sublingual nitroglycerin. Demonstrates normal sinus rhythm with nonspecific ST-T wave changes including flattening of T waves in the inferior and lateral leads. Figure 2. 12-lead electrocardiogram from same patient, obtained 90 minutes later, with patient now experiencing 5/10 left-sided chest discomfort. Demonstrates large, symmetric T waves with depressed STsegment take off consistent with hyperacute T waves in the anterior leads V2-V4. Figure 3. 12-lead electrocardiogram from same patient as Figures 1 and 2, obtained 10 minutes after the electrocardiogram in Figure 2. Demonstrates > 1 mm ST-segment elevation in the anterior leads V2-V4, consistent with an acute anterior wall myocardial infarction. Figure 4. 12-lead electrocardiogram from a 73-year-old man with end-stage renal disease and hyperkalemia (serum potassium 7.6 mEq/L). Demonstrates peaked T waves in leads V3 and V4, consistent with hyperkalemia. Joel T Levis, MD, PhD, FACEP, FAAEM, is a Senior Emergency Physician at the Santa Clara Medical Center, and Clinical Assistant Professor of Emergency Medicine (Surgery) at Stanford University. He is the Medical Director for the Foothill College Paramedic Program in Los Altos, CA. E-mail: [email protected]. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 79 SOUL OF THE HEALER So Much Sky Colored pencils on paper 3” x 6” Sharon Lee Hostler, MD This image was sketched outside the Mabel Dodge Luhan House at the 2014 Taos Writing Workshop. The artist, who grew up in the Green Mountains of Vermont and practices medicine near the Blue Ridge Mountains of Virginia, saw the brilliant blue sky over Taos as dwarfing all, even the towering mountains of New Mexico. Dr Hostler is the McLemore Birdsong Professor of Pediatrics at the University of Virginia School of Medicine and Vice Provost for Faculty Development at the University of Virginia in Charlottesville. 80 The Permanente Journal/ Summer 2015/ Volume 19 No. 3 COMMENTARY Does Consuming Sugar and Artificial Sweeteners Change Taste Preferences? Carole Bartolotto, MA, RD Perm J 2015 Summer;19(3):81-84 http://dx.doi.org/10.7812/TPP/14-229 INTRODUCTION ABSTRACT Americans consume a lot of sugar, primarily from sweeteners that are added to processed foods and beverages. Data from the US Department of Agriculture reveals that in 2013, Americans consumed 22.3 teaspoons of added caloric sweeteners a day, which is significantly more than the American Heart Association’s recommendation. Artificial and alternative sweeteners have also been added to a plethora of foods. These sweeteners range from about 180 times sweeter to as much as 13,000 times sweeter than sugar. Consumption of both sugar and artificial sweeteners may be changing our palates or taste preferences over time, increasing our desire for sweet foods. Unfortunately, the data on this are lacking. In the summer of 2014, a group of 20 people from Kaiser Permanente facilities throughout California agreed to cut out all added sugars and artificial sweeteners for 2 weeks and then complete a survey to determine whether their taste preferences had changed. After the 2-week challenge, 95% of participants (18 out of 19 respondents) found that sweet foods and drinks tasted sweeter or too sweet, 75% (15 out of 20 respondents) found that other foods tasted sweeter, and 95% (19 out of 20 respondents) said moving forward they would use less or even no sugar. Additionally, 86.6% of participants (13 out of 15 respondents) stopped craving sugar after 6 days. Although this was a small survey, the results suggest that using a 2-week sugar challenge can help to reset taste preferences and make consuming less or no sugar easier. Physicians should consider recommending a sugar and artificial sweetener challenge to all their patients, especially those with obesity, diabetes, or cardiovascular disease. Figure 1. Sources of added sugars in the diets of the US population, ages 2 years and older, National Health and Nutrition Examination Survey 2005-2006. Sugars are simple carbohydrates found naturally in fruit and milk. Although we do get some of the sugar we consume from these foods, much of our intake comes from sugars that are added to processed foods and beverages. Cane sugar, high-fructose corn syrup, agave, honey, evaporated cane juice, and other forms of sugar are added to products such as sodas, cakes, cookies, and candies. They are also added to many processed foods such as breakfast cereals, pasta sauce, yogurt, soymilk, barbeque sauce, and bottled teas. In fact, using their new online database, the Environmental Working Group has found that almost 60% of the 80,000 products evaluated contained added sugar.1,2 For examples of sugar content in commonly consumed foods, see Sidebar: Examples of the Amounts of Sugar Found in Processed and Restaurant Foods and Drinks. According to the Dietary Guidelines for Americans 2010, our biggest source of sugar is sugary drinks, which supply 35.7% of our intake.3 Almost 13% of the sugar we consume is from grainbased desserts, such as cookies, cakes, muffins, and scones (Figure 1).3 Most people have a natural propensity for sweet foods and beverages. Data from the US Department of Agriculture reveals that in 2013, Americans consumed 22.3 teaspoons of added caloric sweeteners a day. This includes sugar, high-fructose corn syrup, and other sweeteners.4 The consumption of sugars and sugary drinks has been linked with obesity, diabetes, heart disease, hypertension, impaired lipid metabolism, inflammation, and an increase in cravings and feelings of hunger, which is why major health organizations have weighed in on how much we should consume.5-13 Carole Bartolotto, MA, RD, is a Senior Consultant for Regional Health Education for the Southern California Permanente Medical Group. E-mail: [email protected]. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 81 COMMENTARY Does Consuming Sugar and Artificial Sweeteners Change Taste Preferences? New Recommendations for Sugar In 2009, for the first time ever, the American Heart Association came out with recommendations for sugar consumption.7 For women, they recommend consuming no more than 6 teaspoons or 100 calories of added sugar each day. This is equivalent to about 24 g of sugar. For men, they recommend no more than 9 teaspoons or 150 calories of added sugar a day. This is equal to about 35 g of sugar. It is interesting to note that one 12-ounce can of cola has about 10 teaspoons of sugar, putting the drinker, whether a man or a woman, over the limit recommended by the American Heart Association with just one item. The World Health Organization’s new draft guidelines say sugar consumption should be less than 10% of total energy intake per day, but a reduction to below 5% would have added benefits.14 Five percent of 2000 calories would be 100 calories (around 6 teaspoons or 24 g) of sugar per day. Sugar, Artificial Sweeteners, and Health Artificial sweeteners have also been added to a plethora of foods for those who want a sweet taste without the calories. These sweeteners range from about 180 times sweeter to as much as 13,000 times sweeter than sugar.15 Recent research has linked artificial sweeteners to a number of health problems, including metabolic syndrome, a decrease in kidney function, and possibly even a disruption in the regulation of blood sugar caused by changes in the microbiota.16-18 Although more research is needed, these observational and preliminary data have caused many to rethink their use of artificial sweeteners. In addition to the health problems associated with the use of sugars and artificial sweeteners, their consumption may be changing our palates or taste preferences over time, increasing our Examples of the Amounts of Sugar Found in Processed and Restaurant Foods and Drinks • 1 tsp sugar = 4 g • Kiwi Strawberry Vitamin Water, 20 oz bottle—32 g1 • Yoplait Original Mountain Blueberry Yogurt, 6 oz—26 g2 • Oscar Mayer Lunchables Ham and Cheddar Cracker Stackers (with fruit punch)—31 g3 • Silk Very Vanilla Soy Milk, 1 cup—15 g4 • Sweet Baby Rays Barbecue Sauce, 2 tbsp—16 g5 • Kellogg’s Smart Start Strong Heart Antioxidants Cereal, 1 cup—14 g6 • Starbucks Blueberry Scone—20 g7 • Subway 6” BBQ Oven Roasted Chicken Melt—17 g8 • Panda Express Orange Chicken (2 Entrée meal) with chow mein—47 g9 • California Pizza Kitchen Thai Crunch Salad (full)—48 g10 1. Glaceau vitamin water focus kiwi-strawberry nutrient enhanced water beverage from Vitaminwater [Internet]. Washington, DC: Nutritionix; last updated 2014 Dec 30 [cited 2015 Mar 17]. Available from: www.nutritionix. com/vitaminwater/glaceau-vitamin-water-focus-kiwi-strawberry-nutrient-enhanced-water-beverage. 2. Calories in Yoplait Original Mountain Berry Yogurt [Internet]. San Francisco, CA: MyFitnessPal, Inc; 20052015 [cited 2015 Mar 17]. Available from: www.myfitnesspal.com/food/calories/yoplait-original-mountainberry-yogurt-73025358. 3. Nutrition information, diet info and calories in ham and cheddar stackers from Lunchables [Internet]. Spokane, WA: Albertsons; 2015 [cited 2015 Apr 6]. Available from: www.albertsons.com/pd/Oscar-MayerLunchables/Ham-and-Cheddar-Cracker-Stackers-Lower-Fat/11-oz/044700361177/. 4. Silk very vanilla soy milk: nutrition [Internet]. Broomfield, CO: WhiteWave Foods; 2015 [cited 2015 Mar 17]. Available from: http://silk.com/products/very-vanilla-soymilk. 5. Sweet Baby Ray’s Barbecue Sauce nutrition facts [Internet]. Henderson, NV: CalorieLab, Inc; 20002015 [cited 2015 Mar 17]. Available from: http://calorielab.com/brands/sweet-baby-rays-barbecuesauce/136/2005455. 6. Kellogg’s Smart Start Strong Heart Antioxidants cereal [Internet]. Battle Creek, MI: Kellogg Co; 2015 [cited 2015 Mar 17]. Available from: www.kelloggs.com/en_US/kelloggs-smart-start-strong-heart-antioxidants-cereal.html. 7. Blueberry scone [Internet]. Seattle, WA: Starbucks Coffee Company; c2015 [cited 2015 Feb 6]. Available from: www.starbucks.com/menu/food/bakery/blueberry-scone. 8. BBQ oven roasted chicken melt [Internet]. Milford, CT: Doctor’s Associates, Inc; 2015 [cited 2015 Feb 6]. Available from: www.subway.com/menu/product.aspx?CC=USA&LC=ENG&MenuTypeId=1&MenuId=53&ProductId=291. 9. Nutrition & allergen information [Internet]. Rosemead, CA: Panda Restaurant Group, Inc; 2015 [cited 2015 Feb 6]. Available from: https://s3.amazonaws.com/PandaExpressWebsite/files/pdf/Nutrition.pdf . 10. Nutritional menu guide [Internet]. Los Angeles, CA: California Pizza Kitchen, Inc; 2014 Jul [cited 2015 Feb 6]. Available from: http://info.cpk.com/documents/nutrition_facts.pdf. 82 desire for sweet foods. Unfortunately, the data on this are lacking. I asked Marion Nestle, PhD, for her thoughts on the impact of sugar and artificial sweeteners on the palate. She told me, “Sugar is sweet and everyone loves it. Artificial sweeteners give the illusion of sweetness and not everyone loves them. People get used to a level of sweetness that tastes good to them. The more sugar we eat, the more it takes to reach that taste point. To people deprived of sugar (do any still exist?), even a little tastes delicious. At this point, just about everyone would be healthier eating less sugar and enjoying it more” (Marion Nestle, PhD, personal communication; 2014 Oct 24).a AN ALTERED PALATE I have seen for myself the impact that sugar can have on taste preferences. As a child I loved sugar. I was the one who ate 7 cupcakes at a birthday party and would eat all my Easter candy in a day. For a number of reasons, I decided to cut out sugar when I was in my late 20s. Two things happened pretty quickly: 1) I found out I did not crave sugar once I cut it out, and 2) other foods tasted sweeter to me, foods that had never tasted sweet before, such as Wheat Thins. I realized that my palate appeared to be changing in response to the lack of sugar in my diet, just as the palate can change when salt is limited.19 This idea was supported by what happened one day when I made a smoothie for several friends using only strawberries and bananas. The smoothie tasted great to me and was really sweet. However, to my surprise, every one of my friends said it was too sour and they wanted to add sugar. I also noticed that people who consumed a lot of artificial sweeteners seemed to have an altered palate. A case in point is a friend who uses artificial sweeteners every day. One year at Thanksgiving she added several packets of an artificial sweetener to a dessert because it was not sweet enough for her. Although it was more than sweet enough for everyone else, her copious use of artificial sweeteners seemed to have altered her palate and made supersweet foods normal for her. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 COMMENTARY Does Consuming Sugar and Artificial Sweeteners Change Taste Preferences? THE SUGAR CHALLENGE Because there is a lack of data on the impact of sugar and artificial and alternative sweeteners on the palate, I decided to try a 2-week sugar and artificial sweetener challenge and then look at its impact on taste. In the summer of 2014, a group of 20 people from Kaiser Permanente facilities throughout California agreed to try the challenge (see Sidebar: Sugar and Artificial Sweetener Challenge Instructions). After the two-week challenge, I asked the participants to fill out a survey to determine whether their palate had changed (see Sidebar: Survey Results of the Two-Week Challenge). Some comments about the challenge were • “I think this challenge really helped me to reset my palate. Before the challenge I did not eat a lot of sugar, but would put stevia in my Sugar and Artificial Sweetener Challenge Instructions For two weeks, cut out all added sugars and artificial sweeteners. 1.Do not add any form of sugar (see list below) or any alternative sweeteners to foods or drinks! Avoid artificial and alternative sweeteners including Sweet ‘N Low, Equal, Splenda, monk fruit, neotame, stevia, and xylitol, etc. No added sweeteners! 2.Avoid all sweetened sodas, bottled teas, sports drinks, energy drinks, fruit drinks and juice (even 100% juice), specialty coffee drinks, and any other liquid with added sweeteners. 3.Cut out any foods that have a lot of added sugar or any artificial sweeteners such as cookies, cake, candy, yogurt, soy or almond milk, breakfast cereals, energy bars, or other foods. Read labels! Aim for food with 5 g or less of added sugar. Look at the ingredient lists of foods you eat for other names for sugar such as the following: Sucrose High-fructose corn syrup Honey Corn syrup Maple syrup Molasses Agave Evaporated cane juice Barley malt Dextrose Coconut palm sugar Cane sugar Grape sugar Turbinado sugar Raw sugar Brown sugar Powdered sugar Brown rice syrup Date sugar Note: Plain unsweetened milk and yogurt and fruit contain natural sugar, which is fine because it is not added sugar. Limit dried fruits to 2 servings per day and fresh fruits to 4 to 5 servings per day. Survey Results of the Two-Week Challenge Participants craved sugar after cutting it out, but cravings went away for • 53.3% of participants after 3 days (8 out of 15 people responding) • 86.6% of participants after 6 days (13 out of 15 people responding) After the 2-week challenge: • 95% of participants found that sweet foods and drinks tasted sweeter or too sweet (18 out of 19 people responding) • 75% found that other foods, such as baby carrots, apples, or crackers, tasted sweeter (15 out of 20 people responding) • 95% said moving forward, they would use less or even no sugar (19 out of 20 people responding) • 35% said they lost weight (7 out of 20 people responding) Eating out and social events were identified as problematic, so creating a plan of action to deal with these situations, including bringing a healthy dessert such as fresh fruit, was recommended. Because many of the foods participants regularly ate contained more sugar than they anticipated, taking a look at food items such as breakfast cereals, alternative milk drinks, sauces, and drinks and finding lower- or no-sugar options before the challenge was also recommended. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 tea, oatmeal, and yogurt daily. Now I enjoy the flavor of it without the added sweetener.” • “I enjoyed the challenge; it opened my eyes to how many processed products add sugar. Thank you for helping me move on to a healthier lifestyle.” • “I rediscovered that I like my morning espresso unsweetened—used to drink it that way before getting hooked on sweetener. Will not go back. Also found that adding raisins to oatmeal eliminated need to use a couple packets of Splenda.” • “I realized I was emotionally dependent on these evening snacks and they were not contributing to my goals around weight loss/maintenance. It was a good exercise.” Many of us eat and drink too much sugar and would benefit from consuming less of it. Although this was a small survey, the results suggest that we can make consuming less or no sugar easier by cutting out sugar and artificial sweeteners for two weeks. We can also let our patients know that cravings seem to go away for most people after just six days and that food and desserts will taste sweeter for most people after the challenge. Finding processed foods with less added sugar, eating more real foods instead of processed foods, choosing fruit for dessert, and having some tasty dessert recipes that do not add sugar, can also help patients move forward with a low- or no-sugar diet. Two of the best recipes from a Kaiser Permanente healthy dessert contest (banana cream pie and watermelon and berry skewers) follow this article and are worth trying. CONCLUSION Eating fewer processed foods and choosing more real, whole, and plantbased foods make it easy to consume less sugar. These changes will also improve the overall quality of our diet, which is important for optimal health. In a very real sense, we are being set up to desire and consume more and more sugar. Using a two-week challenge to reset our palates can help our patients— and us—more easily transition to a healthier diet with less sugar and alternative and artificial sweeteners. Physicians should consider recommending a sugar 83 COMMENTARY Does Consuming Sugar and Artificial Sweeteners Change Taste Preferences? and artificial sweetener challenge to all their patients to help them limit or avoid added sugars, especially those with obesity, diabetes, or cardiovascular disease. v 5. New York University Professor in the Department of Nutrition, Food Studies, and Public Health, New York, NY. 6. a Disclosure Statement The author(s) have no conflicts of interest to disclose. 7. Acknowledgment Mary Corrado, ELS, provided editorial assistance. References 1. Strom S. Food Scores, a new web service, ranks grocery items on ingredients and nutrition [Internet]. New York, NY: The New York Times; 2014 Oct 27 [cited 2015 Feb 6]. Available from: www.nytimes.com/2014/10/28/business/foodscores-ranks-grocery-items-on-ingredients-andnutrition.html?_r=0. 2. EWG’s food scores [Internet]. Washington, DC: Environmental Working Group; c2015 [cited 2015 Feb 6]. Available from: www.ewg.org/foodscores. 3. US Department of Agriculture; US Department of Health and Human Services. Dietary guidelines for Americans, 2010. 7th ed [Internet]. Washington, DC: US Government Printing Office; 2010 Dec [cited 2015 Feb 6]. Available from: www.health.gov/dietaryguidelines/dga2010/ DietaryGuidelines2010.pdf. 4. Sugar and Sweeteners Yearbook Tables: US Consumption of Caloric Sweeteners: Table 51-53 [Internet]. Washington, DC: US Department of Agriculture Economic Research Service; 2015 Apr 2 [cited 2015 Apr 6]. Available from: 8. 9. 10. 11. www.ers.usda.gov/data-products/sugar-andsweeteners-yearbook-tables.aspx#25512. Vartanian LR, Schwartz MB, Brownell KD. Effects of soft drink consumption on nutrition and health: a systematic review and meta-analysis. Am J Public Health 2007 Apr;97(4):667-75. DOI: http:// dx.doi.org/10.2105/AJPH.2005.083782. Malik VS, Popkin BM, Bray GA, Després JP, Willett WC, Hu FB. Sugar-sweetened beverages and risk of metabolic syndrome and type 2 diabetes: a meta-analysis. Diabetes Care 2010 Nov;33(11):2477-83. DOI: http://dx.doi. org/10.2337/dc10-1079. Johnson RK, Appel LJ, Brands M, et al; American Heart Association Nutrition Committee of the Council on Nutrition, Physical Activity, and Metabolism and the Council on Epidemiology and Prevention. Dietary sugars intake and cardiovascular health: a scientific statement from the American Heart Association. Circulation 2009 Sep 15;120(11):1011-20. DOI: http://dx.doi. org/10.1161/CIRCULATIONAHA.109.192627. Yang Q, Zhang Z, Gregg EW, Flanders WD, Merritt R, Hu FB. Added sugar intake and cardiovascular diseases mortality among US adults. JAMA Intern Med 2014 Apr;174(4):516-24. DOI: http:// dx.doi.org/10.1001/jamainternmed.2013.13563. Brown IJ, Stamler J, Van Horn L, et al; International Study of Macro/Micronutrients and Blood Pressure Research Group. Sugar-sweetened beverage, sugar intake of individuals, and their blood pressure: international study of macro/ micronutrients and blood pressure. Hypertension 2011 Apr;57(4):695-701. DOI: http://dx.doi. org/10.1161/HYPERTENSIONAHA.110.165456. Welsh JA, Sharma A, Abramson JL, Vaccarino V, Gillespie C, Vos MB. Caloric sweetener consumption and dyslipidemia among US adults. JAMA 2010 Apr 21;303(15):1490-7. DOI: http://dx.doi. org/10.1001/jama.2010.449. Fried SK, Rao SP. Sugars, hypertriglyceridemia, and cardiovascular disease. Am J Clin Nutr 2003 Oct;78(4):873S-880S. Banana Cream Pie (adapted with permission from Living on Live Food by Alissa Cohen) Watermelon and Berry Skewers Submitted by Ed Hernandez, Kaiser Permanente, Senior PC/LAN Analyst, Regional Offices, Pasadena, CA Submitted by Darin Kliem, Kaiser Permanente, Senior Consultant, QRM/Quality Operations, Regional Offices, Pasadena, CA Ingredients Crust 1 cup raw almonds 1 cup dates (soaked) 1 cup shredded coconut Filling 6 small ripe bananas 1 cup shredded coconut ½ peeled apple 1 teaspoon pure vanilla ½ teaspoon carob powder (you can also use unsweetened cocoa) Instructions 1. Mix crust ingredients in a food processor and form into a pie plate. 2. Mash 2 bananas and place in a blender with the apple, 3/4 cup of coconut, and vanilla. Blend until smooth. 3. Remove and place in bowl, slice the remaining bananas, and mix into the filling. 4. Pour into pie crust and sprinkle with carob and the remaining coconut. 84 12. Aeberli I, Gerber PA, Hochuli M, et al. Low to moderate sugar-sweetened beverage consumption impairs glucose and lipid metabolism and promotes inflammation in healthy young men: a randomized controlled trial. Am J Clin Nutr 2011 Aug;94(2):479-85. DOI: http:// dx.doi.org/10.3945/ajcn.111.013540. 13. Lennerz BS, Alsop DC, Holsen LM, et al. Effects of dietary glycemic index on brain regions related to reward and craving in men. Am J Clin Nutr 2013 Sep;98(3):641-7. DOI: http://dx.doi. org/10.3945/ajcn.113.064113. 14. Draft guideline: sugars intake for adults and children [Internet]. Geneva, Switzerland: The World Health Organization; c2015 [cited 2015 Feb 9]. Availabe from: www.who.int/nutrition/ sugars_public_consultation/en/. 15. Artificial sweeteners [Internet]. Boston, MA: Harvard T.H. Chan School of Public Health; c2015 [cited 2015 Feb 9]. Available from: www. hsph.harvard.edu/nutritionsource/healthy-drinks/ artificial-sweeteners/. 16. Dhingra R, Sullivan L, Jacques PF. Soft drink consumption and risk of developing cardiometabolic risk factors and the metabolic syndrome in middle-aged adults in the community. Circulation 2007 Jul 31; 116(5):480-8. DOI: http://dx.doi.org/10.1161/ CIRCULATIONAHA.107.689935. 17. Lin J, Curhan GC. Associations of sugar and artificially sweetened soda with albuminuria and kidney function decline in women. Clin J Am Soc Nephrol 2011 Jan;6(1):160-6. DOI: http://dx.doi. org/10.2215/CJN.03260410. 18. Suez J, Korem T, Zeevi D, et al. Artificial sweeteners induce glucose intolerance by altering the gut microbiota. Nature 2014 Oct 9;514(7521):181-6. DOI: http://dx.doi. org/10.1038/nature13793. 19. Beauchamp GK, Bertino M, Engelman K. Modification of salt taste. Ann Intern Med 1983 May;98(5 Pt 2):763-9. DOI: http://dx.doi. org/10.7326/0003-4819-98-5-763. Ingredients 1 small bottle balsamic vinegar reduced over low heat until it has reduced to 25% of its original volume. Let cool. Mint leaves Assorted berries (blueberries, strawberries, and/or raspberries) Watermelon cut into 1-inch cubes Instructions 1. Skewer berries from smaller to larger, then skewer 1 mint leaf, and lastly the watermelon. 2. Drizzle a plate with the balsamic vinegar and place the skewered fruit over the balsamic vinegar. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 COMMENTARY Special Report New Kid on the Block Turns Ten! The Brief, Remarkable History of the National Physicians Alliance Jean Silver-Isenstadt, MD, PhD Perm J 2015 Summer;19(3):85-89 http://dx.doi.org/10.7812/TPP/15-031 ABSTRACT Founded in 2005 by General Surgeon Lydia J Vaias, MD, MPH, the National Physicians Alliance is a 501c3 public charity with a mission to create research and education programs that promote health and foster active engagement of physicians with their communities to achieve high-quality, affordable health care for all. The National Physicians Alliance offers a professional home to physicians across medical specialties who share a commitment to professional integrity and health justice. As the organization celebrates its tenth birthday, the history and scope of this missionaligned group are described. INTRODUCTION It is not a coincidence that the National Physicians Alliance (NPA)—a nonpartisan, multispecialty organization of physicians and others committed to social justice and health care reform—was founded by a surgeon from Kaiser Permanente (KP). To hear Lydia Vaias, MD, MPH talk about KP is to hear the linkages laid bare: “What’s great about [KP] is its alignment. [KP] allows me to practice in a model where I can focus on the values of medicine instead of on money. I get paid to do the right thing for the patient. Years ago, the [KP] system was mocked. People were once embarrassed to say they worked there. It wasn’t until very recently that people have come to see [KP] as a leading light, delivering health care around a set of values.” (Lydia Vaias, MD, MPH, personal communication; 2015 Jan 29.)a National Physicians Alliance logo. Ten years ago, Dr Vaias set out to organize physicians anew. “There are few physicians in this country who practice in settings that align the payors’, providers’, and hospitals’ incentives to keep patients at the center of care. I feel so lucky to be here at this time in history.” (Lydia Vaias, MD, MPH; personal communication; 2015 Jan 29.)a 1993: THE CALL BEYOND CALL Dr Vaias wasn’t looking for me when she called my house back in 2005. She was looking for her old medical school buddy, my husband Ari Silver-Isenstadt, MD, MSEd, with whom she and a few others had organized 6 separate chapters of the American Medical Student Association (AMSA) about a decade earlier. In October 1993, student chapters from Hahnemann, Jefferson, the Medical College of Pennsylvania, the Philadelphia College of Osteopathic Medicine, the University of Pennsylvania, and Temple University joined forces as “Philadelphia AMSA” and delivered an unprecedented regional conference that laid the groundwork for generational change in medicine. They called the conference “Physician Activism: The Call Beyond Call.” Hugely ambitious, the program offered 5 to 6 concurrent tracks during 2 1/2 days and featured 75 Program from the October 1993 Philadelphia American Medical Student Association conference. speakers, including M Joycelyn Elders, MD, the US Surgeon General. Hoangmai Pham, then a 3rd-year student at Temple University and now Director of the Seamless Care Models Group at the Center for Medicare and Medicaid Innovation Center, served as Chair of the Programming Committee. The conference was a smash hit, drawing more than 600 registrants—and it did so without any pharmaceutical industry sponsorship or staff support. AMSA’s national president, David Evans, MD, set the event’s tone in the printed program’s welcome letter: “It is activism that rounds out our education … .” Philadelphia AMSA was the twinkle in the eye—the spark. Twelve years later, Dr Vaias was on the phone, bringing the band back together to launch the NPA. I had helped with the conference too, although in 1993 I was not yet a medical student. At the University of Jean Silver-Isenstadt, MD, PhD, is the Executive Director of the National Physicians Alliance in Washington, DC. E-mail: [email protected]. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 85 COMMENTARY New Kid on the Block Turns Ten! The Brief, Remarkable History of the National Physicians Alliance Pennsylvania, I was a doctoral student, studying the history and sociology of medicine, specifically 19th century health reform movements. I explored social change efforts led by utopian radicals and feminists—progressive troublemakers who challenged the use of corsets and bloodletting, who touted exercise and bathing, who fought for women’s right to education and self-ownership. Across campus, my husband and his medical school classmates got to know their cadavers, took countless exams, and learned their way around the wards. Their professors recycled the old adage: Fifty percent of what we will teach you is wrong; we just don’t know which 50%. The lecturers were playfully referring to the content of their slide sets—acknowledging dynamic scientific change—but they may as well have been referring to the curricular priorities themselves, the physical plant and workflow of the hospital, the food in the cafeteria, the nature of clinical communication, the financing of health care, the workforce … or even the 50% estimate. Dr Vaias went on to become a general surgeon with a master’s degree in public health. She moved to Long Beach, CA, joined the KP system and, in 2005, was just beginning a three-year term on the Board of the Southern California Permanente Medical Group. My husband became a Baltimore-based general pediatrician and I went to medical school myself. It was organized medicine’s muted response to the Terri Schiavo case (a nationally debated legal struggle involving prolonged life support)1 that led Dr Vaias to start rounding up past AMSA leaders. She was dismayed by the political grandstanding but even more so by the house of medicine, which seemed less engaged in repairing its own broken systems than in deepening ties with industry. Like many others, she saw the medical profession drifting from its core values. Patients were not at the heart of health care. I remember Ari and I were chopping stir-fry ingredients that spring evening ten years ago when Dr Vaias called with a characteristically modest proposal: “Let’s fix this.” Make No Small Plans The NPA’s first official organizing effort took place at AMSA’s 55th convention in Washington, DC, where many past student leaders had gathered to honor Paul R Wright, the organization’s beloved Executive Director who was retiring after 30 years in the position. In a dedicated side room reserved for the discussion, approximately thirty former leaders of the organization agreed that the time had come to build a new professional home for physicians across specialties—an organization that would Meeting with lawmakers on Capital Hill, National Physicians Alliance members: (left to right) Charu Sawhney, MD; Lydia Vaias, MD, MPH; Judy Zerzan, MD; Bethany Picker, MD; Marc Dalton, MD; Rupin Thakkar, MD; Stephen R Smith, MD, MPH; Jean Silver-Isenstadt, MD, PhD; Mara Merritt, MD; and Lenny Lesser, MD. 86 not function as a trade association, but rather as a community whose first concern was patients. It was something AMSA members had imagined building since their split from the American Medical Association (AMA) 38 years earlier. (AMSA had begun in 1950 as a student branch of the AMA but split off in 1967 after its parent organization had opposed the creation of Medicare and showed insufficient support for the civil rights and community health movements.)2 The group pledged $20,000 in immediate support of NPA’s launch and scheduled a follow-up meeting at AMSA’s headquarters in Reston, VA. During the next year, an executive planning committee met for 2-hour phone calls every Friday afternoon. It was a monumental gift of volunteer energy from practicing physicians, all inspired by Dr Vaias’s mantra (with a hat-tip to Joan Baez): “The antidote to despair is action.” It helped that the group included longtime friends with a shared organizational history. It also helped that they had taken different professional paths. Stephen S Cha, MD, MHS—currently the Chief Medical Officer for the Center on Medicaid and CHIP Services— had recently completed his internal medicine residency at Montefiore in New York and was a Robert Wood Johnson Foundation Clinical Scholar at Yale. David V Evans, MD—now an attending physician at the University of Washington—had for the previous decade practiced family medicine in the small rural town of Madras, OR. David Grande, MD, MPA—now an attending physician of internal medicine at the University of Pennsylvania—was a Robert Wood Johnson Foundation Health and Society Scholar at the University of Pennsylvania; his policy research focused on the health of vulnerable populations. Kavita Patel, MD, MS—now Fellow and Managing Director at the Brookings Institution after two years at the White House and time on Capitol Hill—was working on health policy at the RAND Corporation. Alexa Oster, MD—now a Medical Epidemiologist in the Centers for Disease Control and Prevention’s Division The Permanente Journal/ Summer 2015/ Volume 19 No. 3 COMMENTARY New Kid on the Block Turns Ten! The Brief, Remarkable History of the National Physicians Alliance of HIV/AIDS Prevention—was in the midst of her residency in primary care internal medicine at the University of California, San Francisco/San Francisco General Hospital. (I remember her often biking between clinical sites during our phone calls.) Stephen R Smith, MD, MPH—now retired from academia and practicing family medicine part-time at a community health center in New London, CT, was an Associate Dean at the Warren Alpert Medical School of Brown University when he joined the NPA’s founding executive committee. After my own years in the medical archives studying the audacious work of 19th-century health reformers, I found myself unexpectedly surrounded by health reformers focused on the 21st century. But more than that, I found myself surrounded by something crystalline and rare: a group of brilliant people who were full of initiative but not full of ego—collaborative, funny, optimistic physicians who were singularly focused on making health care better for their patients. And they worked like demons. Logo for The Unbranded Doctor campaign. Unbranded Doctors Developing an organizational structure, finalizing a mission and bylaws, building a Web site, formally incorporating, and myriad other details involved lengthy discussion. But one decision was easy: the NPA would not accept funding from pharmaceutical or medical device companies. Out of the gate, this made NPA unique among medical organizations. Everywhere, financial conflict of interest was compromising medical research, education, and practice.3 It was not only eroding patients’ trust in their physicians, but also eroding trust within the profession. Commitment to conflict-free leadership was an undisputed core value of the NPA; because it so clearly distinguished the organization The Permanente Journal/ Summer 2015/ Volume 19 No. 3 from others, the “Unbranded Doctor Campaign” became our introductory calling card. Through this advocacy campaign—an ally of the “No Free Lunch” movement and AMSA’s “PharmFree” efforts—NPA voiced loud concern over the scope and influence of pharmaceutical marketing tactics; supported full transparency regarding industry payments to physicians and medical institutions; challenged the AMA’s lucrative sale of personal Physician Masterfile records for industry data mining and the legitimacy of data mining itself; and called on physicians to take the reins and simply stop accepting industry largesse. These efforts all sought to ensure that medical education, research, and clinical decisions are guided by scientific evidence and not by marketing hype. A different issue would have been an easier lift and surely a more enticing recruitment strategy—one that didn’t ask physicians to give up the comforts of free continuing medical education dinners at posh restaurants; coffee and donuts delivered right to the office by cheerful, healthy drug reps; generous speaking fees, etc—but the profession had grown complacent about these entanglements and therefore complicit in the marketing enterprise. This contamination of purpose had to be addressed. Just as the AMA was launching a $60 million new ad campaign depicting physicians as “everyday heroes,” the NPA’s Unbranded Doctor Campaign was pointing out the dirt under the rugs and the mold in the bathroom tiles. We were handing out buckets and mops by way of recruitment: join the NPA—help us clean our house. We knew the only way to restore trust in medicine would be to earn it. Transparency about industry payments to physicians and hospitals is now mandated by the Sunshine Act section of the Affordable Care Act (ACA)4—a component of the law that the NPA fought hard to include and continues to defend. This year, NPA President William B Jordan, MD, MPH, was featured on CSPAN commenting on how far we’ve come but also on what still goes unreported, for example free medication samples that remain at the heart of marketing but are unmentioned in the ACA’s Sunshine Act provisions. These provisions require manufacturers of drugs, medical devices, and biologics that participate in US federal health care programs to report certain payments and items of value given to physicians and teaching hospitals for inclusion in a content management system database known as Open Payments.5 The Open Payments Web site enables anyone to search physicians and institutions by name to learn the details of their financial relationships with industry. Thanks in many ways to the work of the NPA, it has become less comfortable for physicians to accept these payments, let alone make light of them. For the first time, researchers, journalists, policymakers, physicians, and patients are gaining access to alarming data about the magnitude and direction of industry cash flow in the system. It’s a necessary first step in opening up space for substantive reform. Trust in a Trustworthy System This “pharma work” often set the NPA apart from other physician organizations, testifying on panels and working with consumer advocacy groups quite literally opposite our professional siblings who were defending the status quo. It was then that we could most clearly see the void we were filling: patients needed physician allies. From the outset, NPA’s founders were determined to protect the organization from ever becoming a doctors’ lounge. The board of directors was structured to include nonphysicians to ensure that no discussions of patients’ best interests would take place without patients. Very naturally, the NPA found itself working in regular coalition with groups ranging from Community Catalyst and the National Center for Health Research to the National Committee to Preserve Social Security and Medicare and the Law Center to Prevent Gun Violence. The NPA board was proud to be the first physician organization to join the Health Care for America Now! coalition in support of the ACA’s passage—a coordinated effort of more than 1000 national and state-based groups dedicated to achieving federal health reform and defending Medicare and Medicaid. 87 COMMENTARY New Kid on the Block Turns Ten! The Brief, Remarkable History of the National Physicians Alliance In 2014, the NPA was honored to have Consumer Reports host our 9th annual conference at their National Testing and Research Center in Yonkers, NY. Warm relationships with such allies encouraged NPA members—who valued not only the organization’s bridgebuilding instincts, but also the NPA’s willingness to step outside the profession’s usual comfort zones—to struggle publicly with medicine’s problems and to champion civic engagement. I will never forget Gene Copello, MSW, MDiv, PhD, late co-chair of NPA’s Secure Health Care for All campaign, softly assuring other members of the NPA’s board back in 2008: “The NPA will succeed because it has to succeed. Patients need NPA to succeed.” The room fell silent with the weight of this charge. Dr Copello, whose doctorate had focused on medical ethics and public policy, was then serving as the Executive Director of the AIDS Institute. He died that year, unable to see the passage of the … physicians [taking] ACA 4; the NPA’s Comore responsibility pello Health Advocacy Fellowship was named for their role as in his memory. stewards of limited It had become clear clinical resources that if we wanted health … quickly took reporters to interview shape as the NPA’s physicians who voiced Good Stewardship a different perspective Project, funded by from that of traditional the American Board guilds, we would have of Internal Medicine to provide advocacy, Foundation …[which] media, and communihas since blossomed cations training to physicians who viewed policy under the American through the lens of its Board of Internal potential impact on paMedicine Foundation’s tients. Becky Martin, direction into the NPA’s Director of Projcelebrated Choosing ect Management and Wisely campaign. a seasoned community organizer, has for years connected NPA Fellows and other members to local opportunity and opened up relationships that fuel lasting change. Advocacy, let alone “activism,” are terms rarely associated with white-coat professionalism. Yet our democratic society grants enormous social capital to the medical degree, and physicians 88 are coming to understand advocacy skills as part of their responsibility to patients. The white coat itself may have more benefit for patients when worn at a public podium than when worn in the hospital. The NPA’s immediate past president, James Scott, MD, discovered the organization at a 2009 health reform rally in Washington, DC, where NPA leaders David Evans, MD, and Valerie Arkoosh, MD, MPH, spoke boldly in support of federal health reform. Dr Scott had flown from Oregon to take part in the growing movement for quality, affordable health care for all. As he described it in a recent e-mail to me, “At a reception after the rally, I found real soul-mates— progressive doctors passionate about improving the system for everyone. I thought, after 40 years in medicine, I’ve found my people!” (James Scott, MD; personal communication; 2015 Jan 20)b For many physicians, the opportunity to meet with elected officials and to speak to public audiences on behalf of a like-minded cohort became a reason to deepen involvement with the organization. For others, it was the opportunity to focus on individual practice reform. Dr Smith was only half kidding when he first proposed the idea that NPA generate “Top 5” lists–à la David Letterman—to highlight “things doctors keep doing even though they know better.” The Board of Directors was having lunch and brainstorming. A longtime leader of NPA’s work to reduce professional conflicts of interest, Dr Smith wanted to see physicians take more responsibility for their role as stewards of limited clinical resources. This would require acknowledging overtreatment and waste—calling out bad habits. What if NPA developed a “Top 5” list of evidence-based, quality-improving, resource-sparing activities that could be incorporated into the routine practice of primary care physicians in family medicine, internal medicine, and pediatrics? Under Dr Smith’s leadership, the idea quickly took shape as the NPA’s Good Stewardship Project, funded by the American Board of Internal Medicine Foundation. A mouse that roared, this modest initiative has since blossomed under the American Board of Internal Medicine Foundation’s direction into the celebrated Choosing Wisely campaign. Conceiving and piloting this culture-changing project has been one of the NPA’s most significant contributions. More than 60 specialty societies have since developed lists of “tests or procedures commonly used in their field, whose necessity should be questioned and discussed.”6 Similar efforts are now happening abroad. NPA’s Good Stewardship work challenged physicians to acknowledge and address prescribers’ responsibility for systemic waste and consequent patient harm. Organized medicine has begun to embrace stewardship as a core component of professionalism, and consumers have welcomed this awakening. It was no trivial thing to shift the national conversation in this direction. The challenge now is to see these values broadly translated to practice. New and broad-ranging calls for price transparency and fairness are providing wind at the back of this push for high-value care. In short, as a nonprofit organization without a great deal of money, NPA has made a great deal of difference. With little more than stamina, purpose, and a value set that aligns the incentives of physicians with those of patients, the NPA has been able to make important contributions in a short period of time. LOOKING AHEAD At ten years old, the NPA continues to attract physicians who understand that the future of US health care will be shaped by those who show up to shape it—and that working with patients, we now have a historic opportunity to put health at the heart of medicine. There are gains to be defended and new battles to engage. Relatively recent areas of NPA focus also continue to build momentum, including the creation of NPA national taskforces on gun violence prevention and on the FDA’s drug and medical device approval processes—two areas brought to the fore during Cheryl Bettigole, MD, MPH’s, tenure as NPA President. Although these issues may The Permanente Journal/ Summer 2015/ Volume 19 No. 3 COMMENTARY New Kid on the Block Turns Ten! The Brief, Remarkable History of the National Physicians Alliance at first seem to have little to do with one another or with past NPA efforts to expand access to high-quality health care, they are united by the influence of corporate lobbying. The National Rifle Association’s lobbyists have choked off research funding for gun violence prevention7,8 and have successfully backed state laws that forbid physicians from asking standard screening questions about gun ownership and storage.9 Fracking companies have successfully backed the passage of state laws that require physicians to sign confidentiality agreements before learning what chemicals a sick patient may have been exposed to.10,11 Drug companies continue to press the FDA to approve applications on the basis of surrogate endpoint data and mathematical modeling rather than requiring full clinical trials.12 And far too many medical devices continue to reach the market without any clinical trials at all.13 These are areas that cry out for more attention from organized medicine to ensure patient safety. For our federal watchdog agencies, our clinical guidelines, our pharmacopeia, our educational resources, our state laws, and our individual clinical relationships to be grounded in trust and science, physicians and patients will have to claim more power in these debates. It is fair to say that with my background in medicine and medical history, I never expected to become the Executive Director of a nonprofit organization. But I have always been drawn to visionaries. I had the good fortune to help unite this multispecialty band of serious idealists, this growing force for good. NPA’s presidents have included a surgeon, Dr Vaias; four family practice physicians—Drs Evans, Bettigole, Scott, and Jordan; and an obstetric anesthesiologist, Dr Arkoosh. Around the NPA conference table, consensus has always emerged quickly among family physicians, surgeons, pediatricians, internists, cardiologists, anesthesiologists, patient advocates, and more. We have found there is no fighting for turf when the fight is for patients. As Dr Vaias says, “The NPA reminds me why I got into medicine in the first place.”(Lydia Vaias, MD, MPH; personal communication; 2015 Apr 27)a We have a vision for the next ten years: sparking a transformation of the medical profession that returns us to the core value of serving patients. We have seen this vision made real at places like KP, but we will continue to press on until it is the default setting for health care in our country. Join us in October in Washington, DC, as we launch our second decade at our annual meeting, themed Truth to Power: Alliance for the Public Good. You may learn more about the NPA’s past and future work at www.npalliance.org. v a General Surgeon and Founder, the National Physicians Alliance; Washington, DC. b Immediate Past President of the National Physicians Alliance; Washington, DC. 4. 5. 6. 7. 8. 9. 10. 11. 12. References 1. Racine E, Amaram R, Seidler M, Karczewska M, Illes J. Media coverage of the persistent vegetative state and end-of-life decision-making. Neurology 2008 Sep 23;17(13):1027-32. DOI: http:// dx.doi.org/10.1212/01.wnl.0000320507.64683.ee. 2. History of the American Medical Student Association [Internet]. Sterling, VA; 2014 [cited 2015 Apr 28]. Available from: www.amsa.org/ amsa/homepage/About/History.aspx. 3. Wazana A. Physicians and the pharmaceutical industry: is a gift ever just a gift. JAMA 2000 Jan 13. 19;283(3): 373-80. DOI: http://dx.doi.org/10.1001/ jama.283.3.373. The Patient Protection and Affordable Care Act of 2010. Public Law 111-148, 111th Congress, 124 Stat 119, HR 3590, enacted 2010 Mar 23. openpaymentsdata.CMS.gov [Internet]. Washington, DC: US Department of Health and Human Services; 2015 [cited 2015 Apr 28]. Available from: https://openpaymentsdata.cms.gov. Choosing wisely: about us [Internet]. Philadelphia, PA: ABIM Foundation; 2015 [cited 2015 Apr 28]. Available from: www.choosingwisely.org/about-us/. Jamieson C. Gun violence research: history of the federal funding freeze: Newton tragedy may lead to lifting of freeze in place since 1996 [Internet]. Washington, DC: American Psychological Association; 2013 Feb [cited 2015 Apr 28]. Available from: www.apa.org/science/about/ psa/2013/02/gun-violence.aspx. Frankel TC. Why the CDC still isn’t researching gun violence, despite the ban being lifted two years ago [Internet]. Washington, DC: The Washington Post; 2015 Jan 14 [cited 2015 Apr 28]. Available from: www.washingtonpost.com/ news/storyline/wp/2015/01/14/why-the-cdc-stillisnt-researching-gun-violence-despite-the-banbeing-lifted-two-years-ago/. Federal court upholds Fla’s docs vs glocks law [Internet]. Arlington, VA: Politico.com; 2014 Jul 26 [cited 2015 Apr 28]. Available from: www.politico. com/story/2014/07/federal-court-upholds-floridadocs-vs-glocks-law-109403.html Pennsylvania’s disclosure rules: what the frack’s in the ground? [Internet]. Harrisburg, PA: WITF— StateImpact; 2015 [cited 2015 Apr 28]. Available from: http://stateimpact.npr.org/pennsylvania/tag/ fracking-disclosure/. Wilkinson KD, Cawley MJ. Client Alert: In nonprecendential case, Third Circuit affirms fracking trade secrets trump physician’s right to know, absent actual harm [Internet]. White Plains, NY: Wilson-Elser; 2015 Apr 13 [cited 2015 Apr 28]. Available from: www.wilsonelser.com/news_and_ insights/client_alerts/2256-in_non-precedential_ case_third_circuit_affirms. Doshi P. Speeding new antibiotics to market: a fake fix? BMJ 2015 Mar 25;350:h1453. DOI: http://dx.doi.org/10.1136/bmj.h1453. Medical devices and the public’s health: the FDA 510(k) clearance process at 35 years [Internet]. Washington, DC: Institute of Medicine; 2011 Jul [cited 2015 Apr 28]. Available from: www.iom. edu/~/media/Files/Report%20Files/2011/MedicalDevices-and-the-Publics-Health-The-FDA510k-Clearance-Process-at-35-Years/510k%20 Clearance%20Process%202011%20Report%20 Brief.pdf. The True Physician The true physician cannot remain outside the manifold of the events he observes. — Alan Gregg, MD, 1890-1957, Associate Director of the Medical Education Division, Director of Medical Sciences Division and Vice President of the Rockefeller Foundation The Permanente Journal/ Summer 2015/ Volume 19 No. 3 89 NARRATIVE MEDICINE Suicide is a Baobab Tree: A Narrative Medicine Case Study Adriano Machado Facioli, PhD; Fábio Ferreira Amorim, MD, PhD; Karlo Jozefo Quadros de Almeida, MD; Eliana Mendonça Vilar Trindade, PhD Perm J 2015 Summer;19(3):90-94 http://dx.doi.org/10.7812/TPP/14-201 “A baobab is something you will never, never be able to get rid of if you attend to it too late.”1 — Antoine de Saint-Exupéry ABSTRACT This case study is an example of applying narrative medicine as a useful tool for health professionals to manage an existential and complex scenario such as the suicide of a sibling. Some suicides are like baobab trees—these large and resilient trees grow deep roots for many years, only spreading their limbs above ground once they are firmly established. Like the baobab, when suicide or a suicide attempt occurs, suicidal ideations are well cultivated and have often already been repeatedly planted. Consequently, suicide is often difficult to prevent: once the death seed is planted, it is difficult to recreate life. Every year, more than 800,000 people die by suicide worldwide (1.4% of all deaths), which is approximately 1 person every 40 seconds. These unexpected deaths, predominantly occuring among young and middle-aged adults, have a continuing ripple effect and result in a huge economic, social, and psychological burden for individuals, families, communities, and countries. The complexity of suffering and pain experienced by suicidal individuals and their families, regardless of the success or failure of the suicidal act, is intensified by strong stigmas attached to traditional concepts of sin and eternal damnation. This unfortunate reality emerges in the narrative as a tragic family drama, which is permeated by deep feelings of helplessness. But suicide is preventable. Prevention requires 3 important factors: knowledge, public support, and creation of strategies to enact social change. Now is the time to act and make suicide prevention an imperative goal. CASE STUDY Some suicides are like baobab trees—these trees are large and almost indestructible once established. They grow deep roots for many years, only spreading their limbs to the sky when they are firmly entrenched. Like the baobab, when suicide or a suicide attempt occurs, suicidal ideations are well cultivated and have often already been repeatedly planted. Consequently, suicide is often difficult to prevent. How can one prevent something that has become part of an individual’s identity and constitution? Many suicidal individuals have planned their own death for years in the form of impulses and constant thoughts of how they will end their lives. Personally and professionally, I have witnessed the life course of individuals who showed, many years before they actually committed suicide, clear signs that one day they would kill themselves. I remember quite well my older brother, Edu, at age 18 saying life was often not worth it, because it was very unfair and full of suffering. My mother disagreed with him. At that time she said, “I think it [suicide] is an act of extreme selfishness. One kills himself and doesn’t think about the suffering of those who are left behind.” Edu replied, “Selfishness is when people think they are the owners of the life of the one who is killing himself. Whose life is it anyway?” This conversation took place in 1988, ten years before my brother died. Five years before his death, in 1993, Edu also reportedly told a few friends, as they sat at the banks of the university lake, that it was “a beautiful place to die.” His death took place nearby in 1998. I also remember Edu occasionally joking about other people’s suicide threats. “Do you really want to commit suicide?” he would ask mockingly. “So hang yourself with a steel wire coated with grease. If you do that, there is no turning back.” Edu spoke as someone who believed most people who threatened suicide would not really do it, and that they used their threats only as a means to manipulate others. And he never threatened to kill himself. For the ten years before Edu’s death, I dealt with an extremely unpleasant fear that he would one day kill himself, but this dread was not enough to rid me of the devastating surprise of the reality of his suicide. Although we had clearly talked about suicide, I was not spared the shock of dealing with this kind of misfortune. Five years before his death, Edu and I had a conversation in which he expressed concern about the possibility of me being suicidal. I was 21, and he was 23 years old. I said to him, “Brother, let’s make it clear, the suicidal individual here is you and not me.” Adriano Machado Facioli, PhD, is a Psychologist and Professor of Medicine in the Department of Research and Scientific Communication at Escola Superior de Ciências da Saúde in Brasília, Distrito Federal, Brazil. E-mail: [email protected]. Fábio Ferreira Amorim, MD, PhD, is a Professor of Medicine in the Department of Research and Scientific Communication at Escola Superior de Ciências da Saúde in Brasília, Distrito Federal, Brazil. E-mail: [email protected]. Karlo Jozefo Quadros de Almeida, MD, is a Professor of Medicine in the Department of Research and Scientific Communication at Escola Superior de Ciências da Saúde in Brasília, Distrito Federal, Brazil. E-mail: [email protected]. Eliana Mendonça Vilar Trindade, PhD, is a Psychologist and Professor of Medicine in the Department of Research and Scientific Communication at Escola Superior de Ciências da Saúde in Brasília, Distrito Federal, Brazil. E-mail: [email protected]. 90 The Permanente Journal/ Summer 2015/ Volume 19 No. 3 NARRATIVE MEDICINE Suicide is a Baobab Tree: A Narrative Medicine Case Study “And does that disturb you, do you worry too much about it?” he asked. “Yes, it is very distressing. It is very, very unpleasant to imagine one day I will come home and find you hanged yourself, man.” Our conversation continued and he tried to fix it, tried to show me he would take my distress seriously. He demonstrated empathy and realized the whole situation was painful for me. I thought to myself that this conversation had produced some benefits, that his concern for me would be enough to keep him alive. Unfortunately I was wrong. His baobab missed being watered only on that day or on the few days like that one. His baobab had already grown big, very big, and I had no idea of its hugeness in my brother’s life. SINCE EDU’S DEATH I have often said, “Suicide is a little plant. But do not plant it. If you have planted it, do not cultivate it and do not water it because it is a little plant that grows and turns into a baobab. Then it can become quite difficult to remove from your life.” Edu gave birth to his end of everything by hanging himself from a rope tied around his neck and fastened to a branch of a tree at the banks of the lake near the university where he had studied a few years before. My brother somehow anticipated where and how he would die. It was only a matter of time, because he had been planting and cultivating his suicide for several years. A letter addressed to me, but never sent, was found in his drawer just after his death—he had hidden it there for more than nine months before his suicide. In the letter, Edu made it clear he was already very close to death. The letter began like this: “Yes, my brother, I have been talking to death closely and quite often. It whispers in my ear and pulls me by my feet.” He left many other writings in his drawer. They were kept there so no one would mess them up and to keep Edu’s privacy, which was well respected by the entire family. Several of these writings are part of a more complex picture about his motives and his history. In a letter written a few months before his death, he said, “I rode my bike, at night through deserted streets, and pedaled as fast as I could so that my heart would burst.” I never stop thinking and imagining how his last day went by. He was living with some friends, very close to the university. He took his bicycle and went to the university. Inside his backpack there were his documents, a small notebook, and a pair of handcuffs. I figured that, in case of losing his will, he would handcuff himself so there would be no return. I know nothing else about that day: if he was crying; if he was calm; if he had ever visited that tree beside the lake before, to think or plan about ending his life. I do not know whether he stood there for hours, mustering his courage; whether he took the time to appreciate the landscape in an absurd and lonely farewell; or if there was despair and distress until the last moment. He left farewell letters with justifications and apologies, one for me and one for my parents and my brother. “Mother, it is not your fault”; “I know a black shroud of pain will cover all of you, but I cannot bear my suffering any longer”; “It’s nobody’s fault.” Why did he leave a personal letter to me? Why? The Permanente Journal/ Summer 2015/ Volume 19 No. 3 The only thing I can guess is he really cared about me, as the loving older brother he was, and because he worried about how much suffering his suicide would bring me. PREVENTING A SUICIDE Years later I learned, through his death and in my professional practice, the basics of preventing a suicide. Suicide is a very lonely act. Suicidal people are, in general, socially isolated and radically lonely in their pain. In the Sidebar: Years Later, I have included my attempt to further explore Edu’s world of loneliness and pain. Edu loved being with me and our youngest brother, but he was alone in his town, far from us and with no easy communication available. In Brazil in 1998, our family had no cell phones or personal computers or wireless Internet that allowed us to reach anyone at any time. We were separated by hundreds of miles, by several days without talking to each other, by our ignorance about suicide and the danger that was haunting Edu’s life. He suffered with all these distances. During a phone call some days before his death, he said, probably knowing our recent visit was the last time he would see us, “It was very hard for me to see you leaving …” Now I know that in these moments it is crucial to have loved ones close by and part of our lives. Social gratifications are possibly the most relevant ones in a human being’s life. We are social animals, fed by social interactions—healthy social interactions. We need to love and be loved. We need real love, which at its root involves proximity, being close and together, being present, interacting, and pushing the ghosts of unhealthy loneliness away. When suffering comes, life takes a sudden stop and everything starts moving slowly. Time takes too long to pass and weighs on us unbearably. There, at this time, you are, fully and without escape, feeling all the pain you can experience. When this most extreme part of suffering goes away, another wave comes, although less intense: it is the echo of that past suffering. This is when the blanket of love that others weave for us plays a decisive role. If this blanket is effective, real, and supportive, we will feel that life is worthwhile despite all the pain and injustice in the world. This love is not a crumb of pleasure immersed in the suffering soup of existence deluding us. It is actually the base, often subtle, of a happy life. It seems to me that this structure of a happy life remains primarily a history of comfortable and supportive relationships, largely provided by parents (or our first caregivers), that teach us how to love and be loved. Edu felt so safe when in contact with me and our youngest brother. We two seemed to offer a family structure that could support an important part of Edu’s psychological well-being. Long-gestated suicides, thought out and planned numerous times, often for years, grow like a baobab tree, acquiring and building size along with the person’s identity. I think these deep-rooted intentions are the most difficult to prevent. They come from a long daily routine that feeds them for years. For those of us left behind, what remains are the ashes, our feelings of helplessness and guilt, and, in my case, a lot of good 91 NARRATIVE MEDICINE Suicide is a Baobab Tree: A Narrative Medicine Case Study memories. Edu was an inexhaustible source of ideas, beauty, creativity, art, and surprise. Despite all his faults, he was a rare, beautiful, explosive, surprising, and all-too-brief event that passed through our lives and helped form who I am. DISCUSSION We make sense of the world and the things that happen to us by constructing narratives to explain and interpret events both to ourselves and to other people. Furthermore, narratives also play an important role in touching readers. As a literary genre, the narrative is an important field of arts. A fundamental function of arts in our lives is awakening and vivifying our slumbering feelings, inclinations, and passions of every kind.2 In this context, narrative medicine emerges as a medical practice model based on narrative competence: the capacity of human beings to acknowledge, to absorb, to interpret, and to react to stories that provide resources for the understanding of stories’ meanings, leading to solutions and indicating a way to provide better holistic care.3-6 Moreover, narrative medicine uses patient stories as a diagnostic, therapeutic, and educational tool. Our narrative is an example of applying narrative medicine as a useful tool to manage an existential and complex scenario such as the suicide of a sibling. Some suicidal thoughts grow slowly from recurrent unconscious conflicts that do not arise from nothing.7-8 Freud proposed inevitable intrapsychic conflicts from Eros (life drive) and Thanatos (death drive).9 The complexity of suffering and pain experienced by suicidal individuals and their families, regardless of the success or failure of the suicidal act, is intensified by the strong stigmas attached to traditional concepts of sin and eternal damnation.10-12 This unfortunate reality emerges in our narrative as a tragic family drama permeated by profound feelings of helplessness. A GROWING BAOBAB TREE In our narrative, this suicide construction was compared to a growing baobab tree. The baobab is one of nature’s oldest trees, native to Madagascar, mainland Africa, and Australia. Capable of living for thousands of years, this tree grows to 40 to 75 feet tall with a trunk diameter of 35 to 60 feet. Baobabs are hardy and seemingly indestructible—they are renowned for being difficult to kill and will even regrow bark if stripped of it or burnt. In one chapter of The Little Prince,1 the classic novel by Antoine de Saint-Exupéry, the Little Prince and the author have a very important conversation about baobab trees. The Little Prince talks about how they are a constant threat to his tiny planet, and he has to pull up the little baobab saplings every morning. The Little Prince points out that these trees start out as tiny seedlings, but if not uprooted and discarded when they are small, they firmly take root and can even cause a planet to split apart. Saint-Exupéry states that the lesson to be learned from the story of the baobabs is so important that he has drawn them more carefully than any other drawing in the book.1 On a metaphorical level, the baobabs stand for unpleasant things in our human nature—if we don’t spot these unpleasant elements and weed them out early, they will take firm root and distort our personality. Edu’s suicide grew and became like a baobab tree. His suicidal ideation was left to grow stronger and stronger, and it took root in his personality. His ideation grew for ten years or more in silence, in his and his family’s silence. When his suicide happened, his ideation had been repeatedly planted long before. Some members of our family only realized its enormity when it happened. PUBLIC HEALTH PROBLEM Suicide is an important public health problem that causes immeasurable pain, suffering, and loss to individuals, families, friends, and communities in the world.13,14 Every year, more YEARS LATER By Adriano Machado Facioli, PhD Almost 15 years after my brother’s death, I wrote a poetic text, in first person, in which I play the role of a suicide, attempting to further explore my feelings about the world of Edu and others who lived something similar to his existential dilemmas. I am 28 years old and have long been carrying, in the empty space of my dark existence, the constant and raw idea that it makes no difference being dead or alive. Since my adolescence I have been unable to navigate my thoughts otherwise away from the turbid basement of ideologies upon which I have been building the edifice 92 of my soul. Existentially, nothing puts me at a point beyond my morbid desires. The infinity of the universe, its sparkling, dark, and deaf mysteries, or the absurdity of any inconceivable reality, only feed my desire of not existing, of returning the universe to as it once was before my birth. The immensity of everything swallows my soul into the mouth of the most savage impulses of killing myself or launching my existence to unpredictable and uncontrollable heights. I am a man (though I have never felt like a man) who carries on my shoulders the weight of an insignificant history. I carry also envy of the poorest I meet in the sad corners of the world, knowing the reality of life is unfair and that suffering is the first experience of our brutal collision with existence. We exist so little in the scope of the existence of everything, and too much for ourselves. I cannot bear myself. I cannot handle this voracious struggle exploding inside me, yearning to invade the plagued field of my rationality. Loneliness—this has always been my name, my identity from never having met any loving reflection of the starving people on my face in the mirror of life. v The Permanente Journal/ Summer 2015/ Volume 19 No. 3 NARRATIVE MEDICINE Suicide is a Baobab Tree: A Narrative Medicine Case Study than 800,000 people die by suicide worldwide (1.4% of all deaths), approximately one person every 40 seconds.11 It is one of the top 10 causes of death in the US.14 Globally, suicide is the 15th leading cause of death and the 2nd leading cause of death between the ages of 15 and 29 years; and it accounts for 50% of all violent deaths among men and 71% among women.11 Death by suicide is only a small part of the problem—for every person who dies from suicide, there are more than 30 others who attempt it.14 The heavy burden of long-lasting physical and emotional problems associated with suicidal behaviors affects countless individuals: family members of the person with suicidal behaviors, friends, coworkers, and others in the community. There is also a large economic impact, related to medical care costs and productivity loss.11,14 In Canada, it has been estimated that direct and indirect costs due to suicide are over $2.4 billion ($850,000 for each suicide).13 Another concerning fact is that almost 75% of suicides occur in low- and middle-income countries, where health services and resources for identification, treatment, and support are often scarce and limited. Indeed, suicide has a great impact on the most vulnerable populations, especially because of its high prevalence in minority, marginalized, and discriminated-against society groups, such as indigenous peoples, displaced persons, and individuals who are lesbian, gay, bisexual, transgender, or questioning their sexual identity (LGBTQ).10,11 For instance, LGBTQ youths have a 3- to 4-fold higher suicide risk, and those who have been rejected by their families are 8 times more likely to commit suicide.10 These striking facts make suicide a global health problem that must be considered a priority.10,11 “SUICIDE” In 1642, Sir Thomas Browne, a physician and philosopher, coined the term “suicide” in his famous work, Religio Medici.8 People have worked to understand suicide throughout history and across disciplines of knowledge, such as philosophy, sociology, psychoanalysis, and psychiatry. Social representations regarding suicide have also changed with time: a constituent element of tradition or acceptable option in certain cultures such as Rome, a sin in the Middle Ages, and a sign of mental illness in the 19th century.15-17 Currently, the idea that suicide is a legitimate option has permeated individual human rights and dying-with-dignity debates in certain circumstances.18-20 Durkheim,21 the late 19th-century sociologist who classified suicide types as egoistic, altruistic, or anomic, correlated suicide to the degree of social cohesion in a person’s life. He said family, church, and the state ceased to function as social integration factors after the social revolution, and nothing has replaced them to date. This analysis is a modern one in a world filled with conflicts.8,17,21 Although it is imperative to address suicidal behaviors as soon as possible, they are often met with silence and shame. Social reactions related to the stigma and taboo surrounding suicide are often a huge obstacle to those who need help when going through a crisis, which means many at suicide risk are left alone. Furthermore, a large segment of health services are not prepared to provide timely and effective help to those The Permanente Journal/ Summer 2015/ Volume 19 No. 3 who do seek help.10,11,14 Between 2% and 7% of primary care patients have thought about committing suicide; 45% to 76% of individuals who commit suicide visited their primary care clinician in the preceding month.10 Most primary care clinicians know there are suicidal patients in their practice, but they are not prepared to identify and to provide care for these patients.10 This is an alarming situation. Indeed, physicians may avoid the topic of suicide with patients because they feel ill prepared to care for a patient going through a crisis.10 SUICIDES ARE PREVENTABLE Because suicide was historically associated with mental illness, suicide prevention was largely viewed as a mental health service competence. However, mental health is just one factor that can influence suicide risk. It is important to note that the vast majority of individuals with mental disorders do not have suicidal behaviors.11,14 No single factor is sufficient to fully explain why a person commits suicide. Several risk factors frequently act cumulatively to increase vulnerability to suicidal behavior. Suicidal behavior is a complex phenomenon that is determined by the interplay between personal, social, psychological, cultural, biologic, and environmental factors. At the individual level, risk factors include previous suicide attempts, mental disorders, financial loss, chronic pain, family history of suicide, and alcohol and/or drug abuse. Some risk factors linked to community and human relations include wartime and natural disasters; acculturation stresses, such as those found among indigenous peoples or displaced individuals; discrimination; feelings of social isolation; abuse; violence; and conflicting relationships. Suicide prevention requires coordination and collaboration among multiple society sectors, such as education, labor, business, agriculture, justice, law, politics, and the media. These efforts must be comprehensive, synergistic, and integrated because no single approach can address so complex an issue as suicide. All have a role to play in helping make suicide prevention more widely available.11,12,14 The foundation of any effective preventive response lies in the identification of suicide risk factors and the relief of these risk factors by implementing appropriate interventions. Strategies to counter risk factors are of three types: 1) universal prevention strategies, which are designed to reach an entire population; 2) selective prevention strategies, which target vulnerable individuals; and 3) indicated prevention strategies, which target specific vulnerable individuals with community support.11 Among all risk factors for suicide, a prior suicide attempt is the single most important in the general population. In these cases, follow-up care by health caregivers through regular contact, including by phone or home visits, together with community support, is essential. Decreasing access to suicide means is another way to reduce suicide rates. Context is imperative to understanding suicide risk. Many suicides occur impulsively in moments of crisis, and ready access to suicide means (such as pesticides, firearms, and certain medications) can determine whether a person lives or dies.11 Other effective 93 NARRATIVE MEDICINE Suicide is a Baobab Tree: A Narrative Medicine Case Study measures include responsible suicide reporting in the media, avoiding language that sensationalizes suicide and avoiding explicit descriptions of methods used.11,12,22-25 In a recent report, the World Health Organization recommended that countries get a range of government departments involved in the development of a comprehensive coordinated response to prevent suicide.11 Furthermore, high-level commitment is needed, not just in the health care sector but also within the education, social welfare, employment, and judicial sectors.11 One recommended milestone is to place suicide prevention under national strategy, and to develop standards and guidelines with a multidisciplinary approach that addresses suicide in a comprehensive manner. Implementing timely and effective suicide prevention strategies can considerably reduce suicides rates.11 It is necessary to respond rapidly when a person in crisis is identified. Youth-focused efforts to reduce suicide have reported up to a 40% decrease in deaths by suicide. Among the elderly, these strategies have decreased suicide rates by 33%.10,11,13 In the World Health Organization Mental Health Action Plan 2013-2020,26 World Health Organization member states have pledged to implement actions to reduce the suicide rate by 10% by 2020. CONCLUSION Every suicide is a tragedy. These unexpected deaths, occuring predominantly among young and middle-aged adults, have a continuing ripple effect and result in a huge economic, social, and psychological burden for individuals, families, communities, and countries. Suicide is preventable, and prevention requires social change. To create social change, three important factors are required: knowledge (both scientific and informed by practice), public support (political will), and a social strategy (such as a national response to accomplish suicide prevention goals). Every life lost to suicide is one too many. The time to act and to make suicide prevention an imperative goal is now.10,11,14 If we attend to suicide when it is already too late, a baobab forest will have grown and we may never be able to get rid of it. v Disclosure Statement The author(s) have no conflicts of interest to disclose. References 1. de Saint-Exupéry A. Le Petit Prince. 1st ed. Paris, France: Gallimard; 1943. 2. Hegel GWF. Hegel’s aesthetics: lectures on fine art, vol I. Knox TM, translator. New York, NY: Oxford University Press Inc; 1998. 3. Charon R. Narrative medicine: form, function, and ethics. Ann Intern Med 2001 Jan 2;134(1):83-7. DOI: http://dx.doi.org/10.7326/0003-4819-134-1-20010102000024. 4. Charon R. The patient-physician relationship. Narrative medicine: a model for empathy, reflection, profession, and trust. JAMA 2001 Oct 17;286(15):1897-902. DOI: http://dx.doi.org/10.1001/jama.286.15.1897. 5. Charon R. Reading, writing, and doctoring: literature and medicine. Am J Med Sci 2000 May;319(5):285-91. DOI: http://dx.doi.org/10.1097/00000441200005000-00004. 6. Charon R. Narrative and medicine. N Engl J Med 2004 Feb 26;350(9):862-4. DOI: http://dx.doi.org/10.1056/NEJMp038249. 94 7. Beck AT, Steer RA, Kovacs M, Garrison B. Hopelessness and eventual suicide: a 10-year prospective study of patients hospitalized with suicidal ideation. Am J Psychiatry 1985 May;142(5):559-63. DOI: http://dx.doi.org/10.1176/ ajp.142.5.559. 8. Rutz W. Suicide prevention—background, problems, strategies: introductory remarks. In: De Leo D, Bille-Brahe U, Kerkhof A, Schmidtke A, editors. Suicidal behaviour: theories and research findings. 1st ed. Göttingen, Germany: Hogrefe & Huber Publishers; 2004 Oct. p 3-4. 9. Lind L. Thanatos: the drive without a name. The development of the concept of the death drive in Freud’s writings. Scandinavian Psychoanalytic Review 1991;14(1):60-80. DOI: http://dx.doi.org/10.1080/01062301.1991.10592256. 10. Kuehn BM. Preventing suicide’s ripple effects takes coordinated effort. JAMA 2013 Aug 14;310(6):570-1. DOI: http://dx.doi.org/10.1001/jama.2013.117024. 11. World Health Organization. Preventing suicide: a global imperative [Internet]. Geneva, Switzerland: World Health Organization; 2014 [cited 2014 Oct 1]. Available from: http://apps.who.int/iris/bitstream/10665/131056/1/ 9789241564779_eng.pdf?ua=1. 12. Fitzpatrick SJ, Kerridge IH. Challenges to a more open discussion of suicide. Med J Aust 2013 May 20;198(9):470-1. DOI: http://dx.doi.org/10.5694/ mja12.11540. 13. Spiwak R, Elias B, Bolton JM, Martens PJ, Sareen J. Suicide policy in Canada: lessons from history. Can J Public Health 2012 Jul 18;103(5):e338-41. 14. 2012 national strategy for suicide prevention: goals and objectives for action. A report of the US Surgeon General and of the National Action Alliance for Suicide Prevention [Internet]. Washington, DC: US Department of Health and Human Services; 2012 Sep [cited 2014 Oct 1]. Available from: www.surgeongeneral. gov/library/reports/national-strategy-suicide-prevention/full_report-rev.pdf. 15. De Leo D, Burgis S, Bertolote JM, Kerkhof A, Bille-Brahe U. Definitions of suicidal behaviour. In: De Leo D, Bille-Brahe U, Kerkhof A, Schmidtke A, editors. Suicidal behaviour: theories and research findings. 1st ed. Göttingen, Germany: Hogrefe & Huber Publishers; 2004 Oct. p 17-39. 16. Murray A. Suicide in the middle ages: volume I: the violent against themselves. New York, NY: Oxford University Press Inc; 2009 Feb 15. 17. Toscani F, Borreani C, Boeri P, Miccinesi G. Life at the end of life: beliefs about individual life after death and “good death” models—a qualitative study. Health Qual Life Outcomes 2003 Nov 7;1:65. DOI: http://dx.doi.org/10.1186/ 1477-7525-1-65. 18. Nuland SB. Physician-assisted suicide and euthanasia in practice. N Engl J Med 2000 Feb 24;342(8):583-4. DOI: http://dx.doi.org/10.1056/ NEJM200002243420811. 19. Sullivan AD, Hedberg K, Fleming DW. Legalized physician-assisted suicide in Oregon—the second year. N Engl J Med 2000 Feb 24;342(8):598-604. DOI: http://dx.doi.org/10.1056/NEJM200002243420822. 20. Willems DL, Daniels ER, van der Wal G, van der Maas PJ, Emanuel EJ. Attitudes and practices concerning the end of life: a comparison between physicians from the United States and from The Netherlands. Arch Intern Med 2000 Jan 10;160(1):63-8. DOI: http://dx.doi.org/10.1001/archinte.160.1.63. 21. Pickering WSF, Walford G, editors. Durkheim’s suicide: a century of research and debate. 1st ed. London, United Kingdom: Routledge; 2000. 22. Niederkrotenthaler T, Fu KW, Yip PS, et al. Changes in suicide rates following media reports on celebrity suicide: a meta-analysis. J Epidemiol Community Health 2012 Nov;66(11):1037-42. DOI: http://dx.doi.org/10.1136/jech-2011200707. 23. Sisask M, Värnik A. Media roles in suicide prevention: a systematic review. Int J Environ Res Public Health 2012 Jan;9(1):123-38. DOI: http://dx.doi.org/10.3390/ ijerph9010123. 24. Daine K, Hawton K, Singaravelu V, Stewart A, Simkin S, Montgomery P. The power of the Web: a systematic review of studies of the influence of the Internet on self-harm and suicide in young people. PLoS One 2013 Oct 30;8(10):e77555. DOI: http://dx.doi.org/10.1371/journal.pone.0077555. 25. Westerlund M, Hadlaczky G, Wasserman D. The representation of suicide on the Internet: implications for clinicians. J Med Internet Res 2012 Sep 26; 14(5):e122. DOI: http://dx.doi.org/10.2196/jmir.1979. 26. World Health Organization. Comprehensive mental health action plan 20132020 [Internet]. Geneva, Switzerland: World Health Organization; 2013 [cited 2014 Oct 1]. Available from: http://apps.who.int/gb/ebwha/pdf_files/WHA66/ A66_R8-en.pdf. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 NARRATIVE MEDICINE Why a Hanging Man Dances Gurpreet Kaur Padam, MD Perm J 2015 Summer;19(3):95 http://dx.doi.org/10.7812/TPP/14-230 “Do you know why a hanging man His eyes opened wide. Through the dances?” asked Mr B. He was once an glossy haze of the sclera, his baby blue intensely independent man, now 80 pupils dilated and held my gaze as he years old and afflicted with end-stage expressed great fear of eternal suffering lung disease. At first observation, he ap- if he chose to shorten his life. He manpeared tired, repositioning himself with aged to gather together the energy to great effort from lying down and then reveal that he lived alone at home and reclining in his bed. He then shifted to did not think he could return there, sitting at the edge of the bed, tightly as this was the beginning of the end. holding onto the bed sheets as if clenchWe discussed symptom management ing to a life that was slowly escaping options for dyspnea. He let out a sigh him. He positioned his right hand on of relief that there were alternatives to his chest, gasping for air, and appeared suicide but was disappointed that we frighteningly distressed. I picked up the had not figured out a way to circumnasal cannula and the tubing connected vent the dying process.“That is why a to the oxygen tank sitting hanging man dances, he is beside him. He thrust his looking for something to … he is outstretched palm towards step on,” he said. looking for me and said, “No. I don’t In his agony, Mr B knew something to want anything that will make there wasn’t much time left step on … me live longer.” Despite the and when “see you later” explanation that the flowing slipped from my tongue as air would help him with the sensation I bid farewell, he responded swiftly of air hunger, he still refused the readily that he would not be here the next day available oxygen. but perhaps we may meet in another He had a furrowed brow. He was lifetime. The next day at the hospital, clearly trying to catch his breath with I visited Mr B’s empty bed. I bid goodhis mouth open and mentioned that he bye to the unoccupied and neatly made was also in pain from a sacral decubitus bed where I imagined his last moments. ulcer. Working through his anguish, While I hoped that our meeting was he muttered a few bitter words and re- as meaningful to him as it was to me, quested a “magic injection” to end it all. I prayed for him to be at peace. This While gasping for air between words, encounter left me with more questions his pauses for rest seemed like minutes. than answers. Did he appear frightened Mr B debated out loud as if answering and distressed to me because I was? He his own questions, his predicament seemed so comfortable with the notion that his spiritual belief prohibited him of death and knowing that it hovered from taking his own life and risking nearby. Perhaps I perceived him to be reincarnation. To him, rebirth meant clenching to life not because he was inevitably reliving his current situation. scared to die but because I was afraid That would not be tolerable for him. to let him down? Perhaps the one clenching to life was me, while he had resolved to let go. I am humbled with gratitude that Mr B unknowingly assisted in making me a better person and a more compassionate physician. When I find myself sitting at the edge of the bed in the early morning, I often think of him and what he must have felt. An asthmatic yearns for air as the chest becomes tighter with each cough; most of us experience transitional dyspnea or discomfort when we are afflicted with the flu or a cold. This heightened sense of awareness used to cause anxiety, but now I can channel it as motivation to improve the delivery of my care and our system for those who need it the most. Mr B left a mark on my soul as if through the looking glass he gave me another vital glimpse of my own mortality. After all, I will be at the receiving end one day. v Gurpreet Kaur Padam, MD, is a Hospice and Family Medicine Physician at the Redwood City Medical Center in CA. E-mail: [email protected]. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 95 ONLINE ONLY BOOK REVIEW The Body Keeps the Score: Brain, Mind, and Body in the Healing of Trauma by Bessel van der Kolk, MD Review by Albert Ray, MD Perm J 2015 Summer;19(3):e118-e119 http://dx.doi.org/10.7812/TPP/14-211 This valuable book is an informative primer about the ways traumatic life events affect us as human beings. The impact of physical and emotional trauma on brain, mind, and body is examined thoroughly by the author, Bessel van der Kolk, MD, through numerous real life examples that arouse our clinical interest. In our modern age, when we so often hear the term “posttraumatic stress disorder,” this book takes us back in time to its historic origins and the past efforts of some of the icons of psychiatry who attempted to explain and treat trauma in dealing with their patients. What becomes clear very quickly is that individuals can be forever branded with a historic score that travels with them for the remainder of life. The body indeed keeps that score as a permanent record unless something is done to address its tattoo. Although we all deal with the results in our practices, the origins are rarely recognized. As a result, treatment of such traumaaffected patients today is mostly based on the use of powerful medications to lower the score pharmacologically rather than by exploring underlying causality and thereby creating an individual who feels understood. On the surface, it would appear to be easier to deliver treatment as a “medicating practitioner” rather than as a “talking practitioner.” But unless one gets down into the action through discovering and understanding the patient’s experience, one cannot truly help the healing process begin in a successful manner. On the basis of this foundation, this book explores the ways that both patients and healers can develop the skills to appropriately evaluate historic traumatic events and how to successfully begin treating them. For the scientifically oriented physician, the biochemical, physiologic, and anatomic effects of trauma on the body are well explored in this detailed exposé. What is more importantly emphasized, though, is the invisible mark that is embedded permanently on mind and body by past traumatic events. Through its case examples, this book helps us appreciate this over and over again. It is only with this understanding of the toll on the human being that the score can be altered, resulting in victory. Van der Kolk methodically reviews how our body keeps as a permanent record the history of any “adverse experiences” in a locked account. It is imperative for the clinician to find the key to unlocking that safe, so the individual can remember and emote an experience of past trauma, and deal with it in a healing fashion that is permanent and nonthreatening. It is only in this way that the brain, mind, and body can begin to heal and restart the game with no remnant of points left on the scoreboard. Trauma victims are often unable to recover fully on their own without causal understanding and guidance because our minds and bodies have not been trained to open up new pathways to lead us out of the maze. Instead, patients are often numbed with medications to help them live with the stress of trauma, while numerous unsuccessful visits to health care professionals take place for a myriad of somatic complaints. This has had a major effect on the cost of providing health care. The techniques in this book teach New York, NY: Viking Press; 2014. ISBN: 978-0-670-78593-3. Hardcover: 464 pages. $27.95 helpful methods that should instead be considered, including mediation, yoga, eye-movement desensitization and reprocessing, neurofeedback, and play, to return the patient to a healthy state of wellness. It is never too late to learn to help a person tap into their inner strength through teaching the use of breathing, movement, and touch as an art for healing. Ultimately, the goal of this book is to learn how to help traumatized patients, and to guide their healers to bring a feeling of safety, calm, and acceptance to their patients as we assist them with remembering memories of horrible events that they have experienced. Whether that patient is a child, a war veteran, an abused spouse, a sexually traumatized Albert Ray, MD, is a Partner Emeritus of the Southern California Permanente Medical Group and is the Bariatric Surgery Physician Champion, Positive Choice Wellness Center, San Diego, CA. He is a Clinical Professor at the University of California School of Medicine, a former elected Director of the Southern California Permanente Medical Group, and 2008 President of the San Diego County Medical Society. E-mail: [email protected]. e118 The Permanente Journal/ Summer 2015/ Volume 19 No. 3 BOOK REVIEW The Body Keeps the Score: Brain, Mind, and Body in the Healing of Trauma individual, or a victim of poverty, the roadmap for discovery and healing are much the same and can be achieved without the often ineffectiveness of resorting to multiple courses of potent medications or repeated outpatient visits, which avoid the underlying pathology. Those who use this book and who would find its content useful include not only traumatized individuals and their loved ones, but physicians, health care workers, mental health professionals, policy makers, law enforcement, educators, and military personnel. We are all shocked to hear on the daily news, horrific events involving murder and suicide that have past trauma as their underlying The Permanente Journal/ Summer 2015/ Volume 19 No. 3 etiology. We need a new paradigm to effectively deal with this horror, and this book begins to provide that for us. The world has advanced and retreated throughout its history as a result of monumental events, many of which have been quite traumatic. Success and defeat, agony and ecstasy are familiar to all of us, collectively or individually. A thorough reading of The Body Keeps the Score offers us a new window to help recognize, interpret, and better comprehend how a traumatic event in the past, based not on genetics but rather caused by life experiences, can be explored and successfully overcome so that the individual is no longer a victim but a hero. I encourage you to become an active player in the game, and not an observer, by employing the teachings that this enjoyable, easy-to-read book has to offer. I congratulate the author on taking such a complex subject, making it easy to understand and practical at the same time, so that in the end the brain, mind, and body are healed and no longer have to keep the score. v e119 ONLINE ONLY CLINICAL MEDICINE Image Diagnosis: Inferior Mesenteric Vein Thrombosis Avin Aggarwal, MBBS; Shashank Garg, MBBS Perm J 2015 Summer;19(3):e120-e121 http://dx.doi.org/10.7812/TPP/14-239 CASE STUDY A 59-year-old man presented to the gastroenterology clinic with 2 weeks of worsening lower back pain. There was associated poor appetite, fatigue, night sweats, and chills. The patient’s medical history was significant for well-controlled hypertension and sigmoid diverticulosis. He had been smoking half a pack of cigarettes per day for 30 years. Physical examination was remarkable for fever (100.7°F), periumbilical tenderness, and a soft epigastric bruit. Laboratory evaluation, including complete blood count, lipase, liver and renal function, electrolytes, and lactate, were within normal limits. Ultrasound of the abdomen with venous duplex was performed to evaluate the epigastric bruit. The ultrasound revealed a nonocclusive thrombus in the splenic vein (Figure 1). A computed tomography (CT) scan with intravenous contrast confirmed a thrombus in the inferior mesenteric vein (IMV) (Figure 2) extending to the confluence of the IMV with the splenic vein (Figure 3). Inflammatory changes around the sigmoid colon with a hyperdense diverticulum were also noted on CT scan (Figure 4), suggestive of diverticulitis. No evidence of intestinal obstruction or infarction was seen on imaging, which indicated only partial vein occlusion and/or early IMV thrombosis. The thrombosis probably resulted from inflammation in the adjacent diverticulum. The patient was given ciprofloxacin and metronidazole for 10 days and was started on warfarin therapy, initially bridged with heparin. A CT scan of the patient’s abdomen was performed 15 weeks after his initial visit and treatment. The CT scan Figure 2. Coronal view computed tomography scan of the abdomen, with the white arrows indicating the thrombus in the inferior mesenteric vein. Figure 3. Axial view computed tomography scan of the abdomen, with the white arrow indicating the inferior mesenteric vein thrombus extending up to its confluence with the splenic vein. Figure 1. Ultrasound of the abdomen with the white arrow indicating a nonocclusive thrombus in the splenic vein. The distance between the crosshairs is 0.726 cm. Avin Aggarwal, MBBS, is a Resident in the Department of Medicine at Hennepin County Medical Center in Minneapolis, MN. E-mail: [email protected]. Shashank Garg, MBBS, is a Fellow in the Division of Digestive Diseases and Nutrition in the Department of Medicine at the University of Kentucky in Lexington. Email: [email protected]. e120 The Permanente Journal/ Summer 2015/ Volume 19 No. 3 CLINICAL MEDICINE Image Diagnosis: Inferior Mesenteric Vein Thrombosis IMV thrombosis is an uncommon but potentially life-threatening complication of sigmoid diverticulitis. Prompt diagnosis and management of IMV thrombosis can prevent mesenteric infarction or surgical intervention. v Disclosure Statement The authors have no conflict of interest to disclose. References Figure 4. Coronal view computed tomography scan Figure 5. Coronal view computed tomography of the abdomen. Arrow 1 indicates a hyperdense scan of the abdomen 15 weeks after initial diverticulum, arrow 2 indicates edema of the sigmoid treatment. The white arrow indicates a smaller colon wall, and arrow 3 indicates pericolonic fat inferior mesenteric vein, compared with the time of stranding. diagnosis, without thrombus or collaterals. showed a smaller IMV without any collateral vein formation, indicating resolution of the thrombus (Figure 5). At 30 weeks, ultrasound of the patient’s abdomen showed a patent splenic vein with normal flow (Figure 6). The patient had a comprehensive workup for thrombophilia, which was unremarkable. Warfarin therapy was stopped after resolution of the thrombus. DISCUSSION Acute mesenteric vein thrombosis is responsible for 6% to 9% of cases of acute mesenteric ischemia.1 IMV thrombosis is relatively uncommon and constitutes 4% to 11% of cases of acute mesenteric vein thrombosis.2,3 However, IMV thrombosis carries a 15% to 23% risk of mortality.4-6 It is usually seen in the setting of thrombophilia or local inflammation, and IMV thrombosis on abdominal imaging should prompt workup for these conditions.7 Initial management involves bowel rest, pain control, intravenous hydration, and therapeutic anticoagulation with bridging from heparin to warfarin.7 Surgical resection is reserved for patients with progressive intestinal dilatation or peritoneal signs. 1. Harnik IG, Brandt LJ. Mesenteric venous thrombosis. Vasc Med 2010 Oct;15(5):407-18. DOI: http://dx.doi.org/10.1177/1358863X10379673. 2. Grisham A, Lohr J, Guenther JM, Engel AM. Deciphering mesenteric venous thrombosis: imaging and treatment. Vasc Endovascular Surg 2005 Nov-Dec;39(6):473-9. DOI: http://dx.doi. org/10.1177/153857440503900603. 3. Alvi AR, Khan S, Niazi SK, Ghulam M, Bibi S. Acute mesenteric venous thrombosis: improved outcome with early diagnosis and prompt anticoagulation therapy. Int J Surg 2009 Jun;7(3):210-3. DOI: http://dx.doi.org/10.1016/j. ijsu.2009.03.002. 4. Acosta S, Alhadad A, Svensson P, Ekberg O. Epidemiology, risk and prognostic factors in mesenteric venous thrombosis. Br J Surg 2008 Oct;95(10):1245-51. DOI: http://dx.doi. org/10.1002/bjs.6319. 5. Morasch MD, Ebaugh JL, Chiou AC, Matsumura JS, Pearce WH, Yao JS. Mesenteric venous thrombosis: a changing clinical entity. J Vasc Surg 2001 Oct;34(4):680-4. DOI: http:// dx.doi.org/10.1067/mva.2001.116965. 6. Dentali F, Ageno W, Witt D, et al; WARPED consortium. Natural history of mesenteric venous thrombosis in patients treated with vitamin K antagonists: a multi-centre, retrospective cohort study. Thromb Haemost 2009 Sep;102(3):501-4. DOI: http://dx.doi.org/10.1160/TH08-12-0842. 7. Singal AK, Kamath PS, Tefferi A. Mesenteric venous thrombosis. Mayo Clin Proc 2013 Mar;88(3):285-94. DOI: http://dx.doi.org/10.1016/j. mayocp.2013.01.012. Figure 6. Ultrasound of the abdomen 30 weeks after initial treatment. The white arrow indicates the patent splenic vein without any thrombus. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 e121 ONLINE ONLY CASE REPORTS Pneumomediastinum Diagnosed on Ultrasound in the Emergency Department: A Case Report Hilary FH Beason, MD; Joshua E Markowitz, MD, RDMS, FACEP Perm J 2015 Summer;19(3):e122-e124 http://dx.doi.org/10.7812/TPP/14-232 ABSTRACT An emergency ultrasound performed at bedside helped to confirm and expedite the diagnosis of esophageal perforation in a 23-year-old man. Early diagnosis was essential for prompt treatment and consultation because the patient’s underlying pathology created the potential for him to become critically ill. By serving as a quick, bedside tool for the diagnosis and evaluation of patients in the Emergency Department, bedside ultrasound allows emergency physicians to care for critically ill patients without delays or the need to send patients out of the department for imaging studies. Although the use of ultrasound in diagnosing soft-tissue pathologies is a core competency, the diagnosis of pneumomediastinum by ultrasound has been reported in the literature in only a few case reports. To our knowledge, this is the first published report of using ultrasound as an aid in the diagnosis of Boerhaave syndrome by diagnosing pneumomediastinum in an adult male. INTRODUCTION Ultrasound is an essential tool for emergency physicians because of its use for diagnosis, resuscitation, monitoring, and adjunct treatment in core areas of practice, including trauma, deep vein thrombosis, and thoracic, abdominal, and soft-tissue pathologies.1,2 This article presents a case in which the use of bedside ultrasound aided in a prompt diagnosis of pneumomediastinum, which led to a diagnosis of postemesis esophageal rupture. Cases of esophageal rupture have a high risk of morbidity Figure 1. Ultrasound of the neck. The white arrow indicates free air with posterior acoustic shadowing in the soft tissue of the neck. Free air is identified by the hyperechoic white spots. The white “M” indicates sternohyoid and sternothyroid muscles. The white “Thy” indicates the thyroid. The white “Tr” indicates the trachea. and mortality, and early, definitive diagnosis leading to definitive management improves outcomes. Definitive diagnosis is most often made with imaging, including x-ray and computed tomography scans. These modalities may lead to delays in diagnosis or, in many cases, may require the potentially unstable patient to leave the Emergency Department (ED). This case demonstrates that with a high degree of clinical suspicion and utilization of bedside ultrasound, the emergency physician may 1) more confidently provide earlier interventions including antibiotics and surgical consult, and 2) limit time out away from the department (for imaging) in a patient who may be critically ill. CASE REPORT A 23-year-old man with a history of asthma and alcohol and marijuana use presented to the ED with 2 hours of severe, sharp right-sided chest pain. The pain started suddenly after the patient choked on a large piece of steak and subsequently coughed once and vomited forcefully. On physical examination, the patient appeared uncomfortable and was noted to have reproducible tenderness over the right anterior chest wall and anterior neck. Initially, no other findings on physical exam were noted, but on repeat evaluation after an echocardiogram was performed, the patient had crepitus over his anterior neck. No other positive physical findings were noted. His echocardiogram showed normal sinus rhythm. Using a SonoSite MicroMaxx (SonoSite, Inc, Bothell, WA) machine and a P38 probe, a bedside ultrasound of the soft tissue of the neck was performed 26 minutes later to confirm the physical examination finding of crepitus over the anterior neck. Examination of the anterior neck revealed subcutaneous hyperechoic white foci suggestive of air bubbles in the soft tissue (Figure 1). After confirmation of free air in his anterior neck, the patient was given a diagnosis of subcutaneous air from a presumed pneumomediastinum and a diagnosis of likely esophageal rupture consistent with Boerhaave syndrome. The patient was started on piperacillin/tazobactam. Portable x-ray was not Hilary FH Beason, MD, is an Emergency Physician at the DCH Health System Medical Center in Tuscaloosa, AL. E-mail: [email protected]. Joshua E Markowitz, MD, RDMS, FACEP, is an Emergency Physician at the Santa Clara Medical Center in CA. E-mail: [email protected]. e122 The Permanente Journal/ Summer 2015/ Volume 19 No. 3 CASE REPORTS Pneumomediastinum Diagnosed on Ultrasound in the Emergency Department: A Case Report Figure 2. Radiograph of the chest. The white arrow indicates free air in the soft tissues of the neck. initially available; a chest radiograph was obtained 2 hours and 13 minutes after presentation to the ED (Figure 2). The on-call surgeon was notified of the radiograph findings and the patient was admitted to the Surgical Intensive Care Unit. The diagnosis of pneumomediastinum was further evaluated using a computed tomography scan with contrast (Figure 3), and eventually with an esophagram from the Surgical Intensive Care Unit. These images demonstrated a right pleural effusion, mild emphysema and pneumomediastinum in the chest, and subcutaneous emphysema, in the neck. On the day after admission to the ED, a repeat esophagram was performed that showed that the patient’s perforation had spontaneously closed. The patient was managed medically and was discharged home on hospital day 2. DISCUSSION Boerhaave syndrome is defined as spontaneous transmural rupture and perforation of the esophagus or postemesis esophageal rupture.3,4 The most common causes of esophageal rupture include chest trauma (blunt or penetrating), local trauma from swallowed foreign bodies or caustic agents, spontaneous rupture, anastamotic breakdown, The Permanente Journal/ Summer 2015/ Volume 19 No. 3 and iatrogenesis.3 Boerhaave syndrome has a high rate of morbidity and mortality due to mediastinal contamination, with 20% to 50% of cases resulting in death even when properly treated.3,5 If a significant esophageal tear occurs, the definitive management is surgical.3,4 In our case, the patient reported forceful vomiting, which probably caused the esophageal perforation. Our patient had only a small perforation, which closed spontaneously and required no surgical intervention. However, prompt diagnosis was aided by bedside ultrasound, allowing for the early initiation of antibiotic therapy. These were critical steps in this patient’s hospital course. The physical examination finding of crepitus raised our suspicion for free air; ultrasound confirmed this finding, which, in conjunction with the patient’s presenting history, led to a presumptive diagnosis of pneumomediastinum. The diagnosis of Boerhaave syndrome requires a high clinical suspicion and can often be overlooked. Patients typically present with severe chest or abdominal pain that can mirror other pathologies, thus causing early examination findings to be nonspecific. The classic physical findings associated with Boerhaave syndrome often present late and include a systolic crunch (Hamman sign) and crepitus that is palpable in the neck or along the chest wall.3 Common chest x-ray findings include widening of the mediastinum, pneumothorax, pneumomediastinum, and/or pleural effusions (usually left-sided).3,4 Emergency ultrasound is an accepted practice for the primary assessment of ED patients. 6 Although ultrasound may not be able to definitively diagnose Boerhaave syndrome, sonography has been used to identify some of its common features. Using sonography in the diagnosis of pneumothorax and pleural effusion is common practice. Ultrasound has also been used to identify subcutaneous air bubbles in necrotizing fasciitis and subcutaneous air caused by surgical procedures.7,8 However, the ability to diagnose pneumomediastinum with ultrasound has only been reported in a few case reports and is more often associated with children.9-13 The diagnosis of pneumomediastinum can be challenging with bedside ultrasound and is operator dependent. Thoracic ultrasound poses its own challenges because of limitations caused by bone and by air in the lungs. However, the ability to visualize free air in the soft tissue of the neck is often more straight forward. Differential diagnoses to consider for free air in the neck include Figure 3. Computed tomography scan of the neck with contrast. The white arrow indicates free air in the prevertebral space. e123 CASE REPORTS Pneumomediastinum Diagnosed on Ultrasound in the Emergency Department: A Case Report direct local extension (such as from a line placement), infection from a gasproducing bacteria, pneumothorax, or pneumomediastinum. In our case, use of ultrasound led to early treatment and allowed for close patient monitoring before the patient left the department for further imaging. In an unstable patient, transportation to the Radiology Department would increase risk to the patient, and the use of ultrasound could make an even greater difference in patient mortality. Our patient was young and of appropriate body mass index, which allowed for the thorough physical examination that identified crepitus in his neck. In patients with severely elevated body mass indexes and those considered morbidly obese, findings such as subcutaneous emphysema may be equivocal or even absent on palpation, thus making it more difficult to properly diagnose this condition. In these cases, ultrasound is an even greater tool for identifying subcutaneous air because it can have greater sensitivity than physical examination alone. Many facilities have access to portable x-ray machines, a useful tool in diagnosing free air in the soft tissues. However, there are occasions when this modality may be unavailable. Some EDs may not have access to portable x-ray machines at all. In either of these cases, the ability to use ultrasound becomes crucial in helping to identify and to diagnose e124 emergent conditions. Although it may not be the only imaging modality that can diagnose free air, ultrasound may compliment current available technology because there are times when it is the most accessible imaging modality. Early intervention reduces morbidity and mortality in cases of Boerhaave syndrome. The use of ultrasound at bedside can help lead to early diagnosis of certain aspects of the syndrome, such as pneumomediastinum. Although definitive imaging such as computed tomography and barium esophagram may still be required, particularly before surgical intervention, bedside diagnosis with ultrasound allows for prompt initiation of antibiotics, critical in the treatment of Boerhaave syndrome. v Disclosure Statement The author(s) have no conflict of interest to disclose. References 1. American College of Emergency Physicians policy statement: emergency ultrasound guidelines [Internet]. Dallas, TX: American College of Emergency Physicians; 2008 Oct [cited 2015 May 8]. Available from: www.acep.org/WorkArea/linkit.asp x?LinkIdentifier=ID&ItemID=32878. 2. Burgher SW, Tandy TK, Dawdy MR. Transvaginal ultrasonography by emergency physicians decreases patient time in the emergency department. Acad Emerg Med 1998 Aug;5(8):802-7. DOI: http://dx.doi.org/10.1111/j.1553-2712.1998. tb02507.x. 3. Eckstein M, Henderson SO. Thoracic trauma. In: Marx J, Hockberger R, Walls R, et al, editors. Rosen’s emergency medicine: concepts and clinical practice. 7th ed. Vol 1. Philadelphia, PA: Mosby; 2010. p 387-413. 4. Park DR, Vallières E. Tumors and cysts of the mediastinum. In: Mason RJ, Broaddus VC, Martin T, et al, editors. Murray and Nadel’s textbook of respiratory medicine. 5th ed. Vol 2. Philadelphia, PA: Saunders; 2010. p 1836-58. 5. Zun LS, Singh A. Nausea and vomiting. In: Marx J, Hockberger R, Walls R, et al, editors. Rosen’s emergency medicine: concepts and clinical practice. 7th ed. Vol 1. Philadelphia, PA: Mosby; 2010. p 149-58. 6. American College of Emergency Physicians. Use of ultrasound imaging by emergency physicians. Ann Emerg Med 2001 Oct;38(4):469-70. 7. Castleberg E, Jenson N, Dinh VA. Diagnosis of necrotizing fasciitis with bedside ultrasound: the STAFF exam. West J Emerg Med 2014 Feb;15(1):111-3. DOI: http://dx.doi.org/10.5811/ westjem.2013.8.18303. 8. Butcher CH, Dooley RW, Levitov AB. Detection of subcutaneous and intramuscular air with sonography: a sensitive and specific modality. J Ultrasound Med 2011 Jun;30(6);791-5. 9. Dulchavsky SA, Henry SE, Moed BR, et al. Advanced ultrasonic diagnosis of extremity trauma: the FASTER examination. J Trauma 2002 Jul;53(1):28-32. DOI: http://dx.doi. org/10.1097/00005373-200207000-00006. 10. Anantham D, Ernst A. Ultrasonography. In: Mason RJ, Broaddus VC, Martin T, et al, editors. Murray and Nadel’s textbook of respiratory medicine. 5th ed. Vol 2. Philadelphia, PA: Saunders; 2010. p 445-60. 11. Testa A, Candelli M, Pignataro G, Costantini AM, Pirronti T, Silveri NG. Sonographic detection of spontaneous pneumomediastinum. J Ultrasound Med 2008 Oct;27(10):1507-9. 12. Jung AY, Yang I, Go HS, et al. Imaging neonatal spontaneous pneumomediastinum using ultrasound. J Med Ultrason (2001) 2014;41:45-9. DOI: http://dx.doi.org/10.1007/s10396-013-0454-3. 13. Van Gelderen WF. Ultrasound diagnosis of an atypical pneumomediastinum. Pediatr Radiol 1992;22(6):469. DOI: http://dx.doi.org/10.1007/ BF02013517. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 ONLINE ONLY CASE REPORTS Case Report: Pulmonary Papillomatosis in a Patient Presenting with Cough and Hemoptysis Zhou Zhang, MD; Melisa Chang, MD; Luis M Moreta-Sainz, MD Perm J 2015 Summer;19(3):e125-e127 http://dx.doi.org/10.7812/TPP/14-192 ABSTRACT A previously healthy patient was seen in the Emergency Department for evaluation of a one-month history of cough and one-day history of hemoptysis. A computed tomography scan of the thorax found a mass on the right lower pulmonary lobe and a mass on the left upper lobe. A biopsy specimen of the right lobe lung mass, obtained during bronchoscopy, demonstrated papilloma. This case report, from a pulmonologist’s perspective, includes a comprehensive review of the patient’s clinical presentation and outcome, as well as a discussion of recurrent respiratory papillomatosis. INTRODUCTION Recurrent respiratory papillomatosis (RRP) is an uncommon clinical entity. The incidence rate is 1.8 cases per 100,000 adults and 4.3 cases per 100,000 children. Recurrent respiratory papillomatosis is caused by human papillomavirus (HPV) serotypes 6 and 11 (the same serotypes responsible for more than 90% of genital condylomata) and serotypes 16, 18, 31, and 33 (the serotypes associated with genital and aerodigestive tract malignancies). A double-stranded DNA virus in the Papovaviridae family, HPV infects the mucosal basal layer and induces cellular proliferations via activation of host Figure 1. Computed tomography scan of chest showing masses in right lower and left upper pulmonary nodes. replication genes through the epidermal growth factor receptor pathway.1 This results in thickening of the basal layer. Papilloma appears grossly as velvety or exophytic “cauliflower.” Figure 2. Bronchoscopy demonstrating polypoid lesion on right vocal cord. CASE REPORT A 43-year-old man presented to the Emergency Department with a 1-day history of dark burgundy-colored sputum and a cough. The patient had the cough as well as a 2.7-kg (6-pound) weight loss in the month before admission. He denied fever, night sweats, or change in the tone of his voice. He had no remarkable medical history and no prior surgery. He was not taking any medications. He did not know his family history because he is adopted. His social history included substantial secondhand smoking exposure. He had multiple drug use in the past that included marijuana, cocaine, lysergic acid diethylamide, and amphetamine. He had multiple female sexual partners. A chest x-ray film obtained on admission showed a right-sided lung mass. Computed tomography scan of the chest was subsequently performed for better visualization. Chest computed tomography (Figure 1) demonstrated a right lung mass measuring 5.4 cm × 5.2 cm × 6.1 cm at the superior segment Figure 3. Bronchoscopy showing view of endobronchial mass at right lower lobe. of the right lower lobe with associated “tree-in-bud” nodularity, as well as a lesion in the left upper lobe measuring 1.7 cm in diameter. The inpatient pulmonary team was consulted for assistance with the diagnosis. The patient underwent bronchoscopy, which identified a polypoid lesion on the right vocal cord (Figure 2) and an endobronchial mass at the right lower lobe (Figure 3). The right lung mass was biopsied. Pathologic findings revealed squamous cell papillomatosis. Zhou Zhang, MD, is a Third-Year Resident in Internal Medicine at the Los Angeles Medical Center in CA. E-mail: [email protected]. Melisa Chang, MD, is a Second-Year Fellow in Pulmonary and Critical Care at Cedars-Sinai Medical Center in Los Angeles, CA. E-mail: [email protected]. Luis M Moreta-Sainz, MD, is an Attending Physician in the Department of Pulmonary and Critical Care at the Los Angeles Medical Center in CA. E-mail: [email protected] The Permanente Journal/ Summer 2015/ Volume 19 No. 3 e125 CASE REPORTS Case Report: Pulmonary Papillomatosis in a Patient Presenting with Cough and Hemoptysis Figure 4. Gross specimen from right lobectomy demonstrating squamous cell carcinoma. The patient had 4 hospitalizations for treatment of recurrent pneumonia in the next 6 months, with 19 inpatient days accounted for by this complication. A thoracic surgeon was consulted, and the decision was made to perform a right-sided lobectomy via video-assisted thoracoscopic surgery. A biopsy was performed from the gross specimen obtained at the lobectomy (Figure 4). Results demonstrated squamous cell carcinoma. The patient was subsequently referred to an oncologist for a discussion of treatment options for squamous cell carcinoma of the lung. Human papillomavirus has a predilection for the junction between squamous and ciliated epithelium. RRP affects, from the most common site to the least common site, the true vocal cord, oral cavity, trachea, bronchi, and esophagus. Therefore, patients present most commonly with hoarseness followed by stridor, cough, and dyspnea. Pediatric patients may present with failure to thrive as well. Talierco et al4 reported 100% of patients with adultonset RRP had concurrent HPV infection of the oral cavity; however, our patient had no evidence of oral cavity HPV infection on physical examination or bronchoscopy findings. The diagnosis of lesions typically is first made through visualization by imaging modalities such as computed tomography of the chest, followed by biopsy of suspicious lesions through laryngoscopy, nasopharyngolaryngoscopy, or bronchoscopy. The gross appearance of papilloma is exophytic, with white or pink lesions with frondlike projections. Histologically, papilloma is described as projections of nonkeratinized stratified squamous epithelium over a fibrovascular core (Figure 5). The primary treatment of RRP is surgical removal of the papilloma to reduce the tumor burden. Surgical techniques include cold steel excision, carbon dioxide or argon laser, endoscopic microdebrider, and pulsed dye laser.5 Potential side effects of carbon dioxide or argon laser include active viral DNA in the laser smoke, which potentially can expose the practitioner performing the procedure and the staff to HPV and spread HPV to the patient’s previously unaffected body parts. Other side effects of laser therapy include damage to surrounding tissue causing vocal glottis edema or vocal cord scarring, as well as the potential for the laser to cause an explosion when mixed with oxygen-rich supply from the DISCUSSION The incidence of RRP is bimodal, with the juvenile-onset form typically first occurring in children aged 2 to 4 years and adult-onset RRP typically occurring in adults aged 20 to 40 years. Juvenile-onset RRP is thought to be caused from peripartum exposure through an infected birth canal. Cesarean delivery appears to lower the risk of RRP in newborns but does not eliminate the risk. Risk factors for juvenile-onset RRP include being firstborn, being born via normal spontaneous vaginal delivery, and being born to a teenage mother.2 Risk factors for adult-onset RRP include multiple lifetime sexual partners as well as a high frequency of oral sex. There was no statistically significant difference in illicit drug use between patients with adult-onset RRP vs a control group in a study by Ruiz et al.3 e126 Figure 5. Pathologic specimen from right lower lobe lesion demonstrating squamous cell papillomatosis. Immunostaining was positive for tumor suppressor protein p16. Fingerlike projections of nonkeratinized stratified squamous epithelium appear with fibrovascular core. The Permanente Journal/ Summer 2015/ Volume 19 No. 3 CASE REPORTS Case Report: Pulmonary Papillomatosis in a Patient Presenting with Cough and Hemoptysis Table 1. Comparison of our case report to case reports from the literature Author, year Martina et al, 201410 Azadarmaki et al, 201311 Hasegawa et al, 201312 Lin et al, 201013 Comparison Their patient had a history of laryngeal papillomatosis since childhood. Our patient did not have a history of papillomatosis from childhood. Both our patient and theirs had malignant transformation of respiratory papillomatosis. However, their case report featured a transplant recipient. Both patients had malignant transformation of respiratory papillomatosis to squamous cell carcinoma. However, their patient had tracheal papilloma diagnosed ten years before transformation. Our patient was diagnosed with respiratory papillomatosis about six months before evidence of malignant transformation. Both patients had malignant transformation of respiratory papillomatosis to squamous cell carcinoma. However, their patient had human papillomavirus infection of the larynx and trachea since childhood, years before malignant transformation. Our patient was diagnosed with respiratory papillomatosis about six months before evidence of malignant transformation. endotracheal tube. Tracheostomy might be needed for patients with airway obstruction. However, tracheostomy is to be avoided if at all possible because of a risk of activating or contributing to the spread of RRP because tracheostomy creates a squamocolumnar junction. Medical therapy is considered adjuvant to surgical therapy. The criteria for medical therapy include more than 4 surgeries performed per year, spread of the disease to a distant site, or rapid growth of lesions. Medical therapy includes interferon, ribavirin, acyclovir, and intralesional injection of cidofovir.6 Additional new adjuvant medical therapy under investigation includes bevacizumab and HPV vaccine. Injection of bevacizumab to vocal cord RRP lesions enhanced photoangiolytic laser treatment of RRP and was found to be safe without additional complications related to laser treatment.7,8 For patients who had rapidly growing laryngeal papilloma, adjuvant therapy with 3 doses of quadrivalent prophylactic HPV vaccine (Silgard, Merck, Sharp & Dohme Corp, Merck Co, New York, NY) prolonged the interval between surgical procedures, from a mean interval of 272.1 days before vaccination to 537.4 days after vaccination (p = 0.034) in a study by Hočevar-Boltežar et al.9 There is no cure for RRP, and in 3% to 5% of patients with RRP, it will undergo malignant transformation to squamous cell carcinoma. A quadrivalent The Permanente Journal/ Summer 2015/ Volume 19 No. 3 HPV vaccine (Gardasil, Merck Co, New York, NY) was approved in the US for prevention of cervical cancer caused by HPV infection. Gardasil theoretically should prevent RRP, and future studies should focus on the role of vaccination to prevent RRP. A literature review of RRP case reports10-13 (Table 1) revealed that patients usually have the diagnosis of RRP many years before evidence of malignant transformation. In contrast, our patient had evidence of malignant transformation about six months after diagnosis of respiratory papillomatosis. Our patient received primary therapy for RRP, which was surgical removal of papilloma that was causing infectious complications. However, once malignant transformation to squamous cell carcinoma was diagnosed in the surgical specimen, adjuvant therapy for RRP would have been inappropriate, and the focus was therefore shifted toward treatment of squamous cell carcinoma. v Disclosure Statement The author(s) have no conflicts of interest to disclose. Acknowledgment The authors would like to thank the Kaiser Permanente Los Angeles Medical Center Department of Pulmonary and Critical Care for supporting its resident and fellow writing this case report. Kathleen Louden, ELS, of Louden Health Communications provided editorial assistance. References 1. Derkay CS, Wiatrak B. Recurrent respiratory papillomatosis: a review. Laryngoscope 2008 Jul;118(7):1236-47. DOI: http://dx.doi. org/10.1097/MLG.0b013e31816a7135. 2. Kashima HK, Shah F, Lyles A, et al. A comparison of risk factors in juvenile-onset and adultonset recurrent respiratory papillomatosis. Laryngoscope 1992 Jan;102(1):9-13. DOI: http:// dx.doi.org/10.1288/00005537-199201000-00002. 3. Ruiz R, Achlatis S, Verma A, et al. Risk factors for adult-onset recurrent respiratory papillomatosis. Laryngoscope 2014 Oct;124(10):2338-44. DOI: http://dx.doi.org/10.1002/lary.24730. 4. Taliercio S, Cespedes M, Born H, et al. Adultonset recurrent respiratory papillomatosis: a review of disease pathogenesis and implications for patient counseling. JAMA Otolaryngol Head Neck Surg 2015 Jan 1;141(1):78-83. DOI: http:// dx.doi.org/10.1001/jamaoto.2014.2826. 5. Andrus JG, Shapshay SM. Contemporary management of laryngeal papilloma in adults and children. Otolaryngol Clin North Am 2006 Feb;39(1):135-58. DOI: http://dx.doi. org/10.1016/j.otc.2005.10.009. 6. Chadha NK, James AL. Antiviral agents for the treatment of recurrent respiratory papillomatosis: a systemic review of the English-language literature. Otolaryngol Head Neck Surg 2007 Jun;136(6):863-9. DOI: http://dx.doi.org/10.1016/j. otohns.2006.09.007. 7. Zeitels SM, Barbu AM, Landau-Zemer T, et al. Local injection of bevacizumab (Avastin) and angiolytic KTP laser treatment of recurrent respiratory papillomatosis of the vocal cords: a prospective study. Ann Otol Rhinol Laryngol 2011 Oct;120(10):627-34. 8. Best SR, Friedman AD, Landau-Zemer T, et al. Safety and dosing of bevacizumab (avastin) for the treatment of recurrent respiratory papillomatosis. Ann Otol Rhinol Laryngol 2012 Sep;121(9):587-93. DOI: http://dx.doi. org/10.1177/000348941212100905. 9. Hočevar-Boltežar I, Matičič M, Sereg-Bahar M, et al. Human papilloma virus vaccination in patients with an aggressive course of recurrent respiratory papillomatosis. Eur Arch Otorhinolaryngol 2014 Dec;271(12):3255-62. DOI: http://dx.doi.org/10.1007/s00405-014-3143-y. 10. Martina D, Kurniawan A, Pitoyo CW. Pulmonary papillomatosis: a rare case of recurrent respiratory papillomatosis presenting with multiple nodular and cavitary lesions. Acta Med Indones 2014 Jul:46(3):238-43. 11. Azadarmaki R, Lango MN. Malignant transformation of respiratory papillomatosis in a solid-organ transplant patient: case report and literature review. Ann Otol Rhinol Laryngol 2013 Jul;122(7):457-60. 12. Hasegawa Y, Sato N, Niikawa H, et al. Lung squamous cell carcinoma arising in a patient with adult-onset recurrent respiratory papillomatosis. Jpn J Clin Oncol 2013 Jan;43(1):78-82. DOI: http://dx.doi.org/10.1093/jjco/hys179. 13. Lin HW, Richmon JD, Emerick KS, et al. Malignant transformation of a highly aggressive human papillomavirus type 11-associated recurrent respiratory papillomatosis. Am J Otolaryngol 2010 Jul-Aug;31(4):291-6. DOI: http://dx.doi.org/10.1016/j.amjoto.2009.02.019. e127 Physicians may earn up to 1 AMA PRA Category 1 CreditTM per article for reading and analyzing the designated CME articles published in each edition of TPJ. Each edition has four articles available for review. Other clinicians for whom CME is acceptable in meeting educational requirements may report up to four hours of participation. The CME evaluation form may be completed online or via mobile Web at www.tpjcme.org. The Certification of Credit form will be e-mailed immediately upon successful completion. Alternatively, this paper form may be completed and returned via fax or mail to the address listed below. All Sections must be completed to receive credit. Certification of Credit will be mailed within two months of receipt of the paper form. Completed forms will be accepted until November 2016. To earn CME for reading each article designated for AMA PRA Category 1 Credit, you must: • Score at least 50% in the posttest • Complete the evaluation and provide your contact information This form is also available online: www.thepermanentejournal.org Summer 2015 CME Evaluation Program Section A. Article 1. (page 21) “Getting off the Bus Closer to Your Destination”: Patients’ Views about Pharmacogenetic Testing Article 3. (page 54) Relationship between Participation in Patient- and Family-Centered Care Training and Communication Adaptability among Medical Students: Changing Hearts, Changing Minds Which of the following was not a main finding of this article? a.participants saw the potential value of pharmacogenetic testing but expressed concerns about privacy and discrimination based on genetic information b.participants worried that physicians might overvalue pharmacogenetic test results and dismiss patients’ reports about how a medication is working c. participants did not believe that pharmacogenetic testing should be implemented d.participants wanted to know whether the results of pharmacogenetic testing could be used for purposes other than guiding prescribing decisions According to this study, Families as Faculty education: a.increases medical students’ awareness of best practices for clinical communication techniques b.improves medical students’ awareness of how much information about themselves is necessary for meaningful communication exchanges with patients c. increases anxiety in patients d.compromises HIPAA standards Which of the following did participants not identify as potential risks of pharmacogenetic testing? a.employment discrimination b.breach of confidentiality c. inability to obtain disability or long-term care insurance d.misuse of genetic information by law enforcement e.cloning Article 2. (page 29) A Community-Based Hip Fracture Registry: Population, Methods, and Outcomes What are the most common surgical procedures used to treat fractures of the femoral neck subtrochanteric region? a.internal fixation and hemiarthroplasty b.total hip arthroplasty and hemiarthroplasty c. hip resurfacing and internal fixation d.internal fixation and total hip arthroplasty The Hip Fracture Registry monitors primary hip fractures treated surgically and subsequent revisions for what period of time? a.for 1 year b.for 2 years after surgery c. for 5 years after surgery d.for the patient’s lifetime The author of this study uses a theoretical foundation that supposes: a.patients need to be protected from information b.successful communication between cultures depends on deep understanding of other cultures c. patients and physicians do not represent different cultures d.communication adaptability is comprised of factors that include social composure, wit, appropriate disclosure, articulation, social experience, and social confirmation Article 4. (page 64) 2014 Hypertension Guideline: Recommendation for a Change in Goal Systolic Blood Pressure Strong supportive evidence for the 8th Joint National Committee recommendation favoring goal systolic blood pressure < 150 mmHg in the general elderly population beginning at age 60, exclusive of patients with chronic kidney disease and diabetes, comes from which 2 trials? a.Systolic Hypertension in the Elderly Program (SHEP) and Systolic Hypertension in Europe (Syst-Eur) b.HYpertension in the Very Elderly Trial (HYVET) and Systolic Hypertension in Europe (Syst-Eur) c. JApanese Trial to Assess Optimal Systolic Blood Pressure (JATOS) and HYpertension in the Very Elderly Trial (HYVET) d.Systolic Hypertension in the Elderly Program (SHEP) and Valsartan in Elderly Isolated Hypertension Study (VALISH) In confirmatory hypertension treatment trials supportive of goal systolic blood pressure < 150 mmHg in the general elderly beginning at age 60, exclusive of patients with chronic kidney disease and diabetes, which of the following highly significant endpoint reductions occurred? a.stroke was reduced by 25% to 30% and major cardiovascular events were reduced by 20% b.stroke was reduced by 15% to 20% and major cardiovascular events were reduced by 30% c. stroke was reduced by 35% to 40% and major cardiovascular events were reduced by 30% d.stroke was reduced by 20% to 25% and major cardiovascular events were reduced by 25% Section C. Section B. Referring to the CME articles, how likely is it that you will implement this learning to improve your practice within the next 3 months? Objective 1 Objective 2 Objective 3 What other changes, if any, do you plan to make in your practice as a result of reading these articles? Integrate learned knowledge and increase competence/ confidence to support improvement and change in specific practices, behaviors, and performance. Lead in further developing “PatientCentered Care” activities by acquiring new skills and methods to overcome barriers, improve physician/patient relationships, better identify diagnosis and treatment of clinical conditions, as well as, efficiently stratify health needs of varying patient populations. Implement changes and apply updates in services and practice/policy guidelines, incorporate systems and quality improvements, and effectively utilize evidencebased medicine to produce better patient outcomes. ______________________________________________________ Article 1 210 543 5 4 3 2 1 0 5 4 3 2 1 0 Name _____________________________________________ Article 2 210 543 5 4 3 2 1 0 5 4 3 2 1 0 Article 3 210 543 5 4 3 2 1 0 5 4 3 2 1 0 Article 4 210 543 5 4 3 2 1 0 5 4 3 2 1 0 Key 5 = highly likely 4 = likely 3 = unsure 2 = unlikely 1 = highly unlikely 0 = I already did this ______________________________________________________ ______________________________________________________ Section D. (Please print) Physician Non-Physician Title _____________________________________________ E-mail _____________________________________________ Address _____________________________________________ The Kaiser Permanente National CME Program is accredited by the Accreditation Council for Continuing Medical Education (ACCME) to provide continuing medical education for physicians. The Kaiser Permanente National CME Program designates this journal-based CME activity for 4 AMA PRA Category 1 Credits™. Physicians should claim only the credit commensurate with the extent of their participation in the activity. 96 Mail or fax completed form to: The Permanente Journal 500 NE Multnomah St, Suite 100 Portland, Oregon 97232 Phone: 503-813-3286 Fax: 503-813-2348 _____________________________________________ Signature _____________________________________________ Date _____________________________________________ The Permanente Journal/ Summer 2015/ Volume 19 No. 3 BOOKS PUBLISHED BY PERMANENTE AUTHORS: Summer 2015/ Volume 19 No. 3 PermanenteJournal The Mission: The Permanente Journal advances knowledge in scientific research, clinical medicine, and innovative health care delivery. Circulation: 25,000 print readers per quarter, 6900 eTOC readers, and in 2014, TPJ content had 1 million page views—760,000 of those on TPJ articles on PubMed. Viewers visited from 187 countries/territories. ON THE COVER: Rocky Perspective by David L Shenson, MD This photograph was taken at Ruby Beach, on the Olympic Peninsula in Washington. The contrast in depth of field creates an interesting perspective of these stones ground smooth by the elements and the passage of time. Dr Shenson is an Internist at the Mt Scott Medical Office in Clackamas, OR. More of his photography may be viewed at: www.davidshenson.com. ORIGINAL RESEARCH & CONTRIBUTIONS 4 Characteristics of Newly Enrolled Members of an Integrated Delivery System after the Affordable Care Act. Elizabeth A Bayliss, MD, MSPH; Jennifer L Ellis, MSPH; Mary Jo Strobel, RN, MBA; Deanna B McQuillan, MA; Irena B Petsche, PhD; Jennifer C Barrow, MSPH; Arne Beck, PhD Of 89,289 newly enrolled non-Medicare members, 25.3% completed the Brief Health Questionnaire between 1/1/2014, and 8/31/2014. Of these, 3593 respondents were insured through Medicaid, 9434 through the individual health exchange, and 9521 through primarily commercial plans. Of Medicaid, exchange, and commercial members, 19.5%, 7.1%, and 5.3%, respectively, self-reported fair or poor health; 12.9%, 2.0%, and 3.3% of each group self-reported 2 or more Emergency Department visits during the previous year; and 8.1%, 4.3%, and 4.4% self-reported an inpatient admission during the previous year. 11 A Metrics Taxonomy and Reporting Strategy for Rule-Based Alerts. Michael Krall, MD, MS; Alexander Gerace An action-oriented alerts taxonomy according to structure, actions, and implicit intended process outcomes using a set of 333 rule-based alerts at Kaiser Permanente Northwest (KPNW) was developed. The authors identified 9 major and 17 overall classes of alerts and developed a specific metric approach for 5 of these classes, including the 3 most numerous ones in KPNW, accounting for 224 (67%) of the alerts. 21 “Getting off the Bus Closer to Your Destination”: Patients’ Views about Pharmacogenetic Testing. Susan Brown Trinidad, MA; Tara B Coffin, MEd; Stephanie M Fullerton, DPhil; James Ralston, MD, MPH; Gail P Jarvik, MD, PhD; Eric B Larson, MD, MPH 96 CME EVALUATION FORM The Permanente Journal 500 NE Multnomah St, Suite 100 Portland, Oregon 97232 www.thepermanentejournal.org The authors conducted focus groups with patients prescribed antidepressants (pilot session plus 2 focus groups, n = 27); patients prescribed carbamazepine (2 focus groups, n = 17); and healthy patients (2 focus groups, n = 17). Although participants understood the potential advantages of pharmacogenetic testing, many felt that the risks (discrimination, stigmatization, physician overreliance on genomic results, and denial of certain medications) may outweigh the benefits. These concerns were shared across groups but were more strongly expressed among participants with chronic mental health diagnoses. 29 A Community-Based Hip Fracture Registry: Population, Methods, and Outcomes. Maria C S Inacio, PhD; Jennifer M Weiss, MD; Alex Miric, MD; Jessica J Hunt, MA; Gary L Zohman, MD; Elizabeth W Paxton, MA Cases of hip fracture recorded from 1/2009 to 12/2011 were ascertained using the Kaiser Permanente Hip Fracture Registry. The registry collects information on patient, procedure, surgeon, facility, and surgical outcomes. The population (N = 12,562) was predominantly white, women, and older (≥ 75 years), and 32% had at least 5 comorbidities. The average length of follow-up was 1.1 years. Hemiarthroplasty was the most common procedure (33.1%). Most fractures were treated by medium-volume surgeons at high-volume facilities. The 90-day readmission rate was 22.1%, and the mortality rate was 12.3%. 37 Utility of the Multinational Association for Supportive Care in Cancer (MASCC) Risk Index Score as a Criterion for Nonadmission in Febrile Neutropenic Patients with Solid Tumors. Roger A Bitar, MD, MPH Febrile neutropenic episodes in patients with solid tumors were identified electronically from 10/1/2008 to 11/15/2010. Inclusion criteria were met in 198 episodes. Sensitivity, specificity, and positive and negative predictive values of the MASCC risk index score vs complications were, respectively, 94%, 29.6%, 57.7%, and 82.9%. An MASCC risk index score of 21 or greater could not be used as a criterion for “no complication/ do not admit.” Inability to eat should be an admission criterion. 48 Evidence-Based Referral: Effects of the Revised “Youth Fit 4 Life” Protocol on Physical Activity Outputs: A Randomized Controlled Trial. James J Annesi, PhD, FAAHB, FTOS, FAPA; Linda L Vaughn, MS, MBA The authors contrasted 2 physical activity/ nutrition treatments on the basis of social cognitive and self-efficacy theory, and a comparison condition, on time in moderateto-vigorous physical activity (MVPA) during the 45-min/day physical activity segment of elementary after-school care. The Revised Youth Fit 4 Life protocol that sought to maximize participants’ cardiovascular physical activity appeared to improve upon the Original Youth Fit For Life treatment on time in MVPA. Thus, pediatricians might have confidence in referring their patients to such evidence-based approaches. Instant Work-Ups: A Clinical Guide to Obstetric and Gynecologic Care Theodore X O’Connell, Kathleen Dor ISBN-10: 1416054618 ISBN-13: 978-1416054610 Philadelphia, PA; Saunders: 2008 Paperback: 268 pages $31.95 Glimpses in Time Nicholas Morell ISBN-10: 1483690202 ISBN-13: 978-1483690209 Bloomington, IN: Xlibris; 2013 Paperback: 228 pages $19.99 If you are a Permanente author and would like your book cited here, send an e-mail to [email protected]. NOW AVAILABLE! The new Web mobile CME application from The Permanente Journal. - Read articles. - Take quizzes. - Earn credit. - Get your CME certificate immediately. www.tpjcme.org ISSN 1552-5767 Follow @PermanenteJ The Permanente Journal/ Summer 2015/ Volume 19 No. 3 For information and/or rates for placing an announcement here, please contact [email protected].