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Drug Information Journal, Vol. 30, pp. 601-608, 1996 Printed in the USA. All rights reserved. 0092-8615/% Copyright 0 1996 Drug Information Association Inc. NEW YORK CITY PHARMACISTS AND PROSPECTIVE DRUG UTILIZATION REVIEW UNDER OBRA '90 MARTHAM. RUMORE,PHARMD,JD, RAC, FAPHA Associate Professor, Pharmacy Administration, Arnold & Marie Schwartz College of Pharmacy and Health Sciences, Brooklyn, New York STANLEY FEIFER,RPH, MS Associate Professor, Pharmacy Practice and Director, Community Externship Program, Arnold & Marie Schwartz College of Pharmacy and Health Sciences, Brooklyn, New York JOSEPHS. RUMORE,RPH, MS Assistant Director of Pharmacy, Wyckoff Heights Medical Center, Brooklyn, New York New York regulations to implement the Omnibus Budget Reconciliation Act of 1990 (OBRA '90) have been in effect more than one year yet little is known aboutpharmacists' experience with, or effectiveness oJ the prospective drug utilization review (DUR) mandate. A n anonymous questionnaire distributed to 287 New York City pharmacists and interns achieved a 67% (194) response rate. Time, personnel, and expense constraints were the most frequently mentioned implementation problems. A number of pharmacists and interns misinterpreted various prospective DUR requirements of the New York regulation. Some erroneously believe the requirement to review the drug therapy only applies to new prescriptions but not renewals. Others do not believe the pharmacist must ascertain a complete listing of all medications. Half of the respondents indicated their pharmacy has had to hire more personnel or purchase computer software to comply. Interns appeared more optimistic than pharmacists about the future success of OBRA '90. Approximately two thirds of respondents believe the regulations will increase pharmacists' liability. Key Words: OBRA; Pharmacists; New York City; Drug utilization review; Liability INTRODUCTION UNDER OBRA '90 are required to perform prospective drug use review for all Medicaid patients (1). New York regulations became effective on December 4, 1992 and apply to all patients Presented at the American Pharmaceutical Association 141~tAnnual Meeting, March 19-23.1994. Seattle, Washington. Reprint address: Martha M. Rumore, PharmD, JD, RAC, FAPhA, Associate Professor, Pharmacy Administration, Arnold & Marie Schwartz College of Pharmacy and Health Sciences, Brooklyn, NY. (2). Under the New York regulation a review of drug therapy is required before each prescription is filled or delivered to the patient. This review shall include screening for potential drug therapy problems due to therapeutic duplication, drugdrug interactions, including serious interactions with over-the-counter drugs, incorrect drug dosage or duration of treatment, drug-allergy interactions, and clinical abuse or misuse (2). In addition, a patient medication profile and an offer to patients regarding their medicstion Are required. The pharmacist's desknee may obtain the information for the Downloaded from dij.sagepub.com at PENNSYLVANIA STATE UNIV on March 5, 2016 601 Martha M . Rumore. Stanley Fever, and Joseph S . Rumore 602 profile and make the offer to counsel but the actual counseling and prospective DUR must be conducted by the pharmacist: For the counseling and DUR provisions, in New York patient refusals must be documented and kept in a retrievable form for five years (2,3). Several studies have shown that pharmacists are not aware of the requirements that affect them under OBRA '90 and little is known about the attitudes of pharmacists with regard to implementation of the act ( 4 3 ) . This study attempted to identify the ramifications of the prospective DUR requirements and their impact on pharmacy practice in New York City. METHODOLOGY The instrument for this study was a 15item questionnaire (Appendix 1) that was pretested for clarity on 20 pharmacists and graduate students. Based on the pretest several questions were reworded. Multiple choice responses were included in the following major categories: demographic data, law interpretation, and perceptions regarding liability. The target population was New York City-based interns and pharmacists. The sample selected was a convenience rather than a random sample. A letter of transmittal guaranteeing anonymity and a copy of the survey were mailed in Fall 1993 to 100 community or hospital pharmacists. In addition, 200 questionnaires were distributed in fifth year undergraduate and graduate classes. Students were instructed to distribute the survey to a pharmacist for completion or, if a pharmacist was not readily available to them, they were to complete the survey themselves. Only practicing interns or pharmacists were eligible to participate. The results were tabulated and statistically analyzed (6). Chi Square analyses were conducted to determine if the responses differed between pharmacists and interns or because of practice setting. The level of significance was set at p < 0.05. A limitation of the study is that respon- dents, who volunteered to participate, may differ from nonrespondents. The findings, therefore, may not be generalizable to all New York City pharmacists or interns. The authors did not explore information regarding the size of the pharmacy, volume of prescriptions, or number of employees. RESULTS Forty-eight of the mailed and 146 of the classroom distributed surveys were returned to provide 48% and 73% response rates, respectively. Since a number of graduate students were pharmacists and some surveys were given to pharmacists by the students, the number of pharmacist respondents was 95. Demographic details concerning the New York City sample are provided in Table 1. The majority of respondents (69%) indicated 'independent' TABLE 1 Demographic Information Practice Site Pharmacists (n = 95)' Interns (n = 99). 72 11 62 22 14 16 7 Independent Chain Hospital/clinic/ HMO Not specified * 10 respondents indicated multiple practice sites. Pharmacists' Years in Practice ~~ Years n 0-3 4-7 8-1 1 12-15 16-19 20-23 24-27 28-31 32-35 36-39 > 40 15 19 14 12 9 7 6 6 3 3 1 Mean = 13.9 + I - 5.9 Downloaded from dij.sagepub.com at PENNSYLVANIA STATE UNIV on March 5, 2016 Pharmacists and Prospective DUR Under OBRA ’90 as a practice site. There was an approximately equal number of pharmacists and interns (49% vs. 51%). Questions 1-6, 8, 10, and 14 specifically addressed the OBRA ’90counseling requirement and are discussed elsewhere (7). Question 7 sought to identify problemddeficiencies in implementation of the law. Time, personnel, and expense constraints were the most frequently mentioned. Table 2 shows a complete listing of the responses to this question. In question 9 respondents were requested to identify the following statement as true or false, because the law does not only apply to renewal prescriptions: “The pharmacist shall review the drug therapy before each prescription is filled or refilled.” The vast majority (96%) (92/ 96) of pharmacists and interns (89%) (87/ 98) correctly identified the statement as true. Although more pharmacists correctly identified the statement as true, 603 based on Chi Square analysis there was no significant difference in responses between pharmacists and interns (X’ = 3.38; df = 1; p = 0.05). Question 11 requested respondents to indicate whether or not they feel pharmacists are skillful enough in history taking to be able to interview patients. An overwhelming majority of pharmacists (86%) (81/94) and interns (82%) (82/100) indicated that pharmacists possess the needed skills. Based on Chi Square analysis, there was no significant difference in responses between pharmacists and interns ( X 2 = 0.6276; df = 1; p = 0.05). Question 12 asked if the respondent felt that the time, reimbursement, and professional education issues are so great to overcome that OBRA ’90 will never be a reality. The respondents were almost evenly split; 60 agreed that the barriers are too great to overcome and 70 disagreed. There was a significant difference, how- TABLE 2 ProblemslDeficIencles Observed in Implementation of the Law Reason n Time constraints Lack of pharmacist reimbursement Expense constraints Patient indifference Information provided may decrease patient compliance Lack of privacy or space for counseling Lack of pharmacist knowledge No standardization Patient not willing to supply information Conflicts with what physician has told patient Language barriers Patients refuse to wait Patient confusion over what term ‘counseling’ means Redundant Increases patient wait time Inadequate patient profiles Increases paperwork Belligerenthude patients Raises too many nonpeninent questions Not supported by upper management Law not being taken seriously Increased pharmacist liability Other 5 76 18 18 13 13 13 11 10 10 9 9 8 8 6 6 5 Downloaded from dij.sagepub.com at PENNSYLVANIA STATE UNIV on March 5, 2016 5 5 4 4 4 3 20 Martha M. Rumore, Stanley Fever, and Joseph S. Rumore 604 ever, in the opinions of interns and pharmacists. A majority of the interns were optimistic whereas a majority of the bharmacists took the pessimistic view. This difference was statistically significant (x’ = 9.49; df = 1; p < 0.01). Chi Square analysis by practice site revealed no significant effect in response (X2 = 1.28; df = 1; p = 0.05). The second part of this question asked if the pharmacy has had to hire more personnel or purchase computer software to comply. Sixty-eight respondents indicated that they did and 64 respondents did not, indicating that half of respondents have hired more personnel or upgraded computers to comply and half have not. Because of the ambiguity of the question the authors could not split out what was done, either more personnel and/or a computer upgrade. Question 13 tested the respondent’s knowledge of the prospective DUR requirement via the following statement: “In order to fulfill the prospective DUR obligations of the law, the pharmacist (or intern) must interview every patient each time a prescription is dispensed, to ascertain a complete listing of all medications, both prescription and OTC.” Only 68% (63/93) of pharmacists and 71% (71/100) of interns correctly identified the statement as true. Chi Square analysis did not reveal any significant differences in the responses of interns and pharmacists to this question ( X 2 = 0.24; df = 1; p = 0.05). Question 15 asked whether or not the respondent feared that the new law would prompt increased lawsuits. Almost 66% (128/194) of respondents believe that OBRA ’90 will lead to increased lawsuits of pharmacists whereas 32% (63/194) do not. DISCUSSION The results of this survey reveal both positive and negative responses to the prospective DUR requirement by New York City pharmacists. It revealed differences in responses between interns and pharmacists as well as obstacles and misinterpretations regarding the obligations under the law. Interns’ attitudes were much more optimistic with regard to the ability of pharmacists to interview patients and intervene with physicians. Apparently, many pharmacists erroneously believe that only new prescriptions require medication review. As revealed in question 13, only 68% of pharmacists correctly identified the statement as a prospective DUR requirement. Therefore, almost a third of the pharmacists surveyed erroneously believe that they do not need to interview every patient each time a prescription is dispensed to ascertain a complete listing of all medications, both prescription and OTC. For renewals, questioning about any over the counter (OTC) or prescription additions to the profile would appear extremely pertinent. Some respondents, however, probably interpreted question 13 differently than intended. While all pharmacists should know that they must keep a record of all medications taken by their patients, some respondents may have answered ‘false’ to this question because they do not have to ‘interview’ each patient to obtain this information. Therefore, the number of pharmacists who actually understand the requirements was probably understated. Many obstacles to implementation of the law were identified. A study to ascertain pharmacists’ ability to comply with the OBRA ’90 DUR provisions revealed that 82% of the 12,456 pharmacists have a computer system for DUR. The results also showed, however, that the majority of pharmacists ( > 5 5 % ) could not screen for drug-disease contraindications, drugOTC interactions, incorrect drug dosage, duration of treatment, clinical abuse/misuse, or underutilization. Therefore, a majority of the respondents could not screen for six out of nine drug therapy items listed in the prospective DUR requirement (8). Online claims processors in New York City (eg, PAID, PCS) have the capability to perform DUR in seconds and let the Downloaded from dij.sagepub.com at PENNSYLVANIA STATE UNIV on March 5, 2016 Pharmacists and Prospective DUR Under OBRA '90 pharmacist know if there is a potential drug interaction, duplicate therapy, or refill discrepancy (9): Due to inherent limitations in the software that most pharmacies currently use, all the information required for the patient profile will not fit on the pharmacists' comments section of the computer profile. Many of the current pharmacy computer systems allow the recording of only limited information about the patient, suchas a profile of prescriptions dispensed by the pharmacy for the patient. T o carry out prospective DUR, however, the pharmacy will need to maintain and process a detailed patient profile. The Health Care Financing Administration (HCFA) predicts that to meet the statutory requirements for prospective DUR, software could cost anywhere from $1 ,OOO to $2,000 to upgrade, but it doubts that pharmacists will have to completely revamp their hardware to meet the DUR requirement of the act (10). In this study, only half of the respondents have upgraded their software. By implication, therefore, the other half of the respondents either already had such software in place, are using a manual system, or are not complying with the prospective DUR provisions of the act. Lack of reimbursement for cognitive services and time limitations were strongly identified as barriers to implementation. In addition to the one to two dollar HCFA counseling estimate per patient, other costs include establishing a patient profile, calling physicians, and upgrading computers. In one study, hourly prescription volume was negatively correlated to the rate of pharmacist intervention, suggesting that pharmacists' willingness or ability to intervene in problematic prescriptions decreases as the prescription volume increases ( 5 ) . It seems logical that highvolume pharmacies are especially burdened by the OBRA '90 obligations. There were no differences by practice site, however, when respondents were asked if the time, reimbursement, and professional ed- 605 ucation issues were too great to overcome t o make OBRA '90 a reality. Chain pharmacists were not more likely to respond affirmatively to this question. Some pharmacists appear hopeful that the HCFA demonstration projects may help provide a rationale for pharmacist reimbursement. On June 24, 1994 Senator David Pryor (D-Ark.) and Senator Jim Sasser (D-Tenn.) introduced The Pharmaceutical Marketplace Reform Act of 1994 (S.2239) which would require pharmacists to provide DUR under the current Medicare program, as well as under state Medicaid plans. The secretary of Health and Human Services (HHS) would be required to establish a method to pay pharmacists for these services. The bill uses language adopted from OBRA '90 and requires a DUR allowance to reimburse pharmacists ( 1 1). This bill, however, was not enacted into law. Almost two thirds of the respondents indicated the risk for increased liability because of the OBRA '90 requirements. The prospective screening requirement of the act appears to create a duty to warn (12). Although OBRA '90 does not specify what the pharmacist should d o once a problem is identified, the legally expected action is for the pharmacist to try to resolve it if possible (13). The act, therefore, imposes the duty to warn; as there would be no need to require screening for drug therapy problems if the pharmacist does not warn the prescriber or patient (13). Failure to monitor and correct drug underutilization is an emerging source of pharmacist malpractice liability (14). Other potential OBRA '90 liability issues include: confidentiality, duty to counsel, and recordkeeping and maintenance. A pharmacy litigation group has recently been created at the Association of Trial Lawyers of America to assess the changing standards of patient care that have come about because of OBRA '90. Approximately one third of the respondents (and the authors) believe that the act will not lead to increased lawsuits. Al- Downloaded from dij.sagepub.com at PENNSYLVANIA STATE UNIV on March 5, 2016 Martha M. Rumore, Stanley Feger, and Joseph S. Rumore 606 though none of the respondents mentioned it, the regulations may actually decrease liability as failure to counsel had led to liability. Many of the misfilling or wrong directions cases could have been avoided if the pharmacist had counseled the patient. CONCLUSION Some pharmacists and interns in New York City perceive the requirements of OBRA '90 as directives that erode independent professional judgement, mandate uncompensatable services, and lead to increased liability. Others believe that OBRA is going to move pharmacy from a product-oriented practice to a cognitive-oriented practice. It has the potential to restore pharmacists' historical role of providing care directly to the patient. REFERENCES 1. The Omnibus Budget Reconciliation Act of 1990. Pub L. No. 101-508, 104 Stat 1388. 2. Education Law Clarified. N.Y.S. Council of Hospital Pharmacists Newsletter 1992; 11(4):1. 3. New York State enacts rules to implement OBRA. N . Y.S. Council of Hospital Pharmacists Newsletter. 1993; 12(1):1,5. 4. Reutzel TJ, Wilson LA, Mickel M. Inner-city pharmacies: can they meet the OBRA '90 mandates? A m Pharm. 1993;33:44-51. 5 . Anon. Pharmacists report problems caused by OBRA '90. Pharmacy Today. Nov 22, 1991:3-4. 6. Dixon WJ, Massey FJ. Introduction to StatisticalAnalysis. Third ed. New York: McGraw Hill; 1969. 7. Rumore MM, Feifer S, Rumore JS. New York City pharmacists and OBRA '90- One year later. A m Pharm. 1995;35:29-34,66. 8. Nardi KM, Dix Smith M. National Pharmacy Forum on Medicaid Drug Amendments: Pharmacist's survey report. Med Inter. (Aug) 1992: 38-49. 9. Salma R. Confronting the information gap: Pharmacist's emerging hot issues. Pharm Times. 1993;59:37-42. 10. Martin S . What you need to know about OBRA '90. A m Pharm. 1993;33:26-28. 11. Pryor introduces bill to pay pharmacists for counseling. Pharm Today. July 4, 1994,33:1,7. 12. Holleran MJ. The Pharmaceutical Access and Prudent Purchasing Act of 1990: Federal law shifts the duty to warn from the physician to the pharmacist. Res Ipsa Loquitur. 1993;20:4. 13. Brushwood DB. Pharmaco-legal considerations in the clinical use of decongestants. Pharmacother. 1993;13:1355-1428. 14. Vivian JC. The new liability. Drug Topics. Nov 22, 1993:48. APPENDIX I ARNOLD & MARIE SCHWARTZ COLLEGE OF PHARMACY OBRA '90 Survey The Omnibus Budget Reconciliation Act of 1990 (OBRA '90) was signed into law and became effective January 1, 1993. In recognition of the OBRA requirements, N.Y.S. amended section 63.6 of Title 8 NYCRR to clarify standards of practice in pharmacy, require pharmacists to maintain patient medication profiles and offer to counsel patients regarding their medication therapy. These requirements became effective December 4, 1992. Please take a few minutes to complete this research survey based on your experience with the new law. Responses are anonymous and will be used strictly for academic research being conducted jointly by the Departments of Pharmacy Administration and Pharmacy Practice. Thank you in advance for your commitment to excellence in pharmacy. Martha M. Rumore, Pharm.D., J.D., MBA Associate Professor, Pharmacy Administration Downloaded from dij.sagepub.com at PENNSYLVANIA STATE UNIV on March 5, 2016 Pharmacists and Prospective DUR Under OBRA ’90 607 Demographic Info: Pharmacist (# years in practice) Intern ~ ~ Practice Site -Independent -Chain -HospitaVClinic 1. Has the counseling requirement of the law been implemented correctly? Explain. 2. Who makes the offer to counsel more than 50% of the time? __ Pharmacist -Technician __ Intern -Clerk 3. Approximately what percentage of patients choose not to supply information necessary for maintenance of a medication profile or to accept counseling: -All accept counseling -25-50’70 -<lo% 50-75% ~ ~ 10-25% ~ >75% 4. Please list the reason(s) given, if any, for not accepting counseling. 5 . How do you document such refusals in the records of the pharmacy? 6. How long does the typical counseling session take and is there a separate counseling area? 7. What are some of the problems/deficiencies you have observed in implementation of the law? 8. Is there a “wait” for patients to receive counseling once they accept the offer to counsel? 9. Is the following statement true or false: “The pharmacist shall review the drug therapy before each prescription is filled or refilled.” -True -False. The law only applies to new prescriptions. 10. Do you support the inclusion of pharmacy interns in thedefinition of “pharmacist” under the state regulation for the purpose of patient counseling, insofar as the intern’s actions are under the direct supervision of a pharmacist? __ Yes. -No. 1 1 . Do you feel pharmacists are skillful in history taking to be able to interview and effectively counsel pa- tients? __ Yes. ~ No. Downloaded from dij.sagepub.com at PENNSYLVANIA STATE UNIV on March 5, 2016 Martha M . Rumore, Stanley Fever, and Joseph S. Rumore 608 12. Do you think the time, reimbursement and professional education issues are so great to overcome that OBRAPO will never be a reality? Has your pharmacy had to hire more help or buy computer software to i comply? Explain. 13. Is the following statement true or false: "In order to fulfill the prospective DUR obligations of the new law, the pharmacist (or intern) must interview every patient each time a prescription is dispensed, to ascertain a complete listing of all medications, both Rx and OTC." -True -False 14. Which of the following are discussed each time a prescription is dispensed: Always Often Rarely Never Medication name & description ~ ~ ~~ ~ Dosage form, route, duration of therapy Proper storage Special directions & precautions for preparation, administration & use ~ Common severe side effects or interactions including their avoidance & action if they occur Techniques for self-monitoring ~~~ Refill information Actions to be taken in the event of a missed dose 15. Do you fear that the new law will prompt increased lawsuits against pharmacists? -Yes. -No. Thank you on behalf of the Department of Pharmacy Administration. Downloaded from dij.sagepub.com at PENNSYLVANIA STATE UNIV on March 5, 2016