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Preventive Health Partnership Our organizations came together in 2004 to: – Harness the individual strengths of each to collectively engage the issue of prevention – Create consistent prevention and screening guidelines – Reach widest constituency to increase awareness and inspire action – Further collective goals through joint initiatives Prevalence of Chronic Diseases • 81 million American adults have one or more types of cardiovascular disease1 • As many as 1 in 3 American adults will have diagnosed diabetes in 2050 if present trends continue2 • Approximately 1/3 of cancer deaths are related to overweight or obesity, physical inactivity and poor nutrition, and nearly 1/3 are caused by tobacco use; more than 2/3 of cancer deaths are potentially preventable3 • Improved screening and counseling can result in prevention, treatment and early detection 1 Heart Disease and Stroke Statistics 2010 2 http://www.pophealthmetrics.com/content/8/1/29 3 ACS Cancer Facts and Figures 2010 Framework for Collaboration Focus on four things that can help prevent cancer, diabetes, heart disease and stroke: • Be physically active • Eat well (maintain a healthy weight) • Don’t smoke • See your health care provider regularly The Tri-Agency Relationship What is The Guideline Advantage? Program Advantages – A joint program of the American Cancer Society, the American Diabetes Association, and the American Heart Association – Each organization has long developed scientific statements and guidelines specific to prevention and disease management – Shared goals: – Sets national goals and objectives that compliment their guidelines – Common interest in translating those guidelines into practice Multiple participation models Expanded feedback for quality improvement Reaching a broad range of patients Research and Recognition opportunities Online improvement tools Working with existing technology Vision & Goal Vision Goal To improve the health of all patients through widespread application of primary and secondary prevention guidelines in the United States through data collection, analysis, feedback and quality improvement in the ambulatory setting. To improve the long-term compliance with the ACS, ADA and AHA/ACC guidelines, which in turn supports our shared organizational mission to prevent chronic diseases and to improve the lives of those living with the nation’s most prevalent chronic diseases. The Guideline Advantage is based on the success of nearly 10 years experience in inpatient quality improvement and over 2 millions lives touched. Program Model 2• Technology vendors submit collective clinical data to DCRI for The Guideline Advantage 3• Data are processed, analyzed and sent back to the providers or medical practices 1• Providers can use several different technology platforms 4• Performance is measured, Professionals can set measureable goals and chart improvements in performance What are the different participation models? There are three main approaches to populating the registry with clinical data: Description Direct Vendor Model Practice Managed Model Zero Configuration Model • The electronic health records (EHR) vendor enables the data to flow by mapping to the data warehouse on behalf of its customers (the practices); • Medical practices that have technical staff on site can map to the warehouse directly; • Medical practices that do not have technical staff on site can submit a “flat file” of data, and DCRI will map those data into the warehouse for the practice. Additional information at: www.guidelineadvantage.org Important Things to Understand 1. Data quality and performance reports are then generated on a quarterly basis to help practices identify where they may have areas for improvement. 2. The Guideline Advantage offers an array of CE/CME opportunities, better practices, tools and resources for health care professionals to consider incorporating into their practices to improve. Technically speaking… how does it work? As a part of quality improvement, clinical data must be aggregated into a data warehouse to facilitate analysis and reporting. DATA WAREHOUSE AND REPORTING ELECTRONIC MEDICAL RECORD Data Staging Area Data import Key activities include: - Cleaning data - Reconciling data - Standardizing data - Transforming data De-identification & Data Extract (data submission process) Report Data Database Feedback Reports Research & Analytics The Guideline Advantage’s Ideal Data Elements (2011) Demographics Risk Factor Mortality Contraindications Medical History Ideal Data Elements Medications Hospitalizations Vital Signs Labs *full list of elements can be found at http://guidelineadvantage.org Mock Report New Data Elements New Measures •Cervical cancer screening •Breast cancer screening •Colon cancer screening •Pneumococcal Vaccine •Influenza Vaccine •Sodium •Dental exam in previous 12 months •Currently Pregnant •Mortality •Cancer Prevention Measures: Cervical Cancer Screening Breast Cancer Screening Colon Cancer Screening •ABCS (Aspirin, Blood Pressure, Cholesterol, Smoking), including those measures used in initiatives like Million Hearts. A: Aspirin or other antithrombotic in IVD B: Screening for high blood pressure B: Controlling High Blood Pressure C: Cholesterol: Fasting LDL and riskstratified LDL C: Complete lipid panel and LDL control in IVD S: Smoking: Tobacco use screening and cessation intervention • Pneumococcal vaccine • Influenza Vaccine The Guideline Advantage Alignment with PQRS The difference in The Guideline Advantage metrics and those reported by PQRS is the code sets used to calculate them. To date the program has faced challenges in receiving all of the codes sets required to calculate PQRS measures (specifically, CPT codes). Efforts to further align with PQRS measures - Continue to ask for CPT codes from all participants (just received our first ones!) - Exploring creation of a limited report focusing on the cardiac prevention measures for QIO’s What specialties are eligible to participate? • Cardiology • OB/GYNs • Family Medicine • Osteopathic Medicine • Geriatric Medicine • Oncology • Internal Medicine • Endocrinology • Neurology Patient Inclusion Criteria ALL Patients 18 and Over How does a provider register? Key Takeaways Additional information at GuidelineAdvantage.org • Register on our website at guidelineadvantage.org to express your interest. • Upon registration, a member of our team will contact you and begin work to identify which data transfer model may be best for your practice. Site Implementation Timeline DCRI Shares Contracts (Participation Agreement and Business Associate Agreement) and Technical Specifications and Implementation Packet with Site (3-5 days following registration) Site Registers online Site Gather Glossary/Fields (1 day) Site Map Coded Fields (3 days) DCRI DCRI Verify/Validate Data Test Data Sample Transfer (5 days) (3 days) Site Site Transfer Data Completes Sample Contracts (2 days) Site Submit Historical Data (3 days) HIPAA HIPAA applies to The Guideline Advantage since Protected Health Information (PHI) is used in the program. The Guideline Advantage is considered Quality Improvement as opposed to a clinical trial/research, so the disclosure of PHI to DCRI, including direct patient identifiers, falls under healthcare operations. Leading practices for effective participation Use existing EHR platform; don’t interrupt work flow to collect data; offer multiple ways for data to flow (from EHR vendor, from intermediary vendor, directly from practice, etc.) Provide tools and resources (Webinars, CME programs, etc.) to help develop a culture of quality improvement Provide feedback reports and consult with practices on how to share information Encourage focus on 1-2 areas only Direct practices to resources to support improvement Recognize and link to incentives These are just a few of the best practices shared by the program.