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The Promise of Clinical Data Registries: Using Data to Improve Patient Health Outcomes. Tuesday, SEPTEMBER 9, 2014 12:30 pm - 2:00pm Eastern. Agenda. Welcome and Introductions Registries: brief overview C-P Alliance’s criteria for registries Speaker Presentations FEEDBACK FROM CMS
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The Promise of Clinical Data Registries: Using Data to Improve Patient Health Outcomes Tuesday, SEPTEMBER 9, 2014 12:30 pm - 2:00pm Eastern
Agenda Welcome and Introductions Registries: brief overview C-P Alliance’s criteria for registries Speaker Presentations FEEDBACK FROM CMS PARTICIPANT DISCUSSION
Definition of a Patient Registry The Agency for Healthcare Research and Quality (AHRQ) defines patient registries as a collection of uniform data (clinical and other) used to evaluate outcomes in specific populations for scientific, clinical or policy purposes. Registries for Evaluating Patient Outcomes: A User's Guide
Overview of Patient Registries Defining Characteristics of a “Patient Registry” Types of Patient Registries • Multiple purposes • Varying levels of sophistication
Guiding Principles C-P Alliance criteria in four areas: • Performance measures • Data quality and interoperability • Accountability • Quality improvement
Webinar Objectives We designed this webinar to help consumer, labor, and employer advocates understand: • What defines a clinical quality data registry; • How registries can be used to improve quality and benchmark performance; • How registries can be used to support accountability and meaningful information for consumers; • Key challenges and opportunities.
Speakers • Dr. Elliott Main, Medical Director of the California Maternal Quality Care Collaborative (CMQCC) • Dr. William Rich, Medical Director of Health Policy for the American Academy of Ophthalmology (AAO) • Chris Queram, President and Chief Executive Officer of the Wisconsin Collaborative for Healthcare Quality (WCHQ) • Dr. Daniel Green, Medical Officer at Office of Clinical Standards and Quality at the Center for Medicare and Medicaid Services (CMS)
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