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CathPCI Registry

10 Years and We Keep Going

CathPCI Registry

10 Years and We Keep Going

What is the CathPCI Registry™?

• 10 years in Evolution• Benchmarks and Quality Improvement

– Standardized, evidence-based data collection– Quarterly benchmark reports

• Replacement for Outdated Quality Assurance Programs– Supports P4P– Replaces the traditional CON regulations

• Platform for Outcomes Research• Potential Solution of Post-Market Surveillance

Purpose of the CathPCI Registry™

• National surveillance system to assess the characteristics, treatments, and outcomes

• Optimize outcomes and management of coronary disease patients through implementation of evidence-based guidelines recommendations in clinical practice

• Improve quality and safety of coronary disease care and investigate novel quality improvement methods

• Provide risk-adjusted outcomes

Objectives of the CathPCI Registry™

• Provide data standardization • Provide data that is

– Relevant, Credible, Timely, Actionable

• Present real life outcomes that help providers improve care

• Help Participants meet consumer, payer, and regulator demands for quality care

• Provide data that can be tracked at the local QI level and benchmarked nationally

CathPCI Registry™ Audience:

Cardiologists, emergency medicine physicians, hospitalists, primary care physicians, nurses,

physician assistants, nurse practitioners, pharmacists, case managers, allied health care

personnel, hospital quality improvement personnel and administrators, professional organizations, accrediting organizations, regulatory agencies,

payers, pharmaceutical and device industry, and clinical research organizations

Registry/QI• 906 participants• 4.5 million patient records• Online data entry tool

launch 4/07• Support D2B AllianceData Sharing• States – MA, OH, WV• Payers – United, BCBSA,

WellPointResearch and Publications• DCRI analytic center• Longitudinal Study –

seeking funding (ACHIEVE)• Manuscripts

– 19 published– 2 in press– 17 in development

• 6 abstracts at ACC ’07

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CathPCI Registry Enrollment

Participants

Where do we go from here…

• Online Date Collection Tool (DCT)

• Version 4.0

• ACHIEVE

Online Data Collection Tool• Will be similar to CARE, ICD and ACTION DCT• Free with CathPCI participation in 2007• In v3.04 format• No bells and whistles – basic online data

entry• No access to data currently• Data submission will still go through DQR

process • Will follow format of current v3.0 data

collection form• Will be online beginning May 15, 2007

Version 4.0

• Will have similar admission data fields as ACTION Registry™

• New table for diagnostic devices for diagnostic cath

• Fewer Adverse Event data fields• Cleaner definitions• Fewer data fields than v3.04

ACHIEVE

• Follow up on PCI patients• Alive, deceased, repeat procedure• SAQ – Seattle Angina Questionnaire• Total of 50,000 patients

For Additional Information

NCDR

Website: www.ncdr.com

Service Center: (800) 257-4737Monday –Friday, 8:00 am – 5:00 pm ET

E-mail: ncdr@acc.org

Fax: (202) 375-6843

Mailing address: 2400 N Street NWWashington, DC 20037