Transcript Slide 1

CathPCI Registry
10 Years and We Keep Going
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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• Replacement for Outdated Quality Assurance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
Facilities
• 906 participants
• 4.5 million patient records
• Online data entry tool launch 4/07
• Support D2B Alliance
Data Sharing
• States – MA, OH, WV
• Payers – United, BCBSA,
WellPoint
Research and Publications
• DCRI analytic center
• Longitudinal Study – seeking
funding (ACHIEVE)
• Manuscripts
– 19 published
– 2 in press
– 17 in development
• 6 abstracts at ACC ’07
CathPCI Registry Enrollment
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825
800
700
658
600
500
472
400
300
200
272
321
547
362
190
100
0
1999
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2001
2002
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Participants
2005
2006
2007
Where do we go from here…
• Online Date Collection Tool (DCT)
• Version 4.0
• ACHIEVE
Online Data Collection Tool
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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
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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) 257-4737
Monday –Friday, 8:00 am – 5:00 pm ET
E-mail:
[email protected]
Fax:
(202) 375-6843
Mailing address:
2400 N Street NW
Washington, DC 20037