What Each Registry Collects

Hospital Registries

The ACTION Registry collects:

  • STEMI and NSTEMI patient demographics
  • Provider and facility characteristics
  • Adverse event rates
  • AMI performance measures and selected quality measures and outcomes
  • All other test measures, including medication dosing errors and risk-adjusted metrics*
  • Transfer facility therapies and reperfusion strategies*
  • Compliance with ACC/AHA clinical guideline recommendations*
  • Data needed to qualify registry performance achievement award recognition*

*Features available to Premier level participants.

Download the ACTION Registry Premier Data Collection Form
Download the ACTION Registry Limited Data Collection Form
Download the ACTION Registry Data Coder's Dictionary

The AFib Ablation Registry collects:

  • Patient demographics for atrial fibrillation ablation procedures
  • Procedure prevalence and acute management approaches
  • Provider and facility characteristics
  • History/risk factors
  • Device utilization and adverse event rates
  • Data will support the development of evidence-based guidelines for atrial fibrillation treatments

Download the AFib Ablation Registry Data Collection Form
Download the AFib Ablation Registry Data Coder's Dictionary

The CathPCI Registry collects:

  • Patient demographics for cardiac catheterization and PCI procedures
  • Provider and facility characteristics
  • History/risk factors, cardiac status, treated lesions
  • Intracoronary device utilization and adverse event rates
  • Appropriate use criteria for coronary revascularization
  • Compliance with ACC/AHA clinical guideline recommendations

Download the CathPCI Registry Data Collection Form
Download the CathPCI Registry Data Coder's Dictionary

The ICD Registry collects:

  • Demographics for implantable cardiac defibrillator patients
  • Provider and facility characteristics
  • Device type and characteristics for ICD implantation
  • Atrial, ventricular, defibrillator and left-heart lead data
  • Adverse event rates
  • Compliance with ACC/AHA/HRS clinical guideline recommendations
  • Data necessary for meeting the Centers for Medicare and Medicaid Services requirements for hospitals that perform ICD implantation procedures

Download the ICD Registry Generator & Leads Data Collection Form
Download Version 2.2 (For patient discharges starting April 1, 2016)

Download the ICD Registry Leads Only Data Collection Form
Download Version 2.2 (For patient discharges starting April 1, 2016)

Download the ICD Registry Coder's Data Dictionary
Download Version 2.2 (For patient discharges starting April 1, 2016)

Download the Version 2.1 ICD Registry Generator & Leads Data Collection Form (Data submission for this version retires September 30, 2016)
Download Version 2.1 (For patient discharges prior to April 1, 2016)‚Äč

The IMPACT Registry collects:

  • Demographics for all pediatric and adult congenital heart disease patients undergoing diagnostic catheterizations and catheter-based interventions
  • Provider and facility characteristics
  • Data for diagnostic catheterization procedures and six defined interventional procedures
  • Adverse events rates
  • Data necessary to participate in the American Board of Pediatrics MOC Part IV Credit self-directed performance improvement program Reducing Radiation Risk
  • EP ablation
  • Transcatheter pulmonary valve replacement

Download the IMPACT Registry Data Collection Form
Download Version 2.0.1

Download the IMPACT Coder's Data Dictionary
Download Version 2.0.1

The LAAO Registry collects:

  • Patient demographics for left atrial appendage (LAA) occlusion procedures
  • Procedure prevalence and acute management approaches
  • Provider and facility characteristics
  • History/risk factors
  • Adverse event rates
  • Data necessary for meeting the Centers for Medicare and Medicaid Services requirements for hospitals that perform percutaneous left atrial appendage closure procedures

Download the LAAO Registry Data Collection Form
Download the LAAO Registry Coder's Dictionary
Download the LAAO Registry FAQ Document

The PVI Registry collects:

  • Patient demographics for lower extremity peripheral vascular interventions, carotid artery stenting and carotid endarterectomy procedures
  • Provider and facility characteristics
  • Comparisons for high-risk surgical patients treated with CAS versus surgical intervention
  • The use of balloons, stents and embolic protection devices
  • A comprehensive list of CAS, CEA and lower extremity procedure outcome metrics
  • Adverse event rates
  • Data necessary for meeting the 2005 Centers for Medicare and Medicaid Services reporting requirements for patients receiving carotid artery stenting procedures

Download the PVI Registry CAS and CEA Data Collection Form
Download the PVI Registry Lower Extremity Data Collection Form
Download the PVI Registry Data Coder’s Dictionary

STS/ACC TVT Registry

  • Visit tvtregistry.org for details about data collection and links to data collection forms.

Outpatient Registries

Diabetes Collaborative Registry

The PINNACLE Registry collects and provides:

  • Data on coronary artery disease, hypertension, heart failure, diabetes and atrial fibrillation
  • Practice, provider, and patient characteristics
  • Program Metrics endorsed by the ACC, AHA and the Physician Consortium for Performance Improvement (PCPI)

Download the PINNACLE Registry Data Collection Form 
Download the PINNACLE Registry Data Dictionary