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Cardiovascular care facts: a report from the national cardiovascular data registry: 2011.

Publication ,  Journal Article
Masoudi, FA; Ponirakis, A; Yeh, RW; Maddox, TM; Beachy, J; Casale, PN; Curtis, JP; De Lemos, J; Fonarow, G; Heidenreich, P; Koutras, C; Wei, J ...
Published in: J Am Coll Cardiol
November 19, 2013

OBJECTIVES: The aim of this report was to characterize the patients, participating centers, and measures of quality of care and outcomes for 5 NCDR (National Cardiovascular Data Registry) programs: 1) ACTION (Acute Coronary Treatment and Intervention Outcomes Network) Registry-GWTG (Get With The Guidelines) for acute coronary syndromes; 2) CathPCI Registry for coronary angiography and percutaneous coronary intervention; 3) CARE (Carotid Artery Revascularization and Endarterectomy) Registry for carotid revascularization; 4) ICD Registry for implantable cardioverter defibrillators; and the 5) PINNACLE (Practice INNovation And CLinical Excellence) Registry for outpatients with cardiovascular disease (CVD). BACKGROUND: CVD is a leading cause of death and disability in the United States. The quality of care for patients with CVD is suboptimal. National registry programs, such as NCDR, permit assessments of the quality of care and outcomes for broad populations of patients with CVD. METHODS: For the year 2011, we assessed for each of the 5 NCDR programs: 1) demographic and clinical characteristics of enrolled patients; 2) key characteristics of participating centers; 3) measures of processes of care; and 4) patient outcomes. For selected variables, we assessed trends over time. RESULTS: In 2011 ACTION Registry-GWTG enrolled 119,967 patients in 567 hospitals; CathPCI enrolled 632,557 patients in 1,337 hospitals; CARE enrolled 4,934 patients in 130 hospitals; ICD enrolled 139,991 patients in 1,435 hospitals; and PINNACLE enrolled 249,198 patients (1,436,328 individual encounters) in 74 practices (1,222 individual providers). Data on performance metrics and outcomes, in some cases risk-adjusted with validated NCDR models, are presented. CONCLUSIONS: The NCDR provides a unique opportunity to understand the characteristics of large populations of patients with CVD, the centers that provide their care, quality of care provided, and important patient outcomes.

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Published In

J Am Coll Cardiol

DOI

EISSN

1558-3597

Publication Date

November 19, 2013

Volume

62

Issue

21

Start / End Page

1931 / 1947

Location

United States

Related Subject Headings

  • United States
  • Risk Factors
  • Registries
  • Percutaneous Coronary Intervention
  • Humans
  • Guideline Adherence
  • Cardiovascular System & Hematology
  • Cardiovascular Diseases
  • 3201 Cardiovascular medicine and haematology
  • 1117 Public Health and Health Services
 

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Masoudi, F. A., Ponirakis, A., Yeh, R. W., Maddox, T. M., Beachy, J., Casale, P. N., … Rumsfeld, J. S. (2013). Cardiovascular care facts: a report from the national cardiovascular data registry: 2011. J Am Coll Cardiol, 62(21), 1931–1947. https://doi.org/10.1016/j.jacc.2013.05.099
Masoudi, Frederick A., Angelo Ponirakis, Robert W. Yeh, Thomas M. Maddox, Jim Beachy, Paul N. Casale, Jeptha P. Curtis, et al. “Cardiovascular care facts: a report from the national cardiovascular data registry: 2011.J Am Coll Cardiol 62, no. 21 (November 19, 2013): 1931–47. https://doi.org/10.1016/j.jacc.2013.05.099.
Masoudi FA, Ponirakis A, Yeh RW, Maddox TM, Beachy J, Casale PN, et al. Cardiovascular care facts: a report from the national cardiovascular data registry: 2011. J Am Coll Cardiol. 2013 Nov 19;62(21):1931–47.
Masoudi, Frederick A., et al. “Cardiovascular care facts: a report from the national cardiovascular data registry: 2011.J Am Coll Cardiol, vol. 62, no. 21, Nov. 2013, pp. 1931–47. Pubmed, doi:10.1016/j.jacc.2013.05.099.
Masoudi FA, Ponirakis A, Yeh RW, Maddox TM, Beachy J, Casale PN, Curtis JP, De Lemos J, Fonarow G, Heidenreich P, Koutras C, Kremers M, Messenger J, Moussa I, Oetgen WJ, Roe MT, Rosenfield K, Shields TP, Spertus JA, Wei J, White C, Young CH, Rumsfeld JS. Cardiovascular care facts: a report from the national cardiovascular data registry: 2011. J Am Coll Cardiol. 2013 Nov 19;62(21):1931–1947.
Journal cover image

Published In

J Am Coll Cardiol

DOI

EISSN

1558-3597

Publication Date

November 19, 2013

Volume

62

Issue

21

Start / End Page

1931 / 1947

Location

United States

Related Subject Headings

  • United States
  • Risk Factors
  • Registries
  • Percutaneous Coronary Intervention
  • Humans
  • Guideline Adherence
  • Cardiovascular System & Hematology
  • Cardiovascular Diseases
  • 3201 Cardiovascular medicine and haematology
  • 1117 Public Health and Health Services