The Global Registry of Acute Coronary Events, 1999 to 2009--GRACE

K A A Fox1, K A Eagle, J M Gore

  • 1Centre for Cardiovascular Science, University of Edinburgh, Chancellor's Building, 49 Little France Crescent, Edinburgh EH16 4SB, UK. k.a.a.fox@ed.ac.uk

Insights

The GRACE registry collected data on over 100,000 acute coronary syndrome (ACS) patients globally to understand patient profiles and outcomes. This led to the development of predictive risk scores for better patient management.

Area of Science:

  • Cardiology
  • Epidemiology
  • Outcomes Research

Background:

  • Acute coronary syndromes (ACS) require comprehensive understanding of patient characteristics and outcomes.
  • Multinational registries are crucial for defining the spectrum of ACS and improving patient care.
  • Predictive risk scores aid in stratifying patients and guiding treatment decisions.

Purpose of the Study:

  • To establish a large, multinational registry of acute coronary syndrome (ACS) patients.
  • To define patient demographics, clinical characteristics, and treatment patterns.
  • To derive predictive risk scores for ACS patient outcomes.

Main Methods:

  • The GRACE (Global Registry of Acute Coronary Events) registry enrolled 102,341 patients from 123 hospitals in 14 countries (GRACE) and 154 hospitals (GRACE2).
  • Data collection occurred between 1999 and 2009 using standardized case report forms, capturing demographic factors, comorbidities, treatments, and in-hospital/6-month events.
  • Prospective individual patient follow-up and site audits ensured data quality, with 85% 6-month follow-up completion.

Main Results:

  • The registry successfully characterized a large and diverse ACS patient population.
  • Data facilitated the development and validation of predictive risk scores for ACS.
  • Performance feedback and benchmark data were provided to participating hospitals.

Conclusions:

  • The GRACE registry provided valuable insights into ACS patient characteristics and outcomes.
  • The derived risk scores are instrumental in clinical decision-making for ACS management.
  • Multinational registries are essential for advancing cardiovascular research and improving global ACS care.

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