Validation of the Academic Research Consortium High Bleeding Risk Definition in Contemporary PCI Patients

Davide Cao1, Roxana Mehran2, George Dangas2

  • 1The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, New York; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.

Insights

The Academic Research Consortium (ARC) high bleeding risk (HBR) definition accurately identifies patients undergoing percutaneous coronary intervention at increased risk for bleeding and mortality. Multiple HBR criteria indicate additive prognostic value.

Area of Science:

  • Cardiology
  • Interventional Cardiology
  • Clinical Risk Stratification

Background:

  • Bleeding after percutaneous coronary intervention (PCI) significantly impacts patient prognosis.
  • The Academic Research Consortium (ARC) developed clinical criteria to identify patients at high bleeding risk (HBR).

Purpose of the Study:

  • To validate the ARC-HBR definition in a contemporary, real-world patient cohort undergoing coronary stenting.
  • To assess the prognostic implications of the ARC-HBR definition beyond bleeding events.

Main Methods:

  • A cohort of 9,623 patients undergoing coronary stenting (2014-2017) was analyzed.
  • Patients were classified as HBR based on ARC criteria (≥1 major or ≥2 minor).
  • Primary endpoint: composite bleeding at 1 year; secondary endpoints: myocardial infarction, all-cause mortality.

Main Results:

  • 44.4% of patients met HBR criteria; anemia and age ≥75 were most common.
  • HBR patients had significantly higher 1-year bleeding rates (9.1% vs. 3.2%) compared to non-HBR.
  • A stepwise increase in bleeding risk was observed with more fulfilled HBR criteria; HBR also linked to higher mortality.

Conclusions:

  • The ARC-HBR definition is validated in a contemporary PCI cohort.
  • ARC-HBR identifies patients at elevated risk for bleeding, thrombotic events, and mortality.
  • Multiple HBR criteria demonstrate additive prognostic value for adverse outcomes.
Abstract

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