CHA2 DS2 -VASc impact on risk following percutaneous coronary intervention in atrial fibrillation

Thomas Jensen1, Pernille Gro Thrane1, Kevin Kris Warnakula Olesen1

  • 1Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark.

Insights

The CHA₂DS₂-VASc score increased oral anticoagulation use in atrial fibrillation (AF) patients undergoing PCI. This led to reduced major adverse cardiac events without increasing bleeding risk.

Area of Science:

  • Cardiology
  • Clinical Practice Guidelines
  • Pharmacology

Background:

  • The CHA₂DS₂-VASc score was introduced in 2010 European guidelines to guide oral anticoagulation in atrial fibrillation (AF).
  • Triple therapy (oral anticoagulation + dual antiplatelet therapy) is used in AF patients undergoing percutaneous coronary intervention (PCI) to mitigate ischemic risk.

Purpose of the Study:

  • To evaluate the impact of the CHA₂DS₂-VASc score on oral anticoagulation use in AF patients undergoing PCI.
  • To assess the association between CHA₂DS₂-VASc score implementation and the risks of ischemic events and hospitalized bleeding.

Main Methods:

  • A cohort of 6,014 patients with AF undergoing first-time PCI in Denmark (2003-2017) was analyzed.
  • Patients were grouped by PCI year to assess trends in oral anticoagulation use and risks of major adverse cardiac events (MACE) and bleeding hospitalizations.

Main Results:

  • Oral anticoagulation use increased from 48-49% (2003-2010) to 59% (2011-2014) and 77% (2015-2017) after CHA₂DS₂-VASc score implementation.
  • Major adverse cardiac events (MACE) risk decreased by 23% in 2015-2017 compared to 2003-2006.
  • Hospitalizations for bleeding did not increase despite wider adoption of triple therapy.

Conclusions:

  • The CHA₂DS₂-VASc score's implementation correlated with increased oral anticoagulation and triple therapy use in AF patients undergoing PCI.
  • These treatment changes were linked to a progressive reduction in MACE risk.
  • The risk of hospitalized bleeding remained stable, indicating a favorable risk-benefit profile.
Abstract

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