Dual antiplatelet therapy for secondary prevention of coronary artery disease

Sophie Degrauwe1, Thomas Pilgrim2, Adel Aminian3

  • 1Department of Cardiology, Lausanne University Hospital, Lausanne, Switzerland.

Open Heart
|October 31, 2017
PubMed

Insights

Dual antiplatelet therapy (DAPT) reduces cardiovascular events but increases bleeding. Optimal DAPT duration for coronary artery disease (CAD) prevention is uncertain, requiring personalized treatment and further research into shorter or longer regimens.

Area of Science:

  • Cardiology
  • Vascular Medicine
  • Pharmacology

Background:

  • Dual antiplatelet therapy (DAPT) with aspirin and a P2Y12 inhibitor reduces major adverse cardiovascular events (MACE) in acute coronary syndrome (ACS) and percutaneous coronary intervention (PCI) patients.
  • However, DAPT increases major bleeding risk, and its optimal duration for secondary prevention in coronary artery disease (CAD) remains debated due to conflicting trial results.

Purpose of the Study:

  • To review current evidence on DAPT duration for secondary prevention in CAD.
  • To discuss the balance between ischemic event reduction and bleeding risk.
  • To explore future directions and ongoing trials in antiplatelet therapy post-PCI.

Main Methods:

  • Systematic review of large randomized trials on DAPT duration.
  • Analysis of comparative effectiveness of short-term (3-6 months) versus long-term (12-48 months) DAPT.
  • Evaluation of patient-specific factors influencing DAPT regimen choice.

Main Results:

  • Shorter DAPT (3-6 months) in stable CAD post-PCI was non-inferior for MACE and reduced bleeding compared to longer durations.
  • Prolonged DAPT (18-48 months) reduced myocardial infarction and stent thrombosis but increased bleeding and mortality.
  • Current guidelines recommend 12 months for ACS, but shorter durations are under investigation for newer drug-eluting stents.

Conclusions:

  • Optimal DAPT duration requires individualized patient assessment based on clinical presentation, ischemic, and bleeding risk.
  • Further research is needed to identify patient subgroups benefiting from tailored DAPT durations.
  • Emerging research on P2Y12 inhibitors as monotherapy may alter future antiplatelet strategies post-PCI.

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