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Published on: March 15, 2022
Dual antiplatelet therapy for secondary prevention of coronary artery disease
Sophie Degrauwe1, Thomas Pilgrim2, Adel Aminian3
1Department of Cardiology, Lausanne University Hospital, Lausanne, Switzerland.
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.
Abstract:
Dual antiplatelet therapy (DAPT) combining aspirin and a P2Y12 receptor inhibitor has been consistently shown to reduce recurrent major adverse cardiovascular events (MACE) in patients with acute coronary syndrome (ACS) or undergoing percutaneous coronary intervention (PCI) for stable coronary artery disease (CAD) compared with aspirin monotherapy, but at the expense of an increased risk of major bleeding. Nevertheless, the optimal duration of DAPT for secondary prevention of CAD remains uncertain, owing to the conflicting results of several large randomised trials. Among patients with stable CAD undergoing PCI with drug-eluting stents (DES), shorter durations of DAPT (3-6 months) were shown non-inferior to 12 or 24 months duration with respect to MACE, but reduced the rates of major bleeding. Contrariwise, prolonged DAPT durations (18-48 months) reduced the incidence of myocardial infarction and stent thrombosis, but at a cost of an increased risk of major bleeding and all-cause mortality. Until more evidence becomes available, the choice of optimal DAPT regimen and duration for patients with CAD requires a tailored approach based on the patient clinical presentation, baseline risk profile and management strategy. Future studies are however needed to identify patients who may derive benefit from shortened or extended DAPT courses for secondary prevention of CAD based on their individual ischaemic and bleeding risk. Based on limited evidence, 12 months duration of DAPT is currently recommended in patients with ACS irrespective of their management strategy, but large ongoing randomised trials are currently assessing the efficacy and safety of a short-term DAPT strategy (3-6 months) for patients with ACS undergoing PCI with newer generation DES. Finally, several ongoing, large-scale, randomised trials are challenging the current concept of DAPT by investigating P2Y12 receptor inhibitors as single antiplatelet therapy and may potentially shift the paradigm of antiplatelet therapy after PCI in the near future. This article provides a contemporary state-of-the-art review of the current evidence on DAPT for secondary prevention of patients with CAD and its future perspectives.
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