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Published on: March 15, 2022
Republished: Antiplatelet therapy for secondary prevention of coronary artery disease
Thomas Pilgrim1, Stephan Windecker1
1Department of Cardiology, Bern University Hospital, Bern, Switzerland.
Insights
Choosing antiplatelet therapy for coronary artery disease (CAD) secondary prevention depends on clinical context. Aspirin, clopidogrel, prasugrel, and ticagrelor are key agents, with specific durations recommended based on patient condition.
Area of Science:
- Cardiology
- Pharmacology
- Internal Medicine
Background:
- Secondary prevention of coronary artery disease (CAD) relies on antiplatelet therapy.
- Key oral agents include aspirin (COX-1 inhibitor) and P2Y12 inhibitors (clopidogrel, prasugrel, ticagrelor).
Purpose of the Study:
- To review the choice and duration of antiplatelet therapy for secondary prevention in CAD.
- To compare the efficacy and safety of different antiplatelet agents in various clinical scenarios.
Main Methods:
- Literature review and synthesis of current evidence on antiplatelet therapy in CAD.
- Comparison of clinical outcomes, including ischemic events and bleeding risk, associated with different antiplatelet agents.
Main Results:
- Aspirin is foundational for CAD secondary prevention, often combined with clopidogrel for stable CAD post-percutaneous coronary intervention.
- Prasugrel and ticagrelor offer improved net clinical outcomes in acute coronary syndrome (ACS) by reducing ischemic events, despite increased bleeding risk compared to clopidogrel.
- Prasugrel shows particular benefit in ST-elevation myocardial infarction and in diabetic patients.
- Ticagrelor is linked to reduced mortality without increased CABG-related bleeding versus clopidogrel.
- Dual antiplatelet therapy (DAPT) is recommended for at least 1 year post-ACS.
- For stable CAD with new-generation drug-eluting stents, DAPT beyond 6 months shows no additional benefit.
Conclusions:
- The optimal antiplatelet strategy for CAD secondary prevention is context-dependent.
- Duration of DAPT varies significantly between ACS and stable CAD patients.
- Prasugrel and ticagrelor represent advancements over clopidogrel in specific high-risk ACS populations.
Abstract:
The choice and duration of antiplatelet therapy for secondary prevention of coronary artery disease (CAD) is determined by the clinical context and treatment strategy. Oral antiplatelet agents for secondary prevention include the cyclo-oxygenase-1 inhibitor aspirin, and the ADP dependent P2Y12 inhibitors clopidogrel, prasugrel and ticagrelor. Aspirin constitutes the cornerstone in secondary prevention of CAD and is complemented by clopidogrel in patients with stable CAD undergoing percutaneous coronary intervention. Among patients with acute coronary syndrome, prasugrel and ticagrelor improve net clinical outcome by reducing ischaemic adverse events at the expense of an increased risk of bleeding as compared with clopidogrel. Prasugrel appears particularly effective among patients with ST elevation myocardial infarction to reduce the risk of stent thrombosis compared with clopidogrel, and offered a greater net clinical benefit among patients with diabetes compared with patients without diabetes. Ticagrelor is associated with reduced mortality without increasing the rate of coronary artery bypass graft (CABG)-related bleeding as compared with clopidogrel. Dual antiplatelet therapy should be continued for a minimum of 1 year among patients with acute coronary syndrome irrespective of stent type; among patients with stable CAD treated with new generation drug-eluting stents, available data suggest no benefit to prolong antiplatelet treatment beyond 6 months.
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