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Antiplatelet therapy for secondary prevention of coronary artery disease
Thomas Pilgrim1, Stephan Windecker1
1Department of Cardiology, Bern University Hospital, Bern, Switzerland.
Insights
Antiplatelet therapy choice and duration are key for preventing coronary artery disease (CAD) recurrence. Newer agents like prasugrel and ticagrelor offer benefits over clopidogrel for acute coronary syndrome, but duration varies by clinical context.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Secondary prevention of coronary artery disease (CAD) relies on antiplatelet therapy.
- Key agents include aspirin and P2Y12 inhibitors (clopidogrel, prasugrel, ticagrelor).
Purpose of the Study:
- To review the choice and duration of antiplatelet therapy for secondary CAD prevention.
- To compare the efficacy and safety of different antiplatelet agents in various clinical scenarios.
Main Methods:
- Literature review of clinical trials and guidelines.
- Comparative analysis of antiplatelet agents in stable CAD, acute coronary syndrome, and post-percutaneous coronary intervention.
Main Results:
- Aspirin is foundational; clopidogrel is used with aspirin in stable CAD post-intervention.
- Prasugrel and ticagrelor improve outcomes in acute coronary syndrome but increase bleeding risk versus clopidogrel.
- Prasugrel is effective in ST-elevation myocardial infarction and in diabetic patients. Ticagrelor reduces mortality without increasing CABG bleeding.
- Dual antiplatelet therapy duration: minimum 1 year for acute coronary syndrome; up to 6 months for stable CAD with new-generation drug-eluting stents.
Conclusions:
- Antiplatelet therapy selection and duration must be individualized based on clinical presentation and treatment.
- Newer P2Y12 inhibitors offer advantages in specific high-risk populations but require careful bleeding risk assessment.
- Current evidence supports specific durations for dual antiplatelet therapy to optimize net clinical benefit.
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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