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Antiplatelet therapy in populations at high risk of atherothrombosis
David P Faxon1, Richard W Nesto
1Section of Cardiology, Department of Medicine, University of Chicago, 5841 S. Maryland Ave., Room B-608, MC 6080, Chicago, IL 60637, USA. dfaxon@medicine.bsd.uchicago.edu
Insights
Aspirin and clopidogrel are key antiplatelet agents for preventing atherothrombosis. Dual therapy with aspirin and clopidogrel offers additional benefits for high-risk patients, reducing thrombotic events.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Atherothrombosis is a leading cause of acute ischemic events.
- Antiplatelet agents are crucial for preventing atherothrombosis.
Purpose of the Study:
- To review the use of antiplatelet agents in high-risk patients for atherothrombotic events.
- To identify key studies on antiplatelet therapy in this population.
Main Methods:
- Literature search for key studies on antiplatelet agents in high-risk patients.
- Analysis of data from trials such as CAPRIE, CURE, and PCI-CURE.
Main Results:
- Aspirin reduces thrombotic events by approximately 25%.
- Clopidogrel, alone or with aspirin, provides additional risk reduction.
- CAPRIE: Clopidogrel showed 8.7% greater risk reduction than aspirin.
- CURE: Adding clopidogrel to aspirin reduced cardiovascular events by 20%.
Conclusions:
- Aspirin and clopidogrel are fundamental in managing secondary thrombotic events.
- Dual antiplatelet therapy shows significant benefits in high-risk populations, particularly post-PCI.
- Ongoing trials like CHARISMA and REACH investigate further benefits and epidemiological data.
Abstract:
Atherothrombosis is the most common cause of an acute ischemic event. Antiplatelet agents form the cornerstone of atherothrombosis prevention. The purpose of this article is to review the use of antiplatelet agents in patients that are at particularly high risk of atherothrombotic events. To undertake this review, we searched the literature to identify key studies on the use of antiplatelet agents in this group of patients. Antiplatelet agents, such as aspirin and clopidogrel, play a fundamental role in the treatment and management of secondary thrombotic events. The routine use of aspirin is recommended, as it has been shown to reduce the risk of thrombotic events by approximately 25%. Additional benefit has been demonstrated with clopidogrel, both as a monotherapy and in combination with aspirin. In the CAPRIE trial, 19,185 patients with atherosclerotic vascular disease were randomized to receive clopidogrel (75 mg/day) or aspirin (325 mg/day) for a mean duration of follow-up of 1.91 years. Clopidogrel provided an additional 8.7% relative risk reduction in the primary composite endpoint of ischemic stroke, myocardial infraction or vascular death compared with aspirin. In the CURE trial, the addition of clopidogrel to background aspirin was associated with a 20% relative risk reduction in a composite of death from cardiovascular causes, nonfatal myocardial infarction or stroke compared with aspirin alone. In patients undergoing PCI as part of the PCI-CURE substudy, clopidogrel was associated with a 30% relative reduction in the incidence of cardiovascular events in the first 30 days after intervention compared with aspirin. The benefits of antiplatelet therapy continue to be investigated. Whether dual antiplatelet therapy is superior to aspirin monotherapy for high-risk primary prevention is unknown. The ongoing CHARISMA trial aims to determine the relative efficacies of aspirin monotherapy and aspirin/clopidogrel combination therapy in a broad range of high-risk patient populations. In addition, the REACH registry, a worldwide survey of symptomatic and high-risk patients, has been set up to provide vital epidemiological information regarding the risks of atherothrombosis in order to contribute to the development of better preventive strategies and management regimens for at-risk patients.
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