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Published on: February 28, 2012
Antithrombotic therapy in the secondary prevention of myocardial infarction
1Division of Medicine, University of Leeds, General Infirmary, United Kingdom.
Insights
Antiplatelet and anticoagulant therapies effectively prevent vascular events after myocardial infarction. Aspirin and oral anticoagulants show significant benefits, with aspirin being more commonly used due to ease of administration.
Area of Science:
- Cardiology
- Thrombosis Research
- Pharmacology
Background:
- Myocardial infarction is frequently caused by coronary artery occlusion due to thrombus formation, often linked to ruptured atherosclerotic plaques.
- Thrombi comprise platelets and fibrin, suggesting dual antiplatelet and anticoagulant therapy could prevent recurrent thrombotic events.
Purpose of the Study:
- To review clinical trial evidence on the efficacy of antiplatelet and anticoagulant therapies in preventing secondary thrombotic vascular events post-myocardial infarction.
- To compare the effectiveness and practical considerations of aspirin versus oral anticoagulants, and to explore the potential of combination therapy.
Main Methods:
- Systematic review and analysis of existing clinical trials investigating antiplatelet (aspirin) and anticoagulant therapies.
- Examination of data regarding vascular mortality, total vascular events, and patient compliance.
Main Results:
- Aspirin reduces vascular mortality by approximately 12% and vascular events by 25%.
- Oral anticoagulants decrease total mortality by up to 20% and vascular events by about 40%, though with wider confidence intervals due to fewer large-scale trials.
- The EPSIM trial indicated equal efficacy between aspirin and oral anticoagulants, with superior patient compliance for aspirin.
Conclusions:
- Both aspirin and oral anticoagulants are beneficial in managing post-myocardial infarction patients.
- Aspirin is more widely used due to practical advantages in administration and control.
- Combined antiplatelet and anticoagulant therapy shows promise but requires further large-scale trials due to increased hemorrhage risk.
Abstract:
There is now convincing evidence that the majority of myocardial infarcts are caused by acute occlusion of the coronary artery with a thrombus, often originating from a ruptured atherosclerotic plaque. The thrombus is composed of both platelets and fibrin, so it is logical to expect that both antiplatelet and anticoagulant therapy would be effective for the prevention of reinfarction and other thrombotic vascular events following myocardial infarction. A review of clinical trials confirms this suggestion. Aspirin is beneficial in that it reduces vascular mortality by about 12% and total vascular events by 25%. Similarly, oral anticoagulants reduce total mortality by up to 20% and vascular events by about 40%. However, relatively few large scale trials of oral anticoagulants after infarction have been carried out, and the confidence intervals are wider than those for the aspirin trials. In practice aspirin is used more widely than oral anticoagulants as it is easier to administer and control. Only one trial (EPSIM) has directly compared oral anticoagulants and aspirin. This trial showed that both drugs had equal efficacy but that compliance with aspirin was better. Finally, the question of giving antiplatelet agents and anticoagulants together, to block both platelet aggregation and fibrin formation, is considered. A preliminary trial in prosthetic heart-valve patients has been encouraging but more large, long-term trials are required before recommendations can be made, as the use of both drugs together carries an increased risk of severe hemorrhage.
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