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Published on: August 18, 2015
Secondary stroke prevention with antiplatelet drugs: have we reached the ceiling?
1Department of Neurology, University of Essen, Hufelandstrasse 55, D-45122 Essen, Germany. h.diener@uni-essen.de
Insights
Antiplatelet drugs reduce stroke risk in TIA and ischemic stroke patients. Aspirin is effective and safe, while other agents offer marginal benefits with increased bleeding risks, necessitating careful patient selection.
Area of Science:
- Neurology
- Cardiology
- Pharmacology
Background:
- Patients with transient ischemic attack (TIA) or ischemic stroke face a significant annual risk of recurrent stroke (5-20%).
- Antiplatelet therapy is crucial for secondary stroke prevention, particularly in non-cardiac origin cases, reducing stroke risk and major vascular events.
Purpose of the Study:
- To evaluate the efficacy and safety of various antiplatelet agents for secondary stroke prevention.
- To compare aspirin with combination therapies and newer agents in reducing recurrent stroke and vascular death.
Main Methods:
- Systematic review and meta-analysis of clinical trials on antiplatelet therapies for stroke prevention.
- Comparison of aspirin, aspirin-dipyridamole, clopidogrel, and GP IIb/IIIa antagonists regarding efficacy and bleeding risk.
Main Results:
- Low-dose aspirin (50-325 mg) is effective and safer than higher doses for stroke prevention.
- Aspirin plus dipyridamole showed superior stroke prevention compared to aspirin alone, without increased bleeding.
- Clopidogrel was not superior to aspirin in unselected patients but beneficial in high-risk individuals; combination therapies and GP IIb/IIIa antagonists offered limited additional benefit with higher bleeding risks.
Conclusions:
- Aspirin remains a cornerstone of antiplatelet therapy for TIA and ischemic stroke.
- More potent antiplatelet agents offer marginal efficacy gains over aspirin, often accompanied by increased bleeding complications.
- Careful patient selection is essential to optimize the benefits of antiplatelet therapy and minimize risks.
Abstract:
Patients with transient ischemic attack (TIA) or ischemic stroke carry a risk of recurrent stroke of between 5% and 20% per year. In patients with TIA or ischemic stroke of non-cardiac origin, antiplatelet drugs are able to decrease the relative risk of stroke by 11-15% and the risk of stroke, myocardial infarction, and vascular death by 15-22%. Aspirin is the most widely used drug. It is affordable and effective. Low doses of 50-325 mg aspirin are as effective as high doses and cause less gastrointestinal side-effects. The combination of aspirin with slow-release dipyridamole is superior to aspirin alone for stroke prevention but not for the prevention of cardiac events. The risk of major bleeding complications is not increased with the combination, which suggests that dipyridamole might act in another way than as antiplatelet drug. Clopidogrel is not superior to aspirin in unselected stroke patients but is superior in patients at high risk of recurrence. The combination of aspirin plus clopidogrel is not more effective than clopidogrel alone, but carries a higher bleeding risk. The most effective antiplatelet drugs, the GP IIb/IIIa antagonists, are not superior to aspirin and carry a higher risk of bleeding. These results indicate that any antiplatelet therapy with a more potent drug than aspirin will only have a marginally higher efficacy, which might be offset by a higher bleeding rate. Therefore, selection of patients who might benefit from antiplatelet therapy other than aspirin is important.
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