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A Clinical Update on Antiplatelet Therapy in Secondary Prevention of Ischemic Stroke
Katelyn Marsden1, Hannah Y Mak2, C Patrick Crooks3
1Department of Neurology, University of Washington, Seattle, SA, USA. krlm@uw.edu.
Insights
Dual antiplatelet therapy effectively prevents recurrent stroke in patients with non-cardioembolic ischemic stroke or transient ischemic attack (TIA). Genetic factors may influence treatment effectiveness, and optimal duration requires further study.
Area of Science:
- Neurology
- Cardiology
- Pharmacology
Background:
- Antiplatelet therapy is crucial for secondary stroke prevention.
- Non-cardioembolic ischemic stroke and transient ischemic attack (TIA) management relies on antiplatelet agents.
Purpose of the Study:
- To review clinical trials and meta-analyses on antiplatelet agents for secondary stroke prevention.
- To provide commentary on current practices in antiplatelet therapy for stroke prevention.
Main Methods:
- Review of key clinical trials (POINT, CHANCE, THALES) and meta-analyses.
- Analysis of dual antiplatelet therapy versus aspirin monotherapy.
- Consideration of genetic polymorphisms' impact on treatment efficacy.
Main Results:
- Dual antiplatelet therapy (aspirin plus P2Y12 inhibitors like clopidogrel or ticagrelor) reduced recurrent stroke compared to aspirin alone.
- Sub-analyses suggest genetic polymorphisms may affect clopidogrel effectiveness.
- Ticagrelor-aspirin combination showed better outcomes than aspirin monotherapy in THALES.
Conclusions:
- Combination antiplatelet therapy is effective in reducing stroke recurrence for mild ischemic stroke or high-risk TIA.
- Genetic factors may influence the choice of antiplatelet regimen.
- Optimal duration of combination therapy for different stroke etiologies needs further investigation.
Purpose Of Review:
Antiplatelet therapy remains the standard of care in secondary stroke prevention for non-cardioembolic ischemic stroke and transient ischemic attack. We aim to examine the use of antiplatelet agents in secondary prevention through highlighting relevant clinical trials and meta-analyses as well as providing commentary regarding our practice.
Recent Findings:
In the POINT and CHANCE trials, dual antiplatelet therapy reduced recurrent stroke compared to aspirin monotherapy. Sub-analyses of these trials suggest that genetic polymorphisms could play a role in diminishing the effectiveness of clopidogrel. Similarly, THALES demonstrated better outcomes with ticagrelor-aspirin combination therapy over aspirin monotherapy. Combination antiplatelet therapy with aspirin and the P2Y12 inhibitors, clopidogrel and ticagrelor, reduced stroke recurrence in those presenting with mild ischemic stroke or high risk TIA. Genetic polymorphisms may play a role in determining the appropriate regimen. Questions remain regarding the optimal duration of combination antiplatelet therapy for various stroke etiologies.
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