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Optimized Management of Endovascular Treatment for Acute Ischemic Stroke
Published on: January 18, 2018
Multiple Antiplatelet Therapy in Ischemic Stroke Already on Antiplatelet Agents Based on the Linked Big Data for
Tae Jung Kim1,2, Ji Sung Lee3, Jae Sun Yoon1
1Department of Neurology, Seoul National University Hospital, Seoul, Korea.
Insights
Adding more antiplatelet therapy to single antiplatelet therapy (SAPT) for non-cardioembolic stroke did not lower vascular risks. However, triple antiplatelet therapy significantly increased major bleeding complications in patients already on SAPT.
Area of Science:
- Neurology
- Cardiology
- Pharmacology
Background:
- Optimal antiplatelet strategy for ischemic stroke patients on single antiplatelet therapy (SAPT) is unclear.
- This study evaluates antiplatelet regimens in patients with non-cardioembolic stroke previously on SAPT.
Purpose of the Study:
- To assess the impact of dual antiplatelet therapy (DAPT) and triple antiplatelet therapy (TAPT) versus continued SAPT on vascular and safety outcomes at one year.
- To determine if intensified antiplatelet therapy improves outcomes after non-cardioembolic stroke in patients already on SAPT.
Main Methods:
- Retrospective analysis of 9,284 patients with acute non-cardioembolic ischemic stroke on SAPT.
- Patients were stratified into SAPT, DAPT, or TAPT groups based on discharge medication.
- One-year outcomes included recurrent ischemic stroke, a composite of vascular events and death, and major bleeding.
Main Results:
- Multiple antiplatelet therapy (DAPT/TAPT) did not significantly reduce the risk of recurrent ischemic stroke or the composite outcome at one year.
- Triple antiplatelet therapy (TAPT) was associated with a significantly increased risk of major bleeding complications (HR 4.65).
- Dual antiplatelet therapy (DAPT) showed a non-significant trend towards increased bleeding risk (HR 1.23).
Conclusions:
- Intensifying antiplatelet therapy beyond SAPT does not improve 1-year vascular outcomes in non-cardioembolic stroke patients.
- Triple antiplatelet therapy significantly elevates the risk of major bleeding complications in this patient population.
- The findings suggest that continued SAPT may be a safer strategy for selected patients.
Background:
Optimal antiplatelet strategy for patients with ischemic stroke who were already on single antiplatelet therapy (SAPT) remains to be elucidated. This study aimed to evaluate the effect of different antiplatelet regimens on vascular and safety outcomes at 1 year after non-cardioembolic stroke in patients previously on SAPT.
Methods:
We identified 9,284 patients with acute non-cardioembolic ischemic stroke that occurred on SAPT using linked data. Patients were categorized into three groups according to antiplatelet strategy at discharge: 1) SAPT; 2) dual antiplatelet therapy (DAPT); and 3) triple antiplatelet therapy (TAPT). One-year outcomes included recurrent ischemic stroke, composite outcomes (recurrent ischemic stroke, myocardial infarction, intracerebral hemorrhage, and death), and major bleeding.
Results:
Of 9,284 patients, 5,565 (59.9%) maintained SAPT, 3,638 (39.2%) were treated with DAPT, and 81 (0.9%) were treated with TAPT. Multiple antiplatelet therapy did not reduce the risks of 1-year recurrent stroke (DAPT, hazard ratio [HR], 1.08, 95% confidence interval [CI], 0.92-1.27, P = 0.339; TAPT, HR, 0.71, 95% CI, 0.27-1.91, P = 0.500) and 1-year composite outcome (DAPT, HR, 1.09, 95% CI, 0.68-1.97, P = 0.592; TAPT, HR, 1.46, 95% CI, 0.68-1.97, P = 0.592). However, the TAPT groups showed an increased risk of major bleeding complications (DAPT, HR, 1.23, 95% CI, 0.89-1.71, P = 0.208; TAPT, HR, 4.65, 95% CI, 2.01-10.74, P < 0.001).
Conclusion:
Additional use of antiplatelet agents in patients with non-cardioembolic ischemic stroke who were already on SAPT did not reduce the 1-year incidence of vascular outcomes, although it increased the risk of bleeding complications.
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