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Optimized Management of Endovascular Treatment for Acute Ischemic Stroke
Published on: January 18, 2018
Extending Dual Antiplatelet Therapy Beyond 3 Months in Acute Ischemic Stroke Due to Large-Artery Atherosclerosis
Minwoo Lee1, Mi-Sun Oh1, Kyung-Ho Yu1
1Department of Neurology Hallym University Sacred Heart Hospital Anyang-si Republic of Korea.
Insights
Dual antiplatelet therapy (DAPT) duration for acute ischemic stroke from large-artery atherosclerosis has increased. Continuing DAPT beyond 3 months offers clinical benefits without raising bleeding risk.
Area of Science:
- Cardiology
- Neurology
- Clinical Pharmacy
Background:
- Optimal duration of dual antiplatelet therapy (DAPT) for acute ischemic stroke due to large-artery atherosclerosis is not well-defined.
- Aspirin plus clopidogrel is a common DAPT regimen.
- Large-artery atherosclerosis is a significant cause of ischemic stroke.
Purpose of the Study:
- To evaluate trends in DAPT duration for acute ischemic stroke patients.
- To assess the clinical outcomes associated with extended DAPT.
- To determine if longer DAPT duration increases bleeding risk.
Main Methods:
- Retrospective analysis of a prospective, multicenter stroke registry (2011-2018) linked to a national health insurance claims database.
- Inclusion criteria: acute ischemic stroke, large-artery atherosclerosis, DAPT initiation within 48 hours, no primary outcome events in the first 30 days.
- Landmark analyses assessed DAPT continuation up to 6 months; primary outcome: recurrent stroke, myocardial infarction, major bleeding, all-cause death within 1.5 years.
Main Results:
- Median DAPT duration increased from 36 days (2011) to 122 days (2018).
- Continuing DAPT beyond 3 months reduced the primary outcome risk (aHR 0.78 [95% CI, 0.64-0.94] at 3 months; 0.78 [95% CI, 0.61-0.98] at 6 months).
- DAPT continuation did not significantly increase stroke recurrence or major bleeding but reduced all-cause death.
Conclusions:
- DAPT duration for acute ischemic stroke due to large-artery atherosclerosis has lengthened over time.
- Continuation of DAPT beyond 3 months appears to provide net clinical benefits.
- Extended DAPT does not increase the risk of major bleeding in this patient population.
Background:
The optimal duration of dual antiplatelet therapy (DAPT) with aspirin plus clopidogrel following acute ischemic stroke due to large-artery atherosclerosis remains uncertain.
Methods:
We retrospectively analyzed data from a prospective, multicenter stroke registry (2011-2018) linked to a national health insurance claims database. Patients included had acute ischemic stroke attributable to large-artery atherosclerosis, initiated DAPT within 48 hours of admission and remained free of primary outcome events during the first 30 days. Temporal trends in DAPT usage were evaluated, and landmark analyses assessed the impact of DAPT continuation for up to 6 months after stroke on clinical outcomes. The primary outcome was a composite of recurrent stroke, myocardial infarction, major bleeding, and all-cause death within 1.5 years post-stroke.
Results:
A total of 4814 patients (mean age, 68.1±11.8 years; 64.1% men) were analyzed. The median duration of DAPT significantly increased from 36 days in 2011 to 122 days in 2018 (P<0.001). Continuing DAPT beyond 3 months reduced the risk of the primary outcome, with benefits sustained for up to 6 months (adjusted hazard ratios, 0.78 [95% CI, 0.64-0.94] at 3 months; and 0.78 [95% CI, 0.61-0.98] at 6 months). In the analysis of secondary outcomes, DAPT continuation did not significantly affect stroke recurrence or major bleeding, but was associated with a significant reduction in all-cause death.
Conclusions:
In patients with acute ischemic stroke due to large-artery atherosclerosis, DAPT duration has lengthened over time and continuation beyond 3 months appears to confer net clinical benefits, without increasing the risk of major bleeding.
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