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Clopidogrel plus Aspirin for Symptomatic Intracranial Atherosclerotic Stenosis: A Pilot Study
Tareq Kass-Hout1, Melanie Winningham2, Omar Kass-Hout3
1Department of Neurology, Emory University School of Medicine, Atlanta, Ga, USA; Department of Neurosciences, Rochester Regional Health, Rochester, N.Y, USA.
Insights
Prolonged dual antiplatelet therapy for symptomatic intracranial atherosclerotic disease showed 0% vascular events at 1 year. This approach for secondary stroke prevention may reduce risks without increasing bleeding complications.
Area of Science:
- Neurology
- Cardiology
- Vascular Medicine
Background:
- Limited data exist on optimal dual antiplatelet therapy (DAPT) duration for secondary stroke prevention.
- Symptomatic intracranial atherosclerotic disease poses a significant risk for recurrent cerebrovascular events.
Purpose of the Study:
- To evaluate the efficacy and safety of a prolonged DAPT course (12 months) in patients with symptomatic intracranial atherosclerotic disease.
- To compare outcomes with the Stenting and Aggressive Medical Management for Preventing Recurrent Stroke in Intracranial Stenosis (SAMMPRIS) trial.
Main Methods:
- Retrospective analysis of 25 patients with high-grade (70-99%) symptomatic intracranial stenosis treated with aspirin plus clopidogrel for 12 months.
- Aggressive medical management following the SAMMPRIS protocol, including gastrointestinal prophylaxis.
- Comparison of clinical and safety outcomes with the medical arm of the SAMMPRIS trial.
Main Results:
- No stroke, myocardial infarction, or vascular death occurred in the cohort at 1 year (0% vs. 16% in SAMMPRIS, p=0.03).
- Major bleeding rates were similar between the study cohort and the SAMMPRIS cohort (4% vs. 2.2%, p=1.0).
- Achievement of blood pressure and LDL cholesterol targets was comparable between cohorts.
Conclusions:
- A prolonged duration of dual antiplatelet therapy may be associated with reduced vascular events in symptomatic intracranial atherosclerotic disease.
- This extended DAPT strategy appears safe, with no significant increase in major bleeding complications.
- Further research is warranted to confirm these findings and establish optimal DAPT duration.
Background And Purpose:
There are limited data on the optimal duration of dual antiplatelet therapy for secondary stroke prevention in patients with symptomatic intracranial atherosclerotic disease.
Methods:
Consecutive patients presenting with high-grade (70-99%) symptomatic intracranial stenosis from January 1, 2011, to December 31, 2013, and evaluated within 30 days of the index event were eligible for this analysis. All patients underwent treatment with aspirin plus clopidogrel for a target duration of 12 months along with aggressive medical management based on the Stenting and Aggressive Medical Management for Preventing Recurrent Stroke in Intracranial Stenosis (SAMMPRIS) protocol; all patients were given gastrointestinal prophylaxis for the duration of their aspirin and clopidogrel treatment. Clinical and safety outcomes of our cohort were compared with the medical arm of the SAMMPRIS trial cohort (n = 227).
Results:
Our cohort included 25 patients that met the inclusion criteria. Achievement of blood pressure and LDL cholesterol targets were similar between our cohort and the SAMMPRIS cohort. At 1 year, the rates of stroke, myocardial infarction or vascular death were 0% in our cohort and 16% in the SAMMPRIS cohort (p = 0.03). At 1 year, major bleeding rates were similar between our cohort and the SAMMPRIS cohort (4 vs. 2.2%, p = 1.0).
Conclusion:
A prolonged course of dual antiplatelet therapy for symptomatic intracranial atherosclerotic disease may be associated with less vascular events with no increase in hemorrhagic complications.
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