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Updated: May 29, 2026

Optimized Management of Endovascular Treatment for Acute Ischemic Stroke
Published on: January 18, 2018
Stenting versus aggressive medical therapy for intracranial arterial stenosis
Marc I Chimowitz1, Michael J Lynn, Colin P Derdeyn
1Department of Neurosciences, Medical University of South Carolina, Charleston, SC 29425, USA. mchimow@musc.edu
Insights
Aggressive medical management is superior to percutaneous transluminal angioplasty and stenting (PTAS) for intracranial arterial stenosis. PTAS showed a higher risk of early stroke, while medical therapy alone proved more effective in preventing recurrent stroke.
Area of Science:
- Neurology
- Cardiovascular Medicine
- Interventional Neuroradiology
Background:
- Atherosclerotic intracranial arterial stenosis is a significant cause of stroke.
- Percutaneous transluminal angioplasty and stenting (PTAS) is used to prevent recurrent stroke but lacks randomized trial comparison with medical management.
Purpose of the Study:
- To compare the efficacy of aggressive medical management versus aggressive medical management plus PTAS in preventing stroke in patients with intracranial arterial stenosis.
Main Methods:
- Randomized trial comparing aggressive medical management alone versus aggressive medical management plus PTAS using the Wingspan stent system.
- Patients with 70-99% stenosis of a major intracranial artery were enrolled.
- Primary endpoint included stroke or death within 30 days, or stroke in the qualifying artery territory beyond 30 days.
Main Results:
- The 30-day stroke or death rate was significantly higher in the PTAS group (14.7%) compared to the medical management group (5.8%).
- Beyond 30 days, stroke occurred in 13 patients in each group.
- The 1-year rate of the primary endpoint was 20.0% for PTAS and 12.2% for medical management.
Conclusions:
- Aggressive medical management alone is superior to PTAS with the Wingspan stent system for intracranial arterial stenosis.
- The high early stroke risk associated with PTAS and the lower-than-expected stroke risk with medical therapy contribute to this finding.
Background:
Atherosclerotic intracranial arterial stenosis is an important cause of stroke that is increasingly being treated with percutaneous transluminal angioplasty and stenting (PTAS) to prevent recurrent stroke. However, PTAS has not been compared with medical management in a randomized trial.
Methods:
We randomly assigned patients who had a recent transient ischemic attack or stroke attributed to stenosis of 70 to 99% of the diameter of a major intracranial artery to aggressive medical management alone or aggressive medical management plus PTAS with the use of the Wingspan stent system. The primary end point was stroke or death within 30 days after enrollment or after a revascularization procedure for the qualifying lesion during the follow-up period or stroke in the territory of the qualifying artery beyond 30 days.
Results:
Enrollment was stopped after 451 patients underwent randomization, because the 30-day rate of stroke or death was 14.7% in the PTAS group (nonfatal stroke, 12.5%; fatal stroke, 2.2%) and 5.8% in the medical-management group (nonfatal stroke, 5.3%; non-stroke-related death, 0.4%) (P=0.002). Beyond 30 days, stroke in the same territory occurred in 13 patients in each group. Currently, the mean duration of follow-up, which is ongoing, is 11.9 months. The probability of the occurrence of a primary end-point event over time differed significantly between the two treatment groups (P=0.009), with 1-year rates of the primary end point of 20.0% in the PTAS group and 12.2% in the medical-management group.
Conclusions:
In patients with intracranial arterial stenosis, aggressive medical management was superior to PTAS with the use of the Wingspan stent system, both because the risk of early stroke after PTAS was high and because the risk of stroke with aggressive medical therapy alone was lower than expected. (Funded by the National Institute of Neurological Disorders and Stroke and others; SAMMPRIS ClinicalTrials.gov number, NCT00576693.).
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