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Updated: Jul 19, 2026

A Volumetric Method for Quantification of Cerebral Vasospasm in a Murine Model of Subarachnoid Hemorrhage
Published on: July 28, 2018
Evidence-based cerebral vasospasm management
George W Weyer1, Colum P Nolan, R Loch Macdonald
1Section of Neurosurgery, Department of Surgery, University of Chicago Medical Center and Pritzker School of Medicine, Chicago, Illinois, USA.
Insights
Nimodipine is the only proven therapy for cerebral vasospasm following subarachnoid hemorrhage (SAH). Other treatments show limited or inconclusive efficacy, highlighting the need for improved clinical trials and further research into alternative therapies.
Area of Science:
- Neurology
- Neurosurgery
- Clinical Pharmacology
Background:
- Cerebral vasospasm and delayed cerebral ischemia are frequent, serious complications after aneurysmal subarachnoid hemorrhage (SAH).
- Current therapeutic options for cerebral vasospasm are limited, with only calcium antagonists demonstrating strong evidence of effectiveness.
Purpose of the Study:
- To systematically review the existing literature on therapies for the prevention and treatment of cerebral vasospasm and delayed cerebral ischemia following SAH.
Main Methods:
- A comprehensive literature search was conducted to identify randomized controlled trials (RCTs) evaluating various therapeutic interventions.
- Forty-one articles met the inclusion criteria for the systematic review, and their study characteristics and primary outcomes were analyzed.
Main Results:
- Nimodipine is the only therapy with proven efficacy for vasospasm after SAH; tirilazad was found to be ineffective.
- Studies on hemodynamic maneuvers, magnesium, statins, endothelin antagonists, steroids, anticoagulants/antiplatelets, and intrathecal fibrinolytic drugs yielded inconclusive results.
- The overall quality of clinical trials in this field was initially poor but has shown significant improvement over time.
Conclusions:
- Nimodipine is indicated for patients following SAH, while tirilazad is not recommended.
- Further research is warranted for hemodynamic maneuvers, other calcium channel blockers (e.g., nicardipine), magnesium, statins, endothelin antagonists, and intrathecal fibrinolytic therapy.
- Investigating rescue therapies like balloon angioplasty and intra-arterial vasodilators presents challenges, and improving the quality of future clinical trials is crucial.
Abstract:
Cerebral vasospasm and delayed cerebral ischemia remain common complications of aneurysmal subarachnoid hemorrhage (SAH), and yet therapies for cerebral vasospasm are limited. Despite a large number of clinical trials, only calcium antagonists have strong evidence supporting their effectiveness. The purpose of this work was to perform a systematic review of the literature on the treatment of cerebral vasospasm. A literature search for randomized controlled trials of therapies used for prevention or treatment of cerebral vasospasm and/or delayed cerebral ischemia was conducted, and 41 articles meeting the review criteria were found. Study characteristics and primary results of these articles are reviewed. Key indicators of quality were poor when averaged across all studies, but have improved greatly over time. The only proven therapy for vasospasm is nimodipine. Tirilazad is not effective, and studies of hemodynamic maneuvers, magnesium, statin medications, endothelin antagonists, steroid drugs, anticoagulant/antiplatelet agents, and intrathecal fibrinolytic drugs have yielded inconclusive results. The following conclusions were made: nimodipine is indicated after SAH and tirilazad is not effective. More study of hemodynamic maneuvers, the effectiveness of other calcium channel antagonists such as nicardipine delivered by other routes (for example intrathecally), magnesium, statin drugs, endothelin antagonists, and intrathecal fibrinolytic therapy is warranted. There is less enthusiasm for the study of steroid drugs and anticoagulant/antiplatelet agents because they entail more risks and investigations so far have shown little evidence of efficacy. The study of rescue therapy such as balloon angioplasty and intraarterial vasodilating agents will be difficult. The quality of clinical trials should be improved.
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