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(Stroke. 2008;39:2891.)
© 2008 American Heart Association, Inc.
Research Letters |
From the Department of Neurology (S.H.-Y.C.), Brigham and Womens Hospital, Harvard Medical School, and the Departments of Neurology (E.E.S., R.G.N., J.R.S., G.A.R., C.A.), Radiology (R.G.N., J.R.S., C.A.), and Neurosurgery (C.S.O.), Massachusetts General Hospital, Harvard Medical School, Charlestown, Mass; and the Department of Neurology and Neurosurgery (N.B.), Columbia University College of Physicians and Surgeons, New York.
Correspondence to Cenk Ayata, MD, 149 13th street, Room 6408, Charlestown, MA 02129. E-mail cayata{at}partners.org
Background and Purpose— Studies suggest statins ameliorate aneurysmal subarachnoid hemorrhage (SAH)-induced cerebral vasospasm and ischemic complications. We tested safety and feasibility of simvastatin 80 mg/d for vasospasm prevention in SAH patients.
Methods— Thirty-nine statin-naïve Fisher grade 3 SAH subjects were double-blind randomized to receive simvastatin 80 mg/d (n=19) or placebo (n=20), stratified by Hunt and Hess grade. Primary end points were death and drug morbidity.
Results— Mortality was 3/20 in the placebo and 0/19 in the simvastatin group. Study drug was withdrawn in 1 subject in each treatment group for reversible liver enzyme or creatine phosphokinase elevation. Angiographically-confirmed vasospasm occurred in 8/20 placebo and 5/19 simvastatin-treated subjects. Vasospasm-related ischemic infarcts developed in 5/20 placebo and 2/19 simvastatin-treated subjects.
Conclusion— Simvastatin for the prevention of delayed cerebral ischemia is safe and feasible after SAH. A larger study is needed to test its efficacy.
Key Words: vasospasm delayed cerebral ischemia clinical trial
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