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Resective surgery to treat refractory status epilepticus in children with focal epileptogenesis.

作者信息

Alexopoulos A, Lachhwani D K, Gupta A, Kotagal P, Harrison A M, Bingaman W, Wyllie E

机构信息

Department of Neurology, The Cleveland Clinic Foundation, Cleveland, OH 44195, USA.

出版信息

Neurology. 2005 Feb 8;64(3):567-70. doi: 10.1212/01.WNL.0000150580.40019.63.

DOI:10.1212/01.WNL.0000150580.40019.63
PMID:15699401
Abstract

Prolonged high-dose suppressive therapy (HDST) is a mainstay in the management of refractory status epilepticus (RSE), albeit with high morbidity and mortality. The authors studied 10 patients who were carefully selected for epilepsy surgery after failing prolonged (>2 weeks) HDST. Status epilepticus was stopped acutely in all of them with no mortality and no substantial morbidity. At follow-up (median 7 months), 7 (70%) of 10 patients were seizure free, and 3 (30%) of 10 had significant improvement in their epilepsy.

摘要

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