4.7 Article

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

期刊

NEUROLOGY
卷 64, 期 3, 页码 567-570

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/01.WNL.0000150580.40019.63

关键词

-

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据