Mayer Stephan A, Claassen Jan, Lokin Johnny, Mendelsohn Felicia, Dennis Lyle J, Fitzsimmons Brian-Fred
Division of Critical Care Neurology, Neurological Institute, 710 W 168th St, Unit 39, New York, NY 10032, USA.
Arch Neurol. 2002 Feb;59(2):205-10. doi: 10.1001/archneur.59.2.205.
Refractory status epilepticus (RSE) is a life-threatening condition in which seizures do not respond to first- and second-line anticonvulsant drug therapy. How often RSE occurs, risk factors that predispose to this condition, and the effect of failure to control seizures on clinical outcome are poorly defined.
To determine the frequency, risk factors, and impact on outcome of RSE.
Retrospective cohort study.
Large academic teaching hospital.
Consecutive sample of 83 episodes of status epilepticus in 74 patients (mean age, 63 years).
Refractory status epilepticus was defined as seizures lasting longer than 60 minutes despite treatment with a benzodiazepine and an adequate loading dose of a standard intravenous anticonvulsant drug. Factors associated with RSE were identified using univariate and backward stepwiselogistic regression analyses.
In 57 episodes (69%), seizures occurred after treatment with a benzodiazepine, and in 26 (31%), seizures occurred after treatment with a second-line anticonvulsant drug (usually phenytoin), fulfilling our criteria for RSE. Nonconvulsive SE (P=.03) and focal motor seizures at onset (P=.04) were identified as independent risk factors for RSE. Eleven (42%) of 26 patients with RSE had seizures after receiving a third-line agent (usually phenobarbital). Although mortality was not increased (17% overall), RSE was associated with prolonged hospital length of stay (P<.001) and more frequent functional deterioration at discharge (P=.02).
Refractory status epilepticus occurs in approximately 30% of patients with SE and is associated with increased hospital length of stay and functional disability. Nonconvulsive SE and focal motor seizures at onset are risk factors for RSE. Randomized controlled trials are needed to define the optimal treatment of RSE.
难治性癫痫持续状态(RSE)是一种危及生命的疾病,发作对一线和二线抗惊厥药物治疗无反应。RSE的发生频率、易患此病的危险因素以及癫痫发作控制不佳对临床结局的影响尚不明确。
确定RSE的发生频率、危险因素及其对结局的影响。
回顾性队列研究。
大型学术教学医院。
74例患者(平均年龄63岁)连续发生的83次癫痫持续状态样本。
难治性癫痫持续状态定义为尽管使用了苯二氮䓬类药物和标准静脉抗惊厥药物的足够负荷剂量,但癫痫发作仍持续超过60分钟。使用单因素和向后逐步逻辑回归分析确定与RSE相关的因素。
在57次发作(69%)中,癫痫发作发生在使用苯二氮䓬类药物治疗后,在26次发作(31%)中,癫痫发作发生在使用二线抗惊厥药物(通常为苯妥英钠)治疗后,符合我们对RSE的标准。非惊厥性癫痫持续状态(P=0.03)和发作起始时的局灶性运动性发作(P=0.04)被确定为RSE的独立危险因素。26例RSE患者中有11例(42%)在接受三线药物(通常为苯巴比妥)后仍有癫痫发作。尽管死亡率没有增加(总体为17%),但RSE与住院时间延长(P<0.001)和出院时功能恶化更频繁(P=0.02)相关。
约30%的癫痫持续状态患者会发生难治性癫痫持续状态,且与住院时间延长和功能残疾增加有关。非惊厥性癫痫持续状态和发作起始时的局灶性运动性发作是RSE的危险因素。需要进行随机对照试验来确定RSE的最佳治疗方法。