癫痫持续状态。

Bailliere's clinical neurology Pub Date : 1996-12-01
D M Treiman
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引用次数: 0

摘要

癫痫持续状态是指在另一次癫痫发作发生前,多次癫痫发作未从一次癫痫发作的生理影响中完全恢复的一种状态。SE的种类和癫痫发作的种类一样多。全身性惊厥癫痫持续状态最初表现为反复的全身性惊厥,在癫痫发作之间没有完全恢复意识。如果未经治疗或治疗不足,抽搐活动逐渐变得微妙,并伴有一系列可预测的进行性脑电图变化。非惊厥性SE是指复杂的部分SE或无SE,两者都表现出与环境接触改变的癫痫性暮光状态。单纯性部分SE患者没有意识障碍,行为改变反映了局限于一个皮质区域的局灶性脑顶放电。美国每年有6.5万至15万例SE病例。急性和远端脑损伤均可引起SE,严重的全身性疾病继发于毒性代谢性脑病也可引起SE。死亡率很高,但当SE得到适当和积极的治疗时,很大程度上反映了潜在的病因。治疗的重点是尽快终止正在进行的癫痫活动,因为SE持续的时间越长,就越有可能造成永久性的神经元损伤,也因为强有力的证据表明SE持续的时间越长,治疗就越难。目前最普遍接受的治疗方案包括快速开始静脉注射劳拉西泮(0.1 mg/kg),然后在必要时使用20mg /kg苯妥英,然后在必要时使用20mg /kg苯巴比妥。然而,一些神经科医生仍然使用静脉注射安定(因为它的抗状态作用更快),然后使用苯妥英。在大鼠身上的新实验数据表明,苯妥英和地西泮可能更有效,但这种给药顺序仍然需要在适当设计的临床试验中进行测试。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Status epilepticus.

Status epilepticus is a condition in which multiple epileptic seizures occur without complete recovery from the physiological effects of one seizure before another seizure occurs. There are as many types of SE as there are kinds of epileptic seizures. Generalized convulsive status epilepticus initially presents with repeated generalized convulsions without full recovery of consciousness between seizures. If untreated or undertreated, the convulsive activity becomes progressively subtle and is accompanied by a predictable series of progressive EEG changes. Non-convulsive SE refers to complex partial SE or absence SE, both of which exhibit an epileptic twilight state of altered contact with the environment. In simple partial SE there is no impairment of consciousness, and the behavioural changes reflect focal ictal discharges confined to one area of the cortex. There are between 65,000 and 150,000 cases of the SE in the US each year. Both acute and remote cerebral insults can cause SE, as can severe systemic disease that causes SE secondary to a toxic-metabolic encephalopathy. Mortality is high, but is largely a reflection of underlying aetiology when SE is treated appropriately and aggressively. Treatment is focused on terminating ongoing seizure activity as quickly as possible, both because the longer SE persists the more likely permanent neuronal damage will ensure and also because of strong evidence that the longer SE persists the more refractory to treatment it will be. Currently the most commonly accepted treatment protocol involves rapid initiation of therapy with intravenous lorazepam (0.1 mg/kg), followed, if necessary, by 20 mg/kg of phenytoin, followed, if necessary, by 20 mg/kg of phenobarbital. However, some neurologists still use intravenous diazepam (because of its more rapid antistatus effect) followed by phenytoin. New experimental data in the rat suggest that phenytoin followed by diazepam may be more effective, but this order of administration still has to tested in properly designed clinical trials.

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