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大剂量卡马西平过量:五例临床及药理学观察

Massive carbamazepine overdose: clinical and pharmacologic observations in five episodes.

作者信息

Weaver D F, Camfield P, Fraser A

机构信息

Division of Neurology, I.W. Killam Hospital for Children, Halifax, Nova Scotia, Canada.

出版信息

Neurology. 1988 May;38(5):755-9. doi: 10.1212/wnl.38.5.755.

Abstract

We report five episodes of carbamazepine (CBZ) intoxication in four patients. Clinically, there were four distinct stages: I--coma, seizures (CBZ levels more than 25 micrograms/ml [105 mumol/l]); II--combativeness, hallucinations, choreiform movements (15 to 25 micrograms/ml [65 to 105 mumol/l]); III--drowsiness, ataxia (11 to 15 micrograms/ml [45 to 65 mumol/l]); and IV--potentially catastrophic relapse (less than 11 micrograms/ml [45 mumol/l]). Pharmacokinetic studies revealed a prolongation of the CBZ half-life, elevation of the CBZ-epoxide/CBZ ratio, and emergence of CBZ-epoxide as a significant toxic metabolite. A treatment approach is proposed including repeated gastric lavage, detection of an insoluble tablet coagulum, electrolyte monitoring, avoidance of cathartics, and treatment of seizures with diazepam and phenytoin.

摘要

我们报告了4例患者发生的5次卡马西平(CBZ)中毒事件。临床上,有四个不同阶段:I期——昏迷、癫痫发作(CBZ水平超过25微克/毫升[105微摩尔/升]);II期——好斗、幻觉、舞蹈样动作(15至25微克/毫升[65至105微摩尔/升]);III期——嗜睡、共济失调(11至15微克/毫升[45至65微摩尔/升]);IV期——可能发生灾难性复发(低于11微克/毫升[45微摩尔/升])。药代动力学研究显示CBZ半衰期延长、CBZ-环氧化物/CBZ比值升高,且CBZ-环氧化物成为一种重要的毒性代谢产物。提出了一种治疗方法,包括反复洗胃、检测不溶性片剂凝块、电解质监测、避免使用泻药,以及用地西泮和苯妥英治疗癫痫发作。

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