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两次服用过高剂量卡马西平后出现急性肝毒性。

Acute hepatotoxicity after excessively high doses of carbamazepine on two occasions.

作者信息

Luke D R, Rocci M L, Schaible D H, Ferguson R K

出版信息

Pharmacotherapy. 1986 May-Jun;6(3):108-11. doi: 10.1002/j.1875-9114.1986.tb03463.x.

Abstract

A 2 1/2-year-old child being treated with carbamazepine (CBZ) for a seizure disorder on two separate occasions experienced elevated CBZ serum concentrations (28 and 23.2 mg/L), severe liver damage (SGOT greater than 6000 IU, SGPT greater than 5000 IU), and central nervous system manifestations (coma, lethargy, seizures). During the first episode, the time course of CBZ concentrations exhibited a nonlinear decline and was accompanied by CBZ-10,11-epoxide concentrations that were elevated 4-fold compared to normal values. Cerebrospinal fluid concentrations of CBZ and CBZ-10,11-epoxide were also elevated, although their ratios to serum concentrations did not suggest enhanced permeability of the central nervous system to these substances. The concentrations of CBZ-10,11-epoxide but not CBZ were elevated for the duration of time that the patient was comatose, suggesting that this metabolite may contribute to the neurotoxic side effects observed with CBZ therapy.

摘要

一名2岁半的儿童因癫痫症先后两次接受卡马西平(CBZ)治疗,期间血清卡马西平浓度升高(分别为28和23.2毫克/升),出现严重肝损伤(谷草转氨酶大于6000国际单位,谷丙转氨酶大于5000国际单位),并伴有中枢神经系统症状(昏迷、嗜睡、癫痫发作)。在首次发作期间,卡马西平浓度的时间进程呈现非线性下降,同时卡马西平-10,11-环氧化物浓度比正常值升高了4倍。脑脊液中卡马西平和卡马西平-10,11-环氧化物的浓度也升高了,尽管它们与血清浓度的比值并未表明中枢神经系统对这些物质的通透性增强。在患者昏迷期间,卡马西平-10,11-环氧化物的浓度一直升高,而卡马西平的浓度未升高,这表明这种代谢产物可能导致了卡马西平治疗中观察到的神经毒性副作用。

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