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氯氮平的肝毒性。

Hepatotoxicity of clozapine.

作者信息

Hummer M, Kurz M, Kurzthaler I, Oberbauer H, Miller C, Fleischhacker W W

机构信息

Department of Biological Psychiatry, University Clinics Innsbruck, Austria.

出版信息

J Clin Psychopharmacol. 1997 Aug;17(4):314-7. doi: 10.1097/00004714-199708000-00012.

Abstract

Two hundred thirty-eight patients treated with either haloperidol or clozapine were investigated to shed more light on the incidence and severity of antipsychotic-induced liver enzyme increase. Serum glutamic-pyruvic transaminase (SGPT) increase was most frequently seen in both treatment groups. When analyzing the incidence rates for patients with increased liver enzyme values (serum glutamic-oxaloacetic transaminase, SGPT, gamma-glutamyl transpeptidase) that were higher than twice the upper limit of the normal range, clozapine-treated patients showed an SGPT increase (37.3%) significantly more frequently than patients treated with haloperidol (16.6%). Both patients with higher clozapine plasma levels and male patients were at a higher risk for an SGPT increase. At least 60% of the increase of the different enzymes remitted within the first 13 weeks of treatment. In general, the authors conclude that clozapine-induced liver enzyme elevation seems to be a common and mostly transient phenomenon.

摘要

对238例接受氟哌啶醇或氯氮平治疗的患者进行了调查,以更深入地了解抗精神病药物引起的肝酶升高的发生率和严重程度。血清谷丙转氨酶(SGPT)升高在两个治疗组中最为常见。在分析肝酶值(血清谷草转氨酶、SGPT、γ-谷氨酰转肽酶)高于正常范围上限两倍的患者的发生率时,接受氯氮平治疗的患者SGPT升高(37.3%)的频率明显高于接受氟哌啶醇治疗的患者(16.6%)。氯氮平血浆水平较高的患者和男性患者SGPT升高的风险更高。在治疗的前13周内,至少60%的不同酶升高有所缓解。总体而言,作者得出结论,氯氮平引起的肝酶升高似乎是一种常见且大多为短暂的现象。

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