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氨磺必利与神经阻滞剂恶性综合征

Amisulpride and neuroleptic malignant syndrome.

作者信息

Tu Ming-Che, Hsiao Cheng-Cheng

机构信息

Department of Psychiatry, Chang Gung Memorial Hospital at Keelung, Chang Gung University College of Medicine, Taoyuan, Taiwan.

出版信息

Chang Gung Med J. 2011 Sep-Oct;34(5):536-40.

Abstract

Neuroleptic malignant syndrome (NMS) is a rare but lethal complication of neuroleptics. Its incidence ranges between 0.02% and 3%. Amisulpride, a second generation neuroleptic, was associated with rhabdomyolysis in one report and NMS in 2 reports. Although the precise pathogenesis is still unclear, dopamine receptor blockade is theorized to play a central role. Conventional presentations include hyperthermia, muscle rigidity, and elevated creatine kinase concentrations. However, similar to other second generation neuroleptics, amisulpride induces an atypical form of NMS, which presents with lower degrees of hyperthermia and elevation of creatine kinase than the typical form. This phenomenon makes it difficult to identify early signs of NMS. This study describes the first case of amisulprideinduced NMS in Taiwan, together with a review of the current knowledge on NMS. In this case, the correlation between NMS and amisulpride was categorized as "probable" on the Naranjo adverse drug reaction probability scale.

摘要

抗精神病药恶性综合征(NMS)是一种罕见但致命的抗精神病药并发症。其发病率在0.02%至3%之间。第二代抗精神病药氨磺必利,在一份报告中与横纹肌溶解有关,在两份报告中与NMS有关。尽管确切的发病机制仍不清楚,但理论上多巴胺受体阻断起核心作用。传统表现包括高热、肌肉强直和肌酸激酶浓度升高。然而,与其他第二代抗精神病药类似,氨磺必利会诱发非典型形式的NMS,与典型形式相比,其高热程度和肌酸激酶升高程度较低。这种现象使得难以识别NMS的早期迹象。本研究描述了台湾首例氨磺必利诱发的NMS病例,并对当前关于NMS的知识进行了综述。在该病例中,根据Naranjo药物不良反应概率量表,NMS与氨磺必利之间的相关性被归类为“可能”。

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