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皮下注射利苏瑞肽治疗抗精神病药恶性综合征。

Neuroleptic malignant syndrome treated with subcutaneous lisuride infusion.

作者信息

Rodriguez M E, Luquin M R, Lera G, Delgado G, Salazar J M, Obeso J A

机构信息

Department of Neurology, Clinica Universitaria, University of Navarra, Pamplona, Spain.

出版信息

Mov Disord. 1990;5(2):170-2. doi: 10.1002/mds.870050215.

Abstract

A schizophrenic patient developed a characteristic clinical picture of neuroleptic malignant syndrome (NMS) while admitted to the hospital during an exacerbation of his psychiatric symptoms. Oral treatment of the NMS with bromocriptine (7.5 mg/day) or levodopa/carbidopa (125/12.5 mg) provoked intense vomiting in spite of domperidone (60 mg/day), which led to their discontinuation. In view of the deterioration of the symptoms, treatment was begun with lisuride (1-2 mg/24 h) subcutaneously. An obvious improvement was shown in 24 h, but levodopa/carbidopa (125/12.5 mg t.d.s. orally) had to be added later to achieve complete resolution of the NMS. During the recovery phase, while being treated with subcutaneous lisuride infusion and levodopa (p.o.), the patient presented with confusion, agitation, and hallucination. Lisuride infusion was stopped and levodopa was continued until complete resolution of the NMS. This case indicates that parenteral administration of lisuride or other dopamine agents such as levodopa (i.v.) or apomorphine (s.c.) may be considered an effective and practical way of treating NMS, particularly when the patient's condition makes it difficult or impossible to use other dopaminergic drugs by the oral route.

摘要

一名精神分裂症患者在精神病症状加重期间住院时出现了典型的抗精神病药物恶性综合征(NMS)临床表现。尽管使用了多潘立酮(60毫克/天),用溴隐亭(7.5毫克/天)或左旋多巴/卡比多巴(125/12.5毫克)口服治疗NMS仍引发了剧烈呕吐,导致这些药物停用。鉴于症状恶化,开始皮下注射利舒脲(1 - 2毫克/24小时)进行治疗。24小时内症状明显改善,但后来不得不加用左旋多巴/卡比多巴(125/12.5毫克,每日三次口服)以实现NMS的完全缓解。在恢复阶段,患者在接受皮下注射利舒脲和左旋多巴(口服)治疗时,出现了意识模糊、躁动和幻觉。停止了利舒脲注射,继续使用左旋多巴直至NMS完全缓解。该病例表明,对于NMS的治疗,胃肠外给予利舒脲或其他多巴胺药物如左旋多巴(静脉注射)或阿扑吗啡(皮下注射)可能是一种有效且实用的方法,尤其是当患者病情使得经口服途径使用其他多巴胺能药物困难或不可能时。

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