Harsch H H
J Clin Psychiatry. 1987 Aug;48(8):328-33.
A series of nine cases of neuroleptic malignant syndrome (NMS) are presented with peak measures of autonomic dysfunction and laboratory findings. Urine abnormalities, consisting of proteinuria, casts, or cells, were an associated finding in these cases. Severe hypophosphatemia was present in two patients. Relative dehydration before the onset of the syndrome in eight of the nine patients supports the suggestion that it is a risk factor for the development of NMS. The withdrawal of dopamine agonists was also seen as a trigger for NMS. Autonomic instability and muscular rigidity occurred separately in some cases. Creatine phosphokinase elevation and fever did not necessarily parallel the duration or the degree of muscular rigidity, and this finding supports the idea of a central cause for the symptoms. A systematic approach is presented for the evaluation and treatment of NMS. Observations implicate central dopaminergic mechanisms in the regulation of autonomic functioning and the maintenance of peripheral muscle membrane stability.
本文报告了9例神经阻滞剂恶性综合征(NMS)病例,呈现了自主神经功能障碍的峰值指标和实验室检查结果。这些病例的相关发现包括蛋白尿、管型或细胞等尿液异常。两名患者出现严重低磷血症。9名患者中有8名在综合征发作前存在相对脱水,这支持了脱水是NMS发生的一个危险因素的观点。停用多巴胺激动剂也被视为NMS的一个触发因素。在某些病例中,自主神经不稳定和肌肉僵硬分别出现。肌酸磷酸激酶升高和发热不一定与肌肉僵硬的持续时间或程度平行,这一发现支持了症状由中枢原因引起的观点。本文提出了一种评估和治疗NMS的系统方法。观察结果表明,中枢多巴胺能机制参与自主功能的调节和外周肌肉膜稳定性的维持。