Marelli A, Bodini P, Dizioli P, Chiodelli G, Guarneri M, Boldori L
Divisione di Medicina II, Azienda Ospedaliera, Istituti Ospitalieri, Cremona.
Minerva Med. 1996 Jan-Feb;87(1-2):45-51.
Neuroleptic malignant syndrome (NMS), characterized by catatonic behavior, generalized muscular rigidity, hyperthermia and autonomic dysfunction, can suddenly arise in patients treated with neuroleptic agents and carries a high mortality rate even today. A case of NMS due to i.m. therapy with haloperidol decanoate is reported in this paper, characterized by sustained course and a severe relapse due to a different therapy with another neuroleptic agent. The patient however, after a prolonged remission from the relapse, was able to resume long term therapy with neuroleptic drugs. The importance of monitoring blood levels of CPK during the follow-up and the effectiveness of therapy with bromocriptine and dantrolene in confirmed. Although the patient presented a good clinical response, she developed permanent cerebral and muscular damage. A wide review of the literature on NMS is reported to throw light on this syndrome, whose recognition and prompt diagnosis are necessary to reduce mortality.
抗精神病药恶性综合征(NMS)以紧张症行为、全身肌肉僵硬、高热及自主神经功能障碍为特征,在用抗精神病药治疗的患者中可能突然出现,即使在今天其死亡率仍很高。本文报告1例因肌肉注射癸酸氟哌啶醇治疗导致的NMS,其特点为病程持续,且因换用另一种抗精神病药治疗而出现严重复发。然而,该患者在复发后经过长时间缓解,能够重新开始使用抗精神病药物进行长期治疗。随访期间监测肌酸磷酸激酶(CPK)血药浓度的重要性以及溴隐亭和丹曲林治疗的有效性得到证实。尽管该患者临床反应良好,但仍出现了永久性脑和肌肉损伤。本文对NMS的文献进行了广泛综述,以阐明该综合征,其识别和及时诊断对于降低死亡率至关重要。