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全麻后纳洛酮反应性急性肌张力障碍和帕金森病。

Naloxone-responsive acute dystonia and parkinsonism following general anaesthesia.

机构信息

Department of Anaesthesiology, Geneva University Hospitals and Faculty of Medicine, Genève, Switzerland.

出版信息

Anaesthesia. 2009 Dec;64(12):1359-62. doi: 10.1111/j.1365-2044.2009.06068.x. Epub 2009 Oct 15.

Abstract

Various movement disorders such as dystonia may acutely develop during or at emergence from general anaesthesia in patients with or without pre-existing Parkinson disease. These movements are triggered by a variety of drugs including propofol, sevoflurane, anti-emetics, antipsychotics and opioids. The postulated mechanism involves an imbalance between dopaminergic and cholinergic neurotransmitters in the basal ganglia. We report an acute, severe and generalised dystonic reaction in an otherwise healthy woman at emergence from general anaesthesia, dramatically reversed by the administration of naloxone, pointing to a potential role of the fentanyl and morphine that the patient had received. Recent literature on the mechanisms of abnormal movements induced by opioids are discussed. The severity of the reaction with usual doses of opioids, in a patient with no prior history of parkinsonism, led to further investigation that demonstrated the possibility of an enhanced susceptibility to opioids, involving a genetically determined abnormal function of glycoproteine-P and catechol-O-methyltransferase.

摘要

各种运动障碍,如肌张力障碍,可能在伴有或不伴有帕金森病的患者全身麻醉期间或麻醉苏醒时急性发作。这些运动是由包括丙泊酚、七氟醚、止吐药、抗精神病药和阿片类药物等多种药物引发的。其推测的机制涉及基底节中多巴胺能和胆碱能神经递质之间的不平衡。我们报告了一例在全身麻醉苏醒时出现的急性、严重和全身性肌张力障碍反应的健康女性患者,给予纳洛酮后反应戏剧性逆转,提示患者接受的芬太尼和吗啡可能起作用。讨论了阿片类药物引起异常运动的机制的最新文献。在没有帕金森病病史的患者中,通常剂量的阿片类药物引起的反应的严重程度促使进一步调查,表明对阿片类药物的敏感性增强的可能性,涉及糖蛋白-P 和儿茶酚-O-甲基转移酶的遗传决定的异常功能。

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