Department of Neurology, Baylor College of Medicine, 7200 Cambridge Street, Suite 9A, Houston, TX, 77030, USA.
Corporal Michael J. Crescenz Veterans Affairs Medical Center, Philadelphia, PA, USA.
CNS Drugs. 2024 Apr;38(4):239-254. doi: 10.1007/s40263-024-01078-z. Epub 2024 Mar 19.
Drug-induced movement disorders (DIMDs) are associated with use of dopamine receptor blocking agents (DRBAs), including antipsychotics. The most common forms are drug-induced parkinsonism (DIP), dystonia, akathisia, and tardive dyskinesia (TD). Although rare, neuroleptic malignant syndrome (NMS) is a potentially life-threatening consequence of DRBA exposure. Recommendations for anticholinergic use in patients with DIMDs were developed on the basis of a roundtable discussion with healthcare professionals with extensive expertise in DIMD management, along with a comprehensive literature review. The roundtable agreed that "extrapyramidal symptoms" is a non-specific term that encompasses a range of abnormal movements. As such, it contributes to a misconception that all DIMDs can be treated in the same way, potentially leading to the misuse and overprescribing of anticholinergics. DIMDs are neurobiologically and clinically distinct, with different treatment paradigms and varying levels of evidence for anticholinergic use. Whereas evidence indicates anticholinergics can be effective for DIP and dystonia, they are not recommended for TD, akathisia, or NMS; nor are they supported for preventing DIMDs except in individuals at high risk for acute dystonia. Anticholinergics may induce serious peripheral adverse effects (e.g., urinary retention) and central effects (e.g., impaired cognition), all of which can be highly concerning especially in older adults. Appropriate use of anticholinergics therefore requires careful consideration of the evidence for efficacy (e.g., supportive for DIP but not TD) and the risks for serious adverse events. If used, anticholinergic medications should be prescribed at the lowest effective dose and for limited periods of time. When discontinued, they should be tapered gradually.
药物引起的运动障碍(DIMD)与多巴胺受体阻断剂(DRBA)的使用有关,包括抗精神病药。最常见的形式是药物引起的帕金森病(DIP)、肌张力障碍、静坐不能和迟发性运动障碍(TD)。虽然很少见,但神经阻滞剂恶性综合征(NMS)是 DRBA 暴露的潜在危及生命的后果。抗胆碱能药物在 DIMD 患者中的使用建议是基于与在 DIMD 管理方面具有丰富专业知识的医疗保健专业人员进行的圆桌讨论以及全面的文献回顾。圆桌会议一致认为,“锥体外系症状”是一个非特异性术语,涵盖了一系列异常运动。因此,它导致了一种误解,即所有 DIMD 都可以以相同的方式治疗,可能导致抗胆碱能药物的滥用和过度处方。DIMD 在神经生物学和临床上是不同的,具有不同的治疗模式和抗胆碱能药物使用的不同证据水平。虽然有证据表明抗胆碱能药物对 DIP 和肌张力障碍有效,但不建议用于 TD、静坐不能或 NMS;也不建议用于预防 DIMD,除非个体有急性肌张力障碍的高风险。抗胆碱能药物可能会引起严重的外周不良反应(例如,尿潴留)和中枢效应(例如,认知障碍),所有这些在老年人中都非常令人担忧。因此,抗胆碱能药物的适当使用需要仔细考虑疗效的证据(例如,支持 DIP 但不支持 TD)和严重不良事件的风险。如果使用,抗胆碱能药物应在最低有效剂量下开具,并在有限的时间内使用。停药时,应逐渐减少剂量。