Robinson Samuel
University of Missouri, United States of America.
Am J Emerg Med. 2022 May;55:232.e3-232.e4. doi: 10.1016/j.ajem.2022.02.016. Epub 2022 Feb 8.
Bupropion is an atypical antidepressant often used in the treatment of depression, tobacco cessation, seasonal affective disorder, and off label for ADHD. Its primary mechanism of action is by blocking dopamine and norepinephrine reuptake and it is structurally similar to amphetamines. Toxic effects include, most notably and classically, seizures as well as tachycardia, agitation, nausea and vomiting, QT prolongation, QRS widening, hypertension/hypotension. It has a narrow therapeutic window with maximal daily dosing being 450 mg daily. We are reporting the case of a 14-year-old female who ingested 15 g of extended-release bupropion resulting in agitation, status epilepticus, prolonged QT devolving into pulseless Ventricular Tachycardia and briefly V Fib, requiring a total of 5 cardioversions and 1 defibrillation. The QT interval eventually narrowed after supportive care and lidocaine drip. The patient was able to be extubated just two days later with full cognitive function and echocardiogram without cardiac dysfunction. Seizure and cardiotoxicity (including prolonged QT) have been previously described with massive bupropion overdoses. To our knowledge, deterioration to Ventricular Tachycardia and Ventricular Fibrillation with successful treatment and shortening of QT interval with lidocaine bolus and drip has not been reported. Cardiotoxicity related to bupropion has previously been primarily supportive and avoidance of QT prolonging antiarrhythmics such as amiodarone, and at times requiring VA ECMO. Lidocaine has previously been used in tox cases to shorten QT intervals. The hope is for this information to be helpful to other EM and Critical Care providers when placed in similarly difficult circumstances.
安非他酮是一种非典型抗抑郁药,常用于治疗抑郁症、戒烟、季节性情感障碍,也可用于治疗注意缺陷多动障碍(ADHD)的非适应证用药。其主要作用机制是阻断多巴胺和去甲肾上腺素的再摄取,在结构上与苯丙胺相似。毒性作用最显著且典型的包括癫痫发作,以及心动过速、激动、恶心和呕吐、QT间期延长、QRS波增宽、高血压/低血压。其治疗窗较窄,最大日剂量为每日450毫克。我们报告一例14岁女性病例,该患者摄入15克缓释型安非他酮,导致激动、癫痫持续状态、QT间期延长发展为无脉性室性心动过速,并短暂出现室颤,共需要5次心脏复律和1次除颤。经过支持治疗和利多卡因静脉滴注后,QT间期最终变窄。患者仅在两天后就能够拔管,认知功能完全恢复,超声心动图显示无心脏功能障碍。此前已有大量安非他酮过量导致癫痫发作和心脏毒性(包括QT间期延长)的报道。据我们所知,尚未有因安非他酮过量导致发展为室性心动过速和室颤,经成功治疗后QT间期缩短,且使用利多卡因推注和静脉滴注治疗的报道。此前与安非他酮相关的心脏毒性主要是支持性治疗,避免使用如胺碘酮等可延长QT间期的抗心律失常药物,有时需要体外膜肺氧合(VA ECMO)。利多卡因此前已用于中毒病例以缩短QT间期。希望这些信息能在其他急诊医学和重症监护人员遇到类似困难情况时有所帮助。