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洛哌丁胺中毒的心电图改变:病例报告及文献复习。

Electrocardiographic changes in loperamide toxicity: Case report and review of literature.

机构信息

Division of Cardiac Electrophysiology, Virginia Commonwealth University, Richmond, Virginia.

Capital Cardiology Associates, Albany Medical Center, Albany, New York.

出版信息

J Cardiovasc Electrophysiol. 2019 Nov;30(11):2618-2626. doi: 10.1111/jce.14129. Epub 2019 Aug 29.

Abstract

INTRODUCTION

Loperamide, an antidiarrheal agent, is a µ-opioid receptor agonist increasingly abused to prevent opioid withdrawal or to produce euphoric effects. At supra-therapeutic doses, loperamide can cause cardiac toxicity due to blockade of Na and I channels, resulting in wide QRS rhythms, severe bradycardia, prolonged QTc, polymorphic ventricular tachycardia, cardiac arrest, and death. There are limited data on the cardiotoxic effects of high dose loperamide.

METHODS AND RESULTS

A case report of loperamide toxicity is presented and then added to a contemporary review of the literature. In total, the presentation and management of 36 cases of loperamide cardiotoxicity are summarized. The overall median daily dose (interquartile range) of loperamide was 200 (134-400) mg. The median QRS duration was 160 (125-170) ms. The median QTc duration was 620 (565-701) ms. Ventricular tachycardia was experienced by 24/36 (67%) of patients, 20 of which were specified to be polymorphic. Treatment was supportive, providing advanced cardiopulmonary life support and aggressive electrolyte repletion. Isoproterenol infusion or overdrive pacing was employed in 19/36 (53%) of cases. The median time to electrocardiogram normalization or hospital discharge, whichever came first, was 5 (3.5-10) days.

CONCLUSION

Loperamide overdose is a toxidrome that remains underrecognized, and in patients with unexplained cardiac arrhythmias, loperamide toxicity should be suspected. Prompt recognition is critical due to the delayed recovery and high risk for life-threatening arrhythmias.

摘要

简介

洛哌丁胺是一种止泻药,作为 µ 阿片受体激动剂,其滥用情况日益增多,用于预防阿片类药物戒断或产生欣快感。在超治疗剂量下,洛哌丁胺可通过阻断钠和 I 通道导致心脏毒性,从而引起宽 QRS 节律、严重心动过缓、QTc 延长、多形性室性心动过速、心脏骤停和死亡。关于大剂量洛哌丁胺的心脏毒性作用的数据有限。

方法和结果

报告了 1 例洛哌丁胺中毒病例,并结合当代文献复习进行了讨论。共总结了 36 例洛哌丁胺心脏毒性的表现和处理。洛哌丁胺的每日总剂量(四分位间距)中位数为 200(134-400)mg。QRS 持续时间中位数为 160(125-170)ms。QTc 持续时间中位数为 620(565-701)ms。24/36(67%)的患者发生室性心动过速,其中 20 例为多形性。治疗为支持性的,提供高级心肺生命支持和积极的电解质补充。19/36(53%)的患者使用异丙肾上腺素输注或超速起搏。心电图正常或首次出院的中位时间为 5(3.5-10)天。

结论

洛哌丁胺过量是一种毒理学综合征,目前仍未被充分认识。对于不明原因的心律失常患者,应怀疑洛哌丁胺中毒。由于恢复延迟和发生危及生命的心律失常的风险高,因此及时识别至关重要。

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