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药物性心律失常:临床实践的讨论与思考

Drug-induced proarrhythmia: Discussion and considerations for clinical practice.

作者信息

Klotzbaugh Ralph J, Martin Alejandra, Turner John Rick

机构信息

University of New Mexico College of Nursing, Albuquerque, New Mexico.

Goodwin Community Health Center, Somersworth, New Hampshire.

出版信息

J Am Assoc Nurse Pract. 2020 Feb;32(2):128-135. doi: 10.1097/JXX.0000000000000348.

Abstract

The clinical practice of pharmaceutical medicine includes contributions from physicians, pharmacists, nurse practitioners, and physician assistants. Drug safety considerations are of considerable importance. This article discusses drug-induced proarrhythmia, with a specific focus on Torsade de Pointes (Torsade), a polymorphic ventricular tachycardia that typically occurs in self-limiting bursts that can lead to dizziness, palpitations, syncope, and seizures, but on rare occasions can progress to ventricular fibrillation and sudden cardiac death. A dedicated clinical pharmacology study conducted during a drug's clinical development program has assessed its propensity to induce Torsade using prolongation of the QT interval as seen on the surface electrocardiogram (ECG) as a biomarker. Identification of QT-interval prolongation does not necessarily prevent a drug from receiving marketing approval if its overall benefit-risk balance is favorable, but, if approved, a warning is placed in its Prescribing Information. This article explains why drugs can have a proarrhythmic propensity and concludes with a case presentation.

摘要

药物医学的临床实践涵盖了医师、药剂师、执业护士和医师助理的贡献。药物安全考量至关重要。本文讨论药物诱发的心律失常,特别关注尖端扭转型室速(TdP),这是一种多形性室性心动过速,通常以自限性发作形式出现,可导致头晕、心悸、晕厥和癫痫发作,但在极少数情况下可进展为心室颤动和心源性猝死。在药物临床开发项目期间进行的一项专门临床药理学研究,已将体表心电图(ECG)上QT间期延长作为生物标志物,评估了其诱发TdP的倾向。如果药物的总体获益风险平衡有利,QT间期延长的识别并不一定会阻止其获得上市批准,但如果获批,会在其处方信息中给出警告。本文解释了药物为何会有致心律失常倾向,并以一个病例展示作为结尾。

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