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盐酸决奈达隆:概述。

Dronedarone: an overview.

机构信息

Department of Cardiology and Electrotherapy, Second Chair of Cardiology, Medical University of Gdansk, Poland.

出版信息

Ann Med. 2012 Feb;44(1):60-72. doi: 10.3109/07853890.2011.594808. Epub 2011 Jul 11.

Abstract

Atrial fibrillation (AF) is the most common arrhythmia encountered in clinical practice. Until recently, a rhythm control strategy for AF has been limited by drug toxicity and side-effects, and landmark AF trials have shown that such a strategy is not superior to a rate control one. New antiarrhythmic drugs, free of undesired effects, would enhance the rhythm control strategy, with the possibility of sinus rhythm restoration and maintenance. One of the promising drugs recently approved for clinical use is dronedarone. This drug has amiodarone-like antiarrhythmic and electrophysiological properties, despite it having a modified structure and lacking an iodine moiety. Thus, dronedarone lacks amiodarone's organ toxicity (including adverse thyroid and pulmonary effects). The efficacy of dronedarone has been investigated in several clinical trials, proving its effect in the prevention of AF recurrence, rate control in paroxysmal/persistent and permanent AF, reduction of cardiovascular hospitalization or death from any cause, and others. Indirect comparisons with amiodarone, as well as one head-to-head study of the two drugs, indicate that the relative safety of dronedarone may be at a cost of its lower antiarrhythmic efficacy compared with amiodarone.

摘要

心房颤动(AF)是临床实践中最常见的心律失常。直到最近,AF 的节律控制策略一直受到药物毒性和副作用的限制,并且标志性的 AF 试验表明,这种策略并不优于心率控制策略。没有不良影响的新型抗心律失常药物将增强节律控制策略,有可能恢复和维持窦性节律。最近批准用于临床的一种有前途的药物是决奈达隆。尽管该药物具有改良的结构且不含碘部分,但它具有胺碘酮样抗心律失常和电生理特性。因此,决奈达隆缺乏胺碘酮的器官毒性(包括甲状腺和肺部的不良反应)。决奈达隆的疗效已在几项临床试验中得到证实,证明其在预防 AF 复发、阵发性/持续性和永久性 AF 的心率控制、减少心血管住院或任何原因导致的死亡等方面有效。与胺碘酮的间接比较,以及这两种药物的一项头对头研究表明,与胺碘酮相比,决奈达隆的相对安全性可能是以其较低的抗心律失常疗效为代价的。

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