Cardiology Department, Cumhuriyet University, Sivas, 58100, Turkey.
Cardiovasc Drugs Ther. 2009 Oct;23(5):385-93. doi: 10.1007/s10557-009-6189-0.
Atrial fibrillation (AF) is the most frequently encountered chronic arrhythmia associated with significant morbidity. It is generally encountered in the elderly, and will presumably become more prevalent in the future due to the increasing proportion of the elderly in the population. Major studies on AF have demonstrated no significant difference between rhythm and rate control in terms of mortality. However, young population with new-onset or lone AF, or patients in whom the maintenance of sinus rhythm is a must (due to recurrent thromboembolic events etc.) still gives rise to significant concerns related to the obligatory long-term prophylaxis. The long-term administration of the currently available conventional agents (amiodarone, dofetilide, sotalol, propafenone,flecainide etc.) is considered as a 'double edged sword' due to the presence of life-threatening adverse effects including pro-arrhythmia and organ toxicity associated with these agents. Several molecules are being developed for the management of AF. However, only a few novel agents confer promising results with respect to safety and efficacy issues in the major studies.
Dronedarone is an amiodarone analogue without iodine moiety in its structure, and is similar to amiodarone with regard to its structural and electrophysiological properties. Dronedarone is largely denuded of the potentially life-threatening adverse effects of anti-arrhythmics. Major clinical studies have demonstrated both rhythm and rate-controlling efficacy of dronedarone compared to placebo without any serious adverse effects in patients with AF. However, the ANDROMEDA trial, a large scale study including patients hospitalized for symptomatic congestive heart failure (with severely depressed left ventricular systolic functions) was prematurely terminated due to the increased mortality in the dronedarone arm compared to placebo indicating a lack of safety in this group of patients. Conversely, the recently published ATHENA study (including more than 4,600 high risk patients, but excluding those with severe heart failure) demonstrated a significant reduction in cardiovascular hospitalizations and cardiovascular mortality with dronedarone compared to placebo. In contrast, the DIONYSOS study, comparing dronedarone with amiodarone, demonstrated better safety, but lower efficacy of dronedarone for the maintenance of sinus rhythm in patients with AF.
Further clinical trials (including head to head comparison with other conventional anti-arrhythmics) are still required to determine the place of dronedarone in the management of AF. The present review focuses on basic and clinical aspects of dronedarone, a novel agent for the management of AF.
心房颤动(AF)是最常见的慢性心律失常,与显著的发病率相关。它通常发生在老年人中,并且由于人口中老年人的比例增加,预计未来会更加普遍。关于 AF 的主要研究表明,在死亡率方面,节律控制和心率控制之间没有显著差异。然而,对于新发生或孤立性 AF 的年轻人群,或窦性节律的维持是必须的(由于反复发生血栓栓塞事件等)的患者,仍然会引起与强制性长期预防相关的重大关注。目前可用的常规药物(胺碘酮、多非利特、索他洛尔、普罗帕酮、氟卡尼等)的长期应用被认为是一把“双刃剑”,因为这些药物存在危及生命的不良反应,包括致心律失常和器官毒性。正在开发几种用于治疗 AF 的分子。然而,只有少数新型药物在主要研究中显示出在安全性和疗效方面有希望的结果。
决奈达隆是一种结构中不含碘原子的胺碘酮类似物,其结构和电生理特性与胺碘酮相似。决奈达隆在很大程度上没有抗心律失常药物潜在的危及生命的不良反应。主要临床研究表明,与安慰剂相比,决奈达隆在 AF 患者中具有节律和心率控制作用,且无严重不良反应。然而,ANDROMEDA 试验是一项大型研究,包括因充血性心力衰竭住院的患者(左心室收缩功能严重降低),由于决奈达隆组的死亡率高于安慰剂组,该试验提前终止,表明该组患者的安全性存在问题。相反,最近发表的 ATHENA 研究(包括 4600 多名高危患者,但不包括严重心力衰竭患者)表明,与安慰剂相比,决奈达隆可显著减少心血管住院和心血管死亡率。相比之下,DIONYSOS 研究比较了决奈达隆与胺碘酮,表明决奈达隆在维持 AF 患者窦性节律方面的安全性更好,但疗效较低。
仍需要进一步的临床试验(包括与其他常规抗心律失常药物的头对头比较)来确定决奈达隆在 AF 治疗中的地位。本综述重点介绍了决奈达隆这一治疗 AF 的新型药物的基础和临床方面。