Azimilide, a novel oral class III antiarrhythmic for both supraventricular and ventricular arrhythmias.

Robert A VerNooy, J Michael Mangrum
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引用次数: 11

Abstract

Azimilide is an investigational Class III antiarrhythmic that has been developed for treating both supraventricular and ventricular tachyarrhythmias. Similar to other Class III antiarrhythmics, azimilide prolongs myocardial repolarization in a dose-dependent manner by increasing the action potential duration, QT interval, and effective refractory period. The most frequent reported side effect is headache, with rare serious adverse events of early reversible neutropenia and Torsades de Pointes. In long-term follow up, the patient withdrawal rate has been low. Azimilide has very predictable pharmacokinetics, is predominantly hepatically metabolized, and has no significant drug interactions with digoxin or warfarin. In animal models, azimilide has been shown to be very effective in suppressing both atrial and ventricular tachyarrhythmias, decreasing the defibrillation energy requirement, and preventing post-myocardial infarction ventricular tachycardia and fibrillation. Clinically, in a series of 4 double-blind, randomized, placebo-controlled trials, the Azimilide Supraventricular Arrhythmia Program which included over 1000 patients and approximately 70% with structural heart disease, azimilide showed a significant prolongation in the time to first recurrence of paroxysmal supraventricular tachycardia or atrial fibrillation/flutter. With respect to ventricular tachyarrhythmias, the AzimiLide post-Infarct surVival Evaluation Trial was a large randomized, multinational, prospective, placebo-controlled study in recent survivors of myocardial infarction at high risk for sudden cardiac death. After 1 year of follow-up, this study showed no statistical difference in all-cause mortality between placebo and azimilide. However, azimilide did statistically reduce the incidence of new atrial fibrillation. Further trials are necessary to evaluate the efficacy of azimilide in patients with symptomatic ventricular arrhythmias.

Azimilide,一种新型口服III类抗室上性和室性心律失常药物。
Azimilide是一种III类抗心律失常药物,已被开发用于治疗室上性和室性心动过速。与其他III类抗心律失常药类似,阿齐米胺通过增加动作电位持续时间、QT间期和有效不应期,以剂量依赖的方式延长心肌复极。最常见的副作用是头痛,罕见的严重不良事件是早期可逆性中性粒细胞减少症和角状畸形。在长期随访中,患者退出率低。Azimilide具有非常可预测的药代动力学,主要是肝脏代谢,并且与地高辛或华法林没有明显的药物相互作用。在动物模型中,azimilide已被证明在抑制房性和室性心动过速,降低除颤能量需求,预防心肌梗死后室性心动过速和颤动方面非常有效。临床上,在4个双盲、随机、安慰剂对照试验中,阿兹米利特室上性心律失常项目纳入了1000多例患者,其中约70%为结构性心脏病患者,阿兹米利特在阵发性室上性心动过速或房颤/扑动的首次复发时间显著延长。关于室性心动过速,AzimiLide梗死后生存评估试验是一项大型随机、多国、前瞻性、安慰剂对照研究,研究对象是近期高危心源性猝死的心肌梗死幸存者。经过1年的随访,本研究显示安慰剂组和阿齐米利特组的全因死亡率无统计学差异。然而,azimilide在统计学上确实降低了新发房颤的发生率。需要进一步的试验来评估阿齐米利特对症状性室性心律失常患者的疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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