阿西米利特治疗心房颤动:临床试验结果和意义。

Edward L C Pritchett, Stephen R Marcello
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引用次数: 7

摘要

盐酸阿齐米特(Azimilide dihydrochloride,或Azimilide)是一种III类抗心律失常药物,目前正在研究中,已在四项随机、安慰剂对照的临床试验中对心房颤动进行了测试,以评估其疗效和剂量范围。这些研究性试验表明,阿齐米利100和125 mg每日一次的剂量延长了有症状性心房颤动、心房扑动或两者兼有病史的患者出现症状性心律失常复发的时间。75毫克或更少的剂量在这个适应症中是无效的。阿西米利特的安全性已经在几个不同类型的研究中进行了检验。在一项针对梗死后患者的大型随机临床试验中,阿齐米利特既没有增加也没有降低死亡风险。在室上性心律失常患者中,阿齐米利特患者报告的最常见不良反应与安慰剂患者报告的最常见不良反应的频率大致相同:头痛、乏力、感染、腹泻和头晕。在服用阿齐米利的患者中,报告了罕见的足尖扭转和严重的中性粒细胞减少症。阿齐米利是一种实验性抗心律失常药物,已在心房颤动患者中显示出疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Azimilide for atrial fibrillation: clinical trial results and implications.

Azimilide dihydrochloride (or azimilide) is a class III antiarrhythmic drug currently under investigation that has been tested in atrial fibrillation in four randomized, placebo-controlled clinical trials to assess efficacy and dose range. These investigational trials showed that doses of azimilide 100 and 125 mg once daily prolonged the time to symptomatic arrhythmia recurrence in patients with a history of symptomatic atrial fibrillation, atrial flutter or both. Doses of 75 mg or less were not useful in this indication. Safety of azimilide has been examined in several different types of studies. In a large randomized clinical trial of post-infarct patients, azimilide neither increased nor decreased mortality risk. In patients with supraventricular arrhythmias, the most common adverse effects reported by patients on azimilide were approximately equal in frequency with those on placebo: headache, asthenia, infection, diarrhea and dizziness. Infrequent cases of torsade de pointes and severe neutropenia were reported in patients taking azimilide. Azimilide is an investigational antiarrhythmic drug that has shown efficacy in patients with atrial fibrillation.

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