Doyle James F, Ho Kwok M
Intensive Care Unit, Royal Perth Hospital and School of Population Health, University of Western Australia, Perth, Western Australia, Australia 6000.
Mayo Clin Proc. 2009 Mar;84(3):234-42. doi: 10.4065/84.3.234.
To assess whether amiodarone, as part of a strategy to achieve sinus rhythm, is safe and effective compared with a placebo or rate control drug in patients with persistent atrial fibrillation (AF) of more than 30 days' duration.
Randomized controlled trials comparing amiodarone with a placebo or rate control drug were identified through the EMBASE (January 1, 1988, to October 18, 2008), MEDLINE (January 1, 1966, to October 18, 2008), and Cochrane Controlled Trials Register (second issue 2008) databases with no language restrictions.
Twelve randomized controlled trials that involved a total of 5060 patients with persistent AF were considered. Amiodarone was more effective than a placebo or rate control drug in achieving sinus rhythm (21.3 vs 9.2 per 100 patient-years in sinus rhythm; relative risk [RR], 3.2; 95% confidence interval [CI], 1.9-5.5), and its use was not associated with an increased risk of long-term mortality (4.7 vs 3.9 per 100 patient-years; RR, 0.95; 95% CI, 0.8-1.1; P=.51; I2=0%). Cessation of amiodarone therapy because of intolerable adverse effects was more common compared with a placebo or rate control drug (10.7 vs 1.9 per 100 patient-years; RR, 3.0; 95% CI, 1.4-6.2; P<.001; I2=70%), but amiodarone was not associated with an increased incidence of hospitalizations (RR, 1.1; 95% CI, 0.6-2.1; P=.77; I2=90%).
Amiodarone, as part of a strategy to achieve and maintain sinus rhythm, appears to be safe and effective in patients with persistent AF. However, some patients may not tolerate the adverse effects of this agent.
评估胺碘酮作为恢复窦性心律策略的一部分,与安慰剂或心率控制药物相比,在持续时间超过30天的持续性心房颤动(房颤)患者中是否安全有效。
通过EMBASE(1988年1月1日至2008年10月18日)、MEDLINE(1966年1月1日至2008年10月18日)和Cochrane对照试验注册库(2008年第2期)数据库,识别比较胺碘酮与安慰剂或心率控制药物的随机对照试验,无语言限制。
纳入12项随机对照试验,共涉及5060例持续性房颤患者。胺碘酮在恢复窦性心律方面比安慰剂或心率控制药物更有效(窦性心律每100患者年分别为21.3例和9.2例;相对危险度[RR],3.2;95%置信区间[CI],1.9 - 5.5),且其使用与长期死亡率增加无关(每100患者年分别为4.7例和3.9例;RR,0.95;95% CI,0.8 - 1.1;P = 0.51;I² = 0%)。因无法耐受的不良反应而停用胺碘酮治疗比安慰剂或心率控制药物更常见(每100患者年分别为10.7例和1.9例;RR,3.0;95% CI,1.4 - 6.2;P < 0.001;I² = 70%),但胺碘酮与住院率增加无关(RR,1.1;95% CI,0.6 - 2.1;P = 0.77;I² = 90%)。
胺碘酮作为实现和维持窦性心律策略的一部分,在持续性房颤患者中似乎是安全有效的。然而,一些患者可能无法耐受该药物的不良反应。