Claro Juan Carlos, Candia Roberto, Rada Gabriel, Baraona Fernando, Larrondo Francisco, Letelier Luz M
Department of Internal Medicine and Evidence-Based Healthcare Program, Faculty of Medicine, Pontificia Universidad Católica de Chile, Lira 63, 1st floor, Santiago, Region Metropolitana, Chile.
Cochrane Database Syst Rev. 2015 Dec 8;2015(12):CD008093. doi: 10.1002/14651858.CD008093.pub2.
Sudden cardiac death (SCD) is one of the main causes of cardiac death. There are two main strategies to prevent it: managing cardiovascular risk factors and reducing the risk of ventricular arrhythmias. Implantable cardiac defibrillators (ICDs) constitute the standard therapy for both primary and secondary prevention; however, they are not widely available in settings with limited resources. The antiarrhythmic amiodarone has been proposed as an alternative to ICD.
To evaluate the effectiveness of amiodarone for primary or secondary prevention in SCD compared with placebo or no intervention or any other antiarrhythmic drugs in participants at high risk (primary prevention) or who have recovered from a cardiac arrest or a syncope due to Ventricular Tachycardia/Ventricular Fibrillation, or VT/VF (secondary prevention).
We searched the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE (OVID), EMBASE (OVID), CINAHL (EBSCO) and LILACS on 26 March 2015. We reviewed reference lists of included studies and selected reviews on the topic, contacted authors of included studies, screened relevant meetings and searched in registers for ongoing trials. We applied no language restrictions.
Randomised and quasi-randomised trials assessing the efficacy of amiodarone versus placebo, no intervention, or other antiarrhythmics in adults. For primary prevention we considered participants at high risk for SCD. For secondary prevention we considered participants recovered from cardiac arrest or syncope due to ventricular arrhythmias.
Two authors independently assessed the trials for inclusion and extracted relevant data. We contacted trial authors for missing data. We performed meta-analyses using a random-effects model. We calculated risk ratios (RR) for dichotomous outcomes with 95% confidence intervals (CIs). Three studies included more than one comparison.
We included 24 studies (9,997 participants). Seventeen studies evaluated amiodarone for primary prevention and six for secondary prevention. Only three studies used an ICD concomitantly with amiodarone for the comparison (all of them for secondary prevention).For primary prevention, amiodarone compared to placebo or no intervention (17 studies, 8383 participants) reduced SCD (RR 0.76; 95% CI 0.66 to 0.88), cardiac mortality (RR 0.86; 95% CI 0.77 to 0.96) and all-cause mortality (RR 0.88; 95% CI 0.78 to 1.00). The quality of the evidence was low.Compared to other antiarrhythmics (three studies, 540 participants), amiodarone reduced SCD (RR 0.44; 95% CI 0.19 to 1.00), cardiac mortality (RR 0.41; 95% CI 0.20 to 0.86) and all-cause mortality (RR 0.37; 95% CI 0.18 to 0.76). The quality of the evidence was moderate.For secondary prevention, amiodarone compared to placebo or no intervention (two studies, 440 participants) appeared to increase the risk of SCD (RR 4.32; 95% CI 0.87 to 21.49) and all-cause mortality (RR 3.05; 1.33 to 7.01). However, the quality of the evidence was very low. Compared to other antiarrhythmics (four studies, 839 participants) amiodarone appeared to increase the risk of SCD (RR 1.40; 95% CI 0.56 to 3.52; very low quality of evidence), but there was no effect in all-cause mortality (RR 1.03; 95% CI 0.75 to 1.42; low quality evidence).Amiodarone was associated with an increase in pulmonary and thyroid adverse events.
AUTHORS' CONCLUSIONS: There is low to moderate quality evidence that amiodarone reduces SCD, cardiac and all-cause mortality when compared to placebo or no intervention for primary prevention, and its effects are superior to other antiarrhythmics.It is uncertain if amiodarone reduces or increases SCD and mortality for secondary prevention because the quality of the evidence was very low.
心源性猝死(SCD)是心脏性死亡的主要原因之一。预防SCD主要有两种策略:控制心血管危险因素和降低室性心律失常风险。植入式心脏除颤器(ICD)是一级和二级预防的标准治疗方法;然而,在资源有限的环境中,其普及程度并不高。抗心律失常药物胺碘酮已被提议作为ICD的替代药物。
评估在高危参与者(一级预防)或因室性心动过速/心室颤动(VT/VF)导致心脏骤停或晕厥后已恢复的参与者(二级预防)中,与安慰剂、无干预措施或任何其他抗心律失常药物相比,胺碘酮用于SCD一级或二级预防的有效性。
我们于2015年3月26日检索了Cochrane对照试验中心注册库(CENTRAL)、MEDLINE(OVID)、EMBASE(OVID)、护理学与健康领域数据库(CINAHL,EBSCO)和拉丁美洲及加勒比地区卫生科学数据库(LILACS)。我们查阅了纳入研究的参考文献列表并筛选了关于该主题的综述,联系了纳入研究的作者,筛选了相关会议,并在注册库中检索了正在进行的试验。我们未设语言限制。
评估胺碘酮与安慰剂、无干预措施或其他抗心律失常药物在成人中疗效的随机和半随机试验。对于一级预防,我们考虑SCD高危参与者。对于二级预防,我们考虑因室性心律失常导致心脏骤停或晕厥后已恢复的参与者。
两位作者独立评估试验是否纳入并提取相关数据。我们联系试验作者获取缺失数据。我们使用随机效应模型进行荟萃分析。我们计算二分类结局的风险比(RR)及95%置信区间(CI)。三项研究包含不止一项比较。
我们纳入了24项研究(9997名参与者)。17项研究评估胺碘酮用于一级预防,6项用于二级预防。仅三项研究在比较中同时使用ICD与胺碘酮(均为二级预防)。对于一级预防,与安慰剂或无干预措施相比(17项研究,8383名参与者),胺碘酮降低了SCD(RR 0.76;95%CI 0.66至0.88)、心脏性死亡率(RR 0.86;95%CI 0.77至0.96)和全因死亡率(RR 0.88;95%CI 0.78至1.00)。证据质量低。与其他抗心律失常药物相比(三项研究,540名参与者),胺碘酮降低了SCD(RR 0.44;95%CI 0.(此处原文有误,应为0.19至1.00))、心脏性死亡率(RR 0.41;95%CI 0.20至0.86)和全因死亡率(RR 0.37;95%CI 0.18至0.)(此处原文有误,应为0.76)。证据质量中等。对于二级预防,与安慰剂或无干预措施相比(两项研究,440名参与者),胺碘酮似乎增加了SCD风险(RR 4.32;95%CI 0.87至21.49)和全因死亡率(RR 3.05;1.33至7.01)。然而,证据质量极低。与其他抗心律失常药物相比(四项研究,839名参与者),胺碘酮似乎增加了SCD风险(RR 1.40;95%CI 0.56至3.52;证据质量极低),但对全因死亡率无影响(RR 1.03;95%CI 0.75至1.42;证据质量低)。胺碘酮与肺部和甲状腺不良事件增加相关。
有低至中等质量的证据表明,与安慰剂或无干预措施相比,胺碘酮在一级预防中可降低SCD、心脏性和全因死亡率,且其效果优于其他抗心律失常药物。对于二级预防,胺碘酮是否降低或增加SCD及死亡率尚不确定,因为证据质量极低。