Nichol G, McAlister F, Pham B, Laupacis A, Shea B, Green M, Tang A, Wells G
Clinical Epidemiology Program, Ottawa Health Research Institute, Ottawa Hospital, Ottawa, Ontario, Canada.
Heart. 2002 Jun;87(6):535-43. doi: 10.1136/heart.87.6.535.
To conduct a meta-analysis of randomised controlled trials to estimate the effectiveness of antiarrhythmic drugs at promoting sinus rhythm in patients with atrial fibrillation.
Articles were identified by using a comprehensive search of English language papers indexed in Medline from 1966 to August 2001. For the outcomes of sinus rhythm and death, a random effects model was used to model repeated assessments within a study at different time points.
Emergency departments and ambulatory clinics.
Patients with atrial fibrillation.
Antiarrhythmic agents grouped according to their Vaughan-Williams class.
Sinus rhythm and mortality.
91 articles met a priori criteria for inclusion in the analysis. Median duration of follow up was one day (range 0.04-1096, mean (SD) 46 (136) days). The median proportion of patients in sinus rhythm at follow up was 55% (range 0-100%) and 32% (range 0-90%) receiving active treatment and placebo, respectively. Median survival was 99% (range 55-100%) and 99% (range 55-100%). Compared with placebo, the following drug classes were associated with increased sinus rhythm at follow up: IA (treatment difference 21.5%, 95% confidence interval (CI) 16.3% to 26.8%); IC (treatment difference 33.1%, 95% CI 23.3% to 42.9%); and III (treatment difference 17.4%, 95% CI 11.5% to 23.3%). Class IC drugs were associated with increased sinus rhythm at follow up compared with class IV drugs (treatment difference 43.2%, 95% CI 11.5% to 75.0%). There was no significant difference in mortality between any drug classes.
Class IA, IC, and III drugs are associated with increased sinus rhythm at follow up compared with placebo. It is unclear whether any antiarrhythmic drug class is associated with increased or decreased mortality.
进行一项随机对照试验的荟萃分析,以评估抗心律失常药物促使心房颤动患者恢复窦性心律的有效性。
通过全面检索1966年至2001年8月Medline索引中的英文论文来识别文章。对于窦性心律和死亡结局,采用随机效应模型对研究中不同时间点的重复评估进行建模。
急诊科和门诊诊所。
心房颤动患者。
抗心律失常药物根据其 Vaughan-Williams 分类进行分组。
窦性心律和死亡率。
91篇文章符合纳入分析的预先设定标准。随访的中位持续时间为1天(范围0.04 - 1096天,均值(标准差)46(136)天)。随访时窦性心律患者的中位比例分别为55%(范围0 - 100%)和32%(范围0 - 90%),分别接受积极治疗和安慰剂治疗。中位生存率分别为99%(范围55 - 100%)和99%(范围55 - 100%)。与安慰剂相比,以下药物类别在随访时与窦性心律增加相关:IA类(治疗差异21.5%,95%置信区间(CI)16.3%至26.8%);IC类(治疗差异33.1%,95%CI 23.3%至42.9%);III类(治疗差异17.4%,95%CI 11.5%至23.3%)。与IV类药物相比,IC类药物在随访时与窦性心律增加相关(治疗差异43.2%,95%CI 11.5%至75.0%)。任何药物类别之间的死亡率均无显著差异。
与安慰剂相比,IA类、IC类和III类药物在随访时与窦性心律增加相关。尚不清楚任何抗心律失常药物类别是否与死亡率增加或降低相关。