心房颤动患者窦性心律的预后影响:将心律结果与 CABANA 试验的随机策略结果区分开来

T. Jared Bunch, Jeanne E. Poole, Adam P. Silverstein, Kerry L. Lee, Hussein R. Al-Khalidi, Gerhard Hindricks, Alexander Romanov, Evgeny Pokushalov, Tristram D. Bahnson, Melanie Daniels, Jonathan P. Piccini, Daniel B. Mark, Douglas L. Packer, for the CABANA Investigators
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Since the advent of effective methods for AF rhythm control, investigators have attempted to determine how much these adverse prognostic AF effects could be mitigated by the restoration of sinus rhythm (SR) and whether the method used mattered.METHODS:The CABANA trial (Catheter Ablation versus Antiarrhythmic Drug Therapy for Atrial Fibrillation) randomized 2204 AF patients to ablation versus drug therapy, of which 1240 patients were monitored in follow-up using the CABANA ECG rhythm monitoring system. To assess the prognostic benefits of SR, we performed a prespecified analysis using Cox survival modeling with heart rhythm as a time-dependent variable and a randomized treatment group as a stratification factor.RESULTS:In the 1240 patient study cohort, 883 (71.2%) had documented AF at some point during their postblanking follow-up. 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引用次数: 0

摘要

背景:临床发现的心房颤动(房颤)与死亡率和其他不良心血管事件的显著增加有关。方法:CABANA 试验(心房颤动导管消融与抗心律失常药物治疗)将 2204 名心房颤动患者随机分为消融与药物治疗两组,其中 1240 名患者使用 CABANA 心电图节律监测系统进行随访监测。为了评估 SR 的预后益处,我们使用 Cox 生存模型进行了预先指定的分析,将心律作为时间依赖变量,随机治疗组作为分层因素。在这 883 名患者中,有 671 人(76.0%)在分组后随访的第一年内出现房颤,212 人(24.0%)在分组后随访≥1 年后首次出现房颤。在有房颤记录的 883 例患者中,有 95 例(10.8%)出现了 CABANA 主要终点(死亡、致残性中风、严重出血或心脏骤停),在随访期间没有房颤记录的 357 例患者中,有 29 例(8.1%)出现了 CABANA 主要终点。在多变量时间依赖性分析中,出现 SR(与非 SR 相比)与主要终点风险显著降低相关(调整后危险比为 0.57 [95% CI, 0.38-0.85]; P=0.006;与治疗策略[消融与药物]无关)。结论:在 CABANA 试验中,对患者进行了详细的长期心律随访,SR 时间的延长与死亡率和其他不良预后事件的临床减少有关。SR的预测价值与减少可检测到的房颤负担的治疗方法无关。注册:URL:https://clinicaltrials.gov;唯一标识符:NCT00911508:NCT00911508
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Prognostic Impact of Sinus Rhythm in Atrial Fibrillation Patients: Separating Rhythm Outcomes From Randomized Strategy Findings From the CABANA Trial
BACKGROUND:Clinically detected atrial fibrillation (AF) is associated with a significant increase in mortality and other adverse cardiovascular events. Since the advent of effective methods for AF rhythm control, investigators have attempted to determine how much these adverse prognostic AF effects could be mitigated by the restoration of sinus rhythm (SR) and whether the method used mattered.METHODS:The CABANA trial (Catheter Ablation versus Antiarrhythmic Drug Therapy for Atrial Fibrillation) randomized 2204 AF patients to ablation versus drug therapy, of which 1240 patients were monitored in follow-up using the CABANA ECG rhythm monitoring system. To assess the prognostic benefits of SR, we performed a prespecified analysis using Cox survival modeling with heart rhythm as a time-dependent variable and a randomized treatment group as a stratification factor.RESULTS:In the 1240 patient study cohort, 883 (71.2%) had documented AF at some point during their postblanking follow-up. Among the 883 patients, 671 (76.0%) experienced AF within the first year of postblanking follow-up, and 212 (24.0%) experienced their first AF after ≥1 year of postblanking follow-up. The primary CABANA end point (death, disabling stroke, serious bleeding, or cardiac arrest) occurred in 95 (10.8%) of the 883 patients with documented AF and in 29 (8.1%) of the 357 patients with no AF recorded during follow-up. In multivariable time-dependent analysis, the presence of SR (compared with non-SR) was associated with a significantly reduced risk of the primary end point (adjusted hazard ratio, 0.57 [95% CI, 0.38–0.85]; P=0.006; independent of treatment strategy [ablation versus drugs]). Corresponding results for all-cause mortality were adjusted hazard ratio of 0.59 [95% CI, 0.35–1.01]; P=0.053).CONCLUSIONS:In patients in the CABANA trial with detailed long-term rhythm follow-up, increased time in SR was associated with a clinically consequential decreased in mortality and other adverse prognostic events. The predictive value of SR was independent of the therapeutic approach responsible for reducing the burden of detectable AF.REGISTRATION:URL: https://clinicaltrials.gov; Unique Identifier: NCT00911508
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