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Percutaneous left atrial appendage closure vs warfarin for atrial fibrillation a randomized clinical trial

机译:经皮左心耳封堵术与华法林治疗房颤的一项随机临床试验

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Importance While effective in preventing stroke in patients with atrial fibrillation (AF), warfarin is limited by a narrow therapeutic profile, a need for lifelong coagulation monitoring, and multiple drug and diet interactions. OBJECTIVE To determine whether a local strategy of mechanical left atrial appendage (LAA) closure was noninferior to warfarin. Design, Setting, and Participants Protect AFwas a multicenter, randomized (2:1), unblinded, Bayesian-designed study conducted at 59 hospitals of 707 patients with nonvalvular AF and at least 1 additional stroke risk factor (CHADS2score≥1). Enrollment occurred between February 2005 and June 2008 and included 4-year follow-up through October 2012. Noninferiority required a posterior probability greater than 97.5%and superiority a probability of 95%or greater; the noninferiority margin was a rate ratio of 2.0 comparing event rates between treatment groups. Interventions Left atrial appendage closure with the device (n = 463) or warfarin (n = 244; target international normalized ratio, 2-3). Main Outcomes and Measures A composite efficacy end point including stroke, systemic embolism, and cardiovascular/unexplained death, analyzed by intention-to-treat. Results At a mean (SD) follow-up of 3.8 (1.7) years (2621 patient-years), there were 39 events among 463 patients (8.4%) in the device group for a primary event rate of 2.3 events per 100 patient-years, compared with 34 events among 244 patients (13.9%) for a primary event rate of 3.8 events per 100 patient-years with warfarin (rate ratio, 0.60; 95%credible interval, 0.41-1.05), meeting prespecified criteria for both noninferiority (posterior probability, 99.9%) and superiority (posterior probability, 96.0%). Patients in the device group demonstrated lower rates of both cardiovascular mortality (1.0 events per 100 patient-years for the device group [17/463 patients, 3.7%] vs 2.4 events per 100 patient-years with warfarin [22/244 patients, 9.0%]; hazard ratio [HR], 0.40; 95%CI, 0.21-0.75; P =.005) and all-cause mortality (3.2 events per 100 patient-years for the device group [57/466 patients, 12.3%] vs 4.8 events per 100 patient-years with warfarin [44/244 patients, 18.0%]; HR, 0.66; 95%CI, 0.45-0.98; P =.04). Conclusions and Relevance After 3.8 years of follow-up among patients with nonvalvular AF at elevated risk for stroke, percutaneous LAA closure met criteria for both noninferiority and superiority, compared with warfarin, for preventing the combined outcome of stroke, systemic embolism, and cardiovascular death, as well as superiority for cardiovascular and all-cause mortality.
机译:重要性尽管华法林对预防房颤(AF)患者的卒中有效,但受限于狭窄的治疗方案,需要进行终生凝血监测以及多种药物和饮食相互作用,因此受到了华法林的限制。目的确定机械性左心耳(LAA)闭合的局部策略是否不劣于华法林。贝叶斯设计,设计和参与者保护房颤是一项多中心,随机(2:1),无盲,贝叶斯设计的研究,在707例非瓣膜性房颤且至少有1个额外的卒中危险因素(CHADS2score≥1)的59所医院中进行。入组时间为2005年2月至2008年6月,包括4年的随访期至2012年10月。非自卑要求后验概率大于97.5%,优越性要求后验概率大于95%。非劣效性差的比率为2.0,比较治疗组之间的事件发生率。干预措施左房附件封闭术(n = 463)或华法林(n = 244;国际标准化目标值为2-3)。主要结果和措施通过意向性治疗分析的综合功效终点,包括中风,全身性栓塞和心血管/原因不明的死亡。结果:在平均(SD)随访3.8(1.7)年(2621病人-年)中,设备组463例患者(39%)中有39例事件,每100例患者中2.3例事件发生,年,与之相比,244例患者中有34例(13.9%)发生华法林,其原发事件发生率为每100病人年3.8例(比率,0.60; 95%可信区间,0.41-1.05),均符合既定标准(后验概率,<99.9%)和优越性(后验概率,96.0%)。器械组患者的心血管死亡率均较低(器械组每100名患者年发生1.0次事件[17/463例患者,占3.7%],而华法林的心血管疾病死亡率每100名患者年发生2.4次[22/244名患者,占9.0%] %];危险比[HR],0.40; 95%CI,0.21-0.75; P = .005)和全因死亡率(设备组每100患者年3.2次事件[57/466患者,12.3%]与华法林的每100病人年4.8事件比较[44/244患者,18.0%]; HR,0.66; 95%CI,0.45-0.98; P = .04)。结论与相关性在非瓣膜性AF发生卒中风险较高的患者中进行了3。8年的随访后,与华法林相比,经皮LAA封堵术符合非劣效性和优越性的标准,可预防中风,全身性栓塞和心血管死亡的综合后果,以及心血管和全因死亡率的优势。

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