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首页> 外文期刊>Journal of the American College of Cardiology >Omega-3 fatty acids for the prevention of recurrent symptomatic atrial fibrillation: Results of the forward (randomized trial to assess efficacy of pufa for the maintenance of sinus rhythm in persistent atrial fibrillation) trial
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Omega-3 fatty acids for the prevention of recurrent symptomatic atrial fibrillation: Results of the forward (randomized trial to assess efficacy of pufa for the maintenance of sinus rhythm in persistent atrial fibrillation) trial

机译:Omega-3脂肪酸预防症状性房颤复发的前瞻性研究(随机试验,旨在评估pufa在持续性房颤中维持窦性心律的功效)

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Objectives: The aim of this study was to evaluate the efficacy of polyunsaturated fatty acids (n-3 PUFA) for the prevention of recurrent atrial fibrillation (AF) in patients with normal sinus rhythm. Background: Current pharmacological treatments to limit recurrent AF in patients with previous AF have limited efficacy and high rates of adverse events. Results of trials that tested the efficacy of n-3 PUFA provided heterogeneous results. Methods: This was a prospective, randomized, double-blind, placebo-controlled, multicenter trial involving 586 outpatient participants with confirmed symptomatic paroxysmal AF that required cardioversion (n = 428), at least 2 episodes of AF in the 6 months before randomization (n = 55), or both (103). Patients were randomly allocated to n-3 PUFA (1 g/day) or placebo for 12 months. The primary endpoint was symptomatic recurrence of AF. Results: There were no significant differences between patients allocated to placebo and those who received n-3 PUFA for the main outcome. At 12 months, 56 of 297 participants (18.9%) in the placebo group and 69 of 289 participants (24.0%) in the n-3 PUFA group had a recurrent symptomatic AF (hazard ratio: 1.28, 95% confidence interval: 0.90 to 1.83, p = 0.17). There was no difference between treatment with placebo and n-3 PUFA for any of the other pre-specified endpoints, including the composite of all-cause mortality, nonfatal stroke, nonfatal acute myocardial infarction, systemic embolism, heart failure development, or severe bleeding that occurred in 20 (6.7%) and 16 (5.5%) of patients randomized to placebo or n-3 PUFA, respectively (hazard ratio: 0.86, 95% confidence interval: 0.44 to 1.66, p = 0.65). Conclusions: Pharmacological supplementation with 1 g of n-3 PUFA for 1 year did not reduce recurrent AF. (Randomized Trial to Assess Efficacy of PUFA for the Maintenance of Sinus Rhythm in Persistent Atrial Fibrillation [FORWARD]; NCT00597220) ? 2013 American College of Cardiology Foundation.
机译:目的:本研究的目的是评估多不饱和脂肪酸(n-3 PUFA)预防窦性心律正常的复发性房颤(AF)的疗效。背景:目前限制前房颤患者复发房颤的药物治疗方法疗效有限,不良事件发生率很高。测试n-3 PUFA功效的试验结果提供了异类结果。方法:这是一项前瞻性,随机,双盲,安慰剂对照,多中心试验,涉及586名确诊为阵发性房颤的门诊患者,需要复律(n = 428),在随机分组前6个月内至少发生2次房颤( n = 55),或两者皆是(103)。患者被随机分配到n-3 PUFA(1 g /天)或安慰剂中治疗12个月。主要终点是房颤的症状复发。结果:分配给安慰剂的患者与主要结果为n-3 PUFA的患者之间没有显着差异。在12个月时,安慰剂组297名参与者中的56名(18.9%)和n-3 PUFA组的289名参与者中的69名(24.0%)出现了复发性AF(危险比:1.28,95%置信区间:0.90至1.83,p = 0.17)。安慰剂和n-3 PUFA的治疗在其他任何预先指定的终点之间没有差异,包括全因死亡率,非致命性中风,非致命性急性心肌梗死,全身性栓塞,心力衰竭或严重出血的综合因素随机分别接受安慰剂或n-3 PUFA的患者有20例(6.7%)和16例(5.5%)(危险比:0.86,95%置信区间:0.44至1.66,p = 0.65)。结论:1 g n-3 PUFA的药理补充1年不能降低复发性AF。 (随机试验以评估PUFA维持持续性心房颤动的窦性心律[FORWARD]; NCT00597220)? 2013美国心脏病学会基金会。

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