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首页> 外文期刊>Journal of the American College of Cardiology >Feasibility and safety of dabigatran versus warfarin for periprocedural anticoagulation in patients undergoing radiofrequency ablation for atrial fibrillation: Results from a multicenter prospective registry
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Feasibility and safety of dabigatran versus warfarin for periprocedural anticoagulation in patients undergoing radiofrequency ablation for atrial fibrillation: Results from a multicenter prospective registry

机译:达比加群与华法林联合射频消融治疗房颤的围手术期抗凝的可行性和安全性:多中心前瞻性研究的结果

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Objectives: The purpose of this study was to evaluate the feasibility and safety of periprocedural dabigatran during atrial fibrillation (AF) ablation. Background: AF ablation requires optimal periprocedural anticoagulation for minimizing bleeding and thromboembolic complications. The safety and efficacy of dabigatran as a periprocedural anticoagulant for AF ablation are unknown. Methods: We performed a multicenter, observational study from a prospective registry including all consecutive patients undergoing AF ablation in 8 high-volume centers in the United States. All patients receiving dabigatran therapy who underwent AF ablation on periprocedural dabigatran, with the dose held on the morning of the procedure, were matched by age, sex, and type of AF with an equal number of patients undergoing AF ablation with uninterrupted warfarin therapy over the same period. Results: A total of 290 patients, including 145 taking periprocedural dabigatran and an equal number of matched patients taking uninterrupted periprocedural warfarin, were included in the study. The mean age was 60 years with 79% being male and 57% having paroxysmal AF. Both groups had a similar CHADS 2 score, left atrial size, and left ventricular ejection fraction. Three thromboembolic complications (2.1%) occurred in the dabigatran group compared with none in the warfarin group (p = 0.25). The dabigatran group had a significantly higher major bleeding rate (6% vs. 1%; p = 0.019), total bleeding rate (14% vs. 6%; p = 0.031), and composite of bleeding and thromboembolic complications (16% vs. 6%; p = 0.009) compared with the warfarin group. Dabigatran use was confirmed as an independent predictor of bleeding or thromboembolic complications (odds ratio: 2.76, 95% confidence interval: 1.22 to 6.25; p = 0.01) on multivariate regression analysis. Conclusions: In patients undergoing AF ablation, periprocedural dabigatran use significantly increases the risk of bleeding or thromboembolic complications compared with uninterrupted warfarin therapy.
机译:目的:本研究的目的是评估房颤消融过程中达比加群的可行性和安全性。背景:房颤消融术需要最佳的围手术期抗凝治疗,以最大程度地减少出血和血栓栓塞并发症。达比加群作为房颤消融术中抗凝剂的安全性和有效性尚不清楚。方法:我们从前瞻性注册表中进行了一项多中心的观察性研究,包括在美国8个高容量中心中接受房颤消融的所有连续患者。所有接受达比加群治疗的患者均在手术过程中对达必加群进行围手术期房颤消融,且剂量在手术当天早晨进行,并与年龄,性别和房颤类型相匹配。同一时期。结果:总共290例患者被纳入研究,其中包括145例接受围手术期达比加群治疗,同等数量的匹配患者接受不间断围术期华法林治疗。平均年龄为60岁,其中79%为男性,57%为阵发性AF。两组的CHADS 2评分,左心房大小和左心室射血分数相似。达比加群组发生了三例血栓栓塞并发症(2.1%),而华法林组则没有(P = 0.25)。达比加群组的主要出血率(6%vs. 1%; p = 0.019),总出血率(14%vs. 6%; p = 0.031)以及出血和血栓栓塞并发症的综合发生率(16%vs. 6%; p = 0.009)与华法林组相比。在多因素回归分析中,确认使用达比加群是出血或血栓栓塞并发症的独立预测因子(几率:2.76,95%置信区间:1.22至6.25; p = 0.01)。结论:与不间断的华法林治疗相比,在进行房颤消融的患者中,围手术期使用达比加群显着增加了出血或血栓栓塞并发症的风险。

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