经验性上腔静脉隔离对持续性房颤患者全胸腔镜消融的影响

Hee-Jin Kwon, Dong Seop Jeong, Seung-Jung Park, Kyoung-Min Park, June Soo Kim, Young Keun On
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引用次数: 0

摘要

背景在非阵发性房颤(房颤)患者中,已经尝试了各种消融策略来靶向非肺静脉(PV)病灶或实现肺静脉隔离之外的底物修饰。SVC是最常见的非pv病灶之一,经验消融的效果尚不清楚。本研究的目的是探讨附加上腔静脉(SVC)隔离在接受胸腔镜手术消融的非阵发性房颤患者中的疗效和安全性。方法/结果共纳入191例持续性或长期持续性房颤患者。所有患者均行房颤全胸腔镜手术消融治疗,其中一半患者还行经验性SVC分离。我们比较了两组患者的无房性心动过速(ATa)生存率和手术相关并发症。SVC分离组3年无ata生存率为53%,无SVC分离组为52% (p = 0.644)。两组之间在房颤类型或LA大小方面没有差异。12例(6%)患者发生手术相关并发症。只有SVC隔离组的3名患者植入了起搏器。影响ATa复发的唯一因素是LA直径。结论胸腔镜消融治疗持续性房颤时经验性SVC隔离不能改善患者预后。
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The effect of empirical superior vena cava isolation during total thoracoscopic ablation in patients with persistent atrial fibrillation
Abstract Background In patients with non-paroxysmal AF (atrial fibrillation), various ablation strategies have been attempted to target non-pulmonary vein (PV) foci or to achieve substrate modification beyond pulmonary vein isolation. The efficacy of empirical ablation of the SVC, one of the most common non-PV foci, is unclear. The aim of this study was to investigate the efficacy and safety of additional superior vena cava (SVC) isolation in patients with non-paroxysmal AF undergoing thoracoscopic surgical ablation. Methods/results A total of 191 patients with persistent or long-standing persistent AF was enrolled. All patients underwent total thoracoscopic surgical ablation for AF, and half of them also received empirical SVC isolation. We compared the atrial tachyarrhythmia (ATa)-free survival rate and procedure-related complications in the two groups of patients. The 3-year ATa-free survival rate was 53% in the SVC isolation group and 52% in the no-SVC isolation group ( p = 0.644). There were no differences between the two groups with respect to AF type or LA size. Procedure-related complications occurred in 12 patients (6%). Pacemakers were implanted only in three patients from the SVC isolation group. The only factor influencing recurrence of ATa was LA diameter. Conclusions Empirical SVC isolation during thoracoscopic ablation for persistent AF did not improve patient outcomes.
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审稿时长
31 weeks
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