评估阵发性心房颤动患者心内超声心动图引导的最小荧光镜消融的有效性和安全性的原理和研究设计:一项非劣效、多中心、前瞻性随机对照试验(PAF-ICE试验)

R. Jiang, Xingpeng Liu, Ji-dong Zhang, Yu Chen, Rui Wang, Meng-zuo Wu, Deyong Long, Jia Li, Haixiong Wang, Jie Fan, Weizhu Ju, Weili Ge, X. Liu, Hai Deng, Weijian Wang, Pingzhen Yang, Ding Li, Xiaobo Huang, Xiongtao Liu, Hailong Tao, P. Zei, Roderick Tung, Xunzhang Wang, Chen-yang Jiang
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引用次数: 0

摘要

摘要最近报道了使用最小/零荧光透视法进行心内超声心动图(ICE)引导的心房颤动(AF)导管消融的可行性和安全性。这种方法有助于减少电离辐射暴露和使用铅围裙引起的骨科并发症。这项计划中的前瞻性、多中心随机对照试验(RCT)(阵发性房颤(PAF)-ICE试验;ChiCTR200033624)旨在评估ICE引导的最小荧光透视消融术对PAF患者的疗效和安全性,以及对实验室工作人员职业危害的影响。患者将按1:1的比例随机分为两组:最小荧光检查组(n = 216)和传统方法组(n = 216)。在最小荧光镜检查组中,ICE导管将用于几何结构/解剖结构、经中隔穿刺、导管追踪和积液监测。肺静脉隔离(PVI)将使用开放式灌注射频SmartTouch环绕流或SmartTouch导管(Biosense Webster,Diamond Bar,California,USA)进行,并通过多极Lasso或PentaRay导管(Biosense Webster)进行确认。在传统入路组中,不会使用ICE导管。房间隔穿刺将在荧光镜引导下进行,所有几何形状均通过绘制导管图构建。主要疗效终点是12岁时无房颤复发(无抗心律失常药物) 消融后数月。其他终点包括使用铅围裙的持续时间、术中效率的测量以及围手术期并发症。该随机对照试验将评估ICE引导的最小荧光透视消融术对PAF患者的疗效和安全性,并评估与这种“最小/零荧光透视”和“无引线”模式相关的对实验室工作人员的益处(关于减少职业危害)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rationale and Study Design for Evaluating the Efficacy and Safety of Intracardiac Echocardiography-Guided Minimal-Fluoroscopy Ablation in Patients with Paroxysmal Atrial Fibrillation: A Non-Inferior, Multi-Center, Prospective Randomized Controlled Trial (PAF-ICE Trial)
Abstract The feasibility and safety of intracardiac echocardiography (ICE)-guided catheter ablation for atrial fibrillation (AF) using a minimal/zero-fluoroscopy approach have recently been reported. This approach helps to reduce ionizing radiation exposure and orthopedic complications resulting from using lead aprons. The objectives of this planned prospective, multicenter randomized controlled trial (RCT) (paroxysmal AF (PAF)-ICE trial; ChiCTR2000033624) are to evaluate the efficacy and safety of ICE-guided minimal-fluoroscopy ablation in patients with PAF and the impact on occupational hazards among lab staff. Patients will be randomized in a 1:1 ratio to 2 groups: minimal fluoroscopy group (n = 216) and traditional approach group (n = 216). In the minimal fluoroscopy group, an ICE catheter will be used for geometry/anatomic construction, transseptal puncture, catheter tracking, and effusion monitoring. Pulmonary vein isolation (PVI) will be performed using an open-irrigated radiofrequency SmartTouch Surround Flow or SmartTouch catheter (Biosense Webster, Diamond Bar, California, USA), and confirmed by a multipolar Lasso or PentaRay catheter (Biosense Webster). In the traditional approach group, an ICE catheter will not be used. Transseptal puncture will be performed under fluoroscopic guidance, with all geometries constructed by mapping the catheters. The primary efficacy endpoint is freedom from AF recurrence (without antiarrhythmic medications) at 12 months after ablation. Other endpoints include duration of lead apron use, measures of intra-procedural efficiency, and peri-procedural complications. This RCT will evaluate the efficacy and safety of ICE-guided minimal-fluoroscopy ablation in patients with PAF, also evaluate the benefits to lab staff (regarding reducing occupational hazards) related to this “minimal/zero-fluoroscopy” and “leadless” mode.
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