单独设计的持续性房颤低压区消融术——一项随机对照试验(IDEAL-AF):研究设计和基本原理。

European heart journal open Pub Date : 2025-04-11 eCollection Date: 2025-03-01 DOI:10.1093/ehjopen/oeaf037
Astrid Paul Nordin, Mats Jensen-Urstad, Emmanouil Charitakis, Finn Åkerström, Henrik Almroth, Csaba Herczku, Jari Tapanainen, Niklas Höglund, Nikola Drca
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引用次数: 0

摘要

目的:基于电压的消融是一种很有前途的心房颤动(AF)导管消融策略,其中低压区(LVZs)是肺静脉隔离(PVI)的补充。在一项随机设置中,我们打算研究PVI + LVZs消融与仅PVI相比,是否降低了持续性房颤和LVZs患者心律失常复发的发生率并改善了与健康相关的生活质量(HRQoL)。方法和结果:持续性心房颤动试验(IDEAL-AF;NCT04377594)是一项多中心、随机、对照临床试验。在PVI消融线外LVZ≥3.0 cm²的持续性房颤患者将按1:1的比例随机分配到PVI或PVI + LVZ消融组。主要结果将是在6个月内进行1 - 2次消融手术后12个月内停用抗心律失常药物的房性心律失常复发。第一个程序后,将有3个月的空白期。在整个随访期间,将使用基于智能手机的心电图记录设备对患者进行监测。预计纳入936例患者,该研究有80%的能力检测到主要终点的绝对风险降低20%。此外,HRQoL的改善将使用三份问卷进行评估。结论:IDEAL-AF是一项多中心、随机、对照临床试验,旨在研究与仅消融PVI相比,消融lvz和PVI是否能降低房性心律失常的复发率并改善HRQoL。这项研究有可能修改针对这一特定患者群体的消融技术建议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Individually designed ablation of low-voltage areas in persistent atrial fibrillation-a randomized controlled trial (IDEAL-AF): study design and rationale.

Aims: Voltage-based ablation is a promising catheter ablation strategy for atrial fibrillation (AF) in which low-voltage zones (LVZs) are targeted as a complement to pulmonary vein isolation (PVI). In a randomized setting, we intend to investigate whether PVI plus ablation of LVZs, compared to PVI-only, decreases the incidence of arrhythmia recurrence and improves health-related quality of life (HRQoL) in patients with persistent AF and LVZs.

Methods and results: Individually designed ablation of low-voltage areas in persistent atrial fibrillation trial (IDEAL-AF; NCT04377594) is a multi-centre, randomized, controlled clinical trial. Patients with persistent AF and LVZs ≥ 3.0 cm² outside the PVI ablation lines will be randomized in a 1:1 ratio to either PVI or PVI plus LVZ ablation. The primary outcome will be the recurrence of atrial arrhythmias off anti-arrhythmic drugs during 12 months of follow-up after one to two ablation procedures within 6 months. A 3-month blanking period will be applied after the first procedure. Patients will be monitored using a smart phone-based ECG recording device throughout the follow-up period. With an anticipated enrolment of 936 patients, this study has 80% power to detect a 20% absolute risk reduction in the primary endpoint. Additionally, HRQoL improvement will be assessed using three questionnaires.

Conclusion: IDEAL-AF is a multi-centre, randomized, controlled clinical trial investigating whether ablation of LVZs in addition to PVI reduces the recurrence rate of atrial arrhythmias and improves HRQoL compared to PVI-only in patients with persistent AF and LVZs. This study has the potential to modify recommendations regarding ablation techniques for this specific patient cohort.

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