Inês Martins Esteves, Vinicius Bittar de Pontes, Thierry Trevisan, Sebastian Jaramillo, Wilton F. Gomes
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引用次数: 0
Abstract
Background
Pulsed-field ablation (PFA) is a nonthermal alternative to radiofrequency ablation (RFA) for patients with atrial fibrillation (AF). However, the role of PFA compared to RFA in patients with paroxysmal AF (PAF) remains unclear.
Objective
To compare the efficacy and safety of PFA and RFA in adult patients with PAF.
Methods
A systematic review and meta-analysis were conducted following the Cochrane methodology and reported in accordance with PRISMA guidelines. The PubMed, Embase, and Cochrane databases were searched through February 2025 for studies comparing PFA and RFA in adults with PAF. The outcomes of interest included procedure time, 1-year success rate, and major complications. All the statistical analyses were performed via R version 4.5 with a random effects model.
Results
One randomized controlled trial (RCT) and five observational studies comprising 3163 patients with PAF were included, of whom 972 (30.7%) underwent PFA. The follow-up time ranged from 12 to 30 months. PFA was associated with a significantly shorter procedure time (MD –39.15 min; 95% CI –58.19 to −20.11, p < 0.01), but a significantly longer fluoroscopy time (MD 10.75 min; 95% CI 5.58–15.92, p < 0.01) as compared with RFA. There were no statistically significant differences in terms of the 1-year success rate (RR 1.04; 95% CI 0.77–1.41, p = 0.79) and major complications (RR 0.95; 95% CI 0.60–1.52, p = 0.83) between PFA and RFA.
Conclusion
In this meta-analysis, PFA was associated with a reduced operative time and an increased fluoroscopy time, with comparable 1-year efficacy and overall safety profiles.
背景脉冲场消融(PFA)是心房颤动(AF)患者射频消融(RFA)的一种非热替代方案。然而,与RFA相比,PFA在阵发性房颤(PAF)患者中的作用尚不清楚。目的比较PFA与RFA治疗成人PAF的疗效和安全性。方法采用Cochrane方法学进行系统评价和荟萃分析,并按照PRISMA指南进行报道。到2025年2月,PubMed、Embase和Cochrane数据库检索了比较成人PAF患者PFA和RFA的研究。关注的结果包括手术时间、1年成功率和主要并发症。所有统计分析均采用随机效应模型的R版本4.5进行。结果纳入1项随机对照试验(RCT)和5项观察性研究,共纳入3163例PAF患者,其中972例(30.7%)接受了PFA治疗。随访时间为12 ~ 30个月。PFA与手术时间显著缩短相关(MD -39.15 min;95% CI为-58.19 ~ - 20.11,p < 0.01),但透视时间明显延长(MD 10.75 min;95% CI 5.58-15.92, p < 0.01)。在1年成功率方面,两组间差异无统计学意义(RR 1.04;95% CI 0.77-1.41, p = 0.79)和主要并发症(RR 0.95;PFA和RFA之间95% CI 0.60-1.52, p = 0.83)。在这项荟萃分析中,PFA与手术时间缩短和透视时间增加有关,具有相当的1年疗效和总体安全性。试验注册号:CRD420251000165