Durability of Pulmonary Vein Isolation Using Pulsed-Field Ablation

心房颤动 肺静脉 烧蚀 分离(微生物学) 导管消融 射频消融术 医学 心脏病学 内科学 放射科 外科 生物 微生物学
作者
Thomas Kueffer,Stefano Bordignon,Kars Neven,Yuri Blaauw,Jim Hansen,Raquel Adeliño,Alexandre Ouss,Anna Füting,Laurent Roten,Bart A. Mulder,Martin H. Ruwald,Roberto Mené,Pepijn van der Voort,Nico Reinsch,Serge Bovéda,E Albrecht,Christopher W. Schneider,K.R. Julian Chun,Boris Schmidt,Tobias Reichlin
出处
期刊:JACC: Clinical Electrophysiology [Elsevier BV]
卷期号:10 (4): 698-708 被引量:28
标识
DOI:10.1016/j.jacep.2023.11.026
摘要

Pulsed-field ablation (PFA) is a novel nonthermal ablation technology with high procedural safety and efficiency for pulmonary vein isolation (PVI). Premarket data showed high PVI durability during mandatory remapping studies. Data on lesion durability in real-world patients with clinically indicated redo procedures are scarce. This study sought to report PVI durability rates in patients undergoing a clinically indicated redo procedure after an index PVI using PFA. Patients from 7 European centers undergoing an index PVI using PFA were included the EU-PORIA (European Real-world Outcomes With Pulsed Field Ablation in Patients With Symptomatic Atrial Fibrillation) registry. In patients with subsequent left atrial redo procedures due to arrhythmia recurrence, 3-dimensional electroanatomical maps were acquired. PVI durability was assessed on a per-vein and per-patient level, and sites of reconnections and predictors of lesion durability were identified. Of 1,184 patients (62% paroxysmal atrial fibrillation) undergoing an index PVI using PFA, 272 (23%) had an arrhythmia recurrence. Of these, 144 (53%) underwent a left atrial redo procedure a median of 7 (Q1-Q3: 5-10) months after the first ablation. Three-dimensional electroanatomical maps identified 404 of 567 pulmonary veins (71%) with durable isolation. In 54 patients (38%), all pulmonary veins were durably isolated. Prior operator experience with cryoballoon ablation was associated with a higher PVI durability compared to operators with only point-by-point radiofrequency experience (76% vs 60%; P < 0.001). Neither the operators' cumulative experience in atrial fibrillation ablation (≤5 vs >5 years) nor the size of the PFA device used (31 mm vs 35 mm) had an impact on subsequent lesion durability (both P > 0.50). In 144 patients with arrhythmia recurrence after PFA PVI, durable isolation was observed in 71% of the pulmonary veins during the redo procedure, and 38% of all patients showed durable isolation of all veins.
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