Premium
Circumferential pulmonary vein antrum ablation for the treatment of paroxysmal atrial fibrillation: A randomized controlled trial
Author(s) -
Xu Qiang,
Ju Weizhu,
Xiao Fangyi,
Yang Bing,
Chen Hongwu,
Yang Gang,
Zhang Fengxiang,
Gu Kai,
Li Mingfang,
Wang Daowu,
Chen Minglong
Publication year - 2020
Publication title -
pacing and clinical electrophysiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.686
H-Index - 101
eISSN - 1540-8159
pISSN - 0147-8389
DOI - 10.1111/pace.13863
Subject(s) - medicine , pulmonary vein , antrum , ablation , atrial fibrillation , catheter ablation , sinus rhythm , cardiology , paroxysmal atrial fibrillation , randomized controlled trial , catheter , coronary sinus , surgery , stomach
Background It remains unclear whether the curative result of paroxysmal atrial fibrillation (PAF) is a result of pulmonary vein (PV) isolation, PV antrum modification (PVAM), or both. We hypothesized that sufficient antrum modification (PVAM) is as important as PV isolation (PVI) for atrial fibrillation (AF) control and that PVAM can be evaluated by quantified lesion deployment using a force‐sensing catheter. Methods and Results Patients of symptomatic PAF were randomly assigned 2:1 into a PVAM group or a circumferential PV isolation (CPVI) group. In the PVAM group, circumferential quantitative ablation evaluated by automatical VisiTag module was performed. In the CPVI group, conventional circumferential ablation was performed to achieve the end point of all‐PV isolation. In total, 180 patients with PAF were enrolled and randomly assigned to either the PVAM group ( n = 120) or the CPVI group ( n = 60). A total of 179 patients successfully underwent ablation. In the PVAM group, 68 patients achieved all PVI (PVAM‐PVI), while 51 did not (PVAM‐non‐PVI). At 18 months, there was no significant difference in the maintenance of sinus rhythm between the PVAM and CPVI groups (84.9 vs 79.7%, P = .382). The PVAM‐PVI subgroup demonstrated a higher arrhythmia‐free survival compared with the PVAM‐non‐PVI subgroup (92.6 vs 74.5%, P = .006) and the CPVI group (92.6 vs 79.7%, P = .036). Conclusions The trial shows that sufficient force‐sensing guided PVAM can result in satisfying outcomes in PAF patients. Notably, sufficient PVAM with all‐PV isolated will further increase the success rate.