One-year outcomes of pulmonary vein isolation with a novel cryoballoon: Primary results of the FROZEN AF trial

被引:8
作者
Ellenbogen, Kenneth A. [1 ]
Mittal, Suneet [2 ]
Varma, Niraj [3 ]
Aryana, Arash [4 ]
Marrouche, Nassir [5 ]
Anic, Ante [6 ]
Nair, Devi [7 ]
Champagne, Jean [8 ]
Iacopino, Saverio [9 ]
de Asmundis, Carlo [10 ]
Weiner, Stanislav [11 ]
Makati, Kevin [12 ]
Raybuck, Jonathan D. [13 ]
Richards, Elizabeth [13 ]
Su, Wilber [14 ]
机构
[1] Virginian Commonwealth Univ, Div Cardiol, Richmond, VA 23284 USA
[2] Valley Hosp, Ridgewood, NJ USA
[3] Cleveland Clin, Cleveland, OH USA
[4] Mercy Gen Hosp, Sacramento, CA USA
[5] Tulane Univ, Sch Med, New Orleans, LA USA
[6] Univ Hosp Split, Split, Croatia
[7] Arrhythmia Res Grp, Jonesboro, AR USA
[8] Inst Univ Cardiol & Pneumol Quebec, Quebec City, PQ, Canada
[9] Maria Cecilia Hosp, Cotignola, Italy
[10] UZ Brussel, Brussels, Belgium
[11] Christus Trinity Mother Frances Hlth Syst, Tyler, TX USA
[12] St Josephs Hosp, Tampa, FL USA
[13] Boston Sci, Arden Hills, MN USA
[14] Banner Univ, Med Ctr, Phoenix, AZ USA
关键词
atrial arrhythmias; atrial fibrillation; cryoballoon ablation; ATRIAL-FIBRILLATION; RADIOFREQUENCY ABLATION;
D O I
10.1111/jce.16220
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IntroductionCryoablation therapy for pulmonary vein isolation (PVI) to treat paroxysmal atrial fibrillation (PAF) is well established. A novel 28 mm cryoballoon system designed to operate under low pressure to safely reach a lower nadir temperature and maintain constant balloon size during cooling has not been prospectively studied in a large patient population for safety and efficacy. The FROZEN AF (NCT04133168) trial was an international multicenter, open-label, prospective, single-arm study on the safety and performance of a novel cryoballoon system for treatment of PAF.Methods and ResultsThe study enrolled patients at 44 sites in 10 countries across North America, Europe, and Asia. Subjects were indicated for PVI treatment of PAF and had failed or were intolerant of one or more antiarrhythmic drugs. Procedural outcomes were defined based on the 2017 HRS consensus statement. Follow-up was performed at 7 days, 3, 6, and 12 months. Data are reported as mean +/- SD or median (IQR). PVI was performed with a 28 mm cryoballoon in 325 drug refractory PAF patients. Complete PVI was achieved in 95.7% of patients. In cryoablation lesions longer than 60 s, 60.1% of PV isolations required only a single cryoballoon application. Procedure related complications included: phrenic nerve palsy [temporary 4 (1.2%), persistent 0 (0.0%)], cardiac tamponade/perforation 2 (0.6%), and air embolism 1 (0.3%). Freedom from documented atrial arrhythmia recurrence at 12 months was 79.9% (AF 82.7%, AFL 96.5%, AT 98.1%), antiarrhythmic drugs (AAD) were continued or re-initiated in 26.8% of patients after the 3-month blanking period. Additionally, an extension arm enrolled 50 pts for treatment with 28/31 mm variable size cryoballoon. A single temporary PNP occurred in this group, which resolved before discharge. Freedom from documented recurrence at 12 months in these pts was 82.0%.ConclusionsThis novel cryoballoon may facilitate PVI to treat PAF, providing more options to address the variety of anatomies present in patients with PAF. This cryoballoon system proved to be safe and effective for treatment of patients with drug refractory or drug intolerant PAF. This novel cryoballoon with adjustable size and low compliance successfully achieves pulmonary vein isolation to treat paroxysmal atrial fibrillation (PAF), providing more options for patients with PAF. This cryoballoon system was proven to be safe and effective for treatment of patients with drug refractory or drug intolerant PAF. image
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页码:832 / 842
页数:11
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