Key result
POLARx cryoballoon achieves ~100% acute PVI and high one-year freedom from symptomatic atrial arrhythmias.
Why the study?
A novel cryoballoon ablation catheter showed acute safety and efficacy for de novo PVI in paroxysmal AF, but data demonstrating long-term efficacy were limited.
Does a novel cryoballoon ablation catheter safely and effectively prevent arrhythmia recurrence in patients with paroxysmal atrial fibrillation?
Observational (n=58)
Yes
Does a novel cryoballoon ablation catheter safely and effectively prevent arrhythmia recurrence in patients with paroxysmal atrial fibrillation?
A novel cryoballoon ablation catheter demonstrated high acute procedural success and 77% 1-year arrhythmia-free survival in patients with paroxysmal atrial fibrillation, with an acceptable safety profile.
Supports feasibility of novel cryoballoon for PVI in paroxysmal AF; leaves open need for randomized trials to confirm efficacy and safety.
BACKGROUND: Recently, a novel cryoballoon ablation catheter has demonstrated acute safety and efficacy in de novo pulmonary vein isolation (PVI) procedures in patients with paroxysmal atrial fibrillation (PAF). However, there are limited studies demonstrating the long-term efficacy. The aim of this study was to evaluate the long-term safety and efficacy of this novel cryoballoon in treating PAF. METHODS: This was a non-randomized, prospective, multicentre study enrolling 58 consecutive patients. Cryoablation was delivered for 180 s if time to isolation was ≤ 60 s. Otherwise a 240-s cryoablation was performed. One centre performed pre- and post-ablation high-density mapping (n = 9) to characterize lesion formation. After a 3-month blanking period, recurrence was defined as having any documented, symptomatic episode(s) of AF or atrial tachycardia. All patients were followed for 1 year. RESULTS: Acute PVI was achieved in 230 of 231 pulmonary veins (99.6%) with 5.3 ± 1.6 cryoablations per patient (1.3 ± 0.7 cryoablations per vein). Forty-three (77%) patients remained arrhythmia-free at 1-year follow-up. Four patients (6.9%) experienced phrenic nerve injury (3 resolved during the index procedure; 1 resolved at 6 months). One serious adverse device event was reported: femoral arterial embolism event occurring 2 weeks post-index procedure. For patients who underwent high-density mapping, cryoablation was antral with 50% of the posterior wall ablated. CONCLUSIONS: Initial multicentre clinical experience with a novel cryoballoon has demonstrated safety and efficacy of PVI in patients with PAF. Ablation with this cryoballoon provides a wide, antral lesion set with significant debulking of the posterior wall of the left atrium.
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Martin et al. (2022) conducted an observational in paroxysmal atrial fibrillation (n=58). POLARx cryoballoon system was evaluated on Acute procedural success (pulmonary vein isolation confirmed via exit and entrance block testing). The novel POLARx cryoballoon achieved acute pulmonary vein isolation in 99.6% of targeted veins, with 77% of patients remaining free from symptomatic atrial arrhythmias at 12 months.
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