Key result
An individualized cryoballoon ablation dosing protocol guided by temperature or time-to-pulmonary vein isolation resulted in similar 1-year freedom from atrial arrhythmias (78.75% vs 78.57%) compared to a conventional approach, while significantly reducing procedure and cryotherapy times.
Why the study?
The optimal dosage for cryoablation of AF was unknown.
Does an individualized cryoballoon ablation dosing protocol based on time-to-pulmonary vein isolation or temperature reduce procedure time without compromising freedom from atrial arrhythmia recurrence in patients with paroxysmal atrial fibrillation?
Cohort (n=164)
Open-label
Nonrandomized
No
Does an individualized cryoballoon ablation dosing protocol based on time-to-pulmonary vein isolation or temperature reduce procedure time without compromising freedom from atrial arrhythmia recurrence in patients with paroxysmal atrial fibrillation?
An individualized cryoballoon ablation dosing protocol guided by time-to-pulmonary vein isolation or temperature significantly reduces procedure and left atrial dwell times while maintaining similar 1-year efficacy and safety compared to a conventional 180-second bonus freeze approach.
Answers are grounded in this paper and cite their sources.
May shorten cryoballoon procedures in paroxysmal AF; hypothesis-generating and requires randomized confirmation.
Background The optimal dosage for cryoablation of atrial fibrillation (Cryo-AF) is still unknown. To evaluate the efficacy of an individualized freeze duration, we compared the clinical outcome of patients treated with a time-to-pulmonary vein isolation (TT-PVI) or temperature-guided ablation protocol to the outcome of patients treated with a conventional ablation protocol. Methods A total of 164 consecutive patients were included in the study. One method employed was a conventional dosing protocol (at least 2 applications of 180 s each) (the Cryo-AF Conventional group n = 84), and the second method had a shorter protocol that was based on the TT-PVI or achievement of − 40 °C within 60 s (the Cryo-AF Dosing group n = 80) Results We treated 656 pulmonary veins (PVs) with 1420 cryotherapy applications. The mean number of applications per patient was 8.7 ± 0.8, with no difference between groups (Cryo-AF Conventional , 8.7 ± 0.8 versus Cryo-AF Dosing ,8.6 ± 0.8; P = 0.359). The Cryo-AF Dosing group required significantly less total cryotherapy application time (990.60 ± 137.77versus 1501.58 ± 89.60 s; P < 0.001) and left atrial dwell time (69.91 ± 6.91 versus 86.48 ± 7.03 min; P < 0.001) than the Cryo-AF Conventional group. Additionally, the Cryo-AF Dosing group required significantly less total procedure time (95.03 ± 6.50 versus 112.43 ± 7.11 min; P < 0.001). We observed acute ATP-induced or spontaneous vein electric reconnections in 13 veins (1.98%) after 20 min. The reconnection rates between the Cryo-AF Conventional and Cryo-AF Dosing groups were similar in that 2.98 and 0.94% of the initially isolated veins were reconnected, respectively, ( P = 0.061). There was no difference in the recurrence rate of free atrial arrhythmia after a 1-year follow-up, which were 78.75% in the Cryo-AF Dosing group versus 78.57% in the Cryo-AF Conventional group ( P = 0.978). Conclusion A novel Cryo-AF dosing protocol guided by temperature or the TT-PVI can be used to individualize an ablation strategy. This new protocol can lead to a significant reduction in duration of the procedure, the cryoenergy dosage and the left atrial dwell time. The procedure had equal safety and similar acute and 1-year follow-up outcomes compared to the conventional approach.
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Ding et al. (2019) conducted a cohort in Paroxysmal atrial fibrillation (n=164). Individualized cryoballoon ablation dosing protocol (guided by TT-PVI or temperature) vs. Conventional cryoballoon ablation dosing protocol (180-s freeze plus 180-s bonus) was evaluated on Freedom from recurrent atrial arrhythmias at 1 year (p=0.978). An individualized cryoballoon ablation dosing protocol guided by temperature or time-to-pulmonary vein isolation resulted in similar 1-year freedom from atrial arrhythmias (78.75% vs 78.57%) compared to a conventional approach, while significantly reducing procedure and cryotherapy times.
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