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Contact force and catheter stability are predictive metrics of successful pulmonary vein isolation with high‐power short duration ablation in atrial fibrillation

医学 烧蚀 肺静脉 心房颤动 导管消融 导管 心脏病学 内科学 外科 核医学
作者
Shohreh Honarbakhsh,Claire Martin,Gurpreet Dhillon,Mark M. Gallagher,Manav Sohal,Anthony Chow,Syed Ahsan,Hakam Abbass,Sarah Whittaker‐Axon,Pier D. Lambiase,Mark J. Davies,Matthew Ginks,Ross J. Hunter
出处
期刊:Journal of Cardiovascular Electrophysiology [Wiley]
卷期号:34 (5): 1141-1151 被引量:4
标识
DOI:10.1111/jce.15867
摘要

Preliminary data suggest that high power short duration (HPSD) ablation for pulmonary vein isolation (PVI) are safe. Limited data are available on its effectiveness. Aim was to evaluate HPSD ablation in atrial fibrillation ablation using a novel Qdot Micro catheter.Prospective multicenter study evaluating safety and efficacy of PVI with HPSD ablation. First pass isolation (FPI) and sustained PVI was assessed. If FPI was not achieved additional ablation index (AI)-guided ablation with 45 W was performed and metrics predictive of this were determined. Sixty-five patients and 260 veins were treated. Procedural and LA dwell time was 93.9 ± 30.4 and 60.5 ± 23.1 min, respectively. FPI was achieved in 47 (72.3%) patients and 231 veins (88.8%) with an ablation duration of 4.6 ± 1.0 min. Twenty-nine veins required additional AI-guided ablation to achieve initial PVI with 24 anatomical sites ablated with the right posterior carina being the most common site (37.5%). A contact force of ≥8 g (area under the curve [AUC]: 0.81; p < 0.001) and catheter position variation of ≤1.2 mm (AUC: 0.79; p < 0.001) with HPSD were strongly predictive of not requiring additional AI-guided ablation. Out of the 260 veins, only 5 (1.9%) veins showed acute reconnection. HPSD ablation was associated with shorter procedure times (93.9 vs. 159.4 min; p < 0.001), ablation times (6.1 vs. 27.7 min; p < 0.001), and lower rates of PV reconnection (9.2% vs. 30.8%; p = 0.004) compared to moderate power cohort.HPSD ablation is an effective ablation modality which results in effective PVI whilst maintaining a safety profile. Its superiority needs to be evaluated in randomized controlled trials.

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