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Initial clinical experience of pulmonary vein isolation using the ultra‐low temperature cryoablation catheter for patients with atrial fibrillation

医学 肺静脉 低温消融 烧蚀 心房颤动 导管消融 外科 心脏病学
作者
Shota Tohoku,Boris Schmidt,Stefano Bordignon,Shaojie Chen,Fabrizio Bologna,K. R. Julian Chun
出处
期刊:Journal of Cardiovascular Electrophysiology [Wiley]
卷期号:33 (7): 1371-1379 被引量:12
标识
DOI:10.1111/jce.15519
摘要

Abstract Background The iCLAS ultra‐low temperature cryoablation (ULTC) system has recently been brought to the market. A combination of a newly exploited cryogen and interchangeable stylet enables flexible and continuous lesion creation in atrial fibrillation (AF) ablation. The use of an esophageal warming balloon is recommended when using the system to reduce the potential for collateral esophageal injury. Objective To describe the initial clinical experience when using ULTC in the AF treatment without general anesthesia (GA). Methods Consecutive patients undergoing AF ablation using ULTC under deep sedation without GA were enrolled. We assessed the procedural data focusing on “single‐shot isolation” defined as successful pulmonary vein (PV) isolation after the first application. Esophagogastroduodenoscopy was systematically performed the day after ablation. Results A total of 27 AF patients (67% paroxysmal AF) were analyzed. Onehundred four out of 106 PVs (98.1%) were isolated solely using ULTC. The mean procedure time was 79 ± 30 min. The mean number of applications per PV was 2.6 ± 1.0. Single‐shot isolation was achieved in 57 PVs (54%) varying across PVs from left superior to inferior PVs (40%–64%). The single procedure 6‐month recurrence‐free rate was 84%. No major complication (cerebrovascular event, pericardial effusion/tamponade, esophageal damage on esophagogastroduodenoscopy) occurred. A single transient phrenic nerve palsy occurred during the right superior PV ablation, which had recovered by the 3‐month follow‐up appointment. Conclusions AF ablation using the novel ULTC system seemed feasible without GA and enabled a >50% single‐shot isolation rate. The promising safety profile has to be confirmed in large‐scale studies.
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