Suppr超能文献

新型冷冻球囊行肺静脉隔离术的一年随访结果:FROZEN AF 试验的主要结果。

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

机构信息

Division of Cardiology, Virginian Commonwealth University, Richmond, Virginia, USA.

Valley Hospital, Ridgewood, New Jersey, USA.

出版信息

J Cardiovasc Electrophysiol. 2024 Apr;35(4):832-842. doi: 10.1111/jce.16220. Epub 2024 Mar 6.

Abstract

INTRODUCTION

Cryoablation 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 RESULTS

The 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%.

CONCLUSIONS

This 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.

摘要

简介

冷冻消融治疗肺静脉隔离(PVI)以治疗阵发性心房颤动(PAF)已得到广泛认可。一种新型 28mm 冷冻球囊系统旨在低压下运行,以安全达到更低的最低点温度并在冷却过程中保持恒定的球囊大小,尚未在大量患者中前瞻性研究其安全性和有效性。FROZEN AF(NCT04133168)试验是一项国际多中心、开放性、前瞻性、单臂研究,旨在评估一种新型冷冻球囊系统治疗 PAF 的安全性和性能。

方法和结果

该研究在北美、欧洲和亚洲的 10 个国家的 44 个地点招募了患者。受试者符合 PVI 治疗 PAF 的指征,且对一种或多种抗心律失常药物不耐受或无效。根据 2017 年 HRS 共识声明定义了程序结果。在 7 天、3、6 和 12 个月时进行随访。数据以平均值±标准差或中位数(IQR)报告。在 325 例药物难治性 PAF 患者中进行了 28mm 冷冻球囊的 PVI。95.7%的患者实现了完全 PVI。在冷冻消融时间超过 60s 的病变中,60.1%的 PV 隔离仅需单次应用冷冻球囊。与手术相关的并发症包括:膈神经麻痹[暂时性 4 例(1.2%),持续性 0 例(0.0%)]、心脏压塞/穿孔 2 例(0.6%)和空气栓塞 1 例(0.3%)]。在 12 个月时,无记录的房性心律失常复发率为 79.9%(AF 82.7%,AFL 96.5%,AT 98.1%),在 3 个月的空白期后,26.8%的患者继续或重新开始使用抗心律失常药物(AAD)。此外,一个扩展臂招募了 50 名患者,使用 28/31mm 可变大小的冷冻球囊进行治疗。在该组中,出现了一例暂时性的暂时性膈神经麻痹,在出院前已得到解决。这些患者在 12 个月时无记录的复发率为 82.0%。

结论

这种新型冷冻球囊可能有助于 PVI 治疗 PAF,为治疗 PAF 患者提供了更多的选择,以解决 PAF 患者中存在的各种解剖结构问题。这种冷冻球囊系统已被证明对药物难治性或药物不耐受性 PAF 患者的治疗是安全有效的。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验