使用新型 Lotos 脉冲场消融导管进行 "单次 "肺静脉隔离:对可行性、安全性和 30 天疗效的临床前评估

Sijia Pu, Fangzhou Liu, Yuhan Chen, Cihua Luo, Peng Li, Yanlin Chen, Lu Fu, Huiyi Liu, Xingdong Ye, Shulin Wu, Yumei Xue, Weidong Lin
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摘要

目的 脉冲场消融(PFA)正在成为心房颤动治疗中肺静脉隔离(PVI)的一种非热组织特异性技术。这项临床前研究旨在调查使用新型 PFA 系统(包括纳秒级 PFA 发生器、新型 Lotos PFA 导管和定制的 12 法分可转向鞘)进行 PVI 的可行性和安全性。方法和结果 本研究共纳入 11 头约克夏猪,其中 4 头为急性组,7 头为慢性组。在全身麻醉的情况下,首先进行经皮穿刺和肺静脉血管造影。在对左心房进行电解剖重建后,将 PFA 导管导航至左右肺静脉窦的位置。在纺锤形和洛托斯形的 PV 上进行了双相 PFA 应用。在两组患者中,消融后 30 分钟对 PVI 和 PFA 相关安全性进行评估,在慢性组患者中,消融后 30 天对 PVI 和 PFA 相关安全性进行评估。进行了详细的尸体解剖和组织病理学检查。另外还对心内超声心动图和冠状动脉造影进行了安全性评估。所有目标肺静脉(n = 20)均在首次尝试时成功分离。手术过程中未发现冠状动脉痉挛或微泡。在为期 30 天的侵入性研究中,12 条肺静脉中有 11 条(91.6%)仍保持分离状态。未在任何目标中观察到 PV 狭窄的证据。然而,17.6%的目标发生了短暂的膈肌捕获。组织病理学检查未发现侧支损伤的证据。结论 这项研究提供了科学证据,证明新型 PFA 导管和系统用于单次 PVI 的安全性和有效性,显示出巨大的潜力。
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‘Single-shot’ pulmonary vein isolation using a novel lotos pulsed field ablation catheter: a preclinical evaluation of the feasibility, safety and 30-day efficacy
Aims Pulsed field ablation (PFA) is emerging as a nonthermal, tissue-specific technique for pulmonary vein isolation (PVI) in atrial fibrillation therapy. This preclinical study aimed to investigate the feasibility and safety of PVI using a novel PFA system including a nanosecond-scale PFA generator, a novel lotos PFA catheter, and a customized 12-French steerable sheath. Methods and Results A total of 11 Yorkshire swine were included in this study, with 4 in the acute cohort and 7 in the chronic cohort. Under general anesthesia, transseptal puncture and pulmonary vein (PV) angiography was initially performed. The PFA catheter was navigated to position at the right and left PV antrum after the electroanatomic reconstruction of left atrium. Biphasic PFA applications were performed on PVs in both the spindle-shaped and lotos-shaped poses. PVI and PFA-associated safety was assessed 30 minutes after ablation in both cohorts and 30 days later in the chronic cohort. Detailed necropsy and histopathology were performed. Additional intracardiac echocardiography and coronary angiogram were evaluated for safety. All target pulmonary veins (n = 20) were successfully isolated on the first attempt. No spasm of coronary artery or microbubble was seen during the procedure. Eleven of 12 PVs (91.6%) remained isolation at 30-day invasive study. No evidence of PV stenosis was observed in any targets. However, transient diaphragm capture occurred in 17.6%. Histopathological examinations showed no evidence of collateral injury. Conclusion This study provides scientific evidence demonstrating the safety and efficacy of the novel PFA catheter and system for single-shot PVI, which shows great potential.
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