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经 WATCHMAN FLX 和 WATCHMAN 2.5 装置行经皮左心耳封堵术患者的操作和中期结局的对比数据 - OCEAN-LAAC 注册研究的见解。

Comparative Data of Procedural and Midterm Outcomes in Patients Who Underwent Percutaneous Left Atrial Appendage Closure Between the WATCHMAN FLX and WATCHMAN 2.5 Devices - Insight From the OCEAN-LAAC Registry.

机构信息

Department of Cardiology, Sendai Kousei Hospital.

Department of Cardiology, Toyohashi Heart Center.

出版信息

Circ J. 2024 Jun 25;88(7):1187-1197. doi: 10.1253/circj.CJ-24-0062. Epub 2024 May 17.

DOI:10.1253/circj.CJ-24-0062
PMID:38763735
Abstract

BACKGROUND

Limited data are available regarding clinical outcomes after percutaneous left atrial appendage closure using WATCHMAN FLX (WM-FLX) and WATCHMAN-2.5 (WM2.5) devices in Asian patients.

METHODS AND RESULTS

Data of 1,464 consecutive patients (WM-FLX, n=909; WM2.5, n=555) were extracted from a Japanese multicenter registry, and clinical data were compared between the 2 groups. No in-hospital deaths, periprocedural stroke, or device embolization occurred. Procedural success was significantly higher in the WM-FLX than WM2.5 group (95.8% vs. 91.9%; P=0.002) owing to the lower incidence of periprocedural pericardial effusion (0.55% vs. 1.8%; P=0.021). No significant differences in all-cause death, postprocedural stroke, and device-related thrombus were observed between the 2 groups. However, the cumulative bleeding rate at 1 year was substantially lower in the WM-FLX group (7.8% vs. 16.4%; P<0.001). Landmark analysis of bleeding events highlighted lower bleeding rates in the WM-FLX than WM2.5 group within the first 6 months (6.4% vs. 14.8%; P<0.001), with comparable bleeding rates over the 6- to 12-month period (1.5% vs. 3.2%, respectively; P=0.065).

CONCLUSIONS

This study demonstrated higher early safety and lower 1-year bleeding rates in the WM-FLX than WM2.5 group. The lower bleeding events with WM-FLX are likely due to multiple factors other than purely difference in devices, such as postprocedural drug regimen.

摘要

背景

亚洲患者经皮左心耳封堵术(Percutaneous left atrial appendage closure,LAAC)使用 WATCHMAN FLX(WM-FLX)和 WATCHMAN-2.5(WM2.5)装置的临床结局相关数据有限。

方法和结果

一项日本多中心注册研究中提取了 1464 例连续患者的数据(WM-FLX 组 909 例,WM2.5 组 555 例),并比较了两组间的临床数据。两组均无住院期间死亡、围术期卒中或器械栓塞事件发生。WM-FLX 组的手术成功率明显高于 WM2.5 组(95.8% vs. 91.9%;P=0.002),这归因于围术期心包积液发生率较低(0.55% vs. 1.8%;P=0.021)。两组间全因死亡率、术后卒中发生率和器械相关血栓无显著差异。然而,WM-FLX 组 1 年时的累积出血率明显较低(7.8% vs. 16.4%;P<0.001)。对出血事件的里程碑分析突出显示,WM-FLX 组在前 6 个月内的出血率低于 WM2.5 组(6.4% vs. 14.8%;P<0.001),而在 6-12 个月期间的出血率相当(分别为 1.5% vs. 3.2%;P=0.065)。

结论

与 WM2.5 组相比,WM-FLX 组具有更高的早期安全性和更低的 1 年出血率。WM-FLX 组较低的出血事件可能归因于多个因素,而不仅仅是器械的差异,例如术后药物治疗方案。

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