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WATCHMAN左心耳封堵系统用于中国非瓣膜性心房颤动患者预防卒中的疗效与安全性:一项单中心、前瞻性、观察性研究

Efficacy and Safety of the WATCHMAN Left Atrial Appendage System for Stroke Prevention in Chinese Patients with Nonvalvular Atrial Fibrillation: A Single-center, Prospective, Observational Study.

作者信息

Huang Wei-Ping, Zhang Yong-Hua, He Lei, Su Xi, Yang Xin-Wei, Guo Zai-Xiong

机构信息

Department of Cardiology, Wuhan Asia Heart Hospital, Wuhan, Hubei 430022, China.

出版信息

Chin Med J (Engl). 2017 Feb 20;130(4):434-438. doi: 10.4103/0366-6999.199832.

Abstract

BACKGROUND

In patients with nonvalvular atrial fibrillation (NVAF), embolic stroke is thought to be associated with left atrial appendage (LAA) thrombi. The WATCHMAN LAA Occlusion Device has been shown to be noninferior to conventional oral anticoagulation with warfarin for stroke prevention in patients with NVAF. This study aimed to evaluate the procedural feasibility, safety and 12-month outcomes of the WATCHMAN LAA Occlusion Device in NVAF patients with high risk for stroke in China.

METHODS

The clinical data of 106 NVAF patients, who were consecutively underwent LAA closure with the WATCHMAN Device between April 2014 and May 2015, were collected. Patients were followed up at 1, 3, 6, and 12 months after discharge. A transesophageal echocardiograph was performed at 45 days after implantation and repeated in case of an unexpected event during the follow-up period.

RESULTS

This study included 106 NVAF patients with a mean age of 64.2 ± 8.6 years (ranging from 50 to 88 years), and the mean CHA2DS2-VASc score of all patients was 3.6 ± 1.6 (ranging from 2 to 9). Among those 106 NVAF patients, 100 (94.3%) patients were implanted with the device successfully. The procedural success rate was 94.3% (100/106), and the occlusion rate was 100.0% (100/100). There were one tamponade, one ischemic stroke, and eight minor pericardial effusions during hospitalization. During 12-month follow-up period, two patients developed a thrombus layer on the device that resolved with additional anticoagulation: one with visible device-thrombus experienced transient ischemic stroke, and one had a hemorrhagic stroke. There were no deaths in this study. The overall survival rate was 100.0%, and nonmajor adverse event rate was 95.0% (95/100). In this study, the expected annual rate of ischemic stroke risk in these patients according to the CHA2DS2-VASc score was 4.0%, while the observed ischemic stroke rate was 2.0% per year.

CONCLUSIONS

LAA closure with the WATCHMAN Device was feasible, efficient, and safe for NVAF to prevent the accidence of stroke in Chinese patients. During the 12-month follow-up period, the observed ischemic stroke rate (2.0% per year) in our study was lower than the predicted annual stroke risk (4.0%) using the CHA2DS2-VASc score.

摘要

背景

在非瓣膜性心房颤动(NVAF)患者中,栓塞性卒中被认为与左心耳(LAA)血栓有关。已证明WATCHMAN LAA封堵装置在预防NVAF患者卒中方面不劣于传统的华法林口服抗凝治疗。本研究旨在评估WATCHMAN LAA封堵装置在中国具有高卒中风险的NVAF患者中的手术可行性、安全性及12个月的结局。

方法

收集2014年4月至2015年5月期间连续接受WATCHMAN装置LAA封堵的106例NVAF患者的临床资料。患者在出院后1、3、6和12个月进行随访。植入后45天进行经食管超声心动图检查,随访期间如有意外事件则重复检查。

结果

本研究纳入106例NVAF患者,平均年龄64.2±8.6岁(50至88岁),所有患者的平均CHA2DS2-VASc评分为3.6±1.6(2至9分)。在这106例NVAF患者中,100例(94.3%)成功植入该装置。手术成功率为94.3%(100/106),封堵率为100.0%(100/100)。住院期间发生1例心包填塞、1例缺血性卒中和8例少量心包积液。在12个月的随访期内,2例患者装置上形成血栓层,经追加抗凝治疗后消退:1例可见装置血栓的患者发生短暂性脑缺血发作,1例发生出血性卒中。本研究无死亡病例。总生存率为100.0%,非严重不良事件发生率为95.0%(95/100)。在本研究中,根据CHA2DS2-VASc评分,这些患者预期的年度缺血性卒中风险率为4.0%,而观察到的缺血性卒中发生率为每年2.0%。

结论

对于中国NVAF患者,使用WATCHMAN装置进行LAA封堵在预防卒中发生方面是可行、有效且安全的。在12个月的随访期内,本研究观察到的缺血性卒中发生率(每年2.0%)低于使用CHA2DS2-VASc评分预测的年度卒中风险(4.0%)。

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