Left atrial appendage closure with Amplatzer cardiac plug for stroke prevention in atrial fibrillation: Initial Asia-Pacific experience

被引:128
作者
Lam, Yat-Yin [1 ]
Yip, Gabriel W. K. [1 ]
Yu, Cheuk-Man [1 ]
Chan, Wilson W. M. [1 ]
Cheng, Boron C. W. [1 ]
Yan, Bryan P. [1 ]
Clugston, Richard [2 ]
Yong, Gerald [2 ]
Gattorna, Tim [2 ]
Paul, Vincent [2 ]
机构
[1] Chinese Univ Hong Kong, Dept Med & Therapeut, Prince Wales Hosp, Div Cardiol,SH Ho Cardiovasc & Stroke Ctr, Hong Kong, Hong Kong, Peoples R China
[2] Royal Perth Hosp, Perth, WA, Australia
关键词
left atrial appendage occlusion; Amplatzer cardiac plug; atrial fibrillation; stroke; HIGH-RISK PATIENTS; TRANSCATHETER OCCLUSION; WARFARIN THERAPY; SEPTAL OCCLUDER; PLAATO; ANTICOAGULATION; DEVICE; SYSTEM;
D O I
10.1002/ccd.23136
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Left atrial appendage (LAA) is the main source of left atrial thrombus that causes stroke in patients with non-valvular atrial fibrillation (NVAF). This study reported the initial safety, feasibility, and 1-yr clinical outcomes following AMPLATZER cardiac plug (ACP) implantation in Asia-Pacific region.Methods: Twenty NVAF patients (16 males, age 68 +/- 9 yr) with high risk for developing cardioembolic stroke (CHADS2 score: 2.3 +/- 1.3) and contraindications to warfarin received ACP implants from June 2009 to May 2010. Patients received general anesthesia (n = 9) or controlled propofol sedation (n = 11) and the procedures were guided by fluoroscopy and transesophageal echocardiography (TEE). Clinical follow-up was arranged at 1 month and then every 3 months after implantation, whereas, a TEE was scheduled at 1 month upon completion of dual anti-platelet therapy.Results: The LAA was successfully occluded in 19/20 patients (95%) at two Asian centers. One procedure was abandoned because of catheter-related thrombus formation. Other complications included coronary artery air embolism (n = 1) and TEE-attributed esophageal injury (n = 1). The median procedural and fluoroscopic times were 79 (IQR: 59100) and 18 (IQR 1227) minutes, respectively. The mean size of implant was 23.6 +/- 3.1 mm. The average hospital stay was 1.8 +/- 1.1 days. Follow-up TEE showed all the LAA orifices were sealed without device-related thrombus formation. No stroke or death occurred at a mean follow-up of 12.7 +/- 3.1 months. Conclusions: Our preliminary data suggested LAA closure with ACP is safe, feasible with encouraging 1-yr clinical outcomes. Further large-scaled trials are needed to confirm the efficacy of this device. (c) 2011 Wiley Periodicals, Inc.
引用
收藏
页码:794 / 800
页数:7
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