Late Results After Percutaneous Closure of Patent Foramen Ovale for Secondary Prevention of Paradoxical Embolism Using the Amplatzer PFO Occluder Without Intraprocedural Echocardiography Effect of Device Size

被引:62
作者
Wahl, Andreas
Tai, Tony
Praz, Fabien
Schwerzmann, Markus
Seiler, Christian
Nedeltchev, Krassen [1 ]
Windecker, Stephan
Mattle, Heinrich P. [1 ]
Meier, Bernhard [2 ]
机构
[1] Univ Hosp Bern, Dept Neurol, CH-3010 Bern, Switzerland
[2] Univ Hosp Bern, Swiss Cardiovasc Ctr Bern, Dept Cardiol, CH-3010 Bern, Switzerland
关键词
atrial septal aneurysm; patent foramen ovale; cerebral ischemia; embolism; secondary stroke prevention; ATRIAL SEPTAL ANEURYSM; TRANSCATHETER CLOSURE; CRYPTOGENIC STROKE; MEDICAL-TREATMENT; EVENTS; SAFETY; DEFECT; RISK;
D O I
10.1016/j.jcin.2008.09.013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives We sought to assess the safety and clinical efficacy of patent foramen ovale (PFO) closure under fluoroscopic guidance only, without intraprocedural echocardiography. Background Percutaneous PFO closure has been shown to be safe and feasible using several devices. It is generally performed using simultaneously fluoroscopic and transesophageal or intracardiac echocardiographic guidance. Transesophageal echocardiography requires sedation or general anesthesia and intubation to avoid aspiration. Intracardiac echocardiography is costly and has inherent risks. Both lengthen the procedure. The Amplatzer PFO Occluder (AGA Medical Corporation, Golden Valley, Minnesota) can be safely implanted without echocardiographic guidance. Methods A total of 620 patients (51 +/- 12 years; 66% male) underwent PFO closure using the Amplatzer PFO Occluder for secondary prevention of presumed paradoxical embolism. Based on size and mobility of the PFO and the interatrial septum, an 18-mm device was used in 50 patients, a 25-mm device in 492, and a 35-mm device in 78. Results All procedures were successful, with 5 procedural complications (0.8%): 4 arteriovenous fistulae requiring elective surgical correction, and 1 transient ischemic attack. Contrast transesophageal echocardiography at 6 months showed complete closure in 91% of patients, whereas a minimal, moderate, or large residual shunt persisted in 6%, 2%, and 1%, respectively. During a mean follow-up period of 3.0 +/- 1.9 years (median: 2.6 years; total patient-years: 1,871), 5 ischemic strokes, 8 transient ischemic attacks, and no peripheral emboli were reported. Freedom from recurrent ischemic stroke, transient ischemic attack, or peripheral embolism was 99% at 1 year, 99% at 2 years, and 97% at 5 years. Conclusions The Amplatzer PFO Occluder affords excellent safety and long-term clinical efficacy of percutaneous PFO closure without intraprocedural echocardiography. (J Am Coll Cardiol Intv 2009; 2:116-23) (C) 2009 by the American College of Cardiology Foundation
引用
收藏
页码:116 / 123
页数:8
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