Amplatzer or Figulla Flex II Occluder: A Comparative Study of Outcomes After Transcatheter Patent Foramen Ovale Closure

被引:0
作者
Toggweiler, Stefan [1 ]
Moccetti, Federico [1 ]
Conrad, Nina [1 ]
Loretz, Lucca [1 ]
Madanchi, Mehdi [1 ]
Bossard, Matthias [1 ]
Attiger-Toller, Adrian [1 ]
Cuculi, Florim [1 ]
Wolfrum, Mathias [1 ,2 ]
机构
[1] Luzerner Kantonsspital, Heart Ctr Lucerne, Luzern, Switzerland
[2] Luzerner Kantonsspital, Heart Ctr Lucerne, Cardiol Div, Spitalstr 16, CH-6000 Luzern, Switzerland
关键词
Patent Foramen Ovale; Closure; Amplatzer Occluder Device; Percutaneous Closure; Outcomes; LONG-TERM OUTCOMES; MEDICAL THERAPY;
D O I
10.25270/jic/23.00291
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives. Percutaneous closure of a patent foramen ovale (PFO) for the prevention of recurrent paradoxical thromboembolic events has been shown to be safe and effective in randomized controlled trials. However, it remains uncertain if differences in the structure and design of the occluder devices impact the outcomes. The aim of this study was to compare results of percutaneous PFO closure using 2 widely used double -disc occluders. Methods. Consecutive patients who underwent percutaneous PFO closure with the Abbott Amplatzer occluder (APO) or the Occlutech Figulla-Flex-II occluder (OPO) at the Heart Center Lucerne between February 2017 and December 2022 were included in a registry. The primary endpoint was effective closure of the PFO, defined as a residual shunt grade 0 or 1, assessed by contrast echocardiogram at 6 -month follow-up. Secondary endpoints included procedural efficacy/safety and major adverse cardiovascular events during the hospital stay and at 6 -month follow-up. Results. One hundred ninety-three consecutive patients (mean age 51.7 +/- 12.5 years; 39% women; Risk of Paradoxical Embolism (RoPE) score = 7, interquartile range [IQR] = 6-8) underwent percutaneous PFO closure with the APO (120 patients, 62.2%) or the OPO (73 patients, 37.8%). Main indications for closure were crypotogenic stroke in 168 patients (87.1%) and peripheral embolism in 13 patients (6.7%). At baseline, right -to -left shunt (RLS) greater than or equal to grade 2 was present in 189 patients (97.9%). Immediate procedural success was 99.5%. In 1 patient, an air embolism occurred during positioning of the APO occluder with transient chest pain and electrocardiogram changes, but without further sequelae to the patient. At 6 -month follow-up, effective closure was achieved in 185 patients (95.8%; APO: 96.6% vs OPO: 94.5%, P = .30). Rates of atrial fibrillation and recurrent thromboembolic events were 4.2% and 0.5%, respectively. Conclusions. PFO closure is safe and effective when performed with either the self -expanding Abbott Amplatzer or Occlutech Figulla Flex II PFO occluder.
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页数:10
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