학술논문

Long-Term Contrast Echocardiography and Clinical Follow-Up after Percutaneous Closure of Patent Foramen Ovale Using Two Different Atrial Septal Occluder Devices.
Document Type
Journal Article
Source
Journal of Interventional Cardiology. Aug2016, Vol. 29 Issue 4, p406-413. 8p.
Subject
*ATRIAL septal defect treatment
*CONTRAST echocardiography
*ELECTROCARDIOGRAPHY
*CARDIAC catheterization
*FOLLOW-up studies (Medicine)
*COMPARATIVE studies
*PATENT foramen ovale
*ECHOCARDIOGRAPHY
*LONGITUDINAL method
*RESEARCH methodology
*EVALUATION of medical care
*MEDICAL cooperation
*RESEARCH
*SURGICAL complications
*PRODUCT design
*EVALUATION research
*TREATMENT effectiveness
*DIAGNOSIS
STROKE risk factors
Language
ISSN
0896-4327
Abstract
Introduction: Percutaneous patent foramen ovale (PFO) closure by means of a septal occluder device (SOD) is a well-known therapeutic strategy for the secondary prevention of paradoxical embolic neurological events. The aim of this study was to provide long-term echocardiographic and clinical follow-up data on patients who had undergone percutaneous PFO closure with 2 different SOD.Methods: We selected 2 groups of patients treated with 2 different SOD: Group A: 52 patients with an Amplatzer(®) PFO Occluder and Group B: 49 patients with a Figulla Flex(®) device. All patients underwent follow-up Bubble Test Transthoracic Echocardiography (BTTE) and clinical examination. The results were compared with those recently reported in a group of patients with similar characteristics, but that had been treated conservatively, which acted as a control group.Results: The mean follow-up after PFO closure was 53 months. The Amplatzer(®) PFO Occluder and the Figulla Flex were used in 52 (51.5%) and 49 (48.5%) of patients, respectively. We found no significant difference in the rate of effective PFO closure between the devices: Amplatzer 91.4%, Figulla 93.9% (P = 0.71). One patient (1.0%) suffered a recurrent neurologic event. BTTE was positive (BTTE+) in 8 patients (8%), 5 with an Amplatzer, and 3 with a Figulla device (P = 0.516). Only 1 patient with BTTE+ had a recurrent TIA (12.5%). No significant relationship was found between device dimensions and BTTE+ (P = 0.062). In the control group (163 patients), the recurrence of neurologic events was 9.2% (15 events), that was significantly higher in respect to the patients who had undergone percutaneous closure of the PFO.Conclusions: Percutaneous PFO closure was associated with a remarkably low risk of recurrent embolic neurological events, and no long-term device-related major complications. No statistically significant difference emerged between the 2 different SODs regarding BTTE positivity. Long-term follow-up showed that the recurrence of neurological events has been significantly higher in the group treated in a conservative way. [ABSTRACT FROM AUTHOR]