{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,8]],"date-time":"2026-02-08T00:47:51Z","timestamp":1770511671745,"version":"3.49.0"},"reference-count":25,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2012,5,21]],"date-time":"2012-05-21T00:00:00Z","timestamp":1337558400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Interven Cardiology"],"published-print":{"date-parts":[[2012,8]]},"abstract":"<jats:p><jats:bold>\n            <jats:italic>Background:<\/jats:italic>\n          <\/jats:bold>\n          <jats:italic>Percutaneous closure of secundum type atrial septal defect (ASD) and patent foramen ovale (PFO) has gained widespread use in recent years. Herein, we evaluated the safety and efficacy of the Occlutech\u00ae Figulla devices for PFO and ASD closure in a reference tertiary center.<\/jats:italic><\/jats:p><jats:p><jats:bold>\n            <jats:italic>Methods:<\/jats:italic>\n          <\/jats:bold>\n          <jats:italic>All 143 patients (46.9% male, mean age 39.3 \u00b1 12.2 years) who underwent transcatheter PFO (n = 85) and ASD (n = 58) closure with Occlutech\u00ae Figulla devices between February 2009 and October 2011 were included in this study. An echocardiographic follow\u2010up examination was performed at the 1st, 6th, and 12th month visits.<\/jats:italic><\/jats:p><jats:p><jats:bold>\n            <jats:italic>Results:<\/jats:italic>\n          <\/jats:bold>\n          <jats:italic>The devices were successfully implanted in all 143 patients (100%). In\u2010hospital periprocedural complications were device embolization (0.7%; 1 ASD patient), atrial fibrillation (1.4%; 1 ASD and 1 PFO patients), supraventricular tachycardia (0.7%; 1 PFO patient), and vascular access hematoma (0.7%; 1 ASD patient). Among ASD patients, 2 patients had trivial (jet width &lt;1 mm in diameter) and 1 patient had small (1\u20132 mm) residual shunts before hospital discharge, which disappeared after the 6\u2010month visit. During the mean 15.4 \u00b1 9.6 months follow\u2010up, all patients were asymptomatic and no ischemic stroke, cardiac perforation, device erosion, embolization, thrombus formation, or malposition of the device was observed.<\/jats:italic><\/jats:p><jats:p><jats:bold>\n            <jats:italic>Conclusions:<\/jats:italic>\n          <\/jats:bold>\n          <jats:italic>Percutaneous PFO and secundum type ASD closure with the novel Occlutech\u00ae Figulla Occluder devices without left atrial central pin and with significantly reduced meshwork was safe, feasible, and effective.<\/jats:italic> (J Interven Cardiol 2012;25:375\u2013381)<\/jats:p>","DOI":"10.1111\/j.1540-8183.2012.00734.x","type":"journal-article","created":{"date-parts":[[2012,5,22]],"date-time":"2012-05-22T03:51:57Z","timestamp":1337658717000},"page":"375-381","source":"Crossref","is-referenced-by-count":22,"title":["Early\u2010Mid Term Follow\u2010Up Results of Percutaneous Closure of the Interatrial Septal Defects with Occlutech Figulla Devices: A Single Center Experience"],"prefix":"10.1111","volume":"25","author":[{"given":"KUDRET","family":"AYTEMIR","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"ALI","family":"OTO","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S\u00dcHEYLA","family":"\u00d6ZKUTLU","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"ERG\u00dcN 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