Short-Term Outcomes of Patent Ductus Arteriosus Closure With New Occlutech (R) Duct Occluder: A Multicenter Study

dc.contributor.authorDedeoglu, Reyhan
dc.contributor.authorBilici, Meki
dc.contributor.authorDemir, Fikri
dc.contributor.authorDemir, Fadli
dc.contributor.authorAcar, Onur Caglar
dc.contributor.authorHallioglu, Olgu
dc.contributor.authorPac, Aysenur
dc.contributor.authorKiziltas, Alev
dc.contributor.authorKarabel, Duran
dc.contributor.authorKula, Serdar
dc.contributor.authorCimen, Derya
dc.contributor.authorBaspinar, Osman
dc.contributor.authorAtik, Sezen Ugan
dc.contributor.authorSaltik, Irfan Levent
dc.contributor.orcIDhttps://orcid.org/0000-0003-4444-0027en_US
dc.contributor.pubmedID27090770en_US
dc.contributor.researcherIDV-1112-2019en_US
dc.date.accessioned2023-06-16T07:50:18Z
dc.date.available2023-06-16T07:50:18Z
dc.date.issued2016
dc.description.abstractAim: Over the past 2 decades, transcatheter occlusion of patent ductus arteriosus (PDA) with coils and the duct occluders evolved to be the procedure of choice. A new device, the Occlutech PDA1 occluder (ODO) device has been designed. Herein, we aimed to evaluate the characteristics and short-term results of patients who underwent transcatheter closure of PDA using the ODO. Methods: We reviewed the clinical records of 60 patients from different centers in Turkey between December 2013 and January 2016. The medical records were reviewed for demographic characteristics and echocardiographic findings. Device size was selected on the narrowest diameter of PDA. Results: The median patient age was 2.5 years (6 months-35 years), and median PDA diameter was 2.5mm (1.2-11 mm). Fifty-eight of 60 patients (96.6%) had successful ODO implantation. The occlusion rates were 37/58 (63.7%) at the end of the procedure, 51/58 (87.9%) at 24-48 hours post-procedure, and 57/58 (98.2%) on echocardiography at a median follow-up of 7.6 months. Conclusion: Our results indicate that transcatheter closure of PDA using the ODO is effective. Larger studies and longer follow-up are required to assess whether its shape and longer length make it superior to other duct occluders in large, tubular, or window-type ducts.en_US
dc.identifier.endpage331en_US
dc.identifier.issn0896-4327en_US
dc.identifier.issue3en_US
dc.identifier.scopus2-s2.0-84964334627en_US
dc.identifier.startpage325en_US
dc.identifier.urihttp://hdl.handle.net/11727/9643
dc.identifier.volume29en_US
dc.identifier.wos000384919800011en_US
dc.language.isoengen_US
dc.relation.isversionof10.1111/joic.12290en_US
dc.relation.journalJOURNAL OF INTERVENTIONAL CARDIOLOGYen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCONGENITAL HEART-DISEASEen_US
dc.subjectTRANSCATHETER CLOSUREen_US
dc.subjectCATHETER CLOSUREen_US
dc.subjectPERCUTANEOUS CLOSUREen_US
dc.subjectCOIL OCCLUSIONen_US
dc.subjectFOLLOW-UPen_US
dc.subjectEXPERIENCEen_US
dc.subjectPDAen_US
dc.subjectIMMEDIATEen_US
dc.subjectINFANTSen_US
dc.titleShort-Term Outcomes of Patent Ductus Arteriosus Closure With New Occlutech (R) Duct Occluder: A Multicenter Studyen_US
dc.typeArticleen_US

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