Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/29235
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dc.contributor.authorTüydeş, Oktay-
dc.contributor.authorYüksel, Ahmet-
dc.contributor.authorŞenol, Sefa-
dc.contributor.authorAkarsu, Serkan-
dc.date.accessioned2022-10-27T08:55:31Z-
dc.date.available2022-10-27T08:55:31Z-
dc.date.issued2016-06-
dc.identifier.citationTok, M. vd. (2016). "Early-term outcomes for treatment of saphenous vein insufficiency with N-butyl cyanoacrylate: A novel, non-thermal, and non-tumescent percutaneous embolization technique". Heart Surgery Forum, 19(3), E118-E122.en_US
dc.identifier.issn1098-3511-
dc.identifier.issn1522-6662-
dc.identifier.urihttps://doi.org/10.1532/hsf.1496-
dc.identifier.urihttps://journal.hsforum.com/index.php/HSF/article/view/1496-
dc.identifier.urihttp://hdl.handle.net/11452/29235-
dc.description.abstractBackground: The purpose of this study was to present early-term outcomes of VariClose r Vein Sealing System, which is a novel, non-thermal, and non-tumescent percutaneous embolization technique for treatment of saphenous vein insufficiency. Methods: Between March 2014 and July 2015, 189 saphenous veins in 141 patients were treated with Variclose Vein Sealing System containing n-butyl cyanoacrylate. Pre-, intra-, post-procedural, and follow-up data of patients were collected and retrospectively reviewed. Results: Mean age of patients was 42.5 +/- 14.0 years, of which 53% were female. Technical success rate of intervention was 98.9%. Mean procedure time was 14.3 +/- 7.5 minutes. Eighty-nine percent of patients (n = 126/ 141) were available at mean follow-up time of 6.7 months. Mean Venous Clinical Severity Score was significantly improved from 8.3 +/- 2.2 at pre-procedure period to 3.3 +/- 1.8 at follow-up. No complete recanalization was observed, but 2 patients were presented with partial recanalization during follow-up. The complete occlusion rate was 98.4%. No serious adverse event related to procedure was observed. Conclusion: Variclose Vein Sealing System appears to be safe and effective in treatment of saphenous vein insufficiency. Further randomized studies with long-term outcomes are required for determining optimal treatment modality in patients with saphenous vein insufficiency.en_US
dc.language.isoenen_US
dc.publisherForum Multimedia Publishingen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCardiovascular system & cardiologyen_US
dc.subjectSurgeryen_US
dc.subjectThermal ablationen_US
dc.subjectVaricose-veinsen_US
dc.subjectFollow-upen_US
dc.subjectPolidocanol foamen_US
dc.subjectGreaten_US
dc.subjectSclerotherapyen_US
dc.subjectMulticenteren_US
dc.subjectTrialen_US
dc.subjectAdhesiveen_US
dc.subjectRefluxen_US
dc.subject.meshAdulten_US
dc.subject.meshAgeden_US
dc.subject.meshEmbolization, therapeuticen_US
dc.subject.meshFemaleen_US
dc.subject.meshHumansen_US
dc.subject.meshMaleen_US
dc.subject.meshMiddle ageden_US
dc.subject.meshRetrospective studiesen_US
dc.subject.meshSaphenous veinen_US
dc.subject.meshVaricose veinsen_US
dc.subject.meshVenous insufficiencyen_US
dc.subject.meshYoung adulten_US
dc.titleEarly-term outcomes for treatment of saphenous vein insufficiency with N-butyl cyanoacrylate: A novel, non-thermal, and non-tumescent percutaneous embolization techniqueen_US
dc.typeArticleen_US
dc.identifier.wos000384793300008tr_TR
dc.identifier.scopus2-s2.0-84977652435tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Kalp Damar Cerrahisi Anabilim Dalı.tr_TR
dc.identifier.startpageE118tr_TR
dc.identifier.endpageE122tr_TR
dc.identifier.volume19tr_TR
dc.identifier.issue3tr_TR
dc.relation.journalHeart Surgery Forumen_US
dc.contributor.buuauthorTok, Mustafa-
dc.relation.collaborationSanayitr_TR
dc.identifier.pubmed27355146tr_TR
dc.subject.wosCardiac & cardiovascular systemsen_US
dc.subject.wosSurgeryen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ4en_US
dc.contributor.scopusid6506976035tr_TR
dc.subject.scopusVaricosis; Saphenous Vein; Sclerotherapyen_US
dc.subject.emtreeAntibiotic agenten_US
dc.subject.emtreeEnbucrilateen_US
dc.subject.emtreeNonsteroid antiinflammatory agenten_US
dc.subject.emtreeAdulten_US
dc.subject.emtreeAgeden_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeArtificial embolizationen_US
dc.subject.emtreeClinical effectivenessen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeDevice embolizationen_US
dc.subject.emtreeEcchymosisen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeFemoral veinen_US
dc.subject.emtreeFollow upen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeIntraoperative perioden_US
dc.subject.emtreeMajor clinical studyen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeMean venous clinical severity scoreen_US
dc.subject.emtreeOcclusionen_US
dc.subject.emtreeOperation durationen_US
dc.subject.emtreePercutaneous emblization techniqueen_US
dc.subject.emtreePostoperative perioden_US
dc.subject.emtreePreoperative perioden_US
dc.subject.emtreePriority journalen_US
dc.subject.emtreeRating scaleen_US
dc.subject.emtreeRecanalizationen_US
dc.subject.emtreeReinterventionen_US
dc.subject.emtreeRetrospective studyen_US
dc.subject.emtreeSafetyen_US
dc.subject.emtreeSaphenofemoral junctionen_US
dc.subject.emtreeSaphenous veinen_US
dc.subject.emtreeSaphenous vein insufficiencyen_US
dc.subject.emtreeThrombophlebitisen_US
dc.subject.emtreeTreatment durationen_US
dc.subject.emtreeTreatment outcomeen_US
dc.subject.emtreeValsalva maneuveren_US
dc.subject.emtreeVasospasmen_US
dc.subject.emtreeVein diameteren_US
dc.subject.emtreeVein insufficiencyen_US
dc.subject.emtreeArtificial embolizationen_US
dc.subject.emtreeMiddle ageden_US
dc.subject.emtreeProceduresen_US
dc.subject.emtreeVaricose veinsen_US
dc.subject.emtreeVenous Insufficiencyen_US
dc.subject.emtreeYoung adulten_US
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