Evaluation of procedural and clinical outcomes of transcatheter aortic valve implantation: A single-center experience

dc.authoridAYHAN, Hüseyin/0000-0002-9991-7307
dc.authorscopusid56655177100
dc.authorscopusid26530826900
dc.authorscopusid6603167404
dc.authorscopusid7003971982
dc.authorwosidKaraduman, Bilge Duran/ABC-1759-2020
dc.authorwosidAYHAN, Hüseyin/A-5176-2018
dc.contributor.authorKaraduman, Bilge Duran
dc.contributor.authorKayaoğlu, Hüseyin Ayhan
dc.contributor.authorKeleş, Telat
dc.contributor.authorBozkurt, Engin
dc.date.accessioned2024-07-05T15:38:38Z
dc.date.available2024-07-05T15:38:38Z
dc.date.issued2020
dc.departmentAtılım Universityen_US
dc.department-tempATILIM ÜNİVERSİTESİ,ATILIM ÜNİVERSİTESİ,ANKARA YILDIRIM BEYAZIT ÜNİVERSİTESİ,T.C. SAĞLIK BAKANLIĞIen_US
dc.descriptionAYHAN, Hüseyin/0000-0002-9991-7307en_US
dc.description.abstractObjective: Transcatheter aortic valve implantation (TAVI) is an established alternative to surgical aortic valve replacement. Our study aimed to evaluate the implementation of TAVI at our large-volume center, having an all-comer patient population with short and long-term follow-ups. Methods: This retrospective, single-center analysis included 556 consecutive patients with symptomatic severe aortic stenosis (AS) who underwent TAVI between July 2011 and December 2019. Results: The mean age of the entire population was 77.6±7.9 years, and 54.9% were women. The Society of Thoracic Surgeons (STS) mean score of the cohort was 6.0%±3.5%. The balloon-expandable valve (Sapien XT, Sapien 3; Edwards Lifesciences, Irvine, California) was the most frequently used valves in this cohort (94.6%). Transfemoral access was used in 96.3% of patients. Implantation success was achieved in 96.6% of cases. During the TAVI procedure, 7.2% of patients required permanent pacemaker implantation, with 37.5% in the Lotus valve group needing the most permanent pacemakers. The mean length of hospital stay for the entire cohort was 4.5±2.3 days. Overall, 22 (3.9%) in-hospital deaths occurred before hospital discharge. The mean follow-up period was 15.1±14.9 months for all patients, and a significant improvement was noted in all echocardiographic parameters and functional capacity. Paravalvular leak (PVL) was documented in 18.9% patients, mild in 17.9%, and moderate in 1% at discharge. No cases with severe PVL, necessitating additional procedures. The multiple logistic regression analysis revealed that sex, STS score, baseline SYNTAX score, bicuspid valve morphology, common femoral artery diameter, and post-TAVI PVL were independent predictors of overall mortality. Conclusion: To our knowledge, this study, which is the largest single-center real-world experience of TAVI in Turkey, demonstrated low complication rates with favorable short- and mid-term THV performance in patients undergoing TAVI.en_US
dc.identifier.citation8
dc.identifier.doi10.14744/AnatolJCardiol.2020.03942
dc.identifier.endpage296en_US
dc.identifier.issn2149-2263
dc.identifier.issn2149-2271
dc.identifier.issue5en_US
dc.identifier.pmid32352409
dc.identifier.scopus2-s2.0-85084171044
dc.identifier.scopusqualityQ3
dc.identifier.startpage288en_US
dc.identifier.trdizinid362154
dc.identifier.urihttps://doi.org/10.14744/AnatolJCardiol.2020.03942
dc.identifier.urihttps://search.trdizin.gov.tr/tr/yayin/detay/362154/evaluation-of-procedural-and-clinical-outcomes-of-transcatheter-aortic-valve-implantation-a-single-center-experience
dc.identifier.volume23en_US
dc.identifier.wosWOS:000535232600009
dc.identifier.wosqualityQ4
dc.institutionauthorKaraduman, Bilge Duran
dc.language.isoenen_US
dc.publisherKare Publen_US
dc.relation.ispartofThe Anatolian Journal of Cardiologyen_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleEvaluation of procedural and clinical outcomes of transcatheter aortic valve implantation: A single-center experienceen_US
dc.typeArticleen_US
dspace.entity.typePublication
relation.isAuthorOfPublication0f73438e-c5d8-48a7-9ee7-f34c94ea2421
relation.isAuthorOfPublication.latestForDiscovery0f73438e-c5d8-48a7-9ee7-f34c94ea2421

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