Structural valve deterioration of the Labcor Dokimos aortic prosthesis: A single-centre experience

dc.contributor.authorIskandarani, Dounia Z.
dc.contributor.authorChaabo, Omar
dc.contributor.authorGharzeddine, Walid
dc.contributor.authorSfeir, Pierre M.
dc.contributor.authorObeid, Mounir Y.
dc.contributor.authorGhazzal, Ziyad M.B.
dc.contributor.authorRebeiz, Abdallah G.
dc.contributor.authorSawaya, Fadi J.
dc.contributor.departmentInternal Medicine
dc.contributor.departmentDivision of Cardiology
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:44:06Z
dc.date.available2025-01-24T11:44:06Z
dc.date.issued2022
dc.description.abstractOBJECTIVES: The goal of this study was to assess the performance and incidence of the deterioration of the Labcor Dokimos bioprosthetic aortic valve. METHODS: We performed a retrospective medical chart review of 116 patients who underwent surgical aortic valve replacement with the Labcor Dokimos aortic valve between 2010 and 2018. Abstracted data included patient demographic and echocardiographic data. Patients were divided into 2 groups: patients with structural valve deterioration (SVD) and patients without SVD. RESULTS: Among the patients with complete follow-up (n = 95), 10 patients were excluded because they died within a year; 85 patients were included in the final analysis. Of the 85 patients, 32 (38%) developed SVD; 22 (26%) had severe SVD, 15 (18%) of whom underwent reintervention. The most common aetiology of SVD was severe central aortic regurgitation, which was detected in 91% of the patients who had severe SVD. The average time from operation to severe SVD was 4.7 years with a minimum of 1.5 years and a maximum of 7.9 years. CONCLUSIONS: Bioprosthetic aortic valve deterioration due to severe aortic regurgitation is common and occurs early with the Labcor Dokimos valve. This occurrence needs to be furthered investigated in larger registries. © 2021 The Author(s). Published by Oxford University Press on behalf of the European Association for Cardio-Thoracic Surgery.
dc.identifier.doihttps://doi.org/10.1093/icvts/ivab286
dc.identifier.eid2-s2.0-85131269572
dc.identifier.pmid34687533
dc.identifier.urihttp://hdl.handle.net/10938/30400
dc.language.isoen
dc.publisherOxford University Press
dc.relation.ispartofInteractive Cardiovascular and Thoracic Surgery
dc.sourceScopus
dc.subjectEducation cardiac
dc.subjectTranscatheter valve therapy
dc.subjectValve disease
dc.subjectAortic valve
dc.subjectAortic valve insufficiency
dc.subjectAortic valve stenosis
dc.subjectBioprosthesis
dc.subjectHeart valve prosthesis
dc.subjectHeart valve prosthesis implantation
dc.subjectHumans
dc.subjectProsthesis design
dc.subjectProsthesis failure
dc.subjectRetrospective studies
dc.subjectTranscatheter aortic valve replacement
dc.subjectTreatment outcome
dc.subjectAnticoagulant agent
dc.subjectAntithrombocytic agent
dc.subjectHydroxymethylglutaryl coenzyme a reductase inhibitor
dc.subjectAged
dc.subjectAortic regurgitation
dc.subjectAortic valve disease
dc.subjectAortic valve replacement
dc.subjectAtrial fibrillation
dc.subjectCause of death
dc.subjectClinical outcome
dc.subjectConfidence interval
dc.subjectControlled study
dc.subjectDemographics
dc.subjectDisease severity
dc.subjectEchocardiography
dc.subjectFemale
dc.subjectFollow up
dc.subjectHuman
dc.subjectHuman tissue
dc.subjectIncidence
dc.subjectLogistic regression analysis
dc.subjectMajor clinical study
dc.subjectMale
dc.subjectOdds ratio
dc.subjectProportional hazards model
dc.subjectReoperation
dc.subjectRetrospective study
dc.subjectReview
dc.subjectValve deterioration
dc.subjectAdverse event
dc.subjectDiagnostic imaging
dc.subjectHeart valve replacement
dc.subjectProsthesis complication
dc.subjectTranscatheter aortic valve implantation
dc.titleStructural valve deterioration of the Labcor Dokimos aortic prosthesis: A single-centre experience
dc.typeReview

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