Publication:
Secondary retensioning of a tether-based device for transapical transcatheter mitral valve implantation.

cris.virtualsource.author-orcide58d604d-1e1c-4387-94ae-cf69dd2a3ea3
datacite.rightsopen.access
dc.contributor.authorBeyer, Martin
dc.contributor.authorMuller, David
dc.contributor.authorDe Marco, Federico
dc.contributor.authorBadhwar, Vinay
dc.contributor.authorObadia, Jean-Francois
dc.contributor.authorPraz, Fabien Daniel
dc.contributor.authorModine, Thomas
dc.contributor.authorTonino, Pim
dc.contributor.authorDahle, Gry
dc.contributor.authorCerillo, Alfredo
dc.contributor.authorLudwig, Sebastian
dc.contributor.authorConradi, Lenard
dc.date.accessioned2024-10-26T16:50:55Z
dc.date.available2024-10-26T16:50:55Z
dc.date.issued2024-01-02
dc.description.abstractOBJECTIVES Relevant paravalvular leakage (PVL) due to prothesis dislodgement is a rare but potentially severe complication after transcatheter mitral valve implantation (TMVI). Due to the epicardial anchoring mechanism of the Tendyne® TMVI-system, repositioning of the valve stent may be possible by retensioning of the tether. This multicentre-study aimed to investigate the procedural and short-term safety as well as efficacy of retensioning-maneuvers. METHODS From 2017 to 2021, N = 18 patients who underwent secondary tether-retensioning were identified. Baseline, procedural and follow-up data were available from N = 11 patients and analyzed according to the Mitral Valve Research Consortium (MVARC) definitions. Continuous variables are shown as median with interquartile range. RESULTS All Patients [age 75 years (73.5, 85.0), 64% male (N = 7), EuroSCORE II 6.2% (5.8, 11.6)] presented with post-procedural PVL [63.6% (N = 7) with PVL ≥ 3+]. Of these, 54% (N = 6) showed signs of hemolysis. The majority were severely symptomatic [NYHA≥III (91%, N = 10)]. Procedural outcomes revealed no acute complications and no mortality. At discharge, PVL was completely eliminated in 91% (N = 10) of patients with one case of remaining moderate PVL. At 30 days, MVARC device success was achieved in 82% (N = 9) of patients. Two patients required open surgical mitral valve replacement due to persistent and recurrent PVL. In 89% (N = 8) of patients with successful retensioning procedure NYHA-class was I/II. There was no 30-day mortality. CONCLUSION This multicentre-study demonstrates technical feasibility, procedural safety and acute efficacy of retensioning-procedures in the majority of patients. The potential to retension the tether in transapical TMVI may provide additional management advantages in populations at high surgical risk.
dc.description.sponsorshipUniversitätsklinik für Kardiologie
dc.identifier.doi10.48350/190902
dc.identifier.pmid38152923
dc.identifier.publisherDOI10.1093/ejcts/ezad430
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/172838
dc.language.isoen
dc.publisherOxford University Press
dc.relation.ispartofEuropean journal of cardio-thoracic surgery
dc.relation.issn1873-734X
dc.relation.organizationDCD5A442BB15E17DE0405C82790C4DE2
dc.subjectTMVI TMVR Tendyne mitral valve paravalvular leakage retensioning
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleSecondary retensioning of a tether-based device for transapical transcatheter mitral valve implantation.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue1
oaire.citation.volume65
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
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unibe.date.embargoChanged2024-01-03 17:10:05
unibe.date.licenseChanged2024-01-03 19:36:12
unibe.description.ispublishedpub
unibe.eprints.legacyId190902
unibe.refereedtrue
unibe.subtype.articlejournal

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