• LOGIN
Repository logo

BORIS Portal

Bern Open Repository and Information System

  • Publication
  • Projects
  • Funding
  • Research Data
  • Organizations
  • Researchers
  • LOGIN
Repository logo
Unibern.ch
  1. Home
  2. Publications
  3. Secondary retensioning of a tether-based device for transapical transcatheter mitral valve implantation.
 

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

Options
  • Details
BORIS DOI
10.48350/190902
Date of Publication
January 2, 2024
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Author
Beyer, Martin
Muller, David
De Marco, Federico
Badhwar, Vinay
Obadia, Jean-Francois
Praz, Fabien Daniel
Universitätsklinik für Kardiologie
Modine, Thomas
Tonino, Pim
Dahle, Gry
Cerillo, Alfredo
Ludwig, Sebastian
Conradi, Lenard
Subject(s)

600 - Technology::610...

Series
European journal of cardio-thoracic surgery
ISSN or ISBN (if monograph)
1873-734X
Publisher
Oxford University Press
Language
English
Publisher DOI
10.1093/ejcts/ezad430
PubMed ID
38152923
Uncontrolled Keywords

TMVI TMVR Tendyne mit...

Description
OBJECTIVES

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.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/172838
Show full item
File(s)
FileFile TypeFormatSizeLicensePublisher/Copright statementContent
ezad430.pdftextAdobe PDF1.98 MBacceptedOpen
BORIS Portal
Bern Open Repository and Information System
Build: d1c7f7 [27.06. 13:56]
Explore
  • Projects
  • Funding
  • Publications
  • Research Data
  • Organizations
  • Researchers
More
  • About BORIS Portal
  • Send Feedback
  • Cookie settings
  • Service Policy
Follow us on
  • Mastodon
  • YouTube
  • LinkedIn
UniBe logo