Balloon-Expandable Versus Self-Expanding Transcatheter Aortic Valve Replacement: A Propensity-Matched Comparison From the FRANCE-TAVI Registry - Université de Rennes Accéder directement au contenu
Article Dans Une Revue Circulation Année : 2020

Balloon-Expandable Versus Self-Expanding Transcatheter Aortic Valve Replacement: A Propensity-Matched Comparison From the FRANCE-TAVI Registry

Thierry Lefèvre
  • Fonction : Auteur
Dominique Himbert
  • Fonction : Auteur
Rene Koning
  • Fonction : Auteur
Jean-Phillipe Collet
  • Fonction : Auteur
Pascal Leprince
  • Fonction : Auteur
Emmanuel Teiger
  • Fonction : Auteur
Benoit Lattuca
Patrick Joly
  • Fonction : Auteur
Said Ghostine
  • Fonction : Auteur
Olivier Bar
  • Fonction : Auteur
Nicolas Amabile
Didier Champagnac
  • Fonction : Auteur
Patrick Ohlmann
  • Fonction : Auteur
Nicolas Meneveau
  • Fonction : Auteur
Lionel Leroux
Florence Leclercq
  • Fonction : Auteur
Thomas Gandet
  • Fonction : Auteur
Bernard Iung
Thierry Folliguet
  • Fonction : Auteur
Philippe Commeau
Guillaume Cayla
  • Fonction : Auteur
Gilles Bayet
  • Fonction : Auteur
Olivier Darremont
  • Fonction : Auteur
Christian Spaulding
  • Fonction : Auteur

Résumé

Background - No randomized study powered to compare balloon expandable (BE) with self expanding (SE) transcatheter heart valves (THVs) on individual end points after transcatheter aortic valve replacement has been conducted to date. Methods - From January 2013 to December 2015, the FRANCE-TAVI nationwide registry (Registry of Aortic Valve Bioprostheses Established by Catheter) included 12 141 patients undergoing BE-THV (Edwards, n=8038) or SE-THV (Medtronic, n=4103) for treatment of native aortic stenosis. Long term mortality status was available in all patients (median 20 months; interquartile range, 14 to 30). Patients treated with BE-THV (n=3910) were successfully matched 1:1 with 3910 patients treated with SE-THV by using propensity score (25 clinical, anatomical, and procedural variables) and by date of the procedure (within 3 months). The first coprimary outcome was ≥ moderate occurrence of paravalvular regurgitation or in-hospital mortality, or both. The second coprimary outcome was 2-year all-cause mortality. Results - In propensity-matched analyses, the incidence of the first coprimary outcome was higher with SE-THV (19.8%) compared with BE-THV (11.9%; relative risk, 1.68 [95% CI, 1.46-1.91]; <0.0001). Each component of the outcome was also higher in patients receiving SE-THV: ≥ moderate paravalvular regurgitation (15.5% versus 8.3%; relative risk, 1.90 [95% CI, 1.63-2.22]; <0.0001) and in hospital mortality (5.6% versus 4.2%; relative risk, 1.34 [95% CI, 1.07-1.66]; =0.01). During follow up, all cause mortality occurred in 899 patients treated with SE-THV (2-year mortality, 29.8%) and in 801 patients treated with BE-THV (2-year mortality, 26.6%; hazard ratio, 1.17 [95% CI, 1.06-1.29]; =0.003). Similar results were found using inverse probability of treatment weighting using propensity score analysis. Conclusion - The present study suggests that use of SE-THV was associated with a higher risk of paravalvular regurgitation and higher in-hospital and 2-year mortality compared with use of BE-THV. These data strongly support the need for a randomized trial sufficiently powered to compare the latest generation of SE-THV and BE-THV. Clinical trial registration - https://www.clinicaltrials.gov. Unique identifier: NCT01777828.
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Dates et versions

hal-02472206 , version 1 (11-02-2020)

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Eric Van Belle, Flavien Vincent, Julien Labreuche, Vincent Auffret, Nicolas Debry, et al.. Balloon-Expandable Versus Self-Expanding Transcatheter Aortic Valve Replacement: A Propensity-Matched Comparison From the FRANCE-TAVI Registry. Circulation, 2020, 141 (4), pp.243-259. ⟨10.1161/CIRCULATIONAHA.119.043785⟩. ⟨hal-02472206⟩
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