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The Coronary Access After TAVI (CAvEAT) Study: A Prospective Registry of CA After TAVR

  • Giuseppe Tarantini*
  • , Luca Nai Fovino
  • , Flavia Belloni
  • , Marco Barbierato
  • , Francesco Gallo
  • , Matteo Vercellino
  • , Carlo Trani
  • , Francesco Burzotta
  • , Lluis Asmarats Serra
  • , Anna Sonia Petronio
  • , Francesco Bedogni
  • , Sergio Berti
  • , Andrea Bertolini
  • , Tommaso Fabris
  • , Antonio Tito
  • , Carmine Musto
  • , Arturo Giordano
  • , Nicola Corcione
  • , Francesco Maisano
  • , Massimo Medda
  • Bruno Loi, Carlo Cernetti, Luca Favero, Emilio Di Lorenzo, Dario Gregori, Giulia Lorenzoni, Mateusz Orzalkiewicz, Giovanni Esposito, Francesco Saia, Francesco Cardaioli, Alfredo Marchese
*Autore corrispondente per questo lavoro
  • University of Padua
  • Ospedale S. Spirito
  • Ospedale dell'Angelo
  • San Martino Hospital Genoa
  • Hematology, Hospital Santa Creu i Sant Pau
  • University Hospital of Pisa
  • IRCCS Policlinico San Donato
  • Ospedale del Cuore
  • San Camillo Hospital
  • Pineta Grande Hospital
  • IRCCS San Raffaele Scientific Institute
  • IRCCS Istituto Ortopedico Galeazzi - Milano
  • AO Brotzu
  • Ospedale V. Monaldi
  • Alma Mater Studiorum University of Bologna
  • University of Naples Federico II

Risultato della ricerca: Contributo in rivistaArticolo

Abstract

Background: As transcatheter aortic valve replacement (TAVR) is now performed in patients with longer life expectancy, the need for coronary access (CA) after TAVR is expected to rise. Objectives: The aim of this study was to evaluate the feasibility of CA after TAVR with 4 different types of transcatheter heart valves (THVs). Methods: In the multicenter, prospective CAvEAT (Coronary Access After TAVI; NCT04647864) registry, coronary angiography was performed immediately following transfemoral TAVR using short-frame SAPIEN 3 or SAPIEN 3 Ultra (SAPIEN 3/Ultra) and tall-frame ACURATE neo or ACURATE neo2 (ACURATE neo/neo2), Portico or Navitor, and Evolut Pro or Evolut Pro+ (Evolut Pro/Pro+) THVs. The primary endpoint was defined as selective CA of both coronary arteries. Results: In total, 632 patients were enrolled (mean age 82 years, 59% women). Selective CA of both coronary arteries was achieved in 89% of SAPIEN 3/Ultra, 63% of ACURATE neo/neo2, 62% of Portico or Navitor, and 45% of Evolut Pro/Pro+ THVs (P < 0.001). Unfeasible CA of at least 1 coronary artery occurred in 2%, 6%, 6%, and 9% of cases, respectively (P = 0.06). In pairwise comparisons, the incidence of the primary endpoint was significantly higher for the SAPIEN 3/Ultra compared with all tall-frame THVs (P < 0.001). Among tall-frame devices, no significant difference was observed between the ACURATE neo/neo2 and the Portico or Navitor (P = 0.9), but both devices demonstrated higher rates of the primary endpoint than the Evolut Pro/Pro+ (P = 0.005 and P = 0.002, respectively). Multivariate analysis identified implantation depth, moderate or severe commissural misalignment, and use of a tall-frame THV as independent predictors of unfeasible or nonselective CA. Conclusions: The short-frame SAPIEN 3/Ultra THV demonstrated the highest rate of selective CA following TAVR. Among tall-frame THVs, the large-cell designs of the Portico or Navitor and ACURATE neo/neo2 outperformed the closed-cell Evolut Pro/Pro+ in terms of selective CA.
Lingua originaleInglese
pagine (da-a)1571-1583
Numero di pagine13
RivistaJACC: Cardiovascular Interventions
Volume18
Numero di pubblicazione12
DOI
Stato di pubblicazionePubblicato - 2025

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  1. SDG 3 - Salute e benessere
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All Science Journal Classification (ASJC) codes

  • Cardiologia e Medicina Cardiovascolare

Keywords

  • aortic stenosis
  • coronary access
  • coronary artery disease
  • transcatheter aortic valve replacement

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