Coronary Artery Disease Clinical Trial
Official title:
Prospective, Observational, Single Center Trial of Reobtaining Coronary Ostia Cannulation Beyond Transcatheter Aortic Valve Stent (RE-ACCESS)
With the upcoming expansion of transcatheter aortic valve replacement (TAVR) indications to younger patients, the feasibility of coronary ostia cannulation beyond different bioprosthesis stent is currently a matter of debate. Purpose of this study is: 1) to assess the feasibility to re-engage coronary ostia after TAVR; 2) to discover potential native anatomical or prosthesis-related features that may preclude proper coronary cannulation after TAVR.
Single-center, prospective, pilot study. Aim of this study is to assess the feasibility of
coronary ostia re-engagement beyond transcatheter aortic valve (TAV) stent through a
transfemoral access in 300 consecutive patients undergoing transfemoral TAVR with
pre-procedural computed tomography assessment available.
The possibility to selectively cannulate each coronary, the amount of time and contrast will
be evaluated in each patient before and after implantation of either balloon-(SAPIEN 3) or
self-expanding (Evolut R/PRO, Acurate Neo or Portico) TAVs, thus generating an internal
comparator.
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