TY - JOUR
T1 - Characteristics and outcomes of patients screened for transcatheter mitral valve implantation
T2 - 1-year results from the CHOICE-MI registry
AU - CHOICE-MI Investigators
AU - Ben Ali, Walid
AU - Ludwig, Sebastian
AU - Duncan, Alison
AU - Weimann, Jessica
AU - Nickenig, Georg
AU - Tanaka, Tetsu
AU - Coisne, Augustin
AU - Vincentelli, Andre
AU - Makkar, Raj
AU - Webb, John G.
AU - Akodad, Mariama
AU - Muller, David W.M.
AU - Praz, Fabien
AU - Wild, Mirjam G.
AU - Hausleiter, Jörg
AU - Goel, Sachin S.
AU - von Ballmoos, Moritz Wyler
AU - Denti, Paolo
AU - Chehab, Omar
AU - Redwood, Simon
AU - Dahle, Gry
AU - Baldus, Stephan
AU - Adam, Matti
AU - Ruge, Hendrik
AU - Lange, Rüdiger
AU - Kaneko, Tsuyoshi
AU - Leroux, Lionel
AU - Dumonteil, Nicolas
AU - Tchetche, Didier
AU - Treede, Hendrik
AU - Flagiello, Michele
AU - Obadia, Jean Francois
AU - Walther, Thomas
AU - Taramasso, Maurizio
AU - Søndergaard, Lars
AU - Bleiziffer, Sabine
AU - Rudolph, Tanja K.
AU - Fam, Neil
AU - Kempfert, Joerg
AU - Granada, Juan F.
AU - Tang, Gilbert H.L.
AU - von Bardeleben, Ralph Stephan
AU - Conradi, Lenard
AU - Modine, Thomas
AU - Kalbacher, Daniel
AU - Blankenberg, Stefan
AU - Koell, Benedikt
AU - Schofer, Niklas
AU - Westermann, Dirk
AU - Weber, Marcel
AU - Vogelhuber, Johanna
AU - Pontana, François
AU - Van Belle, Eric
AU - Yoon, Sung Han
AU - Chuang, Anthony
AU - Boone, Robert H.
AU - Jansz, Paul
AU - Song, Ning
AU - Hungerford, Sara
AU - Windecker, Stephan
AU - Reineke, David
AU - Reardon, Michael
AU - Kleiman, Neal S.
AU - Sala, Alessandra
AU - Agricola, Eustachio
AU - Maisano, Francesco
AU - Rajani, Ronak
AU - Prendergast, Bernard
AU - Rein, Kjell A.
AU - Koerber, Maria I.
AU - Ochs, Laurin
AU - Vitanova, Keti
AU - Erlebach, Magdalena
AU - Shah, Pinak
AU - Harloff, Morgan
AU - Bonnet, Guillaume
AU - Pernot, Mathieu
AU - Jonveaux, Melchior
AU - Kreidel, Felix
AU - Ruf, Tobias
AU - Pozzi, Matteo
AU - Dragulescu, Razvan
AU - Holubec, Tomas
AU - Strohschnitter, Heike
AU - Walther, Claudia
AU - Pozzoli, Alberto
AU - Wong, Ivan
AU - Friedrichs, Kai
AU - Peterson, Mark
AU - Unbehaun, Axel
AU - Kofler, Markus
N1 - Funding Information:
This research was supported by a grant from the German Heart Foundation (DHS). Conflict of interest: W.B.A. received research grants from Medtronic and Edwards Lifesciences. S.L. was supported by a grant from the German Heart Foundation (DHS) and received travel compensation by Edwards Lifesciences. A.D. is a consultant for and has and received honoraria from Abbott Laboratories, Edward Lifesciences and Medtronic. G.H.L.T. is a physician proctor and consultant for Medtronic, consultant and TAVR physician advisory board member for Abbott Structural Heart, consultant for NeoChord and advisory board member for JenaValve. L.C. is advisory board member for Abbott, Medtronic and BostonScientific and has received personal fees from Edwards Lifesciences. All other authors have nothing to disclose. We would like to thank all the CHOICE-MI investigators for their invaluable contributions to this study. Open Access funding enabled and organized by Projekt DEAL. This research was supported by a grant from the German Heart Foundation (DHS). Conflict of interest: W.B.A. received research grants from Medtronic and Edwards Lifesciences. S.L. was supported by a grant from the German Heart Foundation (DHS) and received travel compensation by Edwards Lifesciences. A.D. is a consultant for and has and received honoraria from Abbott Laboratories, Edward Lifesciences and Medtronic. G.H.L.T. is a physician proctor and consultant for Medtronic, consultant and TAVR physician advisory board member for Abbott Structural Heart, consultant for NeoChord and advisory board member for JenaValve. L.C. is advisory board member for Abbott, Medtronic and BostonScientific and has received personal fees from Edwards Lifesciences. All other authors have nothing to disclose.
Funding Information:
: W.B.A. received research grants from Medtronic and Edwards Lifesciences. S.L. was supported by a grant from the German Heart Foundation (DHS) and received travel compensation by Edwards Lifesciences. A.D. is a consultant for and has and received honoraria from Abbott Laboratories, Edward Lifesciences and Medtronic. G.H.L.T. is a physician proctor and consultant for Medtronic, consultant and TAVR physician advisory board member for Abbott Structural Heart, consultant for NeoChord and advisory board member for JenaValve. L.C. is advisory board member for Abbott, Medtronic and BostonScientific and has received personal fees from Edwards Lifesciences. All other authors have nothing to disclose. Conflict of interest
Funding Information:
This research was supported by a grant from the German Heart Foundation (DHS).
Publisher Copyright:
© 2022 The Authors. European Journal of Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.
PY - 2022/5
Y1 - 2022/5
N2 - Aims: Transcatheter mitral valve implantation (TMVI) represents a novel treatment option for patients with mitral regurgitation (MR) unsuitable for established therapies. The CHOICE-MI registry aimed to investigate outcomes of patients undergoing screening for TMVI. Methods and results: From May 2014 to March 2021, patients with MR considered suboptimal candidates for transcatheter edge-to-edge repair (TEER) and at high risk for mitral valve surgery underwent TMVI screening at 26 centres. Characteristics and outcomes were investigated for patients undergoing TMVI and for TMVI-ineligible patients referred to bailout-TEER, high-risk surgery or medical therapy (MT). The primary composite endpoint was all-cause mortality or heart failure hospitalization after 1 year. Among 746 patients included (78.5 years, interquartile range [IQR] 72.0–83.0, EuroSCORE II 4.7% [IQR 2.7–9.7]), 229 patients (30.7%) underwent TMVI with 10 different dedicated devices. At 1 year, residual MR ≤1+ was present in 95.2% and the primary endpoint occurred in 39.2% of patients treated with TMVI. In TMVI-ineligible patients (n = 517, 69.3%), rates of residual MR ≤1+ were 37.2%, 100.0% and 2.4% after bailout-TEER, high-risk surgery and MT, respectively. The primary endpoint at 1 year occurred in 28.8% of patients referred to bailout-TEER, in 42.9% of patients undergoing high-risk surgery and in 47.9% of patients remaining on MT. Conclusion: This registry included the largest number of patients treated with TMVI to date. TMVI with 10 dedicated devices resulted in predictable MR elimination and sustained functional improvement at 1 year. In TMVI-ineligible patients, bailout-TEER and high-risk surgery represented reasonable alternatives, while MT was associated with poor clinical and functional outcomes.
AB - Aims: Transcatheter mitral valve implantation (TMVI) represents a novel treatment option for patients with mitral regurgitation (MR) unsuitable for established therapies. The CHOICE-MI registry aimed to investigate outcomes of patients undergoing screening for TMVI. Methods and results: From May 2014 to March 2021, patients with MR considered suboptimal candidates for transcatheter edge-to-edge repair (TEER) and at high risk for mitral valve surgery underwent TMVI screening at 26 centres. Characteristics and outcomes were investigated for patients undergoing TMVI and for TMVI-ineligible patients referred to bailout-TEER, high-risk surgery or medical therapy (MT). The primary composite endpoint was all-cause mortality or heart failure hospitalization after 1 year. Among 746 patients included (78.5 years, interquartile range [IQR] 72.0–83.0, EuroSCORE II 4.7% [IQR 2.7–9.7]), 229 patients (30.7%) underwent TMVI with 10 different dedicated devices. At 1 year, residual MR ≤1+ was present in 95.2% and the primary endpoint occurred in 39.2% of patients treated with TMVI. In TMVI-ineligible patients (n = 517, 69.3%), rates of residual MR ≤1+ were 37.2%, 100.0% and 2.4% after bailout-TEER, high-risk surgery and MT, respectively. The primary endpoint at 1 year occurred in 28.8% of patients referred to bailout-TEER, in 42.9% of patients undergoing high-risk surgery and in 47.9% of patients remaining on MT. Conclusion: This registry included the largest number of patients treated with TMVI to date. TMVI with 10 dedicated devices resulted in predictable MR elimination and sustained functional improvement at 1 year. In TMVI-ineligible patients, bailout-TEER and high-risk surgery represented reasonable alternatives, while MT was associated with poor clinical and functional outcomes.
KW - Medical therapy
KW - Mitral regurgitation
KW - Mitral valve surgery
KW - Transcatheter edge-to-edge repair
KW - Transcatheter mitral valve implantation
UR - http://www.scopus.com/inward/record.url?scp=85130253539&partnerID=8YFLogxK
U2 - 10.1002/ejhf.2492
DO - 10.1002/ejhf.2492
M3 - Article
C2 - 35338542
AN - SCOPUS:85130253539
SN - 1388-9842
VL - 24
SP - 887
EP - 898
JO - European Journal of Heart Failure
JF - European Journal of Heart Failure
IS - 5
ER -