TY - JOUR
T1 - Haemodynamic performance and clinical outcomes of transcatheter aortic valve replacement with the self-expanding ACURATE neo2
AU - Scotti, Andrea
AU - Pagnesi, Matteo
AU - Kim, Won Keun
AU - Schäfer, Ulrich
AU - Barbanti, Marco
AU - Costa, Giuliano
AU - Baggio, Sara
AU - Casenghi, Matteo
AU - De Marco, Federico
AU - Vanhaverbeke, Maarten
AU - Sondergaard, Lars
AU - Wolf, Alexander
AU - Schofer, Joachim
AU - Ancona, Marco Bruno
AU - Montorfano, Matteo
AU - Kornowski, Ran
AU - Assa, Hana Vaknin
AU - Toggweiler, Stefan
AU - Ielasi, Alfonso
AU - Hildick-Smith, David
AU - Windecker, Stephan
AU - Schmidt, Albrecht
AU - Buono, Andrea
AU - Maffeo, Diego
AU - Siqueira, Dimytri
AU - Giannini, Francesco
AU - Adamo, Marianna
AU - Massussi, Mauro
AU - Wood, David A.
AU - Sinning, Jan Malte
AU - Van Der Heyden, Jan
AU - van Ginkel, Dirk Jan
AU - Van Mieghem, Nicholas
AU - Veulemans, Verena
AU - Mylotte, Darren
AU - Tzalamouras, Vasileios
AU - Taramasso, Maurizio
AU - Estévez-Loureiro, Rodrigo
AU - Colombo, Antonio
AU - Mangieri, Antonio
AU - Latib, Azeem
N1 - Publisher Copyright:
© Europa Digital & Publishing 2022. All rights reserved.
PY - 2022/11/18
Y1 - 2022/11/18
N2 - BACKGROUND: Transcatheter aortic valve replacement (TAVR) with the ACURATE neo device has been associated with a non-negligible incidence of paravalvular aortic regurgitation (AR). The new-generation ACURATE neo2 has been designed to mitigate this limitation. AIMS: The aim of the study was to compare TAVR with the ACURATE neo and neo2 devices. METHODS: The NEOPRO and NEOPRO-2 registries retrospectively included patients undergoing transfemoral TAVR with self-expanding valves at 24 and 20 centres, respectively. Patients receiving the ACURATE neo and neo2 devices (from January 2012 to December 2021) were included in this study. Predischarge and 30-day VARC-3 defined outcomes were evaluated. The primary endpoint was predischarge moderate or severe paravalvular AR. Subgroup analyses per degree of aortic valve calcification were performed. RESULTS: A total of 2,026 patients (neo: 1,263, neo2: 763) were included. Predischarge moderate or severe paravalvular AR was less frequent for the neo2 group (2% vs 5%; p<0.001), resulting in higher VARC-3 intended valve performance (96% vs 90%; p<0.001). Furthermore, more patients receiving the neo2 had none/trace paravalvular AR (59% vs 38%; p<0.001). The reduction in paravalvular AR with neo2 was mainly observed with heavy aortic valve calcification. New pacemaker implantation and VARC-3 technical and device success rates were similar between the 2 groups; there were more frequent vascular and bleeding complications for the neo device. Similar 1-year survival was detected after TAVR (neo2: 90% vs neo: 87%; p=0.14). CONCLUSIONS: TAVR with the ACURATE neo2 device was associated with a lower prevalence of moderate or severe paravalvular AR and more patients with none/trace paravalvular AR. This difference was particularly evident with heavy aortic valve calcification.
AB - BACKGROUND: Transcatheter aortic valve replacement (TAVR) with the ACURATE neo device has been associated with a non-negligible incidence of paravalvular aortic regurgitation (AR). The new-generation ACURATE neo2 has been designed to mitigate this limitation. AIMS: The aim of the study was to compare TAVR with the ACURATE neo and neo2 devices. METHODS: The NEOPRO and NEOPRO-2 registries retrospectively included patients undergoing transfemoral TAVR with self-expanding valves at 24 and 20 centres, respectively. Patients receiving the ACURATE neo and neo2 devices (from January 2012 to December 2021) were included in this study. Predischarge and 30-day VARC-3 defined outcomes were evaluated. The primary endpoint was predischarge moderate or severe paravalvular AR. Subgroup analyses per degree of aortic valve calcification were performed. RESULTS: A total of 2,026 patients (neo: 1,263, neo2: 763) were included. Predischarge moderate or severe paravalvular AR was less frequent for the neo2 group (2% vs 5%; p<0.001), resulting in higher VARC-3 intended valve performance (96% vs 90%; p<0.001). Furthermore, more patients receiving the neo2 had none/trace paravalvular AR (59% vs 38%; p<0.001). The reduction in paravalvular AR with neo2 was mainly observed with heavy aortic valve calcification. New pacemaker implantation and VARC-3 technical and device success rates were similar between the 2 groups; there were more frequent vascular and bleeding complications for the neo device. Similar 1-year survival was detected after TAVR (neo2: 90% vs neo: 87%; p=0.14). CONCLUSIONS: TAVR with the ACURATE neo2 device was associated with a lower prevalence of moderate or severe paravalvular AR and more patients with none/trace paravalvular AR. This difference was particularly evident with heavy aortic valve calcification.
UR - http://www.scopus.com/inward/record.url?scp=85142403593&partnerID=8YFLogxK
U2 - 10.4244/EIJ-D-22-00289
DO - 10.4244/EIJ-D-22-00289
M3 - Article
C2 - 35678222
AN - SCOPUS:85142403593
SN - 1774-024X
VL - 18
SP - 804
EP - 811
JO - EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology
JF - EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology
IS - 10
ER -