Transcatheter aortic valve replacement with the self-expanding ACURATE Neo2 in patients with horizontal aorta: Insights from the ITAL-neo registry

Horizontal aorta (HA), defined by an aortic angulation (AA) ≥48°, is associated with worse outcomes particularly after self-expanding (SE) trans-catheter heart valve (THV) implantation. Although the SE ACURATE Neo THV demonstrated favorable procedural success rates in patients with HA, it remains as...

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Veröffentlicht in:International journal of cardiology 2023-10, Vol.389, p.131236-131236, Article 131236
Hauptverfasser: Barki, Monica, Ielasi, Alfonso, Buono, Andrea, Maffeo, Diego, Montonati, Carolina, Pellegrini, Dario, Pellicano, Mariano, Gorla, Riccardo, Costa, Giuliano, Cozzi, Ottavia, Ancona, Marco, Soriano, Francesco, De Carlo, Marco, Ferrara, Erica, Giannini, Francesco, Massussi, Mauro, Fovino, Luca Nai, Messina, Antonio, Sgroi, Carmelo, Gallo, Francesco, Nerla, Roberto, Saccocci, Matteo, D'Ascenzo, Fabrizio, Conrotto, Federico, Bettari, Luca, Fiorina, Claudia, Castriota, Fausto, Poli, Arnaldo, Petronio, Anna Sonia, Oreglia, Jacopo, Montorfano, Matteo, Regazzoli, Damiano, Reimers, Bernhard, Barbanti, Marco, Tamburino, Corrado, Bedogni, Francesco, Tarantini, Giuseppe, Tespili, Maurizio
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Sprache:eng
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Zusammenfassung:Horizontal aorta (HA), defined by an aortic angulation (AA) ≥48°, is associated with worse outcomes particularly after self-expanding (SE) trans-catheter heart valve (THV) implantation. Although the SE ACURATE Neo THV demonstrated favorable procedural success rates in patients with HA, it remains associated with a non-negligible rate of moderate or greater paravalvular leak (PVL). Aim of the study was to assess the performance of ACURATE Neo2 in the setting of HA. We performed a multicenter cohort analysis on patients with severe aortic valve stenosis and HA undergoing transcatheter aortic valve replacement (TAVR) with the Neo or Neo2 THV enrolled in the ITAL-neo registry. The primary endpoint was a composite of early safety and clinical efficacy at 30 days according to the Valve Academic Research Consortium-3 (VARC-3). Secondary endpoints included the occurrence of moderate or severe PVL and 90-day clinical outcomes. Among 900 patients included in the ITAL-neo registry, 407 exhibited HA; of these, 300 received a Neo THV and 107 a Neo2 THV. HA, irrespective of the THV implanted, emerged as an independent risk factor for developing ≥ moderate PVL. Technical and device success at 30-day follow-up was comparable between groups. However, Neo2 was associated with a significantly lower rate of ≥moderate PVL vs. Neo: (5% vs. 15%; p 
ISSN:0167-5273
1874-1754
DOI:10.1016/j.ijcard.2023.131236