Mixed aortic valve disease: Association with paravalvular leak and reduced survival after TAVR.

Mixed aortic valve disease paravalvular regurgitation after TAVR transcatheter aortic valve replacement

Journal

European heart journal. Cardiovascular Imaging
ISSN: 2047-2412
Titre abrégé: Eur Heart J Cardiovasc Imaging
Pays: England
ID NLM: 101573788

Informations de publication

Date de publication:
17 Jan 2024
Historique:
received: 26 12 2023
accepted: 29 12 2023
medline: 18 1 2024
pubmed: 18 1 2024
entrez: 18 1 2024
Statut: aheadofprint

Résumé

Transcatheter aortic valve replacement (TAVR) revolutionized the therapy of severe aortic stenosis (AS) with rising numbers. Mixed aortic valve disease (MAVD) treated by TAVR is gaining more interest, as those patients represent a more complex cohort as compared to isolated AS. However, concerning long-term outcome for this cohort only limited data is available. To assess the prevalence of MAVD in TAVR patients, investigate its association with paravalvular regurgitation (PVR), and analyse its impact on long-term mortality after TAVR. We conducted a registry-based cohort study using the Vienna TAVR registry, enrolling patients who underwent TAVR at Medical University of Vienna between 01/2007 and 05/2020 with available TTE before and after TAVR (n=880). Data analysis included PVR incidence and long-term survival outcomes. 647 (73.52%) out of 880 patients had > mild AR next to severe AS. MAVD was associated with PVR compared to isolated AS with an OR of 2.06, 95% CI: 1.51- 2.81; p= <0.001. More than mild PVR after TAVR, (n168 out of 880 = 19.09%) was related to higher mortality compared to absence of PVR with a HR of 1.33, 95% CI: 1.05- 1.67; p= 0.016. MAVD patients developing ≥ mild PVR after TAVR was also associated with higher mortality compared to absence of PVR with HR of 1.30 and 95% CI: 1.04-1.62; p= 0.022. MAVD is prevalent among TAVR patients and presents unique challenges, with increased PVR risk and worse outcomes compared to isolated AS. Long-term survival for MAVD patients, not limited to those developing PVR post TAVR is compromised. Earlier intervention before the occurrence of structural myocardial damage or surgical valve replacement might be a potential workaround to improve outcomes.

Sections du résumé

BACKGROUND BACKGROUND
Transcatheter aortic valve replacement (TAVR) revolutionized the therapy of severe aortic stenosis (AS) with rising numbers. Mixed aortic valve disease (MAVD) treated by TAVR is gaining more interest, as those patients represent a more complex cohort as compared to isolated AS. However, concerning long-term outcome for this cohort only limited data is available.
AIMS OBJECTIVE
To assess the prevalence of MAVD in TAVR patients, investigate its association with paravalvular regurgitation (PVR), and analyse its impact on long-term mortality after TAVR.
METHODS METHODS
We conducted a registry-based cohort study using the Vienna TAVR registry, enrolling patients who underwent TAVR at Medical University of Vienna between 01/2007 and 05/2020 with available TTE before and after TAVR (n=880). Data analysis included PVR incidence and long-term survival outcomes.
RESULTS RESULTS
647 (73.52%) out of 880 patients had > mild AR next to severe AS. MAVD was associated with PVR compared to isolated AS with an OR of 2.06, 95% CI: 1.51- 2.81; p= <0.001. More than mild PVR after TAVR, (n168 out of 880 = 19.09%) was related to higher mortality compared to absence of PVR with a HR of 1.33, 95% CI: 1.05- 1.67; p= 0.016. MAVD patients developing ≥ mild PVR after TAVR was also associated with higher mortality compared to absence of PVR with HR of 1.30 and 95% CI: 1.04-1.62; p= 0.022.
CONCLUSIONS AND RELEVANCE CONCLUSIONS
MAVD is prevalent among TAVR patients and presents unique challenges, with increased PVR risk and worse outcomes compared to isolated AS. Long-term survival for MAVD patients, not limited to those developing PVR post TAVR is compromised. Earlier intervention before the occurrence of structural myocardial damage or surgical valve replacement might be a potential workaround to improve outcomes.

Identifiants

pubmed: 38236149
pii: 7571308
doi: 10.1093/ehjci/jeae005
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the European Society of Cardiology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Caglayan Demirel (C)

Department of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Max Paul Winter (MP)

Department of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Christian Nitsche (C)

Department of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Sophia Koschatko (S)

Department of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Charlotte Jantsch (C)

Department of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Katharina Mascherbauer (K)

Department of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Kseniya Halavina (K)

Department of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Gregor Heitzinger (G)

Department of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Carolina Dona (C)

Department of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Varius Dannenberg (V)

Department of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Georg Spinka (G)

Department of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Matthias Koschutnik (M)

Department of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Martin Andreas (M)

Department of Cardiac Surgery, Medical University of Vienna, Vienna, Austria.

Christian Hengstenberg (C)

Department of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Philipp E Bartko (PE)

Department of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Classifications MeSH