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
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.