Predictors of outcome in patients with moderate mixed aortic valve disease.

Aortic Valve Insufficiency Aortic Valve Stenosis Echocardiography Heart Valve Prosthesis Implantation Transcatheter Aortic Valve Replacement

Journal

Heart (British Cardiac Society)
ISSN: 1468-201X
Titre abrégé: Heart
Pays: England
ID NLM: 9602087

Informations de publication

Date de publication:
26 Dec 2023
Historique:
received: 09 08 2023
accepted: 13 12 2023
medline: 27 12 2023
pubmed: 27 12 2023
entrez: 26 12 2023
Statut: aheadofprint

Résumé

Grading the severity of moderate mixed aortic stenosis and regurgitation (MAVD) is challenging and the disease poorly understood. Identifying markers of haemodynamic severity will improve risk stratification and potentially guide timely treatment. This study aims to identify prognostic haemodynamic markers in patients with moderate MAVD. Moderate MAVD was defined as coexisting moderate aortic stenosis (aortic valve area (AVA) 1.0-1.5 cm 207 patients with moderate MAVD were included, aged 78 (66-84) years, 56% male sex, AVA 1.2 (1.1-1.4) cm Patients with truly moderate MAVD have a high incidence of death and heart failure hospitalisation (43% at 3.5 (2.5-4.7) years). Within this group, a high-risk group characterised by disproportionately low aortic Vmax (≤2.8 m/s) and adverse remodelling (LVEF ≤50%) have the worst outcomes.

Identifiants

pubmed: 38148159
pii: heartjnl-2023-323321
doi: 10.1136/heartjnl-2023-323321
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : British Heart Foundation
ID : FS/19/35/34374
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/CRTF/21/24128
Pays : United Kingdom

Informations de copyright

© Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: KPP has an unrestricted research grant from Edwards Lifesciences. TAT is directly and indirectly supported by the UCLH and Barts NIHR Biomedical Research Units. MJM has received grants and personal fees from Edwards Lifesciences and personal fees from Abbott Vascular.

Auteurs

Kush P Patel (KP)

Institute of Cardiovascular Science, University College London, London, UK.
Barts Heart Centre, West Smithfield, London, UK.

Michael McKenna (M)

Barts Heart Centre, West Smithfield, London, UK.

George D Thornton (GD)

Institute of Cardiovascular Science, University College London, London, UK.
Barts Heart Centre, West Smithfield, London, UK.

Sebastian Vandermolen (S)

Institute of Cardiovascular Science, University College London, London, UK.
The William Harvey Research Institute, Queen Mary University, London, UK.

Zaid Ali Abdulelah (ZA)

Barts Heart Centre, West Smithfield, London, UK.

Wael Awad (W)

Barts Heart Centre, West Smithfield, London, UK.

Andreas Baumbach (A)

Barts Heart Centre, West Smithfield, London, UK.
The William Harvey Research Institute, Queen Mary University, London, UK.

Anthony Mathur (A)

Barts Heart Centre, West Smithfield, London, UK.
The William Harvey Research Institute, Queen Mary University, London, UK.

Thomas A Treibel (TA)

Institute of Cardiovascular Science, University College London, London, UK.
Barts Heart Centre, West Smithfield, London, UK.

Guy Lloyd (G)

Barts Heart Centre, West Smithfield, London, UK.

Michael J Mullen (MJ)

Barts Heart Centre, West Smithfield, London, UK.

Sanjeev Bhattacharyya (S)

Barts Heart Centre, West Smithfield, London, UK Sanjeev.Bhattacharyya@nhs.net.

Classifications MeSH