Quantification of anatomical aortic valve area by multi-detector computed tomography: A pilot 3D-morphological modeling of the stenotic aortic valve.

3D AVA Aortic valve model MDCT

Journal

International journal of cardiology
ISSN: 1874-1754
Titre abrégé: Int J Cardiol
Pays: Netherlands
ID NLM: 8200291

Informations de publication

Date de publication:
06 Jul 2024
Historique:
received: 14 05 2024
revised: 20 06 2024
accepted: 01 07 2024
medline: 9 7 2024
pubmed: 9 7 2024
entrez: 8 7 2024
Statut: aheadofprint

Résumé

Aortic-valve-stenosis (AS) is a frequent degenerative valvular-disease and carries dismal outcome under-medical-treatment. Transvalvular pressure gradient reflects severity of the valve-disease but is highly dependent on flow-conditions and on other valvular/aortic characteristics. Alternatively, aortic-valve-area (AVA) represents a measure of aortic-valve lesion severity conceptually essential and practically widely-recognized but exhibits multiple-limitations. We analyzed the 4D multi-detector computed tomography(MDCT) of 20 randomly selected patients with severe AS. For each-patient, we generated the 3D-model of the valve and of its calcifications, and we computed the anatomical AVA accounting for the 3D-morphology of the leaflets in three-different-ways. Finally, we compared our results vs. Doppler-based AVA 3D-reconstruction and identification of the cusps were successful in 90% of the cases. The calcification patterns where highly-variable over patients, ranging from multiple small deposits to wide and c-shaped deposits running from commissure-to-commissure. AVA We described a new-method to obtain a set of flow-independent quantifications that complement pressure gradient measurements and combine the advantages of previously proposed methods, while bypassing the corresponding-limitations.

Sections du résumé

BACKGROUND BACKGROUND
Aortic-valve-stenosis (AS) is a frequent degenerative valvular-disease and carries dismal outcome under-medical-treatment. Transvalvular pressure gradient reflects severity of the valve-disease but is highly dependent on flow-conditions and on other valvular/aortic characteristics. Alternatively, aortic-valve-area (AVA) represents a measure of aortic-valve lesion severity conceptually essential and practically widely-recognized but exhibits multiple-limitations.
METHODS METHODS
We analyzed the 4D multi-detector computed tomography(MDCT) of 20 randomly selected patients with severe AS. For each-patient, we generated the 3D-model of the valve and of its calcifications, and we computed the anatomical AVA accounting for the 3D-morphology of the leaflets in three-different-ways. Finally, we compared our results vs. Doppler-based AVA
RESULTS RESULTS
3D-reconstruction and identification of the cusps were successful in 90% of the cases. The calcification patterns where highly-variable over patients, ranging from multiple small deposits to wide and c-shaped deposits running from commissure-to-commissure. AVA
CONCLUSIONS CONCLUSIONS
We described a new-method to obtain a set of flow-independent quantifications that complement pressure gradient measurements and combine the advantages of previously proposed methods, while bypassing the corresponding-limitations.

Identifiants

pubmed: 38977223
pii: S0167-5273(24)00944-6
doi: 10.1016/j.ijcard.2024.132322
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

132322

Informations de copyright

Copyright © 2024. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of competing interest None.

Auteurs

Pappalardo Omar (P)

3D and Computer Simulation Laboratory, IRCCS Policlinico San Donato, San Donato Milanese, Italy.

Benfari Giovanni (B)

Section of Cardiology, Department of Medicine, Università degli Studi di Verona, Italy; Mayo Clinic, Department of Cardiovascular Diseases, Rochester, USA. Electronic address: giovanni.benfari@gmail.com.

Jenkins Williams (J)

Mayo Clinic, Department of Cardiovascular Diseases, Rochester, USA.

Foley Thomas (F)

Mayo Clinic, Radiology, Rochester, USA.

Araoz Philip (A)

Mayo Clinic, Radiology, Rochester, USA.

Redaelli Alberto (R)

Department of Electronics, Information and Bioengineering, Politecnico di Milano, Italy.

Onorati Francesco (O)

Department of Cardiac Surgery, Università degli Studi di Verona, Italy.

Faggian Giuseppe (F)

Department of Cardiac Surgery, Università degli Studi di Verona, Italy.

Hector I Michelena (HI)

Mayo Clinic, Department of Cardiovascular Diseases, Rochester, USA.

Votta Emiliano (V)

Department of Electronics, Information and Bioengineering, Politecnico di Milano, Italy.

Enriquez-Sarano Maurice (ES)

Mayo Clinic, Department of Cardiovascular Diseases, Rochester, USA; Minneapolis Heart Institute Foundation and the Valve Science Center, Minneapolis, MN, USA.

Classifications MeSH