4D flow cardiovascular magnetic resonance derived energetics in the Fontan circulation correlate with exercise capacity and CMR-derived liver fibrosis/congestion.


Journal

Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance
ISSN: 1532-429X
Titre abrégé: J Cardiovasc Magn Reson
Pays: England
ID NLM: 9815616

Informations de publication

Date de publication:
28 03 2022
Historique:
received: 09 01 2022
accepted: 15 03 2022
entrez: 29 3 2022
pubmed: 30 3 2022
medline: 5 4 2022
Statut: epublish

Résumé

This study explores the relationship between in vivo 4D flow cardiovascular magnetic resonance (CMR) derived blood flow energetics in the total cavopulmonary connection (TCPC), exercise capacity and CMR-derived liver fibrosis/congestion. The Fontan circulation, in which both caval veins are directly connected with the pulmonary arteries (i.e. the TCPC) is the palliative approach for single ventricle patients. Blood flow efficiency in the TCPC has been associated with exercise capacity and liver fibrosis using computational fluid dynamic modelling. 4D flow CMR allows for assessment of in vivo blood flow energetics, including kinetic energy (KE) and viscous energy loss rate (EL). Fontan patients were prospectively evaluated between 2018 and 2021 using a comprehensive cardiovascular and liver CMR protocol, including 4D flow imaging of the TCPC. Peak oxygen consumption (VO Sixty-two Fontan patients were included (53% male, 17.3 ± 5.1 years). Maximal effort CPET was obtained in 50 patients (peak VO Adverse 4D flow CMR derived KE and EL in the TCPC correlate with decreased exercise capacity and increased levels of liver fibrosis/congestion. 4D flow CMR is promising as a non-invasive screening tool for identification of patients with adverse TCPC flow efficiency.

Sections du résumé

AIM
This study explores the relationship between in vivo 4D flow cardiovascular magnetic resonance (CMR) derived blood flow energetics in the total cavopulmonary connection (TCPC), exercise capacity and CMR-derived liver fibrosis/congestion.
BACKGROUND
The Fontan circulation, in which both caval veins are directly connected with the pulmonary arteries (i.e. the TCPC) is the palliative approach for single ventricle patients. Blood flow efficiency in the TCPC has been associated with exercise capacity and liver fibrosis using computational fluid dynamic modelling. 4D flow CMR allows for assessment of in vivo blood flow energetics, including kinetic energy (KE) and viscous energy loss rate (EL).
METHODS
Fontan patients were prospectively evaluated between 2018 and 2021 using a comprehensive cardiovascular and liver CMR protocol, including 4D flow imaging of the TCPC. Peak oxygen consumption (VO
RESULTS
Sixty-two Fontan patients were included (53% male, 17.3 ± 5.1 years). Maximal effort CPET was obtained in 50 patients (peak VO
CONCLUSIONS
Adverse 4D flow CMR derived KE and EL in the TCPC correlate with decreased exercise capacity and increased levels of liver fibrosis/congestion. 4D flow CMR is promising as a non-invasive screening tool for identification of patients with adverse TCPC flow efficiency.

Identifiants

pubmed: 35346249
doi: 10.1186/s12968-022-00854-4
pii: 10.1186/s12968-022-00854-4
pmc: PMC8962091
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

21

Subventions

Organisme : Hartstichting
ID : 2018-T083
Organisme : Hartstichting
ID : CVON-2017-08-RADAR
Organisme : Hartstichting
ID : CVON-2017-08-RADAR

Informations de copyright

© 2022. The Author(s).

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Auteurs

Friso M Rijnberg (FM)

Department of Cardiothoracic Surgery, Leiden University Medical Center, Albinusdreef 2, 2333ZA, Leiden, The Netherlands. f.m.rijnberg@lumc.nl.

Jos J M Westenberg (JJM)

Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands.

Hans C van Assen (HC)

Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands.

Joe F Juffermans (JF)

Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands.

Lucia J M Kroft (LJM)

Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands.

Pieter J van den Boogaard (PJ)

Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands.

Covadonga Terol Espinosa de Los Monteros (C)

Department of Pediatric Cardiology, Leiden University Medical Center, Leiden, the Netherlands.

Evangeline G Warmerdam (EG)

Department of Pediatric Cardiology, Utrecht Medical Center, Utrecht, The Netherlands.

Tim Leiner (T)

Department of Radiology, Utrecht Medical Center, Utrecht, The Netherlands.

Heynric B Grotenhuis (HB)

Department of Pediatric Cardiology, Utrecht Medical Center, Utrecht, The Netherlands.

Monique R M Jongbloed (MRM)

Department of Cardiology and Anatomy and Embryology, Leiden University Medical Center, Leiden, The Netherlands.

Mark G Hazekamp (MG)

Department of Cardiothoracic Surgery, Leiden University Medical Center, Albinusdreef 2, 2333ZA, Leiden, The Netherlands.

Arno A W Roest (AAW)

Department of Pediatric Cardiology, Leiden University Medical Center, Leiden, the Netherlands.

Hildo J Lamb (HJ)

Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands.

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