4D flow cardiac magnetic resonance in children and adults with congenital heart disease: Clinical experience in a high volume center.


Journal

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

Informations de publication

Date de publication:
01 Dec 2020
Historique:
received: 06 04 2020
revised: 29 05 2020
accepted: 13 07 2020
pubmed: 28 7 2020
medline: 15 5 2021
entrez: 27 7 2020
Statut: ppublish

Résumé

Cardiac magnetic resonance (CMR) imaging with velocity encoding along all three directions of flow, known as 4DFlow CMR, provides both anatomical and functional information. Few data are available on the usefulness of 4DFlow CMR in everyday practice. Here, our objective was to investigate the usefulness of 4DFlow CMR for assessing congenital heart disease (CHD) in everyday practice. From 2017 to 2019, consecutive patients who underwent 4DFlow CMR were included prospectively at a single high-volume centre. The parameters recommended by an expert's consensus statement for each diagnosis (congenital valvulopathy, septal defect, complex CHD, tetralogy of Fallot, aortic abnormalities) were assessed by two blinded experienced readers. 4DFlow CMRs that provided all recommended parameters were considered successful. Inter-observer and intra-observer agreement were investigated. We included 187 adults and 60 children covering broad ranges of weight (4.5-142 kg) and age (0.1-67 years). 4DFlow CMR was always the second-line imaging modality, after inconclusive echocardiography, and was successful in 231/247 (91%) patients, with no significant difference between children and adults (54/60, 90%; and 177/187, 95%; respectively; p = .13). Longer time using 4DFlow CMR at our centre was associated with success; in children, older age was also associated with exam success. There was an about 12-month learning curve in children. The success rate was lowest in neonates. Inter-observer and intra-observer agreement were substantial. Our results suggest that 4DFlow CMR usually provides a comprehensive assessment of CHD in adults and children. A learning curve exists for children and the investigation remains challenging in neonates.

Sections du résumé

BACKGROUND BACKGROUND
Cardiac magnetic resonance (CMR) imaging with velocity encoding along all three directions of flow, known as 4DFlow CMR, provides both anatomical and functional information. Few data are available on the usefulness of 4DFlow CMR in everyday practice. Here, our objective was to investigate the usefulness of 4DFlow CMR for assessing congenital heart disease (CHD) in everyday practice.
METHODS METHODS
From 2017 to 2019, consecutive patients who underwent 4DFlow CMR were included prospectively at a single high-volume centre. The parameters recommended by an expert's consensus statement for each diagnosis (congenital valvulopathy, septal defect, complex CHD, tetralogy of Fallot, aortic abnormalities) were assessed by two blinded experienced readers. 4DFlow CMRs that provided all recommended parameters were considered successful. Inter-observer and intra-observer agreement were investigated.
RESULTS RESULTS
We included 187 adults and 60 children covering broad ranges of weight (4.5-142 kg) and age (0.1-67 years). 4DFlow CMR was always the second-line imaging modality, after inconclusive echocardiography, and was successful in 231/247 (91%) patients, with no significant difference between children and adults (54/60, 90%; and 177/187, 95%; respectively; p = .13). Longer time using 4DFlow CMR at our centre was associated with success; in children, older age was also associated with exam success. There was an about 12-month learning curve in children. The success rate was lowest in neonates. Inter-observer and intra-observer agreement were substantial.
CONCLUSION CONCLUSIONS
Our results suggest that 4DFlow CMR usually provides a comprehensive assessment of CHD in adults and children. A learning curve exists for children and the investigation remains challenging in neonates.

Identifiants

pubmed: 32712110
pii: S0167-5273(20)33469-0
doi: 10.1016/j.ijcard.2020.07.021
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

168-177

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Auteurs

Marc-Antoine Isorni (MA)

Diagnostic and Therapeutic Radiology Service, Hopital Marie Lannelongue, 133, avenue de la résistance, 92350 Le Plessis Robinson, France. Electronic address: marco.isorni@gmail.com.

Louis Moisson (L)

Diagnostic and Therapeutic Radiology Service, Hopital Marie Lannelongue, 133, avenue de la résistance, 92350 Le Plessis Robinson, France. Electronic address: l.moisson@hml.fr.

Nidal Ben Moussa (NB)

Pôle des cardiopathies congénitales de l'enfant et de l'adulte, Centre de référence malformations cardiaques congénitales complexes (M3C), hôpital Marie-Lannelongue, université Paris-Sud, université Paris-Saclay, 133, avenue de la Résistance, 92350 Le Plessis-Robinson, France. Electronic address: n.benmoussa@hml.fr.

Sébastien Monnot (S)

Diagnostic and Therapeutic Radiology Service, Hopital Marie Lannelongue, 133, avenue de la résistance, 92350 Le Plessis Robinson, France. Electronic address: s.monnot@hml.fr.

Francesca Raimondi (F)

Pediatric Radiology Unit, Hopital universitaire Necker Enfants-Malades, 149, rue de Sevres, 75743 Paris, Cedex 15, France.

Régine Roussin (R)

Pôle des cardiopathies congénitales de l'enfant et de l'adulte, Centre de référence malformations cardiaques congénitales complexes (M3C), hôpital Marie-Lannelongue, université Paris-Sud, université Paris-Saclay, 133, avenue de la Résistance, 92350 Le Plessis-Robinson, France.

Angèle Boet (A)

Pôle des cardiopathies congénitales de l'enfant et de l'adulte, Centre de référence malformations cardiaques congénitales complexes (M3C), hôpital Marie-Lannelongue, université Paris-Sud, université Paris-Saclay, 133, avenue de la Résistance, 92350 Le Plessis-Robinson, France. Electronic address: a.boet@hml.fr.

Isabelle van Aerschot (I)

Pôle des cardiopathies congénitales de l'enfant et de l'adulte, Centre de référence malformations cardiaques congénitales complexes (M3C), hôpital Marie-Lannelongue, université Paris-Sud, université Paris-Saclay, 133, avenue de la Résistance, 92350 Le Plessis-Robinson, France. Electronic address: i.vanaerschot@hml.fr.

Emmanuelle Fournier (E)

Pôle des cardiopathies congénitales de l'enfant et de l'adulte, Centre de référence malformations cardiaques congénitales complexes (M3C), hôpital Marie-Lannelongue, université Paris-Sud, université Paris-Saclay, 133, avenue de la Résistance, 92350 Le Plessis-Robinson, France. Electronic address: e.fournier@hml.fr.

Sarah Cohen (S)

Pôle des cardiopathies congénitales de l'enfant et de l'adulte, Centre de référence malformations cardiaques congénitales complexes (M3C), hôpital Marie-Lannelongue, université Paris-Sud, université Paris-Saclay, 133, avenue de la Résistance, 92350 Le Plessis-Robinson, France. Electronic address: s.cohen@hml.fr.

Meriem Kara (M)

Pôle des cardiopathies congénitales de l'enfant et de l'adulte, Centre de référence malformations cardiaques congénitales complexes (M3C), hôpital Marie-Lannelongue, université Paris-Sud, université Paris-Saclay, 133, avenue de la Résistance, 92350 Le Plessis-Robinson, France. Electronic address: m.kara@hml.fr.

Sébastien Hascoet (S)

Pôle des cardiopathies congénitales de l'enfant et de l'adulte, Centre de référence malformations cardiaques congénitales complexes (M3C), hôpital Marie-Lannelongue, université Paris-Sud, université Paris-Saclay, 133, avenue de la Résistance, 92350 Le Plessis-Robinson, France. Electronic address: s.hascoet@hml.fr.

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Classifications MeSH