Validation of non-contrast multiple overlapping thin-slab 4D-flow cardiac magnetic resonance imaging.


Journal

Magnetic resonance imaging
ISSN: 1873-5894
Titre abrégé: Magn Reson Imaging
Pays: Netherlands
ID NLM: 8214883

Informations de publication

Date de publication:
12 2020
Historique:
received: 15 04 2020
revised: 31 08 2020
accepted: 04 10 2020
pubmed: 10 10 2020
medline: 25 2 2021
entrez: 9 10 2020
Statut: ppublish

Résumé

Cardiac magnetic resonance (CMR) flow quantification is typically performed using 2D phase-contrast (PC) imaging of a plane perpendicular to flow. 3D-PC imaging (4D-flow) allows offline quantification anywhere in a thick slab, but is often limited by suboptimal signal, potentially alleviated by contrast enhancement. We developed a non-contrast 4D-flow sequence, which acquires multiple overlapping thin slabs (MOTS) to minimize signal loss, and hypothesized that it could improve image quality, diagnostic accuracy, and aortic flow measurements compared to non-contrast single-slab approach. We prospectively studied 20 patients referred for transesophageal echocardiography (TEE), who underwent CMR (GE, 3 T). 2D-PC images of the aortic valve and three 4D-flow datasets covering the heart were acquired, including single-slab, pre- and post-contrast, and non-contrast MOTS. Each 4D-flow dataset was interpreted blindly for ≥moderate valve disease and compared to TEE. Flow visualization through each valve was scored (0 to 4), and aortic-valve flow measured on each 4D-flow dataset and compared to 2D-PC reference. Diagnostic quality visualization was achieved with the pre- and post-contrast 4D-flow acquisitions in 25% and 100% valves, respectively (scores 0.9 ± 1.1 and 3.8 ± 0.5), and in 58% with the non-contrast MOTS (1.6 ± 1.1). Accuracy of detection of valve disease was 75%, 92% and 82%, respectively. Aortic flow measurements were possible in 53%, 95% and in 89% patients, respectively. The correlation between pre-contrast single-slab measurements and 2D-PC reference was weak (r = 0.21), but improved with both contrast enhancement (r = 0.71) and with MOTS (r = 0.67). Although non-contrast MOTS 4D-flow improves valve function visualization and diagnostic accuracy, a significant proportion of valves cannot be accurately assessed. However, aortic flow measurements using non-contrast MOTS is feasible and reaches similar accuracy to that of contrast-enhanced 4D-flow.

Sections du résumé

BACKGROUND
Cardiac magnetic resonance (CMR) flow quantification is typically performed using 2D phase-contrast (PC) imaging of a plane perpendicular to flow. 3D-PC imaging (4D-flow) allows offline quantification anywhere in a thick slab, but is often limited by suboptimal signal, potentially alleviated by contrast enhancement. We developed a non-contrast 4D-flow sequence, which acquires multiple overlapping thin slabs (MOTS) to minimize signal loss, and hypothesized that it could improve image quality, diagnostic accuracy, and aortic flow measurements compared to non-contrast single-slab approach.
METHODS
We prospectively studied 20 patients referred for transesophageal echocardiography (TEE), who underwent CMR (GE, 3 T). 2D-PC images of the aortic valve and three 4D-flow datasets covering the heart were acquired, including single-slab, pre- and post-contrast, and non-contrast MOTS. Each 4D-flow dataset was interpreted blindly for ≥moderate valve disease and compared to TEE. Flow visualization through each valve was scored (0 to 4), and aortic-valve flow measured on each 4D-flow dataset and compared to 2D-PC reference.
RESULTS
Diagnostic quality visualization was achieved with the pre- and post-contrast 4D-flow acquisitions in 25% and 100% valves, respectively (scores 0.9 ± 1.1 and 3.8 ± 0.5), and in 58% with the non-contrast MOTS (1.6 ± 1.1). Accuracy of detection of valve disease was 75%, 92% and 82%, respectively. Aortic flow measurements were possible in 53%, 95% and in 89% patients, respectively. The correlation between pre-contrast single-slab measurements and 2D-PC reference was weak (r = 0.21), but improved with both contrast enhancement (r = 0.71) and with MOTS (r = 0.67).
CONCLUSIONS
Although non-contrast MOTS 4D-flow improves valve function visualization and diagnostic accuracy, a significant proportion of valves cannot be accurately assessed. However, aortic flow measurements using non-contrast MOTS is feasible and reaches similar accuracy to that of contrast-enhanced 4D-flow.

Identifiants

pubmed: 33035638
pii: S0730-725X(20)30607-X
doi: 10.1016/j.mri.2020.10.002
pmc: PMC7931662
mid: NIHMS1671353
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

223-231

Subventions

Organisme : NHLBI NIH HHS
ID : T32 HL007381
Pays : United States

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

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Auteurs

Nina Rashedi (N)

Department of Medicine, University of Chicago Medicine, Chicago, IL, USA.

Luis Landeras (L)

Department of Medicine, University of Chicago Medicine, Chicago, IL, USA.

Victor Mor-Avi (V)

Department of Medicine, University of Chicago Medicine, Chicago, IL, USA. Electronic address: vmoravi@bsd.uchicago.edu.

Davide Genovese (D)

Department of Medicine, University of Chicago Medicine, Chicago, IL, USA; Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padua, Padua, Italy.

Peng Lai (P)

General Electric Healthcare, Chicago, IL, USA.

Haonan Wang (H)

General Electric Healthcare, Chicago, IL, USA.

Kalie Kebed (K)

Department of Medicine, University of Chicago Medicine, Chicago, IL, USA.

Isla McClelland (I)

Department of Medicine, University of Chicago Medicine, Chicago, IL, USA.

Anja Brau (A)

General Electric Healthcare, Chicago, IL, USA.

Martin Janich (M)

General Electric Healthcare, Chicago, IL, USA.

Karima Addetia (K)

Department of Medicine, University of Chicago Medicine, Chicago, IL, USA.

Roberto M Lang (RM)

Department of Medicine, University of Chicago Medicine, Chicago, IL, USA.

Amit R Patel (AR)

Department of Medicine, University of Chicago Medicine, Chicago, IL, USA.

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