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Automated segmentation of 3D cine cardiovascular magnetic resonance imaging

INTRODUCTION: As the life expectancy of children with congenital heart disease (CHD) is rapidly increasing and the adult population with CHD is growing, there is an unmet need to improve clinical workflow and efficiency of analysis. Cardiovascular magnetic resonance (CMR) is a noninvasive imaging mo...

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Autores principales: Tayebi Arasteh, Soroosh, Romanowicz, Jennifer, Pace, Danielle F., Golland, Polina, Powell, Andrew J., Maier, Andreas K., Truhn, Daniel, Brosch, Tom, Weese, Juergen, Lotfinia, Mahshad, van der Geest, Rob J., Moghari, Mehdi H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10613522/
https://www.ncbi.nlm.nih.gov/pubmed/37904806
http://dx.doi.org/10.3389/fcvm.2023.1167500
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author Tayebi Arasteh, Soroosh
Romanowicz, Jennifer
Pace, Danielle F.
Golland, Polina
Powell, Andrew J.
Maier, Andreas K.
Truhn, Daniel
Brosch, Tom
Weese, Juergen
Lotfinia, Mahshad
van der Geest, Rob J.
Moghari, Mehdi H.
author_facet Tayebi Arasteh, Soroosh
Romanowicz, Jennifer
Pace, Danielle F.
Golland, Polina
Powell, Andrew J.
Maier, Andreas K.
Truhn, Daniel
Brosch, Tom
Weese, Juergen
Lotfinia, Mahshad
van der Geest, Rob J.
Moghari, Mehdi H.
author_sort Tayebi Arasteh, Soroosh
collection PubMed
description INTRODUCTION: As the life expectancy of children with congenital heart disease (CHD) is rapidly increasing and the adult population with CHD is growing, there is an unmet need to improve clinical workflow and efficiency of analysis. Cardiovascular magnetic resonance (CMR) is a noninvasive imaging modality for monitoring patients with CHD. CMR exam is based on multiple breath-hold 2-dimensional (2D) cine acquisitions that should be precisely prescribed and is expert and institution dependent. Moreover, 2D cine images have relatively thick slices, which does not allow for isotropic delineation of ventricular structures. Thus, development of an isotropic 3D cine acquisition and automatic segmentation method is worthwhile to make CMR workflow straightforward and efficient, as the present work aims to establish. METHODS: Ninety-nine patients with many types of CHD were imaged using a non-angulated 3D cine CMR sequence covering the whole-heart and great vessels. Automatic supervised and semi-supervised deep-learning-based methods were developed for whole-heart segmentation of 3D cine images to separately delineate the cardiac structures, including both atria, both ventricles, aorta, pulmonary arteries, and superior and inferior vena cavae. The segmentation results derived from the two methods were compared with the manual segmentation in terms of Dice score, a degree of overlap agreement, and atrial and ventricular volume measurements. RESULTS: The semi-supervised method resulted in a better overlap agreement with the manual segmentation than the supervised method for all 8 structures (Dice score 83.23 ± 16.76% vs. 77.98 ± 19.64%; P-value ≤0.001). The mean difference error in atrial and ventricular volumetric measurements between manual segmentation and semi-supervised method was lower (bias ≤ 5.2 ml) than the supervised method (bias ≤ 10.1 ml). DISCUSSION: The proposed semi-supervised method is capable of cardiac segmentation and chamber volume quantification in a CHD population with wide anatomical variability. It accurately delineates the heart chambers and great vessels and can be used to accurately calculate ventricular and atrial volumes throughout the cardiac cycle. Such a segmentation method can reduce inter- and intra- observer variability and make CMR exams more standardized and efficient.
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spelling pubmed-106135222023-10-30 Automated segmentation of 3D cine cardiovascular magnetic resonance imaging Tayebi Arasteh, Soroosh Romanowicz, Jennifer Pace, Danielle F. Golland, Polina Powell, Andrew J. Maier, Andreas K. Truhn, Daniel Brosch, Tom Weese, Juergen Lotfinia, Mahshad van der Geest, Rob J. Moghari, Mehdi H. Front Cardiovasc Med Cardiovascular Medicine INTRODUCTION: As the life expectancy of children with congenital heart disease (CHD) is rapidly increasing and the adult population with CHD is growing, there is an unmet need to improve clinical workflow and efficiency of analysis. Cardiovascular magnetic resonance (CMR) is a noninvasive imaging modality for monitoring patients with CHD. CMR exam is based on multiple breath-hold 2-dimensional (2D) cine acquisitions that should be precisely prescribed and is expert and institution dependent. Moreover, 2D cine images have relatively thick slices, which does not allow for isotropic delineation of ventricular structures. Thus, development of an isotropic 3D cine acquisition and automatic segmentation method is worthwhile to make CMR workflow straightforward and efficient, as the present work aims to establish. METHODS: Ninety-nine patients with many types of CHD were imaged using a non-angulated 3D cine CMR sequence covering the whole-heart and great vessels. Automatic supervised and semi-supervised deep-learning-based methods were developed for whole-heart segmentation of 3D cine images to separately delineate the cardiac structures, including both atria, both ventricles, aorta, pulmonary arteries, and superior and inferior vena cavae. The segmentation results derived from the two methods were compared with the manual segmentation in terms of Dice score, a degree of overlap agreement, and atrial and ventricular volume measurements. RESULTS: The semi-supervised method resulted in a better overlap agreement with the manual segmentation than the supervised method for all 8 structures (Dice score 83.23 ± 16.76% vs. 77.98 ± 19.64%; P-value ≤0.001). The mean difference error in atrial and ventricular volumetric measurements between manual segmentation and semi-supervised method was lower (bias ≤ 5.2 ml) than the supervised method (bias ≤ 10.1 ml). DISCUSSION: The proposed semi-supervised method is capable of cardiac segmentation and chamber volume quantification in a CHD population with wide anatomical variability. It accurately delineates the heart chambers and great vessels and can be used to accurately calculate ventricular and atrial volumes throughout the cardiac cycle. Such a segmentation method can reduce inter- and intra- observer variability and make CMR exams more standardized and efficient. Frontiers Media S.A. 2023-10-13 /pmc/articles/PMC10613522/ /pubmed/37904806 http://dx.doi.org/10.3389/fcvm.2023.1167500 Text en © 2023 Tayebi Arasteh, Romanowicz, Pace, Golland, Powell, Maier, Truhn, Brosch, Weese, Lotfinia, van der Geest and Moghari. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cardiovascular Medicine
Tayebi Arasteh, Soroosh
Romanowicz, Jennifer
Pace, Danielle F.
Golland, Polina
Powell, Andrew J.
Maier, Andreas K.
Truhn, Daniel
Brosch, Tom
Weese, Juergen
Lotfinia, Mahshad
van der Geest, Rob J.
Moghari, Mehdi H.
Automated segmentation of 3D cine cardiovascular magnetic resonance imaging
title Automated segmentation of 3D cine cardiovascular magnetic resonance imaging
title_full Automated segmentation of 3D cine cardiovascular magnetic resonance imaging
title_fullStr Automated segmentation of 3D cine cardiovascular magnetic resonance imaging
title_full_unstemmed Automated segmentation of 3D cine cardiovascular magnetic resonance imaging
title_short Automated segmentation of 3D cine cardiovascular magnetic resonance imaging
title_sort automated segmentation of 3d cine cardiovascular magnetic resonance imaging
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10613522/
https://www.ncbi.nlm.nih.gov/pubmed/37904806
http://dx.doi.org/10.3389/fcvm.2023.1167500
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