Assessment of right ventricular size and function from cardiovascular magnetic resonance images using artificial intelligence.


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:
11 04 2022
Historique:
received: 15 12 2021
accepted: 29 03 2022
entrez: 12 4 2022
pubmed: 13 4 2022
medline: 14 4 2022
Statut: epublish

Résumé

Theoretically, artificial intelligence can provide an accurate automatic solution to measure right ventricular (RV) ejection fraction (RVEF) from cardiovascular magnetic resonance (CMR) images, despite the complex RV geometry. However, in our recent study, commercially available deep learning (DL) algorithms for RVEF quantification performed poorly in some patients. The current study was designed to test the hypothesis that quantification of RV function could be improved in these patients by using more diverse CMR datasets in addition to domain-specific quantitative performance evaluation metrics during the cross-validation phase of DL algorithm development. We identified 100 patients from our prior study who had the largest differences between manually measured and automated RVEF values. Automated RVEF measurements were performed using the original version of the algorithm (DL1), an updated version (DL2) developed from a dataset that included a wider range of RV pathology and validated using multiple domain-specific quantitative performance evaluation metrics, and conventional methodology performed by a core laboratory (CORE). Each of the DL-RVEF approaches was compared against CORE-RVEF reference values using linear regression and Bland-Altman analyses. Additionally, RVEF values were classified into 3 categories: ≤ 35%, 35-50%, and ≥ 50%. Agreement between RVEF classifications made by the DL approaches and the CORE measurements was tested. CORE-RVEF and DL-RVEFs were obtained in all patients (feasibility of 100%). DL2-RVEF correlated with CORE-RVEF better than DL1-RVEF (r = 0.87 vs. r = 0.42), with narrower limits of agreement. As a result, DL2 algorithm also showed increasing accuracy from 0.53 to 0.80 for categorizing RV function. The use of a new DL algorithm cross-validated on a dataset with a wide range of RV pathology using multiple domain-specific metrics resulted in a considerable improvement in the accuracy of automated RVEF measurements. This improvement was demonstrated in patients whose images were the most challenging and resulted in the largest RVEF errors. These findings underscore the critical importance of this strategy in the development of DL approaches for automated CMR measurements.

Sections du résumé

BACKGROUND
Theoretically, artificial intelligence can provide an accurate automatic solution to measure right ventricular (RV) ejection fraction (RVEF) from cardiovascular magnetic resonance (CMR) images, despite the complex RV geometry. However, in our recent study, commercially available deep learning (DL) algorithms for RVEF quantification performed poorly in some patients. The current study was designed to test the hypothesis that quantification of RV function could be improved in these patients by using more diverse CMR datasets in addition to domain-specific quantitative performance evaluation metrics during the cross-validation phase of DL algorithm development.
METHODS
We identified 100 patients from our prior study who had the largest differences between manually measured and automated RVEF values. Automated RVEF measurements were performed using the original version of the algorithm (DL1), an updated version (DL2) developed from a dataset that included a wider range of RV pathology and validated using multiple domain-specific quantitative performance evaluation metrics, and conventional methodology performed by a core laboratory (CORE). Each of the DL-RVEF approaches was compared against CORE-RVEF reference values using linear regression and Bland-Altman analyses. Additionally, RVEF values were classified into 3 categories: ≤ 35%, 35-50%, and ≥ 50%. Agreement between RVEF classifications made by the DL approaches and the CORE measurements was tested.
RESULTS
CORE-RVEF and DL-RVEFs were obtained in all patients (feasibility of 100%). DL2-RVEF correlated with CORE-RVEF better than DL1-RVEF (r = 0.87 vs. r = 0.42), with narrower limits of agreement. As a result, DL2 algorithm also showed increasing accuracy from 0.53 to 0.80 for categorizing RV function.
CONCLUSIONS
The use of a new DL algorithm cross-validated on a dataset with a wide range of RV pathology using multiple domain-specific metrics resulted in a considerable improvement in the accuracy of automated RVEF measurements. This improvement was demonstrated in patients whose images were the most challenging and resulted in the largest RVEF errors. These findings underscore the critical importance of this strategy in the development of DL approaches for automated CMR measurements.

Identifiants

pubmed: 35410226
doi: 10.1186/s12968-022-00861-5
pii: 10.1186/s12968-022-00861-5
pmc: PMC8996592
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

27

Informations de copyright

© 2022. The Author(s).

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Auteurs

Shuo Wang (S)

Department of Medicine, University of Chicago, University of Chicago Medical Center, 5758 S. Maryland Avenue, Chicago, IL, MC906760637, USA.
Peking University Shougang Hospital, Beijing, China.

Daksh Chauhan (D)

Department of Medicine, University of Chicago, University of Chicago Medical Center, 5758 S. Maryland Avenue, Chicago, IL, MC906760637, USA.

Hena Patel (H)

Department of Medicine, University of Chicago, University of Chicago Medical Center, 5758 S. Maryland Avenue, Chicago, IL, MC906760637, USA.

Alborz Amir-Khalili (A)

Circle Cardiovascular Imaging, Calgary, Canada.

Isabel Ferreira da Silva (IF)

Circle Cardiovascular Imaging, Calgary, Canada.

Alireza Sojoudi (A)

Circle Cardiovascular Imaging, Calgary, Canada.

Silke Friedrich (S)

Circle Cardiovascular Imaging, Calgary, Canada.

Amita Singh (A)

Department of Medicine, University of Chicago, University of Chicago Medical Center, 5758 S. Maryland Avenue, Chicago, IL, MC906760637, USA.

Luis Landeras (L)

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

Tamari Miller (T)

Department of Medicine, University of Chicago, University of Chicago Medical Center, 5758 S. Maryland Avenue, Chicago, IL, MC906760637, USA.

Keith Ameyaw (K)

Department of Medicine, University of Chicago, University of Chicago Medical Center, 5758 S. Maryland Avenue, Chicago, IL, MC906760637, USA.

Akhil Narang (A)

Northwestern University, Chicago, IL, USA.

Keigo Kawaji (K)

Illinois Institute of Technology, Chicago, IL, USA.

Qiang Tang (Q)

Peking University Shougang Hospital, Beijing, China.

Victor Mor-Avi (V)

Department of Medicine, University of Chicago, University of Chicago Medical Center, 5758 S. Maryland Avenue, Chicago, IL, MC906760637, USA.

Amit R Patel (AR)

Department of Medicine, University of Chicago, University of Chicago Medical Center, 5758 S. Maryland Avenue, Chicago, IL, MC906760637, USA. amitpatel@uchicago.edu.
Department of Radiology, University of Chicago, Chicago, IL, USA. amitpatel@uchicago.edu.

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