Psychophysical Evaluation of Visual vs. Computer-Aided Detection of Brain Lesions on Magnetic Resonance Images.


Journal

Journal of magnetic resonance imaging : JMRI
ISSN: 1522-2586
Titre abrégé: J Magn Reson Imaging
Pays: United States
ID NLM: 9105850

Informations de publication

Date de publication:
08 2023
Historique:
revised: 25 11 2022
received: 30 08 2022
accepted: 28 11 2022
medline: 11 7 2023
pubmed: 11 12 2022
entrez: 10 12 2022
Statut: ppublish

Résumé

Magnetic resonance imaging (MRI) diagnosis is usually performed by analyzing contrast-weighted images, where pathology is detected once it reached a certain visual threshold. Computer-aided diagnosis (CAD) has been proposed as a way for achieving higher sensitivity to early pathology. To compare conventional (i.e., visual) MRI assessment of artificially generated multiple sclerosis (MS) lesions in the brain's white matter to CAD based on a deep neural network. Prospective. A total of 25 neuroradiologists (15 males, age 39 ± 9, 9 ± 9.8 years of experience) independently assessed all synthetic lesions. A 3.0 T, T MS lesions of varying severity levels were artificially generated in healthy volunteer MRI scans by manipulating T Diagnostic performance of the two approaches was compared using z-tests on TP rates, FP rates, and the logarithm of ORs across severity levels. A P-value <0.05 was considered statistically significant. ORs of identifying pathology were significantly higher for CAD vis-à-vis visual inspection for all lesions' severity levels. For a 6% change in T CAD is capable of detecting the presence or absence of more subtle lesions with greater precision than the representative group of 25 radiologists chosen in this study. 1 TECHNICAL EFFICACY: Stage 3.

Sections du résumé

BACKGROUND
Magnetic resonance imaging (MRI) diagnosis is usually performed by analyzing contrast-weighted images, where pathology is detected once it reached a certain visual threshold. Computer-aided diagnosis (CAD) has been proposed as a way for achieving higher sensitivity to early pathology.
PURPOSE
To compare conventional (i.e., visual) MRI assessment of artificially generated multiple sclerosis (MS) lesions in the brain's white matter to CAD based on a deep neural network.
STUDY TYPE
Prospective.
POPULATION
A total of 25 neuroradiologists (15 males, age 39 ± 9, 9 ± 9.8 years of experience) independently assessed all synthetic lesions.
FIELD STRENGTH/SEQUENCE
A 3.0 T, T
ASSESSMENT
MS lesions of varying severity levels were artificially generated in healthy volunteer MRI scans by manipulating T
STATISTICAL TESTS
Diagnostic performance of the two approaches was compared using z-tests on TP rates, FP rates, and the logarithm of ORs across severity levels. A P-value <0.05 was considered statistically significant.
RESULTS
ORs of identifying pathology were significantly higher for CAD vis-à-vis visual inspection for all lesions' severity levels. For a 6% change in T
DATA CONCLUSION
CAD is capable of detecting the presence or absence of more subtle lesions with greater precision than the representative group of 25 radiologists chosen in this study.
LEVEL OF EVIDENCE
1 TECHNICAL EFFICACY: Stage 3.

Identifiants

pubmed: 36495014
doi: 10.1002/jmri.28559
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

642-649

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2022 The Authors. Journal of Magnetic Resonance Imaging published by Wiley Periodicals LLC on behalf of International Society for Magnetic Resonance in Medicine.

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Auteurs

Chen Solomon (C)

Department of Biomedical Engineering, Tel-Aviv University, Tel-Aviv, Israel.

Omer Shmueli (O)

Department of Biomedical Engineering, Tel-Aviv University, Tel-Aviv, Israel.

Shai Shrot (S)

Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
Department of Diagnostic Imaging, Sheba Medical Center, Ramat-Gan, Israel.

Tamar Blumenfeld-Katzir (T)

Department of Biomedical Engineering, Tel-Aviv University, Tel-Aviv, Israel.

Dvir Radunsky (D)

Department of Biomedical Engineering, Tel-Aviv University, Tel-Aviv, Israel.

Noam Omer (N)

Department of Biomedical Engineering, Tel-Aviv University, Tel-Aviv, Israel.

Neta Stern (N)

Department of Biomedical Engineering, Tel-Aviv University, Tel-Aviv, Israel.

Dominique Ben-Ami Reichman (DB)

Department of Diagnostic Imaging, Sheba Medical Center, Ramat-Gan, Israel.

Chen Hoffmann (C)

Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
Department of Diagnostic Imaging, Sheba Medical Center, Ramat-Gan, Israel.

Moti Salti (M)

Brain Imaging Research Center (BIRC), Ben-Gurion University, Beer-Sheva, Israel.
Zlotowski Center for Neuroscience, Ben-Gurion University of the Negev, Beer-Sheva, Israel.

Hayit Greenspan (H)

Department of Biomedical Engineering, Tel-Aviv University, Tel-Aviv, Israel.

Noam Ben-Eliezer (N)

Department of Biomedical Engineering, Tel-Aviv University, Tel-Aviv, Israel.
Zlotowski Center for Neuroscience, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Center for Advanced Imaging Innovation and Research (CAI2R), New York University, New York, New York, USA.
Sagol School of Neuroscience, Tel Aviv University, Tel Aviv, Israel.

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