Abstract
Objectives
To develop a deep-learning method for whole-body fetal segmentation based on MRI; to assess the method’s repeatability, reproducibility, and accuracy; to create an MRI-based normal fetal weight growth chart; and to assess the sensitivity to detect fetuses with growth restriction (FGR).
Methods
Retrospective data of 348 fetuses with gestational age (GA) of 19–39 weeks were included: 249 normal appropriate for GA (AGA), 19 FGR, and 80 Other (having various imaging abnormalities). A fetal whole-body segmentation model with a quality estimation module was developed and evaluated in 169 cases. The method was evaluated for its repeatability (repeated scans within the same scanner, n = 22), reproducibility (different scanners, n = 6), and accuracy (compared with birth weight, n = 7). A normal MRI-based growth chart was derived.
Results
The method achieved a Dice = 0.973, absolute volume difference ratio (VDR) = 1.8% and VDR mean difference = 0.75% (\({CI}_{95\%}\): − 3.95%, 5.46), and high agreement with the gold standard. The method achieved a repeatability coefficient = 4.01%, ICC = 0.99, high reproducibility with a mean difference = 2.21% (\({CI}_{95\%}\): − 1.92%, 6.35%), and high accuracy with a mean difference between estimated fetal weight (EFW) and birth weight of − 0.39% (\({CI}_{95\%}\): − 8.23%, 7.45%). A normal growth chart (n = 246) was consistent with four ultrasound charts. EFW based on MRI correctly predicted birth-weight percentiles for all 18 fetuses ≤ 10thpercentile and for 14 out of 17 FGR fetuses below the 3rd percentile. Six fetuses referred to MRI as AGA were found to be < 3rd percentile.
Conclusions
The proposed method for automatic MRI-based EFW demonstrated high performance and sensitivity to identify FGR fetuses.
Clinical relevance statement
Results from this study support the use of the automatic fetal weight estimation method based on MRI for the assessment of fetal development and to detect fetuses at risk for growth restriction.
Key Points
• An AI-based segmentation method with a quality assessment module for fetal weight estimation based on MRI was developed, achieving high repeatability, reproducibility, and accuracy.
• An MRI-based fetal weight growth chart constructed from a large cohort of normal and appropriate gestational-age fetuses is proposed.
• The method showed a high sensitivity for the diagnosis of small fetuses suspected of growth restriction.
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Abbreviations
- AGA:
-
Appropriate for gestational age
- aVDR :
-
Absolute volume difference ratio
- EFW:
-
Estimated fetal weight
- FGR:
-
Fetal growth restriction
- FIESTA:
-
Fast imaging employing steady-state acquisition
- GA:
-
Gestational age
- HASTE:
-
Half-Fourier acquisition single-shot turbo spin-echo
- ICC:
-
Intraclass correlation coefficient
- TRUFI:
-
True fast imaging with steady-state free precession
- TTA:
-
Test time augmentations
- VDR :
-
Volume difference ratio
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Acknowledgements
This research was supported by Kamin grants 63418 and 72126 from the Israel Innovation Authority. We are grateful to the MRI technicians for scanning the fetuses, to the mothers who participated, and to those involved in data preparation and annotation: Ori Benzvi helped with data extraction, and Tuvia Ganot, Kerina Krupnik, Cassandra Kapoor, and Shelley Levi helped with the annotation process and data transfer.
Funding
This work was financially supported by Kamin grants of the Israel Innovation Authority.
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The scientific guarantor of this publication is Dafna Ben-Bashat.
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Written informed consent was waived by the Institutional Review Boards of Tel Aviv Sourasky Medical Center and Children’s Hospital of Eastern Ontario for the retrospective data and was obtained from all participants in the prospective data at Tel Aviv Sourasky Medical Center.
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• prospective and retrospective
• cross-sectional study
• multicenter study
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Specktor-Fadida, B., Link-Sourani, D., Rabinowich, A. et al. Deep learning–based segmentation of whole-body fetal MRI and fetal weight estimation: assessing performance, repeatability, and reproducibility. Eur Radiol 34, 2072–2083 (2024). https://doi.org/10.1007/s00330-023-10038-y
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DOI: https://doi.org/10.1007/s00330-023-10038-y