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Automated atlas-based multi-label fetal cardiac vessel segmentation in Congenital Heart Disease

Paula Ramirez Gilliland, Alena Uus, Milou P.M. van Poppel, Irina Grigorescu, Johannes K. Steinweg, David F.A. Lloyd, Kuberan Pushparajah, Andrew P. King, Maria Deprez
doi: https://doi.org/10.1101/2022.01.14.476320
Paula Ramirez Gilliland
1School of Biomedical Engineering and Imaging Sciences, King’s College London, London, UK
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  • For correspondence: paula.ramirez_gilliland@kcl.ac.uk
Alena Uus
1School of Biomedical Engineering and Imaging Sciences, King’s College London, London, UK
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Milou P.M. van Poppel
1School of Biomedical Engineering and Imaging Sciences, King’s College London, London, UK
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Irina Grigorescu
1School of Biomedical Engineering and Imaging Sciences, King’s College London, London, UK
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Johannes K. Steinweg
1School of Biomedical Engineering and Imaging Sciences, King’s College London, London, UK
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David F.A. Lloyd
1School of Biomedical Engineering and Imaging Sciences, King’s College London, London, UK
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Kuberan Pushparajah
1School of Biomedical Engineering and Imaging Sciences, King’s College London, London, UK
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Andrew P. King
1School of Biomedical Engineering and Imaging Sciences, King’s College London, London, UK
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Maria Deprez
1School of Biomedical Engineering and Imaging Sciences, King’s College London, London, UK
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Abstract

Congenital heart disease (CHD) is the most commonly diagnosed birth defect. T2w black blood MRI provides optimal vessel visualisation, aiding prenatal CHD diagnosis. Common clinical practice involves manual segmentation of fetal heart and vessels for visualisation and reporting purposes.

We propose an automated multi-label fetal cardiac vessels deep learning segmentation approach for T2w black blood MRI. Our network is trained using single-label manual segmentations obtained through current clinical practice, combined with a multi-label anatomical atlas with desired multi-label segmentation protocol. Our framework combines deep learning label propagation with 3D residual U-Net segmentation to produce high-quality multi-label output well adapted to the individual subject anatomy.

We train and evaluate the network using forty fetal subjects with suspected coarctation of the aorta, achieving a dice score of 0.79 ± 0.02 for the fetal cardiac vessels region. The proposed network outperforms the label propagation and achieves a statistically equivalent performance to a 3D residual U-Net trained exclusively on manual single-label data (p-value>0.05). This multi-label framework therefore represents an advancement over the single-label approach, providing label-specific anatomical information, particularly useful for assessing specific anomaly areas in CHD.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • PAULA.RAMIREZ_GILLILAND{at}KCL.AC.UK

  • ALENA.UUS{at}KCL.AC.UK

  • MILOU.VAN_POPPEL{at}KCL.AC.UK

  • IRINA.GRIGORESCU{at}KCL.AC.UK

  • JOHANNES.STEINWEG{at}KCL.AC.UK

  • DAVID.LLOYD{at}KCL.AC.UK

  • KUBERAN.PUSHPARAJAH{at}KCL.AC.UK

  • ANDREW.KING{at}KCL.AC.UK

  • MARIA.DEPREZ{at}KCL.AC.UK

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted January 17, 2022.
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Automated atlas-based multi-label fetal cardiac vessel segmentation in Congenital Heart Disease
Paula Ramirez Gilliland, Alena Uus, Milou P.M. van Poppel, Irina Grigorescu, Johannes K. Steinweg, David F.A. Lloyd, Kuberan Pushparajah, Andrew P. King, Maria Deprez
bioRxiv 2022.01.14.476320; doi: https://doi.org/10.1101/2022.01.14.476320
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Automated atlas-based multi-label fetal cardiac vessel segmentation in Congenital Heart Disease
Paula Ramirez Gilliland, Alena Uus, Milou P.M. van Poppel, Irina Grigorescu, Johannes K. Steinweg, David F.A. Lloyd, Kuberan Pushparajah, Andrew P. King, Maria Deprez
bioRxiv 2022.01.14.476320; doi: https://doi.org/10.1101/2022.01.14.476320

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