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Radiomics analysis of early pregnancy ultrasound images to predict viability at the end of first trimester
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  • Published: 28 January 2026

Radiomics analysis of early pregnancy ultrasound images to predict viability at the end of first trimester

  • Sughashini Murugesu1,2,
  • Kristofer Linton-Reid3,4,
  • Jennifer Barcroft1,2,
  • Margaret Pikovsky1,2,
  • Srdjan Saso1,2,
  • Eric O. Aboagye3 &
  • …
  • Tom Bourne1,2 

Scientific Reports , Article number:  (2026) Cite this article

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We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Pregnancy outcome
  • Ultrasonography

Abstract

To determine whether there are radiomic ultrasound features of early pregnancy when viability is unknown, which in combination with clinical features, may predict subsequent loss. Multi-centre retrospective cohort study, which included 500 cases of pregnancies of unknown viability (PUV) collected from January 2021 to January 2023. Longitudinal ultrasound images were identified from Queen Charlotte’s and Chelsea Hospital (QCCH), London (n = 400, split 8:2 for training and validation) and St Mary’s Hospital (SMH), London (test data set n = 100). Images were extracted and segmented to include firstly the gestation sac and secondly the sac endometrial border. A segmentation model was developed using a deep learning (DL) model (multi-task nnUNet v2) and standard Dice Coefficient (DICE) was used to measure performance. A prediction model, using clinical and radiomic features, was developed by comparing several machine learning (ML) methods. The area under the ROC curve (AUC), F1-score, and recall were used to assess model performance. The QCCH and SMH data sets were in the majority well matched and consisted of 53.3% and 53.0% miscarriage cases by the end of first trimester, respectively. The DL segmentation model for gestation sac achieved a mean DICE score of 0.950 and 0.940 in the training and test data sets respectively. The segmentation model for the sac endometrial border achieved a mean DICE score of 0.917 (QCCH) and 0.922 (SMH). The best performing PUV outcome classification model (XGBoost and LASSO) for predicting miscarriage (PUVPS model); achieved an AUC of 1.00 (F1-score 1.00), 0.92 (F1-score 0.79) and 0.84 (F1-score 0.76) in the QCCH training, QCCH validation and SMH test set respectively. We have developed an end-to-end radiomics-based model to segment and predict early pregnancy outcomes. The main limitation of this study is its sample size, which can make a ML model prone to overfitting. This study sets the stage for future trials to prospectively evaluate the performance of the PUVPS model, in a large multi-centre cohort, which can then be used to help patients navigate the uncertainty of a PUV early pregnancy classification.

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Data availability

The anonymised adnexal image datasets and corresponding clinical metadata used for model development and validation in this study are not publicly available due to privacy and ethical considerations. However, thesedatasets can be made accessible to qualified researchers upon reasonable request to the corresponding author.

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Funding

SM was supported by Imperial Health Charity and NIHR Imperial BRC. TB is supported by the National Institute for Health Research(NIHR) Biomedical Research Centre based at Imperial College Healthcare NHS Trust and Imperial College London. The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR or the Department of Health. The Tommy’s National Centre for Miscarriage Research at Imperial College NHS Trust is supported by the Tommy’s charity. EA receives funding from the Imperial College Biomedical Research Centre and Experimental Cancer Medicines Centre, paid to his institution. Tom Bourne and Eric Aboagye provided joint supervision for this work.

Author information

Authors and Affiliations

  1. Queen Charlotte’s and Chelsea Hospital, Imperial College, London, W12 0HS, UK

    Sughashini Murugesu, Jennifer Barcroft, Margaret Pikovsky, Srdjan Saso & Tom Bourne

  2. Department of Metabolism, Digestion and Reproduction, Imperial College London, Du Cane Road, London, W12 0NN, UK

    Sughashini Murugesu, Jennifer Barcroft, Margaret Pikovsky, Srdjan Saso & Tom Bourne

  3. Department of Cancer and Surgery, Imperial College London, London, UK

    Kristofer Linton-Reid & Eric O. Aboagye

  4. Research and Innovation Centre, African Institute for Mathematical Sciences, Kigali, Rwanda

    Kristofer Linton-Reid

Authors
  1. Sughashini Murugesu
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Contributions

S.M., K.L-R., E.A. and T.B. were involved in the study design. S.M., J.B. and M.P. collected the data. S.M. and K.L-R. analysed and interpreted the data. S.M. undertook literature review and wrote the initial draft. S.M. and K.L-R. undertook statistical and machine-learning analysis. T.B. and S.S. provided clinical advice. All authors reviewed, contributed to, and approved the manuscript. All authors had access to the data. S.M., K.L-R., E.A. and T.B. were responsible for the decision to submit the manuscript.

Corresponding author

Correspondence to Sughashini Murugesu.

Ethics declarations

Competing interests

The authors declare no competing interests.

Ethical approval

The study was approved by the Health Research Authority, Research Ethics Committee (HRA REC Reference 22/HRA/4847). All methods were performed in accordance with the guidelines and regulations outlined within the approved study protocol. Due to the retrospective nature of the study, written informed consent was not required based on national research guidance, confirmed by the Research Governance and Integrity Team Imperial College London and approved by the HRA REC committee.

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Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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Cite this article

Murugesu, S., Linton-Reid, K., Barcroft, J. et al. Radiomics analysis of early pregnancy ultrasound images to predict viability at the end of first trimester. Sci Rep (2026). https://doi.org/10.1038/s41598-026-35158-5

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  • Received: 30 April 2025

  • Accepted: 02 January 2026

  • Published: 28 January 2026

  • DOI: https://doi.org/10.1038/s41598-026-35158-5

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