Publication

Doppler-based fetal heart rate analysis markers for the detection of early intrauterine growth restriction

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Last modified
  • 05/22/2025
Type of Material
Authors
    Lisa Stroux, University of OxfordChristopher W. Redman, University of OxfordAntoniya Georgieva, University of OxfordStephen J. Payne, University of OxfordGari Clifford, Emory University
Language
  • English
Date
  • 2017-11-01
Publisher
  • Wiley: 12 months
Publication Version
Copyright Statement
  • © 2017 Nordic Federation of Societies of Obstetrics and Gynecology
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 0001-6349
Volume
  • 96
Issue
  • 11
Start Page
  • 1322
End Page
  • 1329
Grant/Funding Information
  • AG was supported by the Action Medical Research and the Henry Smith Charity.
  • GC acknowledges the support of the National Institutes of Health, the Fogarty International Center and the Eunice Kennedy Shriver National Institute of Child Health and Human Development, grant number 1R21HD084114-01.
  • LS acknowledges the support of the RCUK Digital Economy Programme grant number EP/G036861/1 (Oxford Centre for Doctoral Training in Healthcare Innovation).
Abstract
  • Introduction: One indicator for fetal risk of mortality is intrauterine growth restriction (IUGR). Whether markers reflecting the impact of growth restriction on the cardiovascular system, computed from a Doppler-derived heart rate signal, would be suitable for its detection antenatally was studied. Material and methods: We used a cardiotocography archive of 1163 IUGR cases and 1163 healthy controls, matched for gestation and gender. We assessed the discriminative power of short-term variability and long-term variability of the fetal heart rate, computed over episodes of high and low variation aiming to separate growth-restricted fetuses from controls. Metrics characterizing the sleep state distribution within a trace were also considered for inclusion into an IUGR detection model. Results: Significant differences in the risk markers comparing growth-restricted with healthy fetuses were found. When used in a logistic regression classifier, their performance for identifying IUGR was considerably superior before 34 weeks of gestation. Long-term variability in active sleep was superior to short-term variability [area under the receiver operator curve (AUC) of 72% compared with 71%]. Most predictive was the number of minutes in high variation per hour (AUC of 75%). A multivariate IUGR prediction model improved the AUC to 76%. Conclusion: We suggest that heart rate variability markers together with surrogate information on sleep states can contribute to the detection of early-onset IUGR.
Author Notes
  • Lisa Stroux, Institute of Biomedical Engineering, Department of Engineering Science, University of Oxford, UK, Mobile: 0044 7851696157, lisa.stroux@web.de.
Keywords
Research Categories
  • Engineering, Biomedical
  • Health Sciences, Obstetrics and Gynecology

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