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Autor(en) / Beteiligte
Titel
Accounting for Nulliparity in the Prediction of Hypoxic-Ischemic Encephalopathy Using Cardiotocography
Ist Teil von
  • 2023 IEEE EMBS International Conference on Biomedical and Health Informatics (BHI), 2023, Vol.2023, p.1-4
Ort / Verlag
IEEE
Erscheinungsjahr
2023
Link zum Volltext
Quelle
IEEE Xplore Digital Library
Beschreibungen/Notizen
  • Nulliparous pregnancies, those where the mother has not previously given birth, are associated with longer labors and hence expose the fetus to more contractions and other adverse intrapartum conditions such as chorioamnionitis. The objective of the present study was to test if accounting for nulliparity could improve the detection of fetuses at increased risk of developing hypoxic-ischemic encephalopathy (HIE). During labor, clinicians assess the fetal heart rate and uterine pressure signals to identify fetuses at risk of developing HIE. In this study, we performed random forest classification using fetal heart rate and uterine pressure features from 40,831 births, including 374 that developed HIE. We analyzed a two-path classification approach that analyzed separately the fetuses from nulliparous and multiparous mothers, and a one-path classification approach that included the clinical variable for nulliparity as a classification feature. We compared these two approaches to a one-path classifier that had no information about the parity of the mothers. We also compared our results to the rate of Caesarean deliveries in each group, which is used clinically to interrupt the progression towards HIE. All the classifiers detected more fetuses that developed HIE than the observed Caesarean rate, but accounting for nulliparity did not improve performance.Clinical Relevance- Nulliparity is a well-known risk factor for developing hypoxic-ischemic encephalopathy. This study showed that there is no advantage in accounting solely for it in a classification system based on cardiotocography signals.
Sprache
Englisch
Identifikatoren
ISSN: 2641-3590
eISSN: 2641-3604
DOI: 10.1109/BHI58575.2023.10313456
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10685589

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