# Identifying High-Risk Pre-Term Pregnancies Using the Fetal Heart Rate and Machine Learning

**Authors:** Gabriel Davis Jones, William R. Cooke, Manu Vatish

PMC · DOI: 10.3390/bioengineering13020203 · Bioengineering · 2026-02-11

## TL;DR

This study uses fetal heart rate data and machine learning to accurately identify high-risk pre-term pregnancies, potentially improving clinical decisions.

## Contribution

A machine learning model using fetal heart rate features achieves high accuracy in predicting adverse outcomes in pre-term pregnancies.

## Key findings

- A random forest model achieved an AUC of 0.88 in predicting adverse outcomes in pre-term pregnancies.
- The model's performance was consistent across gestational ages and individual adverse outcomes.
- The model demonstrated good calibration and net benefit across clinically relevant thresholds.

## Abstract

Fetal heart rate (FHR) monitoring is ubiquitous in antenatal care, yet human visual interpretation poorly predicts adverse pregnancy outcomes. Meanwhile, preterm gestations carry a high burden of stillbirth and severe fetal compromise, where earlier identification of high-risk pregnancies may justify iatrogenic preterm delivery to prevent avoidable fetal death. We analyzed 4867 antepartum FHR recordings from pre-term pregnancies meeting at least one of ten adverse outcome criteria alongside 4014 term uncomplicated controls. Seven clinically validated FHR features were extracted from each trace, and six machine-learning classifiers were trained on 80% of the data (7105 samples) using k-fold cross-validation; the remaining 20% (1776 samples) formed an internal validation cohort. The random forest demonstrated the best performance, achieving an area under the receiver-operating characteristic curve (AUC) of 0.88 (95% confidence interval [CI] 0.87–0.88) during training and 0.88 (95% CI 0.86–0.90) on validation, with good calibration (Brier score 0.14). Median AUC across individual adverse outcomes was 0.85 (interquartile range [IQR] 0.81–0.89) and exceeded 0.80 at all gestational ages assessed; sensitivity and specificity at the Youden threshold were 76.2% and 87.5%, respectively. Decision-curve analysis demonstrated net benefit across a range of clinically relevant probability thresholds. These findings indicate that data-driven interpretation of antepartum FHR can stratify risk in pre-term pregnancies with high accuracy and may support earlier, evidence-based clinical decision-making, particularly in resource-limited settings where specialist expertise is limited.

## Full-text entities

- **Diseases:** cord compression (MESH:D013117), deficiency in normal neurological (MESH:D009461), maternal hypotension (MESH:D007022), hypoxia (MESH:D000860), bradycardia (MESH:D001919), neonatal sepsis (MESH:D000071074), respiratory conditions (MESH:D012131), perinatal infection (MESH:D003586), hemorrhage (MESH:D006470), FHR (MESH:D005315), Hypoxaemic ischemic encephalopathy (MESH:D002545), injury to (MESH:D014947), hypoxic ischemic encephalopathy (MESH:D020925), pregnancy disorders (MESH:D011254), stillbirth (MESH:D050497), fetal distress (MESH:D005316), cardiac anomalies (MESH:D006331), fetal death (MESH:D005313), infections (MESH:D007239), preterm birth (MESH:D047928), base deficit (MESH:D019292), placental dysfunction (MESH:D010922), acidosis (MESH:D000138), Asphyxia (MESH:D001237), placental insufficiency (MESH:D010927), death (MESH:D003643), hypertensive disease (MESH:D006973), APO (MESH:D011248)
- **Chemicals:** magnesium sulfate (MESH:D008278)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12937779/full.md

## References

76 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937779/full.md

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Source: https://tomesphere.com/paper/PMC12937779