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Comparative Study
. 2024 Dec 5;9(12):e016088.
doi: 10.1136/bmjgh-2024-016088.

Prediction of low birth weight from fetal ultrasound and clinical characteristics: a comparative study between a low- and middle-income and a high-income country

Affiliations
Comparative Study

Prediction of low birth weight from fetal ultrasound and clinical characteristics: a comparative study between a low- and middle-income and a high-income country

Sergio Sanchez-Martinez et al. BMJ Glob Health. .

Abstract

Introduction: Adverse perinatal outcomes (APO) pose a significant global challenge, particularly in low- and middle-income countries (LMICs). This study aims to analyse two cohorts of high-risk pregnant women for APO to comprehend risk factors and improve prediction accuracy.

Methods: We considered an LMIC and a high-income country (HIC) population to derive XGBoost classifiers to predict low birth weight (LBW) from a comprehensive set of maternal and fetal characteristics including socio-demographic, past and current pregnancy information, fetal biometry and fetoplacental Doppler measurements. Data were sourced from the FeDoC (Fetal Doppler Collaborative) study (Pakistan, LMIC) and theIMPACT (Improving Mothers for a Better PrenAtal Care Trial) study (Spain, HIC), and included 520 and 746 pregnancies assessed from 28 weeks gestation, respectively. The models were trained on varying subsets of the mentioned characteristics to evaluate their contribution in predicting LBW cases. For external validation, and to highlight potential differential risk factors for LBW, we investigated the generalisation of these models across cohorts. Models' performance was evaluated through the area under the curve (AUC), and their interpretability was assessed using SHapley Additive exPlanations.

Results: In FeDoC, Doppler variables demonstrated the highest value at predicting LBW compared with biometry and maternal clinical data (AUCDoppler, 0.67; AUCClinical, 0.65; AUCBiometry, 0.63), and its combination with maternal clinical data yielded the best prediction (AUCClinical+Doppler, 0.71). In IMPACT, fetal biometry emerged as the most predictive set (AUCBiometry, 0.75; AUCDoppler, 0.70; AUCClinical, 0.69) and its combination with Doppler and maternal clinical data achieved the highest accuracy (AUCClinical+Biometry+Doppler, 0.81). External validation consistently indicated that biometry combined with Doppler data yielded the best prediction.

Conclusions: Our findings provide new insights into the predictive role of different clinical and ultrasound descriptors in two populations at high risk for APO, highlighting that different approaches are required for different populations. However, Doppler data improves prediction capabilities in both settings, underscoring the value of standardising ultrasound data acquisition, as practiced in HIC, to enhance LBW prediction in LMIC. This alignment contributes to bridging the health equity gap.

Keywords: Decision Making; Obstetrics; Other diagnostic or tool.

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Conflict of interest statement

Competing interests: None declared.

Figures

Figure 1
Figure 1. Diagram of the methodology followed in this work. AUROC, area under the receiver operating characteristic; FeDoC, Fetal Doppler Collaborative; FPR, false positive rate; IMPACT, Improving Mothers for a Better PrenAtal Care Trial; NPV, negative predictive value; PPV, positive predictive value; SGA, small for gestational age; SHAP, SHapley Additive exPlanations; US, ultrasound.
Figure 2
Figure 2. Accuracy metrics and feature interpretation of the models that achieved the best performance across iterations. The first row displays ROC curves for predictions done within (internal validation) and across (external validation) data sets for each feature set. Dotted vertical lines on each ROC plot represent a 10% false positive rate, and their intersection with each ROC curve indicates the true positive rates (sensitivity scores) reported in the figure. Below these, SHAP values corresponding to the model using the full feature set (Set 7) are reported. Variables are ranked top to bottom according to their impact on model output. Red or blue dots represent higher or lower values of inputs, respectively. AC, abdominal circumference; AUC, area under the curve; BP, blood pressure; BPD, biparietal diameter; CPR, cerebro-placental ratio; FeDoC, Fetal Doppler Collaborative; FL, femur length; GA_meas, gestational age at clinical data collection; GA_US, gestational age at ultrasound scan; HC, head circumference; IMPACT, Improving Mothers for a Better PrenAtal Care Trial; MCA PI, Middle Cerebral Artery Pulsatility Index; ROC, receiver operating characteristic; SHAP, SHapley Additive exPlanations; Sn, sensitivity; UA PI, Umbilical Artery Pulsatility Index.

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