A Composite Risk Scoring Model for Predicting Adverse Perinatal Outcomes in Patients with Pre-Eclampsia- A Pilot Study

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Meenakshi Gothwal
Adhibha Babu
Pratibha Singh
Garima Yadav
Swati Asati
Anubhav Gupta

Keywords

Red Cell Alloimmunization, Pregnancy, Risk Prediction Model, Antenatal Screening, TRIPOD, Clinical Utility

Abstract

Background: Accurate early identification of pregnancies at high risk for adverse fetal outcomes (small-for-gestational-age [SGA], preterm birth, stillbirth) enables targeted interventions. The study aims to pilot the development and internal validation of a point-based Fetal Risk Score (rFRS₅) incorporating ten routine maternal parameters, and to compare its performance against a simpler four-item score (FRS red).


Methodology: In this single-centre, retrospective cohort study of 118 pregnant women, we assigned points based on clinically meaningful ranges for age, parity, BMI, blood pressure, 24-hour proteinuria, haemoglobin, platelets, ALT, AST, and LDH. We computed rFRS₅ (0–19 points) and FRS_red (0–6 points). Discrimination was assessed using the ROC AUC (5-fold cross-validation), and calibration was evaluated using the Brier score and calibration curves. Optimal thresholds were determined by sensitivity/specificity trade-offs. Variables for score development were selected a priori based on clinical relevance and published evidence. Internal validation was performed using five-fold cross-validation and calibration methods.


Results: rFRS₅ achieved ROC AUC 0.80 and Brier score 0.219; FRS red achieved ROC AUC 0.82 and Brier score 0.220. For rule-out (sensitivity 100 %), rFRS₅ < 2 and FRS red < 2 both provided NPV 100 %. For rule-in, FRS red ≥ 6 yielded specificity 94 % and PPV 50 %, outperforming rFRS₅ (specificity 68 %, PPV 40 %).


Conclusion: In this pilot study, both scores effectively stratify fetal risk, with the simpler FRS red offering superior rule-in performance in resource-limited settings. Larger, prospective studies are warranted to confirm these findings.

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