External validation and clinical usefulness of first-trimester prediction models for small- and

Lje Meertens1, Ljm Smits1, Smj van Kuijk2

  • 1Department of Epidemiology, Care and Public Health Research Institute (CAPHRI), Maastricht University, Maastricht, the Netherlands.

Insights

First-trimester prediction models for small- and large-for-gestational-age infants show limited clinical relevance due to moderate predictive performance. Models predicting hypertensive disorders and gestational diabetes may offer greater specificity for fetal growth deviations.

Area of Science:

  • Obstetrics and Gynecology
  • Perinatal Medicine
  • Reproductive Health

Background:

  • Accurate prediction of fetal growth deviations, specifically small-for-gestational-age (SGA) and large-for-gestational-age (LGA) infants, is crucial for optimizing perinatal outcomes.
  • Existing first-trimester prediction models utilizing routinely collected maternal data aim to identify pregnancies at risk for SGA and LGA.

Purpose of the Study:

  • To evaluate the external validity of published first-trimester prediction models for SGA and LGA infant risk.
  • To assess the clinical utility of the best-performing models in a real-world setting.

Main Methods:

  • A multicentre prospective cohort study was conducted in 36 midwifery practices and 6 hospitals in the Netherlands.
  • Prediction models were systematically identified from existing literature, with predictor data collected via web-based questionnaires.
  • Predictive performance was evaluated using discrimination (C-statistic) and calibration, with birthweight centiles adjusted for gestational age, parity, fetal sex, and ethnicity.

Main Results:

  • The validation cohort included 2582 pregnant women, with SGA (<10th percentile) and LGA (>90th percentile) observed in 203 and 224 cases, respectively.
  • The C-statistics for SGA ranged from 0.52 to 0.64, and for LGA from 0.60 to 0.69, with improved performance for more extreme definitions (<5th percentile SGA, >95th percentile LGA).
  • Initial calibration showed poor-to-moderate agreement, which significantly improved after recalibration.

Conclusions:

  • The current prediction models for SGA and LGA infants demonstrate limited clinical relevance due to their moderate predictive accuracy.
  • The definitions of SGA and LGA do not adequately account for constitutional variations in infant size.
  • Prediction models focusing on vascular or metabolic factors, such as those for hypertensive disorders and gestational diabetes, are likely to provide more specific identification of clinically relevant fetal growth abnormalities.
Abstract

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