Evidence map›Paper›PMID 30358080›Full record

ArticleBJOG : an international journal of obstetrics and gynaecology2019

External validation and clinical usefulness of first-trimester prediction models for small- and large-for-gestational-age infants: a prospective cohort study.

Lje Meertens, Ljm Smits, Smj van Kuijk, R Aardenburg, Ima van Dooren, J Langenveld, I M Zwaan, Mea Spaanderman, Hcj Scheepers

Abstract readValidation Study
In one paragraph

Article in BJOG : an international journal of obstetrics and gynaecology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  4. External validation and comparison of Fetal Medicine Foundation competing-risks model for small-for-gestational-age neonate in the first trimester: multicenter cohort study.Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology · 2025
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  5. Observational
  6. Observational
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Lje MeertensDepartment of Epidemiology, Care and Public Health Research Institute (CAPHRI), Maastricht University, Maastricht, the Netherlands.
Ljm SmitsDepartment of Epidemiology, Care and Public Health Research Institute (CAPHRI), Maastricht University, Maastricht, the Netherlands.
Smj van KuijkDepartment of Clinical Epidemiology and Medical Technology Assessment (KEMTA), Maastricht University Medical Centre, Maastricht, the Netherlands.
R AardenburgDepartment of Obstetrics and Gynaecology, Zuyderland Medical Centre, Heerlen, the Netherlands.
Ima van DoorenDepartment of Obstetrics and Gynaecology, Sint Jans Gasthuis Weert, Weert, the Netherlands.
J LangenveldDepartment of Obstetrics and Gynaecology, Zuyderland Medical Centre, Heerlen, the Netherlands.
I M ZwaanDepartment of Obstetrics and Gynaecology, Laurentius Hospital, Roermond, the Netherlands.
Mea SpaandermanDepartment of Obstetrics and Gynaecology, School for Oncology and Developmental Biology (GROW), Maastricht University Medical Centre, Maastricht, the Netherlands.
Hcj ScheepersDepartment of Obstetrics and Gynaecology, School for Oncology and Developmental Biology (GROW), Maastricht University Medical Centre, Maastricht, the Netherlands.

Funding

The Netherlands Organization for Health Research and Development, Pregnancy and Childbirth program 209020007
6 · The paper itself

Abstract

objectiveTo assess the external validity of all published first-trimester prediction models based on routinely collected maternal predictors for the risk of small- and large-for-gestational-age (SGA and LGA) infants. Furthermore, the clinical potential of the best-performing models was evaluated.

designMulticentre prospective cohort.

settingThirty-six midwifery practices and six hospitals (in the Netherlands). POPULATION: Pregnant women were recruited at <16 weeks of gestation between 1 July 2013 and 31 December 2015.

methodsPrediction models were systematically selected from the literature. Information on predictors was obtained by a web-based questionnaire. Birthweight centiles were corrected for gestational age, parity, fetal sex, and ethnicity.

main outcome measuresPredictive performance was assessed by means of discrimination (C-statistic) and calibration.

resultsThe validation cohort consisted of 2582 pregnant women. The outcomes of SGA <10th percentile and LGA >90th percentile occurred in 203 and 224 women, respectively. The C-statistics of the included models ranged from 0.52 to 0.64 for SGA (n = 6), and from 0.60 to 0.69 for LGA (n = 6). All models yielded higher C-statistics for more severe cases of SGA (<5th percentile) and LGA (>95th percentile). Initial calibration showed poor-to-moderate agreement between the predicted probabilities and the observed outcomes, but this improved substantially after recalibration.

conclusionThe clinical relevance of the models is limited because of their moderate predictive performance, and because the definitions of SGA and LGA do not exclude constitutionally small or large infants. As most clinically relevant fetal growth deviations are related to 'vascular' or 'metabolic' factors, models predicting hypertensive disorders and gestational diabetes are likely to be more specific. TWEETABLE ABSTRACT: The clinical relevance of prediction models for the risk of small- and large-for-gestational-age is limited.

Indexed as

Infant, Small for Gestational AgeAdultCohort StudiesFemaleFetal MacrosomiaHumansInfant, NewbornModels, StatisticalNetherlandsPregnancyPregnancy Trimester, FirstProspective StudiesReproducibility of ResultsDecision curve analysisexternsal validationfetal growthfirst trimesterlarge for gestational agepredictionrisk assessmentsmall for gestational age

Identifiers

PMID30358080
PMCPMC6590121

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.