Evidence map›Paper›PMID 35727800›Full record

Trial reportPLoS medicine2022

Evaluation of the Growth Assessment Protocol (GAP) for antenatal detection of small for gestational age: The DESiGN cluster randomised trial.

Matias C Vieira, Sophie Relph, Walter Muruet-Gutierrez, Maria Elstad, Bolaji Coker, Natalie Moitt, Louisa Delaney, Chivon Winsloe, Andrew Healey, Kirstie Coxon and 16 more

Open access · goldAbstract readPragmatic Clinical TrialRandomized Controlled TrialEquivalence Trial
In one paragraph

Trial report in PLoS medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 5% of its field
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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Perinatal outcomes after selective third-trimester ultrasound screening for small-for-gestational age: prospective cohort study nested within DESiGN randomized controlled trial.Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology · 2025
    Trial
  3. Trial
  4. Characteristics associated with antenatally unidentified small-for-gestational-age fetuses: prospective cohort study nested within DESiGN randomized controlled trial.Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology · 2023
    Trial
  5. Trial
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Improving antenatal detection of small-for-gestational-age fetus: economic evaluation of Growth Assessment Protocol.Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology · 2022
    Article
  14. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

26 authors at 10 institutions in 4 countries.

Matias C VieiraDepartment of Women and Children's Health, King's College London, London, United Kingdom.ORCID 0000-0002-8076-4275
Sophie RelphDepartment of Women and Children's Health, King's College London, London, United Kingdom.ORCID 0000-0002-2007-9647
Walter Muruet-GutierrezDepartment of Women and Children's Health, King's College London, London, United Kingdom.ORCID 0000-0003-0610-3505
Maria ElstadSchool of Population Health and Environmental Sciences, King's College London, London, United Kingdom.ORCID 0000-0002-7882-7564
Bolaji CokerSchool of Population Health and Environmental Sciences, King's College London, London, United Kingdom.
Natalie MoittDepartment of Women and Children's Health, King's College London, London, United Kingdom.ORCID 0000-0002-0875-9850
Louisa DelaneyDepartment of Women and Children's Health, King's College London, London, United Kingdom.ORCID 0000-0002-2749-7665
Chivon WinsloeDepartment of Women and Children's Health, King's College London, London, United Kingdom.ORCID 0000-0002-9860-4173
Andrew HealeyCentre for Implementation Science and King's Health Economics, King's College London, London, United Kingdom.ORCID 0000-0003-2013-3161
Kirstie CoxonFaculty of Health, Social Care and Education, Kingston University and St. George's, University of London, London, United Kingdom.ORCID 0000-0001-5480-597X
Alessandro AlagnaLondon Perinatal Morbidity and Mortality Working Group (NHS), London, United Kingdom.
Annette BrileyDepartment of Women and Children's Health, King's College London, London, United Kingdom.ORCID 0000-0002-4266-920X
Mark JohnsonDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, United Kingdom.
Louise M PageWest Middlesex University Hospital, Chelsea & Westminster Hospital NHS Foundation Trust, Isleworth, United Kingdom.ORCID 0000-0001-5568-7135
Donald PeeblesUCL Institute for Women's Health, University College London, London, United Kingdom.
Andrew ShennanDepartment of Women and Children's Health, King's College London, London, United Kingdom.ORCID 0000-0001-5273-3132
Baskaran ThilaganathanFetal Medicine Unit, St George's University Hospitals NHS Foundation Trust, London, United Kingdom.ORCID 0000-0002-5531-4301
Neil MarlowUCL Institute for Women's Health, University College London, London, United Kingdom.ORCID 0000-0001-5890-2953
Lesley McCowanFaculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.ORCID 0000-0001-9915-7873
Christoph LeesDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, United Kingdom.
Deborah A LawlorBristol NIHR Biomedical Research Centre, Bristol, United Kingdom.ORCID 0000-0002-6793-2262
Asma KhalilFetal Medicine Unit, St George's University Hospitals NHS Foundation Trust, London, United Kingdom.ORCID 0000-0003-2802-7670
Jane SandallDepartment of Women and Children's Health, King's College London, London, United Kingdom.ORCID 0000-0003-2000-743X
Andrew CopasCentre for Pragmatic Global Health Trials, University College London, London, United Kingdom.ORCID 0000-0001-8968-5963
Dharmintra PasupathyDepartment of Women and Children's Health, King's College London, London, United Kingdom.ORCID 0000-0002-6722-1006
DESiGN Collaborative Group
King's College London · GBSt George's, University of London · GBUniversity College London · GBImperial College London · GBChelsea and Westminster Hospital NHS Foundation Trust · GBFlinders University · AUThe University of Sydney · AUUniversidade Estadual de Campinas (UNICAMP) · BRUniversity of Auckland · NZUniversity of Bristol · GB

Funding

Department of Health NF-0616-10102
6 · The paper itself

Abstract

backgroundAntenatal detection and management of small for gestational age (SGA) is a strategy to reduce stillbirth. Large observational studies provide conflicting results on the effect of the Growth Assessment Protocol (GAP) in relation to detection of SGA and reduction of stillbirth; to the best of our knowledge, there are no reported randomised control trials. Our aim was to determine if GAP improves antenatal detection of SGA compared to standard care. METHODS AND

findingsThis was a pragmatic, superiority, 2-arm, parallel group, open, cluster randomised control trial. Maternity units in England were eligible to participate in the study, except if they had already implemented GAP. All women who gave birth in participating clusters (maternity units) during the year prior to randomisation and during the trial (November 2016 to February 2019) were included. Multiple pregnancies, fetal abnormalities or births before 24+1 weeks were excluded. Clusters were randomised to immediate implementation of GAP, an antenatal care package aimed at improving detection of SGA as a means to reduce the rate of stillbirth, or to standard care. Randomisation by random permutation was stratified by time of study inclusion and cluster size. Data were obtained from hospital electronic records for 12 months prerandomisation, the washout period (interval between randomisation and data collection of outcomes), and the outcome period (last 6 months of the study). The primary outcome was ultrasound detection of SGA (estimated fetal weight <10th centile using customised centiles (intervention) or Hadlock centiles (standard care)) confirmed at birth (birthweight <10th centile by both customised and population centiles). Secondary outcomes were maternal and neonatal outcomes, including induction of labour, gestational age at delivery, mode of birth, neonatal morbidity, and stillbirth/perinatal mortality. A 2-stage cluster-summary statistical approach calculated the absolute difference (intervention minus standard care arm) adjusted using the prerandomisation estimate, maternal age, ethnicity, parity, and randomisation strata. Intervention arm clusters that made no attempt to implement GAP were excluded in modified intention to treat (mITT) analysis; full ITT was also reported. Process evaluation assessed implementation fidelity, reach, dose, acceptability, and feasibility. Seven clusters were randomised to GAP and 6 to standard care. Following exclusions, there were 11,096 births exposed to the intervention (5 clusters) and 13,810 exposed to standard care (6 clusters) during the outcome period (mITT analysis). Age, height, and weight were broadly similar between arms, but there were fewer women: of white ethnicity (56.2% versus 62.7%), and in the least deprived quintile of the Index of Multiple Deprivation (7.5% versus 16.5%) in the intervention arm during the outcome period. Antenatal detection of SGA was 25.9% in the intervention and 27.7% in the standard care arm (adjusted difference 2.2%, 95% confidence interval (CI) -6.4% to 10.7%; p = 0.62). Findings were consistent in full ITT analysis. Fidelity and dose of GAP implementation were variable, while a high proportion (88.7%) of women were reached. Use of routinely collected data is both a strength (cost-efficient) and a limitation (occurrence of missing data); the modest number of clusters limits our ability to study small effect sizes.

conclusionsIn this study, we observed no effect of GAP on antenatal detection of SGA compared to standard care. Given variable implementation observed, future studies should incorporate standardised implementation outcomes such as those reported here to determine generalisability of our findings.

trial registrationThis trial is registered with the ISRCTN registry, ISRCTN67698474.

Indexed as

Fetal Growth RetardationInfant, Small for Gestational AgePrenatal DiagnosisCluster AnalysisFemaleHumansInfant, NewbornPregnancyStillbirth

Identifiers

PMID35727800
PMCPMC9212153
OpenAlexW4283213546

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LicenceCC BY
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Registered trials

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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.