Evidence map›Paper›PMID 32354021›Full record

SynthesisInternational journal of environmental research and public health2020

Children Born with Congenital Heart Defects and Growth Restriction at Birth: A Systematic Review and Meta-Analysis.

Ali Ghanchi, Neil Derridj, Damien Bonnet, Nathalie Bertille, Laurent J Salomon, Babak Khoshnood

Open access · goldAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in International journal of environmental research and public health, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Birthweight and isolated congenital heart defects - A systematic review and meta-analysis.BJOG : an international journal of obstetrics and gynaecology · 2022
    Pooled it
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  8. Impact of isolated fetal congenital heart disease on pregnancy and perinatal outcomes.International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics · 2025
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  18. Population-Based Birth Cohort Studies in Epidemiology.International journal of environmental research and public health · 2020
    Article
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

6 authors at 2 institutions in 1 country.

Ali GhanchiUniversité de Paris, CRESS, INSERM, INRA, F-75004 Paris, France.ORCID 0000-0002-6082-2140
Neil DerridjUniversité de Paris, CRESS, INSERM, INRA, F-75004 Paris, France.
Damien BonnetDepartment of Pediatric Cardiology, M3C-Necker, APHP, Hôpital Necker-Enfants Malades, F-75015 Paris, France.
Nathalie BertilleUniversité de Paris, CRESS, INSERM, INRA, F-75004 Paris, France.
Laurent J SalomonService d'Obstétrique-Maternité, chirurgie médecine et imagerie fœtales, APHP, Hôpital Necker Enfants Malades, F-75015 Paris, France.
Babak KhoshnoodUniversité de Paris, CRESS, INSERM, INRA, F-75004 Paris, France.
Hôpital Necker-Enfants Malades · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Newborns with congenital heart defects tend to have a higher risk of growth restriction, which can be an independent risk factor for adverse outcomes. To date, a systematic review of the relation between congenital heart defects (CHD) and growth restriction at birth, most commonly estimated by its imperfect proxy small for gestational age (SGA), has not been conducted.

objectiveTo conduct a systematic review and meta-analysis to estimate the proportion of children born with CHD that are small for gestational age (SGA).

methodsThe search was carried out from inception until 31 March 2019 on Pubmed and Embase databases. Studies were screened and selected by two independent reviewers who used a predetermined data extraction form to obtain data from studies. Bias was assessed using the Critical Appraisal Skills Programme (CASP) checklist. The database search identified 1783 potentially relevant publications, of which 38 studies were found to be relevant to the study question. A total of 18 studies contained sufficient data for a meta-analysis, which was done using a random effects model.

resultsThe pooled proportion of SGA in all CHD was 20% (95% CI 16%-24%) and 14% (95% CI 13%-16%) for isolated CHD. Proportion of SGA varied across different CHD ranging from 30% (95% CI 24%-37%) for Tetralogy of Fallot to 12% (95% CI 7%-18%) for isolated atrial septal defect. The majority of studies included in the meta-analysis were population-based studies published after 2010.

conclusionThe overall proportion of SGA in all CHD was 2-fold higher whereas for isolated CHD, 1.4-fold higher than the expected proportion in the general population. Although few studies have looked at SGA for different subtypes of CHD, the observed variability of SGA by subtypes suggests that growth restriction at birth in CHD may be due to different pathophysiological mechanisms.

Indexed as

Fetal Growth RetardationHeart Defects, CongenitalInfant, Small for Gestational AgeParturitionFemaleHumansInfant, NewbornPregnancyRisk Factorscongenital heart defectsmeta-analysispopulation-based studysmall for gestational agesystematic review

Identifiers

PMID32354021
PMCPMC7246925
OpenAlexW3022581882

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.