Evidence map›Paper›PMID 36650449›Full record

ArticleBMC pediatrics2023

Sex-specific percentiles for bodyweight and height in children born with esophageal atresia: a registry-based analysis 2001-2021.

Tatjana Tamara König, Maria-Christina Stefanescu, Melanie Wildermuth, Luisa Maria Frankenbach, Oliver J Muensterer, Emilio Gianicolo

Open access · goldAbstract read
In one paragraph

Article in BMC pediatrics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

0 citing papers in PubMed, 5 citations in OpenAlex.

No citing paper in PubMed yet.

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 4 institutions in 2 countries.

Tatjana Tamara KönigDepartment of Pediatric Surgery, Universitätsmedizin, Johannes Gutenberg-University, 55131, Mainz, Germany. Tatjana.Koenig@unimedizin-mainz.de.
Maria-Christina StefanescuDepartment of Pediatric Surgery, Universitätsmedizin, Johannes Gutenberg-University, 55131, Mainz, Germany.
Melanie WildermuthKinder und Erwachsene mit kranker Speiseröhre, KEKS e.V., Stuttgart, Germany.
Luisa Maria FrankenbachDepartment of Pediatric Surgery, Universitätsmedizin, Johannes Gutenberg-University, 55131, Mainz, Germany.
Oliver J MuenstererDepartment of Pediatric Surgery, Dr. von Haunersches Kinderspital, Ludwig Maximilian-University Munich, Munich, Germany.
Emilio GianicoloInstitute of Medical Biostatistics, Epidemiology and Informatics (IMBEI), Universitätsmedizin, Johannes Gutenberg-University, Mainz, Germany.
Johannes Gutenberg University Mainz · DEInstitut für Krankenhaushygiene & Infektionsprävention · DELudwig-Maximilians-Universität München · DEUniversity Medical Center of the Johannes Gutenberg University Mainz · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEsophageal atresia (EA) is a rare malformation with a wide range of co-morbidity and associated malformations impairing weight gain and growth. The aim of this study was to calculate specific percentiles for body weight and height for children born with esophageal atresia according to sex from birth to the age of 6 years, accounting for prematurity and presence of congenital heart disease (CHD).

methodsData was extracted from an anonymized voluntary national registry for patients born with esophageal atresia between 2001 and 2021, from birth until the age of six years. Missing values were imputed using a multiple imputation approach. In premature infants, chronological age was corrected for gestational week until the age of one year. The impact of sex and additional congenital heart disease on weight gain and growth was analysed using quartile regression models.

resultsIn total, 1812 examinations of 485 patients were considered and 1232 examinations of 301 patients were finally included. Most data was available for children at birth and during the first year of life. Body weight was imputed for 3.3% and height for 12.5% of examinations. The mean body weight-for-age and length-for-age at birth according to gestational age was lower in EA patients and median body weight developed along the tenth percentile compared to the general population. Median height-for-age was at the 50th percentile during the first months of life, before crossing to lower percentiles before the age of one year. CHD had an additional negative impact on growth and weight gain, especially during the first year of life.

conclusionsChildren with EA had a reduced bodyweight and -height compared to the general population. Therefore, specific percentile curves are helpful to evaluate growth and development. Especially during the first year of life, particular attention is necessary and complications leading to a reduced calorie intake should be treated without delay to promote timely development and growth. Cardiac co-morbidities may further compromise weight gain in these patients, implying that such patients should be under even closer surveillance.

Indexed as

Esophageal AtresiaHeart Defects, CongenitalChildChild, PreschoolFemaleHumansInfantInfant, NewbornInfant, PrematureMaleRegistriesWeight GainBody weightEsophageal atresiaGrowthHeightPercentiles

Identifiers

PMID36650449
PMCPMC9847123
OpenAlexW4317000349

What OpenQuestion holds

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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.