Evidence map›Paper›PMID 35990006›Full record

ArticleFrontiers in pediatrics2022

Nutritional status at age 1 year in patients born with esophageal atresia: A population-based, prospective cohort study.

Suzanne Depoortere, Alexandre Lapillonne, Rony Sfeir, Arnaud Bonnard, Thomas Gelas, Nicoleta Panait, Pierre-Yves Rabattu, Audrey Guignot, Thierry Lamireau, Sabine Irtan and 31 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pediatrics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Observational
  2. Article
  3. 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

41 authors at 20 institutions in 3 countries.

Suzanne DepoortereUniv. Lille, CRACMO Reference Center for Rare Esophageal Diseases, CHU Lille, INFINITE U1286, Lille, France.
Alexandre LapillonneUniversity Hospital APHP Necker-Enfants Malades, Paris, France.
Rony SfeirUniv. Lille, CRACMO Reference Center for Rare Esophageal Diseases, CHU Lille, INFINITE U1286, Lille, France.
Arnaud BonnardUniversity Hospital APHP Robert Debré, Paris, France.
Thomas GelasUniversity Hospital of Lyon, Lyon, France.
Nicoleta PanaitUniversity Hospital of Marseille, Marseille, France.
Pierre-Yves RabattuUniversity Hospital of Grenoble Alpes, Grenoble, France.
Audrey GuignotUniversity Hospital of Nantes, Nantes, France.
Thierry LamireauUniversity Hospital of Bordeaux, Bordeaux, France.
Sabine IrtanUniversity Hospital APHP Armand Trousseau, Paris, France.
Edouard HabonimanaUniversity Hospital of Rennes, Rennes, France.
Anne BretonUniversity Hospital of Toulouse, Toulouse, France.
Virginie FouquetUniversity Hospital APHP Kremlin Bicêtre, Paris, France.
Hossein AllalUniversity Hospital of Montpellier, Montpellier, France.
Frédéric ElbazUniversity Hospital of Rouen, Rouen, France.
Isabelle TalonUniversity Hospital of Strasbourg, Strasbourg, France.
Aline RankeUniversity Hospital of Nancy, Nancy, France.
Michel AbelyUniversity Hospital of Reims, Reims, Champagne-Ardenne, France.
Jean-Luc MichelUniversity Hospital of La Réunion, Saint Denis de la Réunion, France.
Joséphine Lirussi BorgnonUniversity Hospital of Dijon, Dijon, France.
Philippe BuissonUniversity Hospital of Amiens, Amiens, France.
Françoise SchmittUniversity Hospital of Angers, Angers, France.
Hubert LardyUniversity Hospital of Tours, Tours, France.
Thierry PetitUniversity Hospital of Caen, Caen, France.
Yann ChaussyUniversity Hospital of Besançon, Besançon, France.
Corinne BorderonUniversity Hospital of Clermont-Ferrand, Clermont-Ferrand, France.
Guillaume LevardUniversity Hospital of Poitiers, Poitiers, France.
Clara CremillieuxUniversity Hospital of Saint-Etienne, Saint-Etienne, France.
Cécilia TolgUniversity Hospital of Fort De France, Martinique, Fort de France, France.
Jean BreaudUniversity Hospital of Nice, Nice, France.
Olivier JabyUniversity Hospital of Créteil, Créteil, France.
Céline GrossosUniversity Hospital of Limoges, Limoges, France.
Philine De VriesUniversity Hospital of Brest, Brest, France.
Myriam ArnouldGeneral Hospital of Orléans, Orléans, France.
Cécile PelatanGeneral Hospital of Le Mans, Le Mans, France.
Stephan GeissGeneral Hospital of Colmar, Colmar, France.
Christophe LaplaceUniversity Hospital of Point à Pitre, Guadeloupe, Point à Pitre, France.
Maéva KyhengCHU Lille-Department of Biostatistics, Lille, France.
Audrey NicolasUniv. Lille, CRACMO Reference Center for Rare Esophageal Diseases, CHU Lille, INFINITE U1286, Lille, France.
Madeleine AumarUniv. Lille, CRACMO Reference Center for Rare Esophageal Diseases, CHU Lille, INFINITE U1286, Lille, France.
Frédéric GottrandUniv. Lille, CRACMO Reference Center for Rare Esophageal Diseases, CHU Lille, INFINITE U1286, Lille, France.
Université de Lille · FRAssistance Publique – Hôpitaux de Paris · FRAssistance Publique Hôpitaux de Marseille · FRCentre Hospitalier du Mans · FRCentre Hospitalier Régional et Universitaire de Nancy · FRCentre Hospitalier Régional Universitaire de Brest · FRCentre Hospitalier Universitaire Amiens-Picardie · FRCentre Hospitalier Universitaire d'Angers · FRCentre Hospitalier Universitaire de Besançon · FRCentre Hospitalier Universitaire de Caen Normandie · FRCentre Hospitalier Universitaire de Clermont-Ferrand · FRCentre Hospitalier Universitaire de Grenoble · FRCentre Hospitalier Universitaire de La Réunion · FRCentre Hospitalier Universitaire de Lille · FRCentre Hospitalier Universitaire de Martinique · MQCentre Hospitalier Universitaire de Montpellier · FRCentre Hospitalier Universitaire de Nantes · FRCentre Hospitalier Universitaire de Nice · FRCentre Hospitalier Universitaire de Reims · FRCentre Hospitalier Universitaire de Rennes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Despite recent progress in caring for patients born with esophageal atresia (EA), undernutrition and stunting remain common. Our study objective was to assess nutritional status in the first year after birth with EA and to identify factors associated with growth failure. Study design: We conducted a population-based study of all infants born in France with EA between 2010 and 2016. Through the national EA register, we collected prenatal to 1 year follow-up data. We used body mass index and length-for-age ratio Z scores to define patients who were undernourished and stunted, respectively. Factors with Results: Among 1,154 patients born with EA, body mass index and length-for-age ratio Z scores at 1 year were available for about 61%. Among these, 15.2% were undernourished and 19% were stunted at the age of 1 year. There was no significant catch-up between ages 6 months and 1 year. Patients born preterm (41%), small for gestational age (17%), or with associated abnormalities (55%) were at higher risk of undernutrition and stunting at age 1 year ( Conclusion: Undernutrition and stunting are common during the first year after birth in patients born with EA. These outcomes are significantly influenced by early factors, regardless of EA type or surgical management. Identifying high-risk patient groups with EA (i.e., those born preterm, small for gestational age, and/or with associated abnormalities) may guide early nutritional support strategies.

Indexed as

catch-upgrowthprematuritysmall for gestational agestuntingsyndromicundernutrition

Identifiers

PMID35990006
PMCPMC9387303
OpenAlexW4289835509

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.