Evidence map›Paper›PMID 28473972›Full record

ArticleFrontiers in pediatrics2017

Importance of an International Registry for and Collaborative Research on Esophageal Atresia.

Frédéric Gottrand, Delphine Ley, Laurent Michaud, Rony Sfeir

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pediatrics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

4 authors at 2 institutions in 1 country.

Frédéric GottrandReference Center for Congenital and Malformative Esophageal Disorders, CHU Lille, Univ. Lille2, Lille, France.
Delphine LeyReference Center for Congenital and Malformative Esophageal Disorders, CHU Lille, Univ. Lille2, Lille, France.
Laurent MichaudReference Center for Congenital and Malformative Esophageal Disorders, CHU Lille, Univ. Lille2, Lille, France.
Rony SfeirReference Center for Congenital and Malformative Esophageal Disorders, CHU Lille, Univ. Lille2, Lille, France.
Université de Lille · FRCentre Hospitalier Universitaire de Lille · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Esophageal atresia (EA) is a rare congenital defect. Data on EA prevalence, management, and long-term outcome are lacking because the available data come from small retrospective series from tertiary referral centers. An international multicenter registry would provide strong epidemiological data from large population-based cohorts on EA prevalence and incidence, treatment, long-term morbidity, and prognosis and would thus provide accurate data for evaluation of the current guidelines for EA management. The future challenge of the new international network on EA, which was created in 2013, is to promote the creation of a collaborative database and further studies.

Indexed as

collaborative researchcongenital defectesophageal atresiainternational registrypopulation-based cohort

Identifiers

PMID28473972
PMCPMC5397510
OpenAlexW2607828750

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.