Evidence map›Paper›PMID 42501267›Full record

ArticleWorld journal of pediatrics : WJP2026

Heterogeneity of the prevalence of congenital hip dislocation in Europe.

Ester Garne, Anke Rissmann, Carlos Matias Dias, Carlotta Buzzoni, Catherine Lynch, Christine Dumoulin, Clara Cavero-Carbonell, David Tucker, Dieuwke Broekstra, Elisa Ballardini and 16 more

Abstract readLetter
PubMed Publisher
In one paragraph

Article in World journal of pediatrics : WJP, 2026. 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
–field-weighted citation impact
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.

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

26 authors.

Ester GarneDepartment of Paediatrics and Adolescent Medicine, Lillebaelt Hospital, University Hospital of Southern Denmark, Kolding, Denmark. Ester.garne@rsyd.dk.
Anke RissmannMedical Faculty, Malformation Monitoring Centre Saxony-Anhalt, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany.
Carlos Matias DiasDepartment of Epidemiology, National Institute of Health, Ministry of Health, Lisbon, Portugal.
Carlotta BuzzoniEpidemiology Unit, Agency for Health Protection of Milan, Via Conca del Naviglio, Milan, Italy.
Catherine LynchDepartment of Public Health Dublin & Southeast, Dublin, Ireland.
Christine DumoulinEUROCAT Hainaut -Namur, Institut de Pathologie Et de Génétique, Charleroi, Belgium.
Clara Cavero-CarbonellRare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.
David TuckerResearch, Data & Digital Directorate, Public Health Wales, Swansea, UK.
Dieuwke BroekstraDepartment of Genetics, University of Groningen, University Medical Center Groningen, EUROCAT Registration Northern Netherlands, Groningen, The Netherlands.
Elisa BallardiniNeonatal Intensive Care Unit, Department of Medical Sciences, University Hospital of Ferrara, IMER Registry (Emilia Romagna Registry of Birth Defects), University of Ferrara, Ferrara, Italy.
Elly Den HondEUROCAT Antwerp, Provincial Institute of Hygiene, Antwerp, Belgium.
Florence RougetBrittany Registry of Congenital Anomalies, CHU Rennes, Univ Rennes, Inserm, EHESP, Irset (Institut de Recherche en Santé, Environnement Et Travail), Rennes, France.
Francisco Rodriguez-RaseroJoint Research Centre, European Commission, Ispra, Italy.
Ianis CousinMaison de La Femme de La Mère Et de L'enfant, CHU de Martinique, La Meynard, France.
Isabelle MonierCenter for Research in Epidemiology and Statistics (CRESS), Université Paris Cité, Obstetric, Perinatal, Paediatric Life Course Epidemiology (OPPaLE) Research Team, INSERM, Paris, France.
Joan MorrisSchool of Health and Medical Sciences, City St George's, University of London, London, UK.
Joanna SichitiuDepartment Woman-Mother-Child, Ultrasound and Fetal Medicine Unit, Lausanne University Hospital, Lausanne, Switzerland.
Kari KlungsøyrDepartment of Global Public Health and Primary Care, University of Bergen and Department of Health Promotion, Norwegian Institute of Public Health, Bergen, Norway.
Ljubica OdakDepartment of Medical and Laboratory Genetics, Endocrinology and Diabetology With Daily Care Unit, Scientific Centre of Excellence for Reproductive and Regenerative Medicine (CERRM), University of Zagreb School of Medicine and Referral Center of the Ministry of Health for Surveillance of Congenital Anomalies, Children's Hospital Zagreb, Zagreb, Croatia.
Marilena CeresolaRegistro Malformazioni Congenite, SC Osservatorio Epidemiologico, ATS Val Padana, Mantua, Italy.
Mary O'MahonyDepartment of Public Health, Public Health Area D, St. Finbarr's Hospital, Cork, Ireland.
Michele SantoroUnit of Epidemiology of Rare Diseases and Congenital Anomalies, Institute of Clinical Physiology, National Research Council, Pisa, Italy.
Nataliia Zymak-ZakutniaOMNI-Net Ukraine and Khmelnytskyi City Children's Hospital, Khmelnytskyi, Ukraine.
Rachel WoodPublic Health Scotland and Usher Institute, University of Edinburgh, Edinburgh, UK.
Riccardo PertileDepartment of Clinical and Evaluative Epidemiology, Healthcare Trust of the Autonomous Province of Trento, APSS, Trento, Italy.
Sarah StevensNHS Health Education England, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID42501267

What OpenQuestion holds

Textmetadata
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.