Evidence map›Paper›PMID 38373775›Full record

ArticleArchives of disease in childhood2024

Hospital care in the first 10 years of life of children with congenital anomalies in six European countries: data from the EUROlinkCAT cohort linkage study.

Joan K Morris, Maria Loane, Charlotte Wahlich, Joachim Tan, Silvia Baldacci, Elisa Ballardini, Clara Cavero-Carbonell, Mads Damkjær, Laura García-Villodre, Mika Gissler and 12 more

Open access · hybridAbstract read
In one paragraph

Article in Archives of disease in childhood, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
5.2field-weighted citation impact, top 4% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. 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

22 authors at 12 institutions in 7 countries.

Joan K MorrisPopulation Health Research Institute, St George's, University of London, London, UK.ORCID 0000-0002-7164-612X
Maria LoaneCentre for Maternal, Fetal and Infant Research, INHR, Ulster University, Belfast, Northern Ireland, UK ma.loane@ulster.ac.uk.ORCID 0000-0002-1206-3637
Charlotte WahlichPopulation Health Research Institute, St George's, University of London, London, UK.
Joachim TanPopulation Health Research Institute, St George's, University of London, London, UK.
Silvia BaldacciUnit of Epidemiology of Rare Diseases and Congenital Anomalies, Institute of Clinical Physiology, National Research Council, Pisa, Italy.ORCID 0000-0002-7626-1202
Elisa BallardiniNeonatal Intensive Care Unit, Paediatric Section, IMER Registry (Emilia Romagna Registry of Birth Defects), Department of Medical Sciences, University of Ferrara, Ferrara, Emilia-Romagna, Italy.
Clara Cavero-CarbonellRare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region FISABIO, Valencia, Valencia, Spain.
Mads DamkjærDepartment of Paediatrics and Adolescent Medicine, Lillebaelt Hospital, University Hospital of Southern Denmark, Kolding, Denmark.
Laura García-VillodreRare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region FISABIO, Valencia, Valencia, Spain.
Mika GisslerDepartment of Knowledge Brokers, THL Finnish Institute for Health and Welfare, Helsinki, Finland.
Joanne GivenCentre for Maternal, Fetal and Infant Research, INHR, Ulster University, Belfast, Northern Ireland, UK.
Francesca GoriniUnit of Epidemiology of Rare Diseases and Congenital Anomalies, Institute of Clinical Physiology, National Research Council, Pisa, Italy.
Anna HeinoDepartment of Knowledge Brokers, THL Finnish Institute for Health and Welfare, Helsinki, Finland.
Elizabeth LimbPopulation Health Research Institute, St George's, University of London, London, UK.
Renee LutkeDepartment of Genetics, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.
Amanda NevilleEmilia Romagna Registry of Birth Defects and Center for Clinical and Epidemiological Research, University of Ferrara, Ferrara, Italy.
Anke RissmannMalformation Monitoring Centre Saxony-Anhalt, Medical Faculty, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany.ORCID 0000-0002-9437-2790
Leuan ScanlonFaculty of Health and Life Sciences, Swansea University, Swansea, UK.
David F TuckerFaculty of Health and Life Sciences, Swansea University, Swansea, UK.
Stine Kjaer UrhojDepartment of Paediatrics and Adolescent Medicine, Lillebaelt Hospital, University Hospital of Southern Denmark, Kolding, Denmark.ORCID 0000-0002-2069-9723
Hermien Ek de WalleDepartment of Genetics, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.
Ester GarneDepartment of Paediatrics and Adolescent Medicine, Lillebaelt Hospital, University Hospital of Southern Denmark, Kolding, Denmark.
St George's, University of London · GBFinnish Institute for Health and Welfare · FIFundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana · ESIstituto di Fisiologia Clinica · ITSwansea University · GBUniversity Medical Center Groningen · NLUniversity of Ferrara · ITUniversity of Ulster · GBLillebaelt Hospital · DKOtto-von-Guericke-Universität Magdeburg · DEUniversity of Copenhagen · DKUniversity of Southern Denmark · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo quantify the hospital care for children born with a major congenital anomaly up to 10 years of age compared with children without a congenital anomaly. DESIGN, SETTING AND PATIENTS: 79 591 children with congenital anomalies and 2 021 772 children without congenital anomalies born 1995-2014 in six European countries in seven regions covered by congenital anomaly registries were linked to inpatient electronic health records up to their 10th birthday.

main outcome measuresNumber of days in hospital and number of surgeries.

resultsDuring the first year of life among the seven regions, a median of 2.4% (IQR: 2.3, 3.2) of children with a congenital anomaly accounted for 18% (14, 24) of days in hospital and 63% (62, 76) of surgeries. Over the first 10 years of life, the percentages were 17% (15, 20) of days in hospital and 20% (19, 22) of surgeries. Children with congenital anomalies spent 8.8 (7.5, 9.9) times longer in hospital during their first year of life than children without anomalies (18 days compared with 2 days) and 5 (4.1-6.1) times longer aged, 5-9 (0.5 vs 0.1 days). In the first year of life, children with gastrointestinal anomalies spent 40 times longer and those with severe heart anomalies 20 times longer in hospital reducing to over 5 times longer when aged 5-9.

conclusionsChildren with a congenital anomaly consume a significant proportion of hospital care resources. Priority should be given to public health primary prevention measures to reduce the risk of congenital anomalies.

Indexed as

Congenital AbnormalitiesHeart Defects, CongenitalChildCohort StudiesEuropeFemaleHumansParturitionPregnancyRegistriesChild Health ServicesHealth services research

Identifiers

PMID38373775
PMCPMC11041558
OpenAlexW4391930349

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.