Evidence mapPaperPMID 42555545Full record

Observational studyPloS one2026

Mortality amongst European children with congenital anomalies: Associations with socio-economic status in the EUROLINKCAT cohort.

Sue Jordan, David Tucker, Ieuan Scanlon, Daniel S Thayer, Elisa Ballardini, Clara Cavero-Carbonell, Mads Damkjaer, Miriam Gatt, Mika Gissler, Lyubov Ostapchuk and 7 more

Abstract readObservational Study
In one paragraph

Observational study in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

17 authors.

Sue JordanFaculty of Medicine, Health and Life Sciences, Swansea University, Swansea, United Kingdom.ORCID https://orcid.org/0000-0002-5691-2987
David TuckerCongenital Anomaly Register & Information Service for Wales (CARIS), Public Health Knowledge and Research, Public Health Wales, Swansea, United Kingdom.
Ieuan ScanlonFaculty of Medicine, Health and Life Sciences, Swansea University, Swansea, United Kingdom.
Daniel S ThayerFaculty of Medicine, Health and Life Sciences, Swansea University, Swansea, United Kingdom.
Elisa BallardiniDepartment of Medical Sciences, Neonatal Intensive Care Unit, University Hospital of Ferrara, IMER Registry (Emilia Romagna Registry of Birth Defects), University of Ferrara, Ferrara, Italy.
Clara Cavero-CarbonellRare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.ORCID https://orcid.org/0000-0002-4858-6456
Mads DamkjaerDepartment of Paediatrics and Adolescent Medicine, Lillebaelt Hospital, University Hospital of Southern Denmark, Kolding, Denmark.ORCID https://orcid.org/0000-0001-7410-8573
Miriam GattMalta Congenital Anomalies Registry, Directorate for Health Information and Research, Pieta, Malta.
Mika GisslerDepartment of Data and Analytics, THL Finnish Institute for Health and Welfare, Helsinki, Finland; Region Stockholm, Academic Primary Health Care Centre, Stockholm, Sweden.
Lyubov OstapchukRivne Medical Diagnostic Center and OMNI-Net Ukraine, Rivne Oblast, Ukraine.
Michel SantoroUnit of Epidemiology of Rare Diseases and Congenital Anomalies, Institute of Clinical Physiology, National Research Council, Pisa, Italy.
Sarah StevensNational Disease Registration Service, NHS, London, England.
Diana WellesleyUniversity of Southampton and Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, United Kingdom.ORCID https://orcid.org/0000-0002-9463-3188
Wladimir WerteleckiRivne Medical Diagnostic Center and OMNI-Net Ukraine, Rivne Oblast, Ukraine.ORCID https://orcid.org/0000-0001-5864-5985
Joanne GivenInstitute of Nursing and Health Research, Ulster University, Belfast, United Kingdom.
Maria LoaneInstitute of Nursing and Health Research, Ulster University, Belfast, United Kingdom.ORCID https://orcid.org/0000-0002-1206-3637
Hywel T EvansFaculty of Medicine, Health and Life Sciences, Swansea University, Swansea, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChildhood mortality is affected by major congenital anomalies and socio-economic status (SES). To our knowledge, their combined impact has not been explored to age 10.

methodsWe analysed the population-based EUROlinkCAT cohort to ascertain the impact of SES on mortality by ages 1 and 10 amongst children with congenital anomalies in ten congenital anomaly registers in seven European countries. Four countries defined SES according to maternal education, and two used their national index of multiple deprivation. The ten registers used a common script to generate data on survival by ages 1 and 1-10 (365-3651 days). Eight registers analysed deaths according to their SES criteria, categorised as low, intermediate and high SES. Linked data were combined in random effects meta-analyses. Finland and Emilia-Romagna held data on single motherhood and EU-nationality.

resultsWe analysed mortality in relation to SES using data on 47,134 live-born children with major congenital anomalies classified and recorded 1996-2014. Mortality by age 1 and ages 1-10 was higher amongst the most than the least deprived, hazard ratios (HR) and 95% confidence intervals (CI) 1.47, 1.19-1.83 and 2.00, 1.32-3.02. Differences between intermediate and least deprived groups were smaller. Differences were statistically significant for all four analyses only in Ukraine and Wales. Mortality rates were higher for children of non-EU nationals, but not single mothers. IMPLICATIONS: Deprivation was more strongly associated with death at ages 1-10 than in infancy. These analyses of the most ill children in Europe indicate that, to achieve sustainable development goals, more resources are needed for the most vulnerable children.

Indexed as

Child MortalityCongenital AbnormalitiesSocial ClassChildChild, PreschoolCohort StudiesEuropeFemaleHumansInfantLow Socioeconomic StatusMaleRegistriesSocioeconomic Disparities in Health

Identifiers

PMID42555545
PMCPMC13440827

What Socratic holds

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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 Socratic graph.