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Risk Factors for hospital admission and length of stay for children with and without congenital anomalies: A EUROlinkCAT cohort study

  • Joanne Given
  • , Ester Garne
  • , Joan K. Morris
  • , Silvia Baldacci
  • , Elisa Ballardini,
  • , Mika Gissler
  • , Francesca Gorini
  • , Sonja Kiuru-Kuhlefelt
  • , Stine Kjaer Urhoj
  • , Marco Manfrini
  • , Joachim Tan
  • , Maria Loane

Research output: Contribution to journalArticlepeer-review

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Abstract

Objective To evaluate risk factors for hospital admission and length of stay (LOS) among children with and without congenital anomalies (CAs).

Design A population-based linkage cohort study including 50 353 children with major CAs and 1 259 925 children without CAs from four EUROCAT registry areas in three countries. Data on children born 1995–2014 were linked to hospital discharge databases 1995–2015. HRs and incidence rate ratios estimated risk of admission and LOS for children aged <1 and 1–4 years by birth cohort, gestational age, sex, maternal age, multiple births and maternal education. Estimates were pooled using random effects meta-analysis.

Results In children <1 year, twins/triplets with CAs were 34% more likely to be admitted and had over two times the LOS compared with singletons, while twins/triplets without CAs were over two and a half times as likely to be admitted and had six times longer stays. Despite this, a higher proportion of twins/triplets with CAs were admitted compared to those without CAs (91% vs 65%) and had longer LOS (20 days vs 10). Smaller increases in risk of admission or LOS were found in boys, young mothers and low maternal education. Preterm birth was a major risk factor for admission and LOS.

Conclusions While the impact of risk factors on hospital admission and LOS was generally greater in children without CAs, a higher proportion of children with CAs were admitted and had longer stays. These findings have implications for health care planning and for counselling parents regarding their child's future healthcare needs.


Original languageEnglish
Article numbere003586
Pages (from-to)1-11
Number of pages11
JournalBMJ Paediatrics Open
Volume9
Issue number1
Early online date14 Aug 2025
DOIs
Publication statusPublished (in print/issue) - 14 Aug 2025

Bibliographical note

Publisher Copyright:
© Author(s) (or their employer(s)) 2025. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ Group.

Data Availability Statement

The data that support the findings of this study are available, but restrictions apply to the availability of these data, which were used under license for the current study and so are not publicly available. Data are, however, available from the authors after the permission of the participating registries of congenital anomalies.

Funding

This work was supported by the European Union\u2019s Horizon 2020 Research and Innovation programme under grant agreement number 733001, from 1 January 2017 to 31 May 2022. The views presented here are those of the authors only, and the European Commission is not responsible for any use that may be made of the information presented here.

Funder number
733001

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Keywords

    • Cohort Studies
    • Congenital Anomalies
    • Registries
    • Risk factors
    • length of stay
    • Episode of care
    • Data Collection
    • Child Health
    • Epidemiology
    • Health services research
    • Information Technology

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