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

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  • Joan K Morris
  • Maria Loane
  • Charlotte Wahlich
  • Joachim Tan
  • Silvia Baldacci
  • Elisa Ballardini
  • Clara Cavero-Carbonell
  • Mads Damkjær
  • Laura García-Villodre
  • Mika Gissler
  • Joanne Given
  • Francesca Gorini
  • Anna Heino
  • Elizabeth Limb
  • Renee Lutke
  • Amanda Neville
  • Anke Rissmann
  • Leuan Scanlon
  • David F Tucker
  • Hermien Ek de Walle
  • Ester Garne

OBJECTIVE: To 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 MEASURES: Number of days in hospital and number of surgeries.

RESULTS: During 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.

CONCLUSIONS: Children 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.

OriginalsprogEngelsk
TidsskriftArchives of Disease in Childhood
Vol/bind109
Udgave nummer5
Antal sider7
ISSN1359-2998
DOI
StatusUdgivet - 2024

Bibliografisk note

© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

ID: 383562091