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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.
Morris, Joan K; Loane, Maria; Wahlich, Charlotte; Tan, Joachim; Baldacci, Silvia; Ballardini, Elisa; Cavero-Carbonell, Clara; Damkjær, Mads; García-Villodre, Laura; Gissler, Mika; Given, Joanne; Gorini, Francesca; Heino, Anna; Limb, Elizabeth; Lutke, Renee; Neville, Amanda; Rissmann, Anke; Scanlon, Leuan; Tucker, David F; Urhoj, Stine Kjaer; de Walle, Hermien Ek; Garne, Ester.
Afiliación
  • Morris JK; Population Health Research Institute, St George's, University of London, London, UK.
  • Loane M; Centre for Maternal, Fetal and Infant Research, INHR, Ulster University, Belfast, Northern Ireland, UK ma.loane@ulster.ac.uk.
  • Wahlich C; Population Health Research Institute, St George's, University of London, London, UK.
  • Tan J; Population Health Research Institute, St George's, University of London, London, UK.
  • Baldacci S; Unit of Epidemiology of Rare Diseases and Congenital Anomalies, Institute of Clinical Physiology, National Research Council, Pisa, Italy.
  • Ballardini E; Neonatal Intensive Care Unit, Paediatric Section, IMER Registry (Emilia Romagna Registry of Birth Defects), Department of Medical Sciences, University of Ferrara, Ferrara, Emilia-Romagna, Italy.
  • Cavero-Carbonell C; Rare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region FISABIO, Valencia, Valencia, Spain.
  • Damkjær M; Department of Paediatrics and Adolescent Medicine, Lillebaelt Hospital, University Hospital of Southern Denmark, Kolding, Denmark.
  • García-Villodre L; Department of Regional Health Research, University of Southern Denmark, Kolding, Denmark.
  • Gissler M; Rare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region FISABIO, Valencia, Valencia, Spain.
  • Given J; Department of Knowledge Brokers, THL Finnish Institute for Health and Welfare, Helsinki, Finland.
  • Gorini F; Centre for Maternal, Fetal and Infant Research, INHR, Ulster University, Belfast, Northern Ireland, UK.
  • Heino A; Unit of Epidemiology of Rare Diseases and Congenital Anomalies, Institute of Clinical Physiology, National Research Council, Pisa, Italy.
  • Limb E; Department of Knowledge Brokers, THL Finnish Institute for Health and Welfare, Helsinki, Finland.
  • Lutke R; Population Health Research Institute, St George's, University of London, London, UK.
  • Neville A; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.
  • Rissmann A; Emilia Romagna Registry of Birth Defects and Center for Clinical and Epidemiological Research, University of Ferrara, Ferrara, Italy.
  • Scanlon L; Malformation Monitoring Centre Saxony-Anhalt, Medical Faculty, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany.
  • Tucker DF; Faculty of Health and Life Sciences, Swansea University, Swansea, UK.
  • Urhoj SK; Faculty of Health and Life Sciences, Swansea University, Swansea, UK.
  • de Walle HE; Congenital Anomaly Register and Information Service for Wales, Public Health Wales, Swansea, UK.
  • Garne E; Department of Paediatrics and Adolescent Medicine, Lillebaelt Hospital, University Hospital of Southern Denmark, Kolding, Denmark.
Arch Dis Child ; 109(5): 402-408, 2024 Apr 18.
Article en En | MEDLINE | ID: mdl-38373775
ABSTRACT

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.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Anomalías Congénitas / Cardiopatías Congénitas Límite: Child / Female / Humans / Pregnancy País/Región como asunto: Europa Idioma: En Revista: Arch Dis Child Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Anomalías Congénitas / Cardiopatías Congénitas Límite: Child / Female / Humans / Pregnancy País/Región como asunto: Europa Idioma: En Revista: Arch Dis Child Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido