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Hospital length of stay among children with and without congenital anomalies across 11 European regions-A population-based data linkage study.
Urhoj, Stine Kjaer; Tan, Joachim; Morris, Joan K; Given, Joanne; Astolfi, Gianni; Baldacci, Silvia; Barisic, Ingeborg; Brigden, Joanna; Cavero-Carbonell, Clara; Evans, Hannah; Gissler, Mika; Heino, Anna; Jordan, Sue; Lutke, Renée; Odak, Ljubica; Puccini, Aurora; Santoro, Michele; Scanlon, Ieuan; de Walle, Hermien E K; Wellesley, Diana; Zurriaga, Óscar; Loane, Maria; Garne, Ester.
Afiliação
  • Urhoj SK; Department of Paediatrics and Adolescent Medicine, Lillebaelt Hospital, University Hospital of Southern Denmark, Kolding, Denmark.
  • Tan J; Population Health Research Institute, St George's, University of London, London, United Kingdom.
  • Morris JK; Population Health Research Institute, St George's, University of London, London, United Kingdom.
  • Given J; Faculty of Life and Health Sciences, Ulster University, Northern Ireland, United Kingdom.
  • Astolfi G; Dept. of Neuroscience and Rehabilitation, University of Ferrara, Ferrara, Italy.
  • Baldacci S; Unit of Epidemiology of Rare diseases and Congenital anomalies, Institute of Clinical Physiology, National Research Council, Pisa, Italy.
  • Barisic I; Children's Hospital Zagreb, Centre of Excellence for Reproductive and Regenerative Medicine, Medical School University of Zagreb, Zagreb, Croatia.
  • Brigden J; Population Health Research Institute, St George's, University of London, London, United Kingdom.
  • Cavero-Carbonell C; Rare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region (UVEG-FISABIO), Valencia, Spain.
  • Evans H; Population Health Research Institute, St George's, University of London, London, United Kingdom.
  • Gissler M; Finnish Institute for Health and Welfare, Information Services Department, Helsinki, Finland.
  • Heino A; Finnish Institute for Health and Welfare, Information Services Department, Helsinki, Finland.
  • Jordan S; Faculty of Medicine, Health and Life Sciences, Swansea University, Wales, United Kingdom.
  • Lutke R; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
  • Odak L; Children's Hospital Zagreb, Centre of Excellence for Reproductive and Regenerative Medicine, Medical School University of Zagreb, Zagreb, Croatia.
  • Puccini A; Territorial Assistance Service-Drug and Medical Device Area, Emilia Romagna Health Department, Bologna, Italy.
  • Santoro M; Unit of Epidemiology of Rare diseases and Congenital anomalies, Institute of Clinical Physiology, National Research Council, Pisa, Italy.
  • Scanlon I; Faculty of Medicine, Health and Life Sciences, Swansea University, Wales, United Kingdom.
  • de Walle HEK; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
  • Wellesley D; Clinical Genetics, Princess Anne Hospital, University of Southampton and Wessex Clinical Genetics Service, Southampton, United Kingdom.
  • Zurriaga Ó; Department of Preventive Medicine and Public Health, Rare Diseases Research Unit UVEG-FISABIO Valencia and Spanish Consortium for Biomedical Research in Epidemiology and Public Health, University of Valencia (Spain) and Valencia Region (Spain) Health Authority (Conselleria de Sanitat Universal I Sal
  • Loane M; Faculty of Life and Health Sciences, Ulster University, Northern Ireland, United Kingdom.
  • Garne E; Department of Paediatrics and Adolescent Medicine, Lillebaelt Hospital, University Hospital of Southern Denmark, Kolding, Denmark.
PLoS One ; 17(7): e0269874, 2022.
Article em En | MEDLINE | ID: mdl-35867669
BACKGROUND: Congenital anomalies are a leading cause of childhood morbidity, but little is known about the long-term outcomes. OBJECTIVE: To quantify the burden of disease in childhood for children with congenital anomalies by assessing the risk of hospitalisation, the number of days spent in hospital and proportion of children with extended stays (≥10 days). METHODS: European population-based record-linkage study in 11 regions in eight countries including children with congenital anomalies (EUROCAT children) and without congenital anomalies (reference children) living in the same regions. The children were born between 1995 and 2014 and were followed to their tenth birthday or 31/12/2015. European meta-analyses of the outcome measures were performed by two age groups, <1 year and 1-4 years. RESULTS: 99,416 EUROCAT children and 2,021,772 reference children were linked to hospital databases. Among EUROCAT children, 85% (95%-CI: 79-90%) were hospitalised in the first year and 56% (95%-CI: 51-61%) at ages 1-4 years, compared to 31% (95%-CI: 26-37%) and 25% (95%-CI: 19-31%) of the reference children. Median length of stay was 2-3 times longer for EUROCAT children in both age groups. The percentages of children with extended stays (≥10 days) in the first year were 24% (95%-CI: 20-29%) for EUROCAT children and 1% (95%-CI: 1-2%) for reference children. The median length of stay varied greatly between congenital anomaly subgroups, with children with gastrointestinal anomalies and congenital heart defects having the longest stays. CONCLUSIONS: Children with congenital anomalies were more frequently hospitalised and median length of stay was longer. The outlook improves after the first year. Parents of children with congenital anomalies should be informed about the increased hospitalisations required for their child's care and the impact on family life and siblings, and they should be adequately supported.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Congênitas / Cardiopatias Congênitas Tipo de estudo: Prevalence_studies / Risk_factors_studies Limite: Child / Child, preschool / Female / Humans / Infant Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Congênitas / Cardiopatias Congênitas Tipo de estudo: Prevalence_studies / Risk_factors_studies Limite: Child / Child, preschool / Female / Humans / Infant Idioma: En Ano de publicação: 2022 Tipo de documento: Article