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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

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 hospit...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9307180/
https://www.ncbi.nlm.nih.gov/pubmed/35867669
http://dx.doi.org/10.1371/journal.pone.0269874
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author 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
author_facet 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
author_sort Urhoj, Stine Kjaer
collection PubMed
description 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.
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spelling pubmed-93071802022-07-23 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 PLoS One Research Article 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. Public Library of Science 2022-07-22 /pmc/articles/PMC9307180/ /pubmed/35867669 http://dx.doi.org/10.1371/journal.pone.0269874 Text en © 2022 Urhoj et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
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
Hospital length of stay among children with and without congenital anomalies across 11 European regions—A population-based data linkage study
title Hospital length of stay among children with and without congenital anomalies across 11 European regions—A population-based data linkage study
title_full Hospital length of stay among children with and without congenital anomalies across 11 European regions—A population-based data linkage study
title_fullStr Hospital length of stay among children with and without congenital anomalies across 11 European regions—A population-based data linkage study
title_full_unstemmed Hospital length of stay among children with and without congenital anomalies across 11 European regions—A population-based data linkage study
title_short Hospital length of stay among children with and without congenital anomalies across 11 European regions—A population-based data linkage study
title_sort hospital length of stay among children with and without congenital anomalies across 11 european regions—a population-based data linkage study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9307180/
https://www.ncbi.nlm.nih.gov/pubmed/35867669
http://dx.doi.org/10.1371/journal.pone.0269874
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