Severe Congenital Heart Defects and Cerebral Palsy
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10400.18/8850 |
Resumo: | Objective: To report the prevalence of cerebral palsy (CP) in children with severe congenital heart defects (sCHD) and the outcome/severity of the CP. Methods: Population-based, data linkage study between CP and congenital anomaly registers in Europe and Australia. The EUROCAT definition of severe CHD (sCHD) was used. Linked data from 4 regions in Europe and 2 in Australia were included. All children born in the regions from 1991 through 2009 diagnosed with CP and/or sCHD were included. Linkage was completed locally. Deidentified linked data were pooled for analyses. Results:The study sample included 4989 children with CP and 3684 children with sCHD. The total number of livebirths in the population was 1 734 612. The prevalence of CP was 2.9 per 1000 births (95% CI, 2.8-3.0) and the prevalence of sCHD was 2.1 per 1000 births (95% CI, 2.1-2.2). Of children with sCHD, 1.5% (n = 57) had a diagnosis of CP, of which 35 (61%) children had prenatally or perinatally acquired CP (resulting from a brain injury at £28 days of life) and 22 (39%) children had a postneonatal cause (a brain injury between 28 days and 2 years). Children with CP and sCHD more often had unilateral spastic CP and more intellectual impairments than children with CP without congenital anomalies.Conclusions: In high-income countries, the proportion of children with CP is much higher in children with sCHD than in the background population. The severity of disease in children with CP and sCHD is milder compared with children with CP without congenital anomalies |
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Severe Congenital Heart Defects and Cerebral PalsyCerebral PalsyCongenital Heart DefectCHDBrain InjuryIntellectual ImpairmentSeverityEUROCATCongenital AnomaliesDeterminantes da Saúde e da DoençaObjective: To report the prevalence of cerebral palsy (CP) in children with severe congenital heart defects (sCHD) and the outcome/severity of the CP. Methods: Population-based, data linkage study between CP and congenital anomaly registers in Europe and Australia. The EUROCAT definition of severe CHD (sCHD) was used. Linked data from 4 regions in Europe and 2 in Australia were included. All children born in the regions from 1991 through 2009 diagnosed with CP and/or sCHD were included. Linkage was completed locally. Deidentified linked data were pooled for analyses. Results:The study sample included 4989 children with CP and 3684 children with sCHD. The total number of livebirths in the population was 1 734 612. The prevalence of CP was 2.9 per 1000 births (95% CI, 2.8-3.0) and the prevalence of sCHD was 2.1 per 1000 births (95% CI, 2.1-2.2). Of children with sCHD, 1.5% (n = 57) had a diagnosis of CP, of which 35 (61%) children had prenatally or perinatally acquired CP (resulting from a brain injury at £28 days of life) and 22 (39%) children had a postneonatal cause (a brain injury between 28 days and 2 years). Children with CP and sCHD more often had unilateral spastic CP and more intellectual impairments than children with CP without congenital anomalies.Conclusions: In high-income countries, the proportion of children with CP is much higher in children with sCHD than in the background population. The severity of disease in children with CP and sCHD is milder compared with children with CP without congenital anomaliesFunding support received for the overarching Comprehensive CA-CP Study: the Cerebral Palsy Alliance Research Foundation (The Comprehensive CA-CP Study PG1215 and PG2816 and salary support from Cerebral Palsy Alliance Research Foundation (S.G., S.M., H.S.S., N.B.).ElsevierRepositório Científico do Instituto Nacional de SaúdeGarne, EsterGoldsmith, ShonaBarisic, IngeborgBraz, PaulaDakovic, IvanaGibson, CatherineHansen, MicheleHoei-Hansen, Christina E.Hollung, Sandra JulsenKlungsøyr, KariSmithers-Sheedy, HayleyVirella, DanielBadawi, NadiaWatson, LindaMcIntyre, Sarah2024-01-04T15:40:41Z2023-07-182023-07-18T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.18/8850engJ Pediatr. 2023 Nov:262:113617. doi: 10.1016/j.jpeds.2023.113617. Epub 2023 Jul 18.0022-347610.1016/j.jpeds.2023.113617info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-01-06T01:34:17Zoai:repositorio.insa.pt:10400.18/8850Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T01:30:30.722616Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Severe Congenital Heart Defects and Cerebral Palsy |
title |
Severe Congenital Heart Defects and Cerebral Palsy |
spellingShingle |
Severe Congenital Heart Defects and Cerebral Palsy Garne, Ester Cerebral Palsy Congenital Heart Defect CHD Brain Injury Intellectual Impairment Severity EUROCAT Congenital Anomalies Determinantes da Saúde e da Doença |
title_short |
Severe Congenital Heart Defects and Cerebral Palsy |
title_full |
Severe Congenital Heart Defects and Cerebral Palsy |
title_fullStr |
Severe Congenital Heart Defects and Cerebral Palsy |
title_full_unstemmed |
Severe Congenital Heart Defects and Cerebral Palsy |
title_sort |
Severe Congenital Heart Defects and Cerebral Palsy |
author |
Garne, Ester |
author_facet |
Garne, Ester Goldsmith, Shona Barisic, Ingeborg Braz, Paula Dakovic, Ivana Gibson, Catherine Hansen, Michele Hoei-Hansen, Christina E. Hollung, Sandra Julsen Klungsøyr, Kari Smithers-Sheedy, Hayley Virella, Daniel Badawi, Nadia Watson, Linda McIntyre, Sarah |
author_role |
author |
author2 |
Goldsmith, Shona Barisic, Ingeborg Braz, Paula Dakovic, Ivana Gibson, Catherine Hansen, Michele Hoei-Hansen, Christina E. Hollung, Sandra Julsen Klungsøyr, Kari Smithers-Sheedy, Hayley Virella, Daniel Badawi, Nadia Watson, Linda McIntyre, Sarah |
author2_role |
author author author author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Repositório Científico do Instituto Nacional de Saúde |
dc.contributor.author.fl_str_mv |
Garne, Ester Goldsmith, Shona Barisic, Ingeborg Braz, Paula Dakovic, Ivana Gibson, Catherine Hansen, Michele Hoei-Hansen, Christina E. Hollung, Sandra Julsen Klungsøyr, Kari Smithers-Sheedy, Hayley Virella, Daniel Badawi, Nadia Watson, Linda McIntyre, Sarah |
dc.subject.por.fl_str_mv |
Cerebral Palsy Congenital Heart Defect CHD Brain Injury Intellectual Impairment Severity EUROCAT Congenital Anomalies Determinantes da Saúde e da Doença |
topic |
Cerebral Palsy Congenital Heart Defect CHD Brain Injury Intellectual Impairment Severity EUROCAT Congenital Anomalies Determinantes da Saúde e da Doença |
description |
Objective: To report the prevalence of cerebral palsy (CP) in children with severe congenital heart defects (sCHD) and the outcome/severity of the CP. Methods: Population-based, data linkage study between CP and congenital anomaly registers in Europe and Australia. The EUROCAT definition of severe CHD (sCHD) was used. Linked data from 4 regions in Europe and 2 in Australia were included. All children born in the regions from 1991 through 2009 diagnosed with CP and/or sCHD were included. Linkage was completed locally. Deidentified linked data were pooled for analyses. Results:The study sample included 4989 children with CP and 3684 children with sCHD. The total number of livebirths in the population was 1 734 612. The prevalence of CP was 2.9 per 1000 births (95% CI, 2.8-3.0) and the prevalence of sCHD was 2.1 per 1000 births (95% CI, 2.1-2.2). Of children with sCHD, 1.5% (n = 57) had a diagnosis of CP, of which 35 (61%) children had prenatally or perinatally acquired CP (resulting from a brain injury at £28 days of life) and 22 (39%) children had a postneonatal cause (a brain injury between 28 days and 2 years). Children with CP and sCHD more often had unilateral spastic CP and more intellectual impairments than children with CP without congenital anomalies.Conclusions: In high-income countries, the proportion of children with CP is much higher in children with sCHD than in the background population. The severity of disease in children with CP and sCHD is milder compared with children with CP without congenital anomalies |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-07-18 2023-07-18T00:00:00Z 2024-01-04T15:40:41Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10400.18/8850 |
url |
http://hdl.handle.net/10400.18/8850 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
J Pediatr. 2023 Nov:262:113617. doi: 10.1016/j.jpeds.2023.113617. Epub 2023 Jul 18. 0022-3476 10.1016/j.jpeds.2023.113617 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier |
publisher.none.fl_str_mv |
Elsevier |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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