Follow-up of the survivors of congenital diaphragmatic hernia

Detalhes bibliográficos
Autor(a) principal: Pinto, Jorge Correia
Data de Publicação: 2012
Outros Autores: Rocha, Gustavo, Azevedo, Inês, Guimarães, Hercília
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/1822/33411
Resumo: INTRODUCTION: Survivors of congenital diaphragmatic hernia have increased with the introduction of new treatment modalities and have been reported to experience ongoing medical morbidity until adulthood. AIM: To describe the long-term functional impact of congenital diaphragmatic repair on the survivors of a single institution cohort of newborns over a 14-year period. METHODS: The follow up medical charts of 39 congenital diaphragmatic hernia survivors treated at a tertiary neonatal intensive care unit, from January 1997 to December 2010, were analyzed. RESULTS: The median age at follow up was 70 (4-162) months. Gastrointestinal sequelae were the most common with 12 (30.7%) patients affected by failure to thrive. Chronic lung disease occurred in 5 (12.8%) patients, neurodevelopmental delay in 5 (12.8%), musculoskeletal sequelae in 6 (15.3%), recurrence of hernia in 4 (10.2%) and 2 (7.6%) were deceased. CONCLUSION: Congenital diaphragmatic hernia survivors are a group of patients that requires long term periodic follow up in a multidisciplinary setting to provide adequate support and improve their quality of life.
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spelling Follow-up of the survivors of congenital diaphragmatic herniaCongenital diaphragmatic herniaSurvivorsFollow-upGastrointestinalNeurodevelopmentalMusculoskeletalScience & TechnologyINTRODUCTION: Survivors of congenital diaphragmatic hernia have increased with the introduction of new treatment modalities and have been reported to experience ongoing medical morbidity until adulthood. AIM: To describe the long-term functional impact of congenital diaphragmatic repair on the survivors of a single institution cohort of newborns over a 14-year period. METHODS: The follow up medical charts of 39 congenital diaphragmatic hernia survivors treated at a tertiary neonatal intensive care unit, from January 1997 to December 2010, were analyzed. RESULTS: The median age at follow up was 70 (4-162) months. Gastrointestinal sequelae were the most common with 12 (30.7%) patients affected by failure to thrive. Chronic lung disease occurred in 5 (12.8%) patients, neurodevelopmental delay in 5 (12.8%), musculoskeletal sequelae in 6 (15.3%), recurrence of hernia in 4 (10.2%) and 2 (7.6%) were deceased. CONCLUSION: Congenital diaphragmatic hernia survivors are a group of patients that requires long term periodic follow up in a multidisciplinary setting to provide adequate support and improve their quality of life.ElsevierUniversidade do MinhoPinto, Jorge CorreiaRocha, GustavoAzevedo, InêsGuimarães, Hercília2012-12-012012-12-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/33411eng0378-378210.1016/j.earlhumdev.2011.08.025http://dx.doi.org/10.1016/j.earlhumdev.2011.08.025info: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:RCAAP2023-07-21T12:03:15Zoai:repositorium.sdum.uminho.pt:1822/33411Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T18:53:21.492730Repositório 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 Follow-up of the survivors of congenital diaphragmatic hernia
title Follow-up of the survivors of congenital diaphragmatic hernia
spellingShingle Follow-up of the survivors of congenital diaphragmatic hernia
Pinto, Jorge Correia
Congenital diaphragmatic hernia
Survivors
Follow-up
Gastrointestinal
Neurodevelopmental
Musculoskeletal
Science & Technology
title_short Follow-up of the survivors of congenital diaphragmatic hernia
title_full Follow-up of the survivors of congenital diaphragmatic hernia
title_fullStr Follow-up of the survivors of congenital diaphragmatic hernia
title_full_unstemmed Follow-up of the survivors of congenital diaphragmatic hernia
title_sort Follow-up of the survivors of congenital diaphragmatic hernia
author Pinto, Jorge Correia
author_facet Pinto, Jorge Correia
Rocha, Gustavo
Azevedo, Inês
Guimarães, Hercília
author_role author
author2 Rocha, Gustavo
Azevedo, Inês
Guimarães, Hercília
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Pinto, Jorge Correia
Rocha, Gustavo
Azevedo, Inês
Guimarães, Hercília
dc.subject.por.fl_str_mv Congenital diaphragmatic hernia
Survivors
Follow-up
Gastrointestinal
Neurodevelopmental
Musculoskeletal
Science & Technology
topic Congenital diaphragmatic hernia
Survivors
Follow-up
Gastrointestinal
Neurodevelopmental
Musculoskeletal
Science & Technology
description INTRODUCTION: Survivors of congenital diaphragmatic hernia have increased with the introduction of new treatment modalities and have been reported to experience ongoing medical morbidity until adulthood. AIM: To describe the long-term functional impact of congenital diaphragmatic repair on the survivors of a single institution cohort of newborns over a 14-year period. METHODS: The follow up medical charts of 39 congenital diaphragmatic hernia survivors treated at a tertiary neonatal intensive care unit, from January 1997 to December 2010, were analyzed. RESULTS: The median age at follow up was 70 (4-162) months. Gastrointestinal sequelae were the most common with 12 (30.7%) patients affected by failure to thrive. Chronic lung disease occurred in 5 (12.8%) patients, neurodevelopmental delay in 5 (12.8%), musculoskeletal sequelae in 6 (15.3%), recurrence of hernia in 4 (10.2%) and 2 (7.6%) were deceased. CONCLUSION: Congenital diaphragmatic hernia survivors are a group of patients that requires long term periodic follow up in a multidisciplinary setting to provide adequate support and improve their quality of life.
publishDate 2012
dc.date.none.fl_str_mv 2012-12-01
2012-12-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/1822/33411
url http://hdl.handle.net/1822/33411
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 0378-3782
10.1016/j.earlhumdev.2011.08.025
http://dx.doi.org/10.1016/j.earlhumdev.2011.08.025
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
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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