Newborns with Suspected Congenital Heart Disease Demanding Emergency Transport: Seven Years Casuistic
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | https://doi.org/10.25754/pjp.2020.17936 |
Resumo: | Introduction: Congenital heart diseases are the most common congenital malformation in Portugal. Fetus diagnosed in utero are referenced to and born in a tertiary care center. Newborns with suspected congenital heart disease missed in the pre-natal screening program and born outside of a referral center that present with clinical severity are transported by the Pediatric Inter-hospital Transport system. Our objective was to analyze the last seven years of inter-hospital transport of newborns with suspected Congenital Heart Disease of Portugal’s northern region and study those who escape the prenatal screening program. Materials and Methods: Newborns with suspected congenital heart disease, transported between April 1st 2011 and March 30th 2018, were identified from the Pediatric Inter-hospital Transport System’s records and individually reviewed in the National Health Service’s informatic system. Results: Were included 195 transports, corresponding to 144 patients. Congenital heart disease was excluded in 46 patients. Of these 144 patients, 87 were born outside of the reference center. Transposition of great arteries was the most common congenital heart disease transported (16/87; 18.4%) and aortic coarctation (14/87; 16.1%) the second. Prenatal diagnosis was present in nine of these patients (10.3%). Discussion: Transport number stability may translate the constant incidence of congenital heart diseases and/or reflect a non-improving prenatal diagnosis rate. Technical challenges in transposition of great arteries’ prenatal diagnosis may explain the higher number of transports. It is necessary to guarantee the prenatal diagnosis of congenital heart diseases by intervening locally. |
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Newborns with Suspected Congenital Heart Disease Demanding Emergency Transport: Seven Years CasuisticRecém-nascidos com Suspeita de Cardiopatia Congénita com Necessidade de Transporte Inter-hospitalar: Revisão Casuística de 7 AnosCase seriesIntroduction: Congenital heart diseases are the most common congenital malformation in Portugal. Fetus diagnosed in utero are referenced to and born in a tertiary care center. Newborns with suspected congenital heart disease missed in the pre-natal screening program and born outside of a referral center that present with clinical severity are transported by the Pediatric Inter-hospital Transport system. Our objective was to analyze the last seven years of inter-hospital transport of newborns with suspected Congenital Heart Disease of Portugal’s northern region and study those who escape the prenatal screening program. Materials and Methods: Newborns with suspected congenital heart disease, transported between April 1st 2011 and March 30th 2018, were identified from the Pediatric Inter-hospital Transport System’s records and individually reviewed in the National Health Service’s informatic system. Results: Were included 195 transports, corresponding to 144 patients. Congenital heart disease was excluded in 46 patients. Of these 144 patients, 87 were born outside of the reference center. Transposition of great arteries was the most common congenital heart disease transported (16/87; 18.4%) and aortic coarctation (14/87; 16.1%) the second. Prenatal diagnosis was present in nine of these patients (10.3%). Discussion: Transport number stability may translate the constant incidence of congenital heart diseases and/or reflect a non-improving prenatal diagnosis rate. Technical challenges in transposition of great arteries’ prenatal diagnosis may explain the higher number of transports. It is necessary to guarantee the prenatal diagnosis of congenital heart diseases by intervening locally.Sociedade Portuguesa de Pediatria2020-04-16info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://doi.org/10.25754/pjp.2020.17936eng2184-44532184-3333Carvalho, CatarinaGrilo, MartaBaptista, Maria Joãoinfo: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:RCAAP2023-08-03T02:58:01Zoai:ojs.revistas.rcaap.pt:article/17936Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:25:32.029790Repositório 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 |
Newborns with Suspected Congenital Heart Disease Demanding Emergency Transport: Seven Years Casuistic Recém-nascidos com Suspeita de Cardiopatia Congénita com Necessidade de Transporte Inter-hospitalar: Revisão Casuística de 7 Anos |
title |
Newborns with Suspected Congenital Heart Disease Demanding Emergency Transport: Seven Years Casuistic |
spellingShingle |
Newborns with Suspected Congenital Heart Disease Demanding Emergency Transport: Seven Years Casuistic Carvalho, Catarina Case series |
title_short |
Newborns with Suspected Congenital Heart Disease Demanding Emergency Transport: Seven Years Casuistic |
title_full |
Newborns with Suspected Congenital Heart Disease Demanding Emergency Transport: Seven Years Casuistic |
title_fullStr |
Newborns with Suspected Congenital Heart Disease Demanding Emergency Transport: Seven Years Casuistic |
title_full_unstemmed |
Newborns with Suspected Congenital Heart Disease Demanding Emergency Transport: Seven Years Casuistic |
title_sort |
Newborns with Suspected Congenital Heart Disease Demanding Emergency Transport: Seven Years Casuistic |
author |
Carvalho, Catarina |
author_facet |
Carvalho, Catarina Grilo, Marta Baptista, Maria João |
author_role |
author |
author2 |
Grilo, Marta Baptista, Maria João |
author2_role |
author author |
dc.contributor.author.fl_str_mv |
Carvalho, Catarina Grilo, Marta Baptista, Maria João |
dc.subject.por.fl_str_mv |
Case series |
topic |
Case series |
description |
Introduction: Congenital heart diseases are the most common congenital malformation in Portugal. Fetus diagnosed in utero are referenced to and born in a tertiary care center. Newborns with suspected congenital heart disease missed in the pre-natal screening program and born outside of a referral center that present with clinical severity are transported by the Pediatric Inter-hospital Transport system. Our objective was to analyze the last seven years of inter-hospital transport of newborns with suspected Congenital Heart Disease of Portugal’s northern region and study those who escape the prenatal screening program. Materials and Methods: Newborns with suspected congenital heart disease, transported between April 1st 2011 and March 30th 2018, were identified from the Pediatric Inter-hospital Transport System’s records and individually reviewed in the National Health Service’s informatic system. Results: Were included 195 transports, corresponding to 144 patients. Congenital heart disease was excluded in 46 patients. Of these 144 patients, 87 were born outside of the reference center. Transposition of great arteries was the most common congenital heart disease transported (16/87; 18.4%) and aortic coarctation (14/87; 16.1%) the second. Prenatal diagnosis was present in nine of these patients (10.3%). Discussion: Transport number stability may translate the constant incidence of congenital heart diseases and/or reflect a non-improving prenatal diagnosis rate. Technical challenges in transposition of great arteries’ prenatal diagnosis may explain the higher number of transports. It is necessary to guarantee the prenatal diagnosis of congenital heart diseases by intervening locally. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-04-16 |
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 |
https://doi.org/10.25754/pjp.2020.17936 |
url |
https://doi.org/10.25754/pjp.2020.17936 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
2184-4453 2184-3333 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
Sociedade Portuguesa de Pediatria |
publisher.none.fl_str_mv |
Sociedade Portuguesa de Pediatria |
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 |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
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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1799133524343652353 |