Congenital Heart Disease Prevalence in Portugal in 2015: Data from the National Register of Congenital Anomalies

Detalhes bibliográficos
Autor(a) principal: Melo, Isabel Saraiva de
Data de Publicação: 2020
Outros Autores: Braz, Paula, Roquette, Rita, Sousa, Paulo, Nunes, Carla, Dias, Carlos
Tipo de documento: Artigo
Idioma: por
eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/12111
Resumo: Introduction: The prevalence at birth of congenital heart disease in Portugal is 8.3/1000 births; undetected critical congenital heart disease may result in adverse outcomes for the fetus/newborn infant. This study describes the reported cases of congenital heart disease in Portugal in 2015 regarding antenatal diagnosis, cardiac defect, and presence of other congenital anomalies/chromosomal abnormalities. These indicators are compared in live births and medical pregnancy terminations. Additionally, postnatal deaths were characterized.Material and Methods: Congenital heart disease data derived from the 2015 Portuguese National Registry of Congenital Birth Defects were analyzed. The prevalence rates per 1000 births were assessed by the chi-square test of independence.Results: The prevalence of congenital heart disease in this study was 5/1000 live-births (339 live-births, 20% with critical defects). The most common defects were ventricular septal defect (38%), atrial septal defect (15%), aortic coarctation (7%), tetralogy of Fallot (7%) and pulmonary stenosis (5%). One third of the live births had antenatal diagnosis of congenital heart disease. In the live-births with critical congenital heart disease, 54% had antenatal diagnosis and 14% were diagnosed at birth. There were records of 84 pregnancy terminations; 49% had critical defects, 75% had non-cardiac congenital anomalies and 40% had chromosomal abnormalities. There were 15 postnatal deaths recorded (3.4% mortality rate), associated with prematurity/low birthweight, critical congenital heart disease, other non-cardiac congenital anomalies and chromosomal abnormalities.Discussion: The data analysis revealed a prevalence of congenital heart disease in this study of 5/1000 births (inferior to other international studies), with a distribution per type of anomaly similar to that reported in previously published work. There were significant regional differences that need further studying.Conclusion: These results are paramount to characterize the Portuguese scenario and improve Healthcare planning. It is important to improve reporting in the Portuguese National Registry of Congenital Birth Defects.
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spelling Congenital Heart Disease Prevalence in Portugal in 2015: Data from the National Register of Congenital AnomaliesPrevalência de Cardiopatias Congénitas em Portugal em 2015: Dados do Registo Nacional de Anomalias CongénitasHeart DefectsCongenital / epidemiologyPortugalRegistriesCardiopatias Congénitas/epidemiologiaPortugalRegistosIntroduction: The prevalence at birth of congenital heart disease in Portugal is 8.3/1000 births; undetected critical congenital heart disease may result in adverse outcomes for the fetus/newborn infant. This study describes the reported cases of congenital heart disease in Portugal in 2015 regarding antenatal diagnosis, cardiac defect, and presence of other congenital anomalies/chromosomal abnormalities. These indicators are compared in live births and medical pregnancy terminations. Additionally, postnatal deaths were characterized.Material and Methods: Congenital heart disease data derived from the 2015 Portuguese National Registry of Congenital Birth Defects were analyzed. The prevalence rates per 1000 births were assessed by the chi-square test of independence.Results: The prevalence of congenital heart disease in this study was 5/1000 live-births (339 live-births, 20% with critical defects). The most common defects were ventricular septal defect (38%), atrial septal defect (15%), aortic coarctation (7%), tetralogy of Fallot (7%) and pulmonary stenosis (5%). One third of the live births had antenatal diagnosis of congenital heart disease. In the live-births with critical congenital heart disease, 54% had antenatal diagnosis and 14% were diagnosed at birth. There were records of 84 pregnancy terminations; 49% had critical defects, 75% had non-cardiac congenital anomalies and 40% had chromosomal abnormalities. There were 15 postnatal deaths recorded (3.4% mortality rate), associated with prematurity/low birthweight, critical congenital heart disease, other non-cardiac congenital anomalies and chromosomal abnormalities.Discussion: The data analysis revealed a prevalence of congenital heart disease in this study of 5/1000 births (inferior to other international studies), with a distribution per type of anomaly similar to that reported in previously published work. There were significant regional differences that need further studying.Conclusion: These results are paramount to characterize the Portuguese scenario and improve Healthcare planning. It is important to improve reporting in the Portuguese National Registry of Congenital Birth Defects.Introdução: A prevalência de cardiopatias congénitas em Portugal é de 8,3/1000 nascimentos; cardiopatias congénitas críticas não detectadas podem resultar em graves consequências para o feto/recém-nascido. O objectivo deste trabalho é descrever os casos de cardiopatia congénita reportados em Portugal em 2015 quanto ao diagnóstico pré-natal, patologia cardíaca e à presença de outras malformações congénitas ou anomalias cromossómicas. Estas características são comparadas nos subgrupos dos nados-vivos e de interrupção médica da gravidez. Por último, caracterizam-se os óbitos.Material e Métodos: Os dados de cardiopatias congénitas reportadas ao Registo Nacional de Anomalias Congénitas em 2015 foram analisados, e calculadas as taxas de prevalência por 1000 nascimentos, comparadas utilizando teste de independência do quiquadrado.Resultados: A prevalência de cardiopatias congénitas neste estudo foi de 5/1000, (339 nados-vivos, 20% com cardiopatias congénitas críticas). As cardiopatias mais frequentes foram as seguintes: comunicação interventricular (38%), comunicação interauricular (15%), coartação da aorta (7%), tetralogia de Fallot (7%) e estenose pulmonar (5%). Um terço dos nados-vivos teve diagnostico pré-natal de cardiopatia. Dos nados-vivos com cardiopatias congénitas críticas, 54% teve diagnostico pré-natal e 14% foi diagnosticado ao nascer. Foram identificados 84 registos de interrupção médica da gravidez; 49% apresentava cardiopatias congénitas críticas, 75% outras malformações associadas, e 40% cromossomopatias. Foram registados 15 óbitos (3,4% de mortalidade) associados a prematuridade e/ou baixo-peso ao nascer, cardiopatias congénitas críticas, outras malformações e anomalias cromossómicas.Discussão: A prevalência de cardiopatias congénitas neste estudo (5/1000 nascimentos) foi inferior ao descrito noutros estudos internacionais, não obstante uma distribuição por tipo de anomalia semelhante ao previamente reportado. Observaram-se assimetrias regionais significativas que necessitam de mais investigação.Conclusão: Este estudo é relevante para melhor conhecimento da realidade nacional e organização dos Cuidados de Saúde. É importante uma maior adesão ao Registo Nacional de Anomalias Congénitas.Ordem dos Médicos2020-07-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfapplication/pdfapplication/pdfapplication/mswordapplication/vnd.openxmlformats-officedocument.wordprocessingml.documentapplication/pdfhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/12111oai:ojs.www.actamedicaportuguesa.com:article/12111Acta Médica Portuguesa; Vol. 33 No. 7-8 (2020): July-August; 491-499Acta Médica Portuguesa; Vol. 33 N.º 7-8 (2020): Julho-Agosto; 491-4991646-07580870-399Xreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPporenghttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/12111https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/12111/6006https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/12111/6707https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/12111/11593https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/12111/11932https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/12111/12003https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/12111/12060Direitos de Autor (c) 2020 Acta Médica Portuguesainfo:eu-repo/semantics/openAccessMelo, Isabel Saraiva deBraz, PaulaRoquette, RitaSousa, PauloNunes, CarlaDias, Carlos2022-12-20T11:06:31Zoai:ojs.www.actamedicaportuguesa.com:article/12111Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:20:08.511613Repositório 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 Congenital Heart Disease Prevalence in Portugal in 2015: Data from the National Register of Congenital Anomalies
Prevalência de Cardiopatias Congénitas em Portugal em 2015: Dados do Registo Nacional de Anomalias Congénitas
title Congenital Heart Disease Prevalence in Portugal in 2015: Data from the National Register of Congenital Anomalies
spellingShingle Congenital Heart Disease Prevalence in Portugal in 2015: Data from the National Register of Congenital Anomalies
Melo, Isabel Saraiva de
Heart Defects
Congenital / epidemiology
Portugal
Registries
Cardiopatias Congénitas/epidemiologia
Portugal
Registos
title_short Congenital Heart Disease Prevalence in Portugal in 2015: Data from the National Register of Congenital Anomalies
title_full Congenital Heart Disease Prevalence in Portugal in 2015: Data from the National Register of Congenital Anomalies
title_fullStr Congenital Heart Disease Prevalence in Portugal in 2015: Data from the National Register of Congenital Anomalies
title_full_unstemmed Congenital Heart Disease Prevalence in Portugal in 2015: Data from the National Register of Congenital Anomalies
title_sort Congenital Heart Disease Prevalence in Portugal in 2015: Data from the National Register of Congenital Anomalies
author Melo, Isabel Saraiva de
author_facet Melo, Isabel Saraiva de
Braz, Paula
Roquette, Rita
Sousa, Paulo
Nunes, Carla
Dias, Carlos
author_role author
author2 Braz, Paula
Roquette, Rita
Sousa, Paulo
Nunes, Carla
Dias, Carlos
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Melo, Isabel Saraiva de
Braz, Paula
Roquette, Rita
Sousa, Paulo
Nunes, Carla
Dias, Carlos
dc.subject.por.fl_str_mv Heart Defects
Congenital / epidemiology
Portugal
Registries
Cardiopatias Congénitas/epidemiologia
Portugal
Registos
topic Heart Defects
Congenital / epidemiology
Portugal
Registries
Cardiopatias Congénitas/epidemiologia
Portugal
Registos
description Introduction: The prevalence at birth of congenital heart disease in Portugal is 8.3/1000 births; undetected critical congenital heart disease may result in adverse outcomes for the fetus/newborn infant. This study describes the reported cases of congenital heart disease in Portugal in 2015 regarding antenatal diagnosis, cardiac defect, and presence of other congenital anomalies/chromosomal abnormalities. These indicators are compared in live births and medical pregnancy terminations. Additionally, postnatal deaths were characterized.Material and Methods: Congenital heart disease data derived from the 2015 Portuguese National Registry of Congenital Birth Defects were analyzed. The prevalence rates per 1000 births were assessed by the chi-square test of independence.Results: The prevalence of congenital heart disease in this study was 5/1000 live-births (339 live-births, 20% with critical defects). The most common defects were ventricular septal defect (38%), atrial septal defect (15%), aortic coarctation (7%), tetralogy of Fallot (7%) and pulmonary stenosis (5%). One third of the live births had antenatal diagnosis of congenital heart disease. In the live-births with critical congenital heart disease, 54% had antenatal diagnosis and 14% were diagnosed at birth. There were records of 84 pregnancy terminations; 49% had critical defects, 75% had non-cardiac congenital anomalies and 40% had chromosomal abnormalities. There were 15 postnatal deaths recorded (3.4% mortality rate), associated with prematurity/low birthweight, critical congenital heart disease, other non-cardiac congenital anomalies and chromosomal abnormalities.Discussion: The data analysis revealed a prevalence of congenital heart disease in this study of 5/1000 births (inferior to other international studies), with a distribution per type of anomaly similar to that reported in previously published work. There were significant regional differences that need further studying.Conclusion: These results are paramount to characterize the Portuguese scenario and improve Healthcare planning. It is important to improve reporting in the Portuguese National Registry of Congenital Birth Defects.
publishDate 2020
dc.date.none.fl_str_mv 2020-07-01
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dc.relation.none.fl_str_mv https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/12111
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/12111/6006
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/12111/6707
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/12111/11593
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/12111/11932
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/12111/12003
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/12111/12060
dc.rights.driver.fl_str_mv Direitos de Autor (c) 2020 Acta Médica Portuguesa
info:eu-repo/semantics/openAccess
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application/pdf
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dc.publisher.none.fl_str_mv Ordem dos Médicos
publisher.none.fl_str_mv Ordem dos Médicos
dc.source.none.fl_str_mv Acta Médica Portuguesa; Vol. 33 No. 7-8 (2020): July-August; 491-499
Acta Médica Portuguesa; Vol. 33 N.º 7-8 (2020): Julho-Agosto; 491-499
1646-0758
0870-399X
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