Risk factors for bronchopulmonary dysplasia in five portuguese neonatal intensive care units

Detalhes bibliográficos
Autor(a) principal: Guimarães, H
Data de Publicação: 2010
Outros Autores: Rocha, G, Vasconcellos, G, Proença, E, Carreira, ML, Sossai, MR, Morais, B, Martins, I, Rodrigues, T, Severo, M
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.10/658
Resumo: The pathogenesis of bronchopulmonary dysplasia (BPD) is clearly multifactorial. Specific pathogenic risk factors are prematurity, respiratory distress, oxygen supplementation, mechanical ventilation (MV), inflammation, patent ductus arteriosus (PDA), etc. AIM: To evaluate BPD prevalence and to identify risk factors for BPD in five Portuguese Neonatal Intensive Care Units in order to develop better practices the management of these newborns. MATERIAL AND METHODS: 256 very low birth weight infants with gestational age (GA) <30 weeks and/or birthweight (BW) <1250 g admitted in five Portuguese NICUs, between 2004 and 2006 were studied. A protocol was filled in based on clinical information registered in the hospital charts. BPD was defined as oxygen dependency at 36 weeks of postconceptional age. RESULTS: BPD prevalence was 12.9% (33/256). BPD risk decreased 46% per GA week and of 39% per 100g BW. BPD risk was significantly higher among newborns with low BW (adj OR= 0.73, 95% CI=0.57- 0.95), severe hyaline membrane disease (adj OR= 9.85, 95% CI=1.05-92.35), and those with sepsis (adj OR=6.22, 95% CI=1.68-23.02), those with longer duration on ventilatory support (42 vs 3 days, respectively in BPD and no BPD patients, p <0.001) and longer duration of FiO2>0.30 (85 vs 5 days, respectively in BPD and no BPD patients, p <0.001). COMMENTS: The most relevant risk factors were low birth weight, severe hyaline membrane disease, duration of respiratory support and oxygen therapy, and nosocomial sepsis. The implementation of potentially better practices to reduce lung injury in neonates must be addressed to improve practices to decrease these risk factors.
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spelling Risk factors for bronchopulmonary dysplasia in five portuguese neonatal intensive care unitsFactores de risco de displasia broncopulmonar em cinco unidades portuguesas de cuidados intensivos neonataisDisplasia broncopulmonarUnidade de cuidados intensivos pediátricosCriançaPortugalBronchopulmonary dysplasiaNeonatal intensive care unitsThe pathogenesis of bronchopulmonary dysplasia (BPD) is clearly multifactorial. Specific pathogenic risk factors are prematurity, respiratory distress, oxygen supplementation, mechanical ventilation (MV), inflammation, patent ductus arteriosus (PDA), etc. AIM: To evaluate BPD prevalence and to identify risk factors for BPD in five Portuguese Neonatal Intensive Care Units in order to develop better practices the management of these newborns. MATERIAL AND METHODS: 256 very low birth weight infants with gestational age (GA) <30 weeks and/or birthweight (BW) <1250 g admitted in five Portuguese NICUs, between 2004 and 2006 were studied. A protocol was filled in based on clinical information registered in the hospital charts. BPD was defined as oxygen dependency at 36 weeks of postconceptional age. RESULTS: BPD prevalence was 12.9% (33/256). BPD risk decreased 46% per GA week and of 39% per 100g BW. BPD risk was significantly higher among newborns with low BW (adj OR= 0.73, 95% CI=0.57- 0.95), severe hyaline membrane disease (adj OR= 9.85, 95% CI=1.05-92.35), and those with sepsis (adj OR=6.22, 95% CI=1.68-23.02), those with longer duration on ventilatory support (42 vs 3 days, respectively in BPD and no BPD patients, p <0.001) and longer duration of FiO2>0.30 (85 vs 5 days, respectively in BPD and no BPD patients, p <0.001). COMMENTS: The most relevant risk factors were low birth weight, severe hyaline membrane disease, duration of respiratory support and oxygen therapy, and nosocomial sepsis. The implementation of potentially better practices to reduce lung injury in neonates must be addressed to improve practices to decrease these risk factors.Sociedade Portuguesa de PneumologiaRepositório do Hospital Prof. Doutor Fernando FonsecaGuimarães, HRocha, GVasconcellos, GProença, ECarreira, MLSossai, MRMorais, BMartins, IRodrigues, TSevero, M2012-08-21T09:08:07Z2010-01-01T00:00:00Z2010-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.10/658engRev Port Pneumol. 2010 May-Jun;16(3):419-300873-2159info: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:RCAAP2022-09-20T15:51:32Zoai:repositorio.hff.min-saude.pt:10400.10/658Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T15:51:53.910280Repositório 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 Risk factors for bronchopulmonary dysplasia in five portuguese neonatal intensive care units
Factores de risco de displasia broncopulmonar em cinco unidades portuguesas de cuidados intensivos neonatais
title Risk factors for bronchopulmonary dysplasia in five portuguese neonatal intensive care units
spellingShingle Risk factors for bronchopulmonary dysplasia in five portuguese neonatal intensive care units
Guimarães, H
Displasia broncopulmonar
Unidade de cuidados intensivos pediátricos
Criança
Portugal
Bronchopulmonary dysplasia
Neonatal intensive care units
title_short Risk factors for bronchopulmonary dysplasia in five portuguese neonatal intensive care units
title_full Risk factors for bronchopulmonary dysplasia in five portuguese neonatal intensive care units
title_fullStr Risk factors for bronchopulmonary dysplasia in five portuguese neonatal intensive care units
title_full_unstemmed Risk factors for bronchopulmonary dysplasia in five portuguese neonatal intensive care units
title_sort Risk factors for bronchopulmonary dysplasia in five portuguese neonatal intensive care units
author Guimarães, H
author_facet Guimarães, H
Rocha, G
Vasconcellos, G
Proença, E
Carreira, ML
Sossai, MR
Morais, B
Martins, I
Rodrigues, T
Severo, M
author_role author
author2 Rocha, G
Vasconcellos, G
Proença, E
Carreira, ML
Sossai, MR
Morais, B
Martins, I
Rodrigues, T
Severo, M
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório do Hospital Prof. Doutor Fernando Fonseca
dc.contributor.author.fl_str_mv Guimarães, H
Rocha, G
Vasconcellos, G
Proença, E
Carreira, ML
Sossai, MR
Morais, B
Martins, I
Rodrigues, T
Severo, M
dc.subject.por.fl_str_mv Displasia broncopulmonar
Unidade de cuidados intensivos pediátricos
Criança
Portugal
Bronchopulmonary dysplasia
Neonatal intensive care units
topic Displasia broncopulmonar
Unidade de cuidados intensivos pediátricos
Criança
Portugal
Bronchopulmonary dysplasia
Neonatal intensive care units
description The pathogenesis of bronchopulmonary dysplasia (BPD) is clearly multifactorial. Specific pathogenic risk factors are prematurity, respiratory distress, oxygen supplementation, mechanical ventilation (MV), inflammation, patent ductus arteriosus (PDA), etc. AIM: To evaluate BPD prevalence and to identify risk factors for BPD in five Portuguese Neonatal Intensive Care Units in order to develop better practices the management of these newborns. MATERIAL AND METHODS: 256 very low birth weight infants with gestational age (GA) <30 weeks and/or birthweight (BW) <1250 g admitted in five Portuguese NICUs, between 2004 and 2006 were studied. A protocol was filled in based on clinical information registered in the hospital charts. BPD was defined as oxygen dependency at 36 weeks of postconceptional age. RESULTS: BPD prevalence was 12.9% (33/256). BPD risk decreased 46% per GA week and of 39% per 100g BW. BPD risk was significantly higher among newborns with low BW (adj OR= 0.73, 95% CI=0.57- 0.95), severe hyaline membrane disease (adj OR= 9.85, 95% CI=1.05-92.35), and those with sepsis (adj OR=6.22, 95% CI=1.68-23.02), those with longer duration on ventilatory support (42 vs 3 days, respectively in BPD and no BPD patients, p <0.001) and longer duration of FiO2>0.30 (85 vs 5 days, respectively in BPD and no BPD patients, p <0.001). COMMENTS: The most relevant risk factors were low birth weight, severe hyaline membrane disease, duration of respiratory support and oxygen therapy, and nosocomial sepsis. The implementation of potentially better practices to reduce lung injury in neonates must be addressed to improve practices to decrease these risk factors.
publishDate 2010
dc.date.none.fl_str_mv 2010-01-01T00:00:00Z
2010-01-01T00:00:00Z
2012-08-21T09:08:07Z
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/10400.10/658
url http://hdl.handle.net/10400.10/658
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Rev Port Pneumol. 2010 May-Jun;16(3):419-30
0873-2159
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 Sociedade Portuguesa de Pneumologia
publisher.none.fl_str_mv Sociedade Portuguesa de Pneumologia
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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collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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