Small for gestational age very preterm infants present a higher risk of developing bronchopulmonary dysplasia

Detalhes bibliográficos
Autor(a) principal: Rocha, G
Data de Publicação: 2019
Outros Autores: Lima, F, Machado, AP, Guimarães, H, Proença, E, Carvalho, C, Barroso, R, et al.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.10/2360
Resumo: INTRODUCTION: Several studies assessed the influence of a low birth weight on bronchopulmonary dysplasia (BPD), but not all could find a significant association. Our aim was to assess the association between low birth weight and BPD in preterm infants, prospectively recruited at 11 level III Portuguese neonatal centers. METHODS: Obstetrical and neonatal data on mothers and preterm infants with gestational ages between 24 and 30 weeks, born during 2015 and 2016 after a surveilled pregnancy, were analyzed. Neonates were considered small for gestational age (SGA) when their birthweight was below the 10th centile of Fenton's growth chats and BPD was defined as the dependency for oxygen therapy until 36 weeks of corrected age. Statistical analysis was performed using IBM SPSS ® statistics 23 and a p-value <0.05 was considered statistically significant. RESULTS: Out of 614, a total of 494 preterm infants delivered from 410 women were enrolled in the study; 40 (8.0% ) infants with SGA criteria. SGA were more often associated with a single pregnancy, had greater use of antenatal corticosteroids, increased prevalence of gestational hypertensive disorders, C-section, rupture of membranes below 18 hours, rate of intubation in the delivery room, use of surfactant treatment, oxygen therapy, mechanical ventilation need, BPD, cystic periventricular leukomalacia, nosocomial sepsis and pneumonia; had lower prevalence of chorioamnionitis, and lower Apgar scores. The multivariate analysis by logistic regression, adjusted for BPD risk factors revealed a significant association between SGA and BPD: OR = 5.2 [CI: 1.46-18.58]; p = 0.01. CONCLUSION: The results of this study increase the scientific evidence that SGA is an independent risk factor for BPD.
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spelling Small for gestational age very preterm infants present a higher risk of developing bronchopulmonary dysplasiaPremature infantBronchopulmonary dysplasia/INTRODUCTION: Several studies assessed the influence of a low birth weight on bronchopulmonary dysplasia (BPD), but not all could find a significant association. Our aim was to assess the association between low birth weight and BPD in preterm infants, prospectively recruited at 11 level III Portuguese neonatal centers. METHODS: Obstetrical and neonatal data on mothers and preterm infants with gestational ages between 24 and 30 weeks, born during 2015 and 2016 after a surveilled pregnancy, were analyzed. Neonates were considered small for gestational age (SGA) when their birthweight was below the 10th centile of Fenton's growth chats and BPD was defined as the dependency for oxygen therapy until 36 weeks of corrected age. Statistical analysis was performed using IBM SPSS ® statistics 23 and a p-value <0.05 was considered statistically significant. RESULTS: Out of 614, a total of 494 preterm infants delivered from 410 women were enrolled in the study; 40 (8.0% ) infants with SGA criteria. SGA were more often associated with a single pregnancy, had greater use of antenatal corticosteroids, increased prevalence of gestational hypertensive disorders, C-section, rupture of membranes below 18 hours, rate of intubation in the delivery room, use of surfactant treatment, oxygen therapy, mechanical ventilation need, BPD, cystic periventricular leukomalacia, nosocomial sepsis and pneumonia; had lower prevalence of chorioamnionitis, and lower Apgar scores. The multivariate analysis by logistic regression, adjusted for BPD risk factors revealed a significant association between SGA and BPD: OR = 5.2 [CI: 1.46-18.58]; p = 0.01. CONCLUSION: The results of this study increase the scientific evidence that SGA is an independent risk factor for BPD.IOS PressRepositório do Hospital Prof. Doutor Fernando FonsecaRocha, GLima, FMachado, APGuimarães, HProença, ECarvalho, CBarroso, R, et al.2019-12-17T14:17:05Z2019-01-01T00:00:00Z2019-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.10/2360engJ Neonatal Perinatal Med. 2019 Jun 251878-442910.3233/NPM-180129metadata only accessinfo: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:RCAAP2022-09-20T15:53:02ZPortal AgregadorONG
dc.title.none.fl_str_mv Small for gestational age very preterm infants present a higher risk of developing bronchopulmonary dysplasia
title Small for gestational age very preterm infants present a higher risk of developing bronchopulmonary dysplasia
spellingShingle Small for gestational age very preterm infants present a higher risk of developing bronchopulmonary dysplasia
Rocha, G
Premature infant
Bronchopulmonary dysplasia/
title_short Small for gestational age very preterm infants present a higher risk of developing bronchopulmonary dysplasia
title_full Small for gestational age very preterm infants present a higher risk of developing bronchopulmonary dysplasia
title_fullStr Small for gestational age very preterm infants present a higher risk of developing bronchopulmonary dysplasia
title_full_unstemmed Small for gestational age very preterm infants present a higher risk of developing bronchopulmonary dysplasia
title_sort Small for gestational age very preterm infants present a higher risk of developing bronchopulmonary dysplasia
author Rocha, G
author_facet Rocha, G
Lima, F
Machado, AP
Guimarães, H
Proença, E
Carvalho, C
Barroso, R, et al.
author_role author
author2 Lima, F
Machado, AP
Guimarães, H
Proença, E
Carvalho, C
Barroso, R, et al.
author2_role 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 Rocha, G
Lima, F
Machado, AP
Guimarães, H
Proença, E
Carvalho, C
Barroso, R, et al.
dc.subject.por.fl_str_mv Premature infant
Bronchopulmonary dysplasia/
topic Premature infant
Bronchopulmonary dysplasia/
description INTRODUCTION: Several studies assessed the influence of a low birth weight on bronchopulmonary dysplasia (BPD), but not all could find a significant association. Our aim was to assess the association between low birth weight and BPD in preterm infants, prospectively recruited at 11 level III Portuguese neonatal centers. METHODS: Obstetrical and neonatal data on mothers and preterm infants with gestational ages between 24 and 30 weeks, born during 2015 and 2016 after a surveilled pregnancy, were analyzed. Neonates were considered small for gestational age (SGA) when their birthweight was below the 10th centile of Fenton's growth chats and BPD was defined as the dependency for oxygen therapy until 36 weeks of corrected age. Statistical analysis was performed using IBM SPSS ® statistics 23 and a p-value <0.05 was considered statistically significant. RESULTS: Out of 614, a total of 494 preterm infants delivered from 410 women were enrolled in the study; 40 (8.0% ) infants with SGA criteria. SGA were more often associated with a single pregnancy, had greater use of antenatal corticosteroids, increased prevalence of gestational hypertensive disorders, C-section, rupture of membranes below 18 hours, rate of intubation in the delivery room, use of surfactant treatment, oxygen therapy, mechanical ventilation need, BPD, cystic periventricular leukomalacia, nosocomial sepsis and pneumonia; had lower prevalence of chorioamnionitis, and lower Apgar scores. The multivariate analysis by logistic regression, adjusted for BPD risk factors revealed a significant association between SGA and BPD: OR = 5.2 [CI: 1.46-18.58]; p = 0.01. CONCLUSION: The results of this study increase the scientific evidence that SGA is an independent risk factor for BPD.
publishDate 2019
dc.date.none.fl_str_mv 2019-12-17T14:17:05Z
2019-01-01T00:00:00Z
2019-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.10/2360
url http://hdl.handle.net/10400.10/2360
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv J Neonatal Perinatal Med. 2019 Jun 25
1878-4429
10.3233/NPM-180129
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dc.publisher.none.fl_str_mv IOS Press
publisher.none.fl_str_mv IOS Press
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instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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