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Perinatal risk factors for neonatal encephalopathy: an unmatched case-control study

OBJECTIVE: Neonatal encephalopathy (NE) is the third leading cause of child mortality. Preclinical studies suggest infection and inflammation can sensitise or precondition the newborn brain to injury. This study examined perinatal risks factor for NE in Uganda. DESIGN: Unmatched case–control study....

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Autores principales: Tann, Cally J, Nakakeeto, Margaret, Willey, Barbara A, Sewegaba, Margaret, Webb, Emily L, Oke, Ibby, Mutuuza, Emmanuel Derek, Peebles, Donald, Musoke, Margaret, Harris, Kathryn A, Sebire, Neil J, Klein, Nigel, Kurinczuk, Jennifer J, Elliott, Alison M, Robertson, Nicola J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916101/
https://www.ncbi.nlm.nih.gov/pubmed/28780500
http://dx.doi.org/10.1136/archdischild-2017-312744
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author Tann, Cally J
Nakakeeto, Margaret
Willey, Barbara A
Sewegaba, Margaret
Webb, Emily L
Oke, Ibby
Mutuuza, Emmanuel Derek
Peebles, Donald
Musoke, Margaret
Harris, Kathryn A
Sebire, Neil J
Klein, Nigel
Kurinczuk, Jennifer J
Elliott, Alison M
Robertson, Nicola J
author_facet Tann, Cally J
Nakakeeto, Margaret
Willey, Barbara A
Sewegaba, Margaret
Webb, Emily L
Oke, Ibby
Mutuuza, Emmanuel Derek
Peebles, Donald
Musoke, Margaret
Harris, Kathryn A
Sebire, Neil J
Klein, Nigel
Kurinczuk, Jennifer J
Elliott, Alison M
Robertson, Nicola J
author_sort Tann, Cally J
collection PubMed
description OBJECTIVE: Neonatal encephalopathy (NE) is the third leading cause of child mortality. Preclinical studies suggest infection and inflammation can sensitise or precondition the newborn brain to injury. This study examined perinatal risks factor for NE in Uganda. DESIGN: Unmatched case–control study. SETTING: Mulago National Referral Hospital, Kampala, Uganda. METHODS: 210 term infants with NE and 409 unaffected term infants as controls were recruited over 13 months. Data were collected on preconception, antepartum and intrapartum exposures. Blood culture, species-specific bacterial real-time PCR, C reactive protein and placental histology for chorioamnionitis and funisitis identified maternal and early newborn infection and inflammation. Multivariable logistic regression examined associations with NE. RESULTS: Neonatal bacteraemia (adjusted OR (aOR) 8.67 (95% CI 1.51 to 49.74), n=315) and histological funisitis (aOR 11.80 (95% CI 2.19 to 63.45), n=162) but not chorioamnionitis (aOR 3.20 (95% CI 0.66 to 15.52), n=162) were independent risk factors for NE. Among encephalopathic infants, neonatal case fatality was not significantly higher when exposed to early neonatal bacteraemia (OR 1.65 (95% CI 0.62 to 4.39), n=208). Intrapartum antibiotic use did not improve neonatal survival (p=0.826). After regression analysis, other identified perinatal risk factors (n=619) included hypertension in pregnancy (aOR 3.77), male infant (aOR 2.51), non-cephalic presentation (aOR 5.74), lack of fetal monitoring (aOR 2.75), augmentation (aOR 2.23), obstructed labour (aOR 3.8) and an acute intrapartum event (aOR 8.74). CONCLUSIONS: Perinatal infection and inflammation are independent risk factors for NE in this low-resource setting, supporting a role in the aetiological pathway of term brain injury. Intrapartum antibiotic administration did not mitigate against adverse outcomes. The importance of intrapartum risk factors in this sub-Saharan African setting is highlighted.
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spelling pubmed-59161012018-04-27 Perinatal risk factors for neonatal encephalopathy: an unmatched case-control study Tann, Cally J Nakakeeto, Margaret Willey, Barbara A Sewegaba, Margaret Webb, Emily L Oke, Ibby Mutuuza, Emmanuel Derek Peebles, Donald Musoke, Margaret Harris, Kathryn A Sebire, Neil J Klein, Nigel Kurinczuk, Jennifer J Elliott, Alison M Robertson, Nicola J Arch Dis Child Fetal Neonatal Ed Original Article OBJECTIVE: Neonatal encephalopathy (NE) is the third leading cause of child mortality. Preclinical studies suggest infection and inflammation can sensitise or precondition the newborn brain to injury. This study examined perinatal risks factor for NE in Uganda. DESIGN: Unmatched case–control study. SETTING: Mulago National Referral Hospital, Kampala, Uganda. METHODS: 210 term infants with NE and 409 unaffected term infants as controls were recruited over 13 months. Data were collected on preconception, antepartum and intrapartum exposures. Blood culture, species-specific bacterial real-time PCR, C reactive protein and placental histology for chorioamnionitis and funisitis identified maternal and early newborn infection and inflammation. Multivariable logistic regression examined associations with NE. RESULTS: Neonatal bacteraemia (adjusted OR (aOR) 8.67 (95% CI 1.51 to 49.74), n=315) and histological funisitis (aOR 11.80 (95% CI 2.19 to 63.45), n=162) but not chorioamnionitis (aOR 3.20 (95% CI 0.66 to 15.52), n=162) were independent risk factors for NE. Among encephalopathic infants, neonatal case fatality was not significantly higher when exposed to early neonatal bacteraemia (OR 1.65 (95% CI 0.62 to 4.39), n=208). Intrapartum antibiotic use did not improve neonatal survival (p=0.826). After regression analysis, other identified perinatal risk factors (n=619) included hypertension in pregnancy (aOR 3.77), male infant (aOR 2.51), non-cephalic presentation (aOR 5.74), lack of fetal monitoring (aOR 2.75), augmentation (aOR 2.23), obstructed labour (aOR 3.8) and an acute intrapartum event (aOR 8.74). CONCLUSIONS: Perinatal infection and inflammation are independent risk factors for NE in this low-resource setting, supporting a role in the aetiological pathway of term brain injury. Intrapartum antibiotic administration did not mitigate against adverse outcomes. The importance of intrapartum risk factors in this sub-Saharan African setting is highlighted. BMJ Publishing Group 2018-05 2017-08-05 /pmc/articles/PMC5916101/ /pubmed/28780500 http://dx.doi.org/10.1136/archdischild-2017-312744 Text en © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/
spellingShingle Original Article
Tann, Cally J
Nakakeeto, Margaret
Willey, Barbara A
Sewegaba, Margaret
Webb, Emily L
Oke, Ibby
Mutuuza, Emmanuel Derek
Peebles, Donald
Musoke, Margaret
Harris, Kathryn A
Sebire, Neil J
Klein, Nigel
Kurinczuk, Jennifer J
Elliott, Alison M
Robertson, Nicola J
Perinatal risk factors for neonatal encephalopathy: an unmatched case-control study
title Perinatal risk factors for neonatal encephalopathy: an unmatched case-control study
title_full Perinatal risk factors for neonatal encephalopathy: an unmatched case-control study
title_fullStr Perinatal risk factors for neonatal encephalopathy: an unmatched case-control study
title_full_unstemmed Perinatal risk factors for neonatal encephalopathy: an unmatched case-control study
title_short Perinatal risk factors for neonatal encephalopathy: an unmatched case-control study
title_sort perinatal risk factors for neonatal encephalopathy: an unmatched case-control study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916101/
https://www.ncbi.nlm.nih.gov/pubmed/28780500
http://dx.doi.org/10.1136/archdischild-2017-312744
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