Cargando…
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....
Autores principales: | , , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1783316961383415808 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5916101 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT tanncallyj perinatalriskfactorsforneonatalencephalopathyanunmatchedcasecontrolstudy AT nakakeetomargaret perinatalriskfactorsforneonatalencephalopathyanunmatchedcasecontrolstudy AT willeybarbaraa perinatalriskfactorsforneonatalencephalopathyanunmatchedcasecontrolstudy AT sewegabamargaret perinatalriskfactorsforneonatalencephalopathyanunmatchedcasecontrolstudy AT webbemilyl perinatalriskfactorsforneonatalencephalopathyanunmatchedcasecontrolstudy AT okeibby perinatalriskfactorsforneonatalencephalopathyanunmatchedcasecontrolstudy AT mutuuzaemmanuelderek perinatalriskfactorsforneonatalencephalopathyanunmatchedcasecontrolstudy AT peeblesdonald perinatalriskfactorsforneonatalencephalopathyanunmatchedcasecontrolstudy AT musokemargaret perinatalriskfactorsforneonatalencephalopathyanunmatchedcasecontrolstudy AT harriskathryna perinatalriskfactorsforneonatalencephalopathyanunmatchedcasecontrolstudy AT sebireneilj perinatalriskfactorsforneonatalencephalopathyanunmatchedcasecontrolstudy AT kleinnigel perinatalriskfactorsforneonatalencephalopathyanunmatchedcasecontrolstudy AT kurinczukjenniferj perinatalriskfactorsforneonatalencephalopathyanunmatchedcasecontrolstudy AT elliottalisonm perinatalriskfactorsforneonatalencephalopathyanunmatchedcasecontrolstudy AT robertsonnicolaj perinatalriskfactorsforneonatalencephalopathyanunmatchedcasecontrolstudy |