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Associations between birth at, or after, 41 weeks gestation and perinatal encephalopathy: a cohort study

BACKGROUND: Preterm birth causes long-term problems, even for infants born 1 or 2 weeks early. However, less is known about infants born after their due date and over a quarter of infants are born over 1 week late, and many still remain undelivered after 2 weeks. The aim of this work is to quantify...

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Autores principales: Odd, David E, Yau, Christopher, Winter, Cathy, Draycott, Timothy, Rasmussen, Finn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5842989/
https://www.ncbi.nlm.nih.gov/pubmed/29637179
http://dx.doi.org/10.1136/bmjpo-2017-000010
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author Odd, David E
Yau, Christopher
Winter, Cathy
Draycott, Timothy
Rasmussen, Finn
author_facet Odd, David E
Yau, Christopher
Winter, Cathy
Draycott, Timothy
Rasmussen, Finn
author_sort Odd, David E
collection PubMed
description BACKGROUND: Preterm birth causes long-term problems, even for infants born 1 or 2 weeks early. However, less is known about infants born after their due date and over a quarter of infants are born over 1 week late, and many still remain undelivered after 2 weeks. The aim of this work is to quantify the risks of infants developing encephalopathy when birth occurs after the due date, and if other proposed risk factors modify this relationship. METHODS: The dataset contain information on 4 036 346 infants born in Sweden between 1973 and 2012. Exposure was defined as birth 7, or more, days after the infants’ due date. The primary outcome was the development of neonatal encephalopathy (defined as seizures, encephalopathy or brain injury caused by asphyxia or with unspecified cause). Covariates were selected as presumed confounders a priori. RESULTS: 28.4% infants were born 1 or more weeks after their due date. An infant’s risk of being born with encephalopathy was higher in the post 41 weeks group in the unadjusted (OR 1.40 (95% CI 1.32 to 1.49)) and final model (OR 1.38 (95% CI 1.29 to 1.47)), with the relative odds of encephalopathy increasing by an estimated 20% per week after the due date, and modified by maternal age (P=0.022). CONCLUSIONS: Singleton infants born at, or after, 41 weeks gestation have lower Apgar scores and higher risk of developing encephalopathy in the newborn period, and the association appeared more marked in older mothers. These data could be useful if provided to women as part of their decision-making.
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spelling pubmed-58429892018-04-10 Associations between birth at, or after, 41 weeks gestation and perinatal encephalopathy: a cohort study Odd, David E Yau, Christopher Winter, Cathy Draycott, Timothy Rasmussen, Finn BMJ Paediatr Open Original Article BACKGROUND: Preterm birth causes long-term problems, even for infants born 1 or 2 weeks early. However, less is known about infants born after their due date and over a quarter of infants are born over 1 week late, and many still remain undelivered after 2 weeks. The aim of this work is to quantify the risks of infants developing encephalopathy when birth occurs after the due date, and if other proposed risk factors modify this relationship. METHODS: The dataset contain information on 4 036 346 infants born in Sweden between 1973 and 2012. Exposure was defined as birth 7, or more, days after the infants’ due date. The primary outcome was the development of neonatal encephalopathy (defined as seizures, encephalopathy or brain injury caused by asphyxia or with unspecified cause). Covariates were selected as presumed confounders a priori. RESULTS: 28.4% infants were born 1 or more weeks after their due date. An infant’s risk of being born with encephalopathy was higher in the post 41 weeks group in the unadjusted (OR 1.40 (95% CI 1.32 to 1.49)) and final model (OR 1.38 (95% CI 1.29 to 1.47)), with the relative odds of encephalopathy increasing by an estimated 20% per week after the due date, and modified by maternal age (P=0.022). CONCLUSIONS: Singleton infants born at, or after, 41 weeks gestation have lower Apgar scores and higher risk of developing encephalopathy in the newborn period, and the association appeared more marked in older mothers. These data could be useful if provided to women as part of their decision-making. BMJ Publishing Group 2018-01-24 /pmc/articles/PMC5842989/ /pubmed/29637179 http://dx.doi.org/10.1136/bmjpo-2017-000010 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 Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Original Article
Odd, David E
Yau, Christopher
Winter, Cathy
Draycott, Timothy
Rasmussen, Finn
Associations between birth at, or after, 41 weeks gestation and perinatal encephalopathy: a cohort study
title Associations between birth at, or after, 41 weeks gestation and perinatal encephalopathy: a cohort study
title_full Associations between birth at, or after, 41 weeks gestation and perinatal encephalopathy: a cohort study
title_fullStr Associations between birth at, or after, 41 weeks gestation and perinatal encephalopathy: a cohort study
title_full_unstemmed Associations between birth at, or after, 41 weeks gestation and perinatal encephalopathy: a cohort study
title_short Associations between birth at, or after, 41 weeks gestation and perinatal encephalopathy: a cohort study
title_sort associations between birth at, or after, 41 weeks gestation and perinatal encephalopathy: a cohort study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5842989/
https://www.ncbi.nlm.nih.gov/pubmed/29637179
http://dx.doi.org/10.1136/bmjpo-2017-000010
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