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Impact of adolescent age on maternal and neonatal outcomes in the Born in Bradford cohort

OBJECTIVES: Explore associations between maternal and neonatal outcomes and maternal age, with particular reference to adolescent women. DESIGN: Population-based cohort study. SETTING: Maternity department of a large hospital in Northern England. PARTICIPANTS: Primiparous women delivering a singleto...

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Autores principales: Marvin-Dowle, Katie, Kilner, Karen, Burley, Victoria Jane, Soltani, Hora
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5857698/
https://www.ncbi.nlm.nih.gov/pubmed/29549196
http://dx.doi.org/10.1136/bmjopen-2017-016258
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author Marvin-Dowle, Katie
Kilner, Karen
Burley, Victoria Jane
Soltani, Hora
author_facet Marvin-Dowle, Katie
Kilner, Karen
Burley, Victoria Jane
Soltani, Hora
author_sort Marvin-Dowle, Katie
collection PubMed
description OBJECTIVES: Explore associations between maternal and neonatal outcomes and maternal age, with particular reference to adolescent women. DESIGN: Population-based cohort study. SETTING: Maternity department of a large hospital in Northern England. PARTICIPANTS: Primiparous women delivering a singleton at Bradford Royal Infirmary between March 2007 and December 2010 aged ≤19 years (n=640) or 20–34 years (n=3951). Subgroup analysis was performed using women aged ≤16 years (n=68). Women aged 20–34 years were used as the reference group. PRIMARY OUTCOME MEASURES: Maternal and neonatal outcomes. RESULTS: The odds of extremely low birth weight (<1000 g) were significantly higher in the adolescent group (≤19 years) compared with the reference group (adjusted OR (aOR) 4.13, 95% CI 1.41 to 12.11). The odds of very (<32 weeks) and extremely (<28 weeks) preterm delivery were also higher in the adolescent group (aOR 2.12, 95% CI 1.06 to 4.25 and aOR 5.06, 95% CI 1.23 to 20.78, respectively). Women in the adolescent group had lower odds of gestational diabetes (aOR 0.35, 95% CI 0.20 to 0.62), caesarean delivery (aOR 0.53, 95% CI 0.42 to 0.67 and instrumental delivery (aOR 0.53, 95% CI 0.41 to 0.67). CONCLUSIONS: This study identifies important differences in maternal and neonatal outcomes between women by age group. These findings could help in identifying at-risk groups for additional support and tailored interventions to minimise the risk of adverse outcomes for these vulnerable groups. Further work is needed to identify the causal mechanisms linking age with outcomes in adolescent women where significant gaps in the literature exist.
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spelling pubmed-58576982018-03-20 Impact of adolescent age on maternal and neonatal outcomes in the Born in Bradford cohort Marvin-Dowle, Katie Kilner, Karen Burley, Victoria Jane Soltani, Hora BMJ Open Obstetrics and Gynaecology OBJECTIVES: Explore associations between maternal and neonatal outcomes and maternal age, with particular reference to adolescent women. DESIGN: Population-based cohort study. SETTING: Maternity department of a large hospital in Northern England. PARTICIPANTS: Primiparous women delivering a singleton at Bradford Royal Infirmary between March 2007 and December 2010 aged ≤19 years (n=640) or 20–34 years (n=3951). Subgroup analysis was performed using women aged ≤16 years (n=68). Women aged 20–34 years were used as the reference group. PRIMARY OUTCOME MEASURES: Maternal and neonatal outcomes. RESULTS: The odds of extremely low birth weight (<1000 g) were significantly higher in the adolescent group (≤19 years) compared with the reference group (adjusted OR (aOR) 4.13, 95% CI 1.41 to 12.11). The odds of very (<32 weeks) and extremely (<28 weeks) preterm delivery were also higher in the adolescent group (aOR 2.12, 95% CI 1.06 to 4.25 and aOR 5.06, 95% CI 1.23 to 20.78, respectively). Women in the adolescent group had lower odds of gestational diabetes (aOR 0.35, 95% CI 0.20 to 0.62), caesarean delivery (aOR 0.53, 95% CI 0.42 to 0.67 and instrumental delivery (aOR 0.53, 95% CI 0.41 to 0.67). CONCLUSIONS: This study identifies important differences in maternal and neonatal outcomes between women by age group. These findings could help in identifying at-risk groups for additional support and tailored interventions to minimise the risk of adverse outcomes for these vulnerable groups. Further work is needed to identify the causal mechanisms linking age with outcomes in adolescent women where significant gaps in the literature exist. BMJ Publishing Group 2018-03-16 /pmc/articles/PMC5857698/ /pubmed/29549196 http://dx.doi.org/10.1136/bmjopen-2017-016258 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 Obstetrics and Gynaecology
Marvin-Dowle, Katie
Kilner, Karen
Burley, Victoria Jane
Soltani, Hora
Impact of adolescent age on maternal and neonatal outcomes in the Born in Bradford cohort
title Impact of adolescent age on maternal and neonatal outcomes in the Born in Bradford cohort
title_full Impact of adolescent age on maternal and neonatal outcomes in the Born in Bradford cohort
title_fullStr Impact of adolescent age on maternal and neonatal outcomes in the Born in Bradford cohort
title_full_unstemmed Impact of adolescent age on maternal and neonatal outcomes in the Born in Bradford cohort
title_short Impact of adolescent age on maternal and neonatal outcomes in the Born in Bradford cohort
title_sort impact of adolescent age on maternal and neonatal outcomes in the born in bradford cohort
topic Obstetrics and Gynaecology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5857698/
https://www.ncbi.nlm.nih.gov/pubmed/29549196
http://dx.doi.org/10.1136/bmjopen-2017-016258
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