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Adverse maternal outcomes associated with fetal macrosomia: what are the risk factors beyond birthweight?

BACKGROUND: To identify risk factors, beyond fetal weight, associated with adverse maternal outcomes in delivering infants with a birthweight of 4000 g or greater, and to quantify their role in maternal complications. METHODS: All women (n = 1564) with singleton pregnancies who attempted vaginal del...

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Autores principales: Fuchs, Florent, Bouyer, Jean, Rozenberg, Patrick, Senat, Marie-Victoire
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3623722/
https://www.ncbi.nlm.nih.gov/pubmed/23565692
http://dx.doi.org/10.1186/1471-2393-13-90
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author Fuchs, Florent
Bouyer, Jean
Rozenberg, Patrick
Senat, Marie-Victoire
author_facet Fuchs, Florent
Bouyer, Jean
Rozenberg, Patrick
Senat, Marie-Victoire
author_sort Fuchs, Florent
collection PubMed
description BACKGROUND: To identify risk factors, beyond fetal weight, associated with adverse maternal outcomes in delivering infants with a birthweight of 4000 g or greater, and to quantify their role in maternal complications. METHODS: All women (n = 1564) with singleton pregnancies who attempted vaginal delivery and delivered infants weighing at least 4000 g, in two French tertiary care centers from 2005 to 2008, were included in our study. The studied outcome was maternal complications defined as composite item including the occurrence of a third- or fourth-degree perineal laceration, or the occurrence of severe postpartum hemorrhage requiring the use of prostaglandins, uterine artery embolization, internal iliac artery ligation or haemostatic hysterectomy, or the occurrence of blood transfusion. Univariate analysis, multivariable logistic regression and estimation of attributable risk were used. RESULTS: Maternal complications were increased in Asian women (adjusted odds ratio [aOR], 3.1; 95% confidence interval [CI], 1.1–9.3, Attributable risk (AR): 3%), in prolonged labor (aOR = 1.9 [95% CI; 1.1–3.4], AR = 12%) and in cesarean delivery during labor (aOR = 2.2 [95% CI; 1.3–3.9], AR = 17%). Delivering infants with a birthweight > 4500 g also increased the occurrence of maternal complications (aOR = 2.7 [95% CI; 1.4–5.1]) but with an attributable risk of only 10%. Multiparous women with a previous delivery of a macrosomic infant were at lower risk of maternal complications (aOR = 0.5 [95% CI; 0.2–0.9]). CONCLUSION: In women delivering infants with a birthweight of 4000 g or greater, some maternal characteristics as well as labor parameters may worsen maternal outcome beyond the influence of increased fetal weight.
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spelling pubmed-36237222013-04-12 Adverse maternal outcomes associated with fetal macrosomia: what are the risk factors beyond birthweight? Fuchs, Florent Bouyer, Jean Rozenberg, Patrick Senat, Marie-Victoire BMC Pregnancy Childbirth Research Article BACKGROUND: To identify risk factors, beyond fetal weight, associated with adverse maternal outcomes in delivering infants with a birthweight of 4000 g or greater, and to quantify their role in maternal complications. METHODS: All women (n = 1564) with singleton pregnancies who attempted vaginal delivery and delivered infants weighing at least 4000 g, in two French tertiary care centers from 2005 to 2008, were included in our study. The studied outcome was maternal complications defined as composite item including the occurrence of a third- or fourth-degree perineal laceration, or the occurrence of severe postpartum hemorrhage requiring the use of prostaglandins, uterine artery embolization, internal iliac artery ligation or haemostatic hysterectomy, or the occurrence of blood transfusion. Univariate analysis, multivariable logistic regression and estimation of attributable risk were used. RESULTS: Maternal complications were increased in Asian women (adjusted odds ratio [aOR], 3.1; 95% confidence interval [CI], 1.1–9.3, Attributable risk (AR): 3%), in prolonged labor (aOR = 1.9 [95% CI; 1.1–3.4], AR = 12%) and in cesarean delivery during labor (aOR = 2.2 [95% CI; 1.3–3.9], AR = 17%). Delivering infants with a birthweight > 4500 g also increased the occurrence of maternal complications (aOR = 2.7 [95% CI; 1.4–5.1]) but with an attributable risk of only 10%. Multiparous women with a previous delivery of a macrosomic infant were at lower risk of maternal complications (aOR = 0.5 [95% CI; 0.2–0.9]). CONCLUSION: In women delivering infants with a birthweight of 4000 g or greater, some maternal characteristics as well as labor parameters may worsen maternal outcome beyond the influence of increased fetal weight. BioMed Central 2013-04-08 /pmc/articles/PMC3623722/ /pubmed/23565692 http://dx.doi.org/10.1186/1471-2393-13-90 Text en Copyright © 2013 Fuchs et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Fuchs, Florent
Bouyer, Jean
Rozenberg, Patrick
Senat, Marie-Victoire
Adverse maternal outcomes associated with fetal macrosomia: what are the risk factors beyond birthweight?
title Adverse maternal outcomes associated with fetal macrosomia: what are the risk factors beyond birthweight?
title_full Adverse maternal outcomes associated with fetal macrosomia: what are the risk factors beyond birthweight?
title_fullStr Adverse maternal outcomes associated with fetal macrosomia: what are the risk factors beyond birthweight?
title_full_unstemmed Adverse maternal outcomes associated with fetal macrosomia: what are the risk factors beyond birthweight?
title_short Adverse maternal outcomes associated with fetal macrosomia: what are the risk factors beyond birthweight?
title_sort adverse maternal outcomes associated with fetal macrosomia: what are the risk factors beyond birthweight?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3623722/
https://www.ncbi.nlm.nih.gov/pubmed/23565692
http://dx.doi.org/10.1186/1471-2393-13-90
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