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Risk factors for obstetric anal sphincter injuries at vaginal birth after caesarean: a retrospective cohort study

INTRODUCTION AND HYPOTHESIS: Vaginal birth after caesarean (VBAC) is associated with an increased risk of obstetric anal sphincter injuries (OASIS). However, specific factors that influence the risk of OASIS at VBAC have not been studied, particularly whether there are specific baseline characterist...

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Autores principales: D’Souza, Joanna C., Monga, Ash, Tincello, Douglas G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6795633/
https://www.ncbi.nlm.nih.gov/pubmed/31267138
http://dx.doi.org/10.1007/s00192-019-03978-x
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author D’Souza, Joanna C.
Monga, Ash
Tincello, Douglas G.
author_facet D’Souza, Joanna C.
Monga, Ash
Tincello, Douglas G.
author_sort D’Souza, Joanna C.
collection PubMed
description INTRODUCTION AND HYPOTHESIS: Vaginal birth after caesarean (VBAC) is associated with an increased risk of obstetric anal sphincter injuries (OASIS). However, specific factors that influence the risk of OASIS at VBAC have not been studied, particularly whether there are specific baseline characteristics of the first delivery which affect the subsequent perineal outcomes. METHODS: Retrospective analysis of prospectively collected data from University of Southampton NHS Foundation Trusts’ maternity database. This included secundiparous women with a previous caesarean delivery (CS) who achieved a singleton, term, cephalic vaginal delivery from 2004 to 2014. Univariate analysis compared maternal, intrapartum and neonatal factors of those who suffered OASIS at VBAC with those who did not. A binary logistic regression model calculated the adjusted, independent odds ratio (OR) of OASIS. RESULTS: A total of 1375 women met the inclusion criteria. The OASIS rate was 8.1%, a 1.4-fold increase compared with primiparous women [difference 2.4% (95% CI 1.1, 3.6)]. Those sustaining OASIS at VBAC were older (p = 0.011) and had infants of greater birth weight at initial caesarean (p < 0.001) and VBAC (p = 0.04). Analysis of odds ratios revealed that mediolateral episiotomy (MLE) at VBAC halved the risk of OASIS [37.5% VBAC with OASIS vs. 52.2% VBAC without OASIS (OR 0.51, 95% CI 0.32–0.81)], whereas an urgent CS at initial delivery doubled the risk [52.3% VBAC with OASIS vs. 34.9% VBAC without OASIS (OR 2.05, 95% CI 1.31–3.21)]. CONCLUSIONS: Advanced maternal age, increased infant birth weight and an urgent category of initial CS increase the risk of OASIS at VBAC, whereas MLE is protective.
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spelling pubmed-67956332019-10-25 Risk factors for obstetric anal sphincter injuries at vaginal birth after caesarean: a retrospective cohort study D’Souza, Joanna C. Monga, Ash Tincello, Douglas G. Int Urogynecol J Original Article INTRODUCTION AND HYPOTHESIS: Vaginal birth after caesarean (VBAC) is associated with an increased risk of obstetric anal sphincter injuries (OASIS). However, specific factors that influence the risk of OASIS at VBAC have not been studied, particularly whether there are specific baseline characteristics of the first delivery which affect the subsequent perineal outcomes. METHODS: Retrospective analysis of prospectively collected data from University of Southampton NHS Foundation Trusts’ maternity database. This included secundiparous women with a previous caesarean delivery (CS) who achieved a singleton, term, cephalic vaginal delivery from 2004 to 2014. Univariate analysis compared maternal, intrapartum and neonatal factors of those who suffered OASIS at VBAC with those who did not. A binary logistic regression model calculated the adjusted, independent odds ratio (OR) of OASIS. RESULTS: A total of 1375 women met the inclusion criteria. The OASIS rate was 8.1%, a 1.4-fold increase compared with primiparous women [difference 2.4% (95% CI 1.1, 3.6)]. Those sustaining OASIS at VBAC were older (p = 0.011) and had infants of greater birth weight at initial caesarean (p < 0.001) and VBAC (p = 0.04). Analysis of odds ratios revealed that mediolateral episiotomy (MLE) at VBAC halved the risk of OASIS [37.5% VBAC with OASIS vs. 52.2% VBAC without OASIS (OR 0.51, 95% CI 0.32–0.81)], whereas an urgent CS at initial delivery doubled the risk [52.3% VBAC with OASIS vs. 34.9% VBAC without OASIS (OR 2.05, 95% CI 1.31–3.21)]. CONCLUSIONS: Advanced maternal age, increased infant birth weight and an urgent category of initial CS increase the risk of OASIS at VBAC, whereas MLE is protective. Springer International Publishing 2019-07-02 2019 /pmc/articles/PMC6795633/ /pubmed/31267138 http://dx.doi.org/10.1007/s00192-019-03978-x Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
D’Souza, Joanna C.
Monga, Ash
Tincello, Douglas G.
Risk factors for obstetric anal sphincter injuries at vaginal birth after caesarean: a retrospective cohort study
title Risk factors for obstetric anal sphincter injuries at vaginal birth after caesarean: a retrospective cohort study
title_full Risk factors for obstetric anal sphincter injuries at vaginal birth after caesarean: a retrospective cohort study
title_fullStr Risk factors for obstetric anal sphincter injuries at vaginal birth after caesarean: a retrospective cohort study
title_full_unstemmed Risk factors for obstetric anal sphincter injuries at vaginal birth after caesarean: a retrospective cohort study
title_short Risk factors for obstetric anal sphincter injuries at vaginal birth after caesarean: a retrospective cohort study
title_sort risk factors for obstetric anal sphincter injuries at vaginal birth after caesarean: a retrospective cohort study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6795633/
https://www.ncbi.nlm.nih.gov/pubmed/31267138
http://dx.doi.org/10.1007/s00192-019-03978-x
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