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Risk factors associated with cesarean section and adverse fetal outcomes in intrahepatic cholestasis of pregnancy
BACKGROUND: To determine the risk factors for cesarean section (CS) and adverse fetal outcomes (AFOs) in patients with intrahepatic cholestasis of pregnancy (ICP) based on the severity of maternal hypercholanemia. METHODS: A hospital-based retrospective cohort study was performed between January 1,...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349544/ https://www.ncbi.nlm.nih.gov/pubmed/37456565 http://dx.doi.org/10.3389/fped.2023.1136244 |
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author | Kong, Chengcai Zhu, Zonghao Mei, Fenglin |
author_facet | Kong, Chengcai Zhu, Zonghao Mei, Fenglin |
author_sort | Kong, Chengcai |
collection | PubMed |
description | BACKGROUND: To determine the risk factors for cesarean section (CS) and adverse fetal outcomes (AFOs) in patients with intrahepatic cholestasis of pregnancy (ICP) based on the severity of maternal hypercholanemia. METHODS: A hospital-based retrospective cohort study was performed between January 1, 2015, and December 31, 2019. A total of 227 nulliparous women with a singleton fetus complicated by ICP were included. The patients were divided into two groups according to the levels of total bile acids, that is, mild (10 μmol/L < total bile acids < 40 μmol/L) and severe (≥40 μmol/L). The patients' clinical characteristics and fetal outcomes were assessed. RESULTS: Among the 227 eligible women, 177 (78.0%) were allocated to the mild group and 50 (22.0%) were in the severe group. Women with severe ICP also had a significantly higher incidence of planned and unplanned CS compared with mild ICP subjects (52.0% vs. 23.7% and 22.0% vs. 6.8%, respectively; p < 0.001). The indications for CS showed that fetal intolerance (65.4% vs. 14.3%) was higher in severe ICP compared with mild ICP (p < 0.001). Severe ICP was associated with an increased risk of preterm delivery (p < 0.001), low birthweight (p = 0.001), and neonatal intensive care unit (NICU) admission (p < 0.001). Women with severe ICP (OR 6.397, 95%CI 3.041–13.455, p < 0.001) or preeclampsia (OR 12.434, 95%CI 5.166–29.928, p < 0.001) had increased risks of AFOs compared to controls. CONCLUSIONS: Severe ICP and preeclampsia are associated with a higher incidence of AFOs. |
format | Online Article Text |
id | pubmed-10349544 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103495442023-07-16 Risk factors associated with cesarean section and adverse fetal outcomes in intrahepatic cholestasis of pregnancy Kong, Chengcai Zhu, Zonghao Mei, Fenglin Front Pediatr Pediatrics BACKGROUND: To determine the risk factors for cesarean section (CS) and adverse fetal outcomes (AFOs) in patients with intrahepatic cholestasis of pregnancy (ICP) based on the severity of maternal hypercholanemia. METHODS: A hospital-based retrospective cohort study was performed between January 1, 2015, and December 31, 2019. A total of 227 nulliparous women with a singleton fetus complicated by ICP were included. The patients were divided into two groups according to the levels of total bile acids, that is, mild (10 μmol/L < total bile acids < 40 μmol/L) and severe (≥40 μmol/L). The patients' clinical characteristics and fetal outcomes were assessed. RESULTS: Among the 227 eligible women, 177 (78.0%) were allocated to the mild group and 50 (22.0%) were in the severe group. Women with severe ICP also had a significantly higher incidence of planned and unplanned CS compared with mild ICP subjects (52.0% vs. 23.7% and 22.0% vs. 6.8%, respectively; p < 0.001). The indications for CS showed that fetal intolerance (65.4% vs. 14.3%) was higher in severe ICP compared with mild ICP (p < 0.001). Severe ICP was associated with an increased risk of preterm delivery (p < 0.001), low birthweight (p = 0.001), and neonatal intensive care unit (NICU) admission (p < 0.001). Women with severe ICP (OR 6.397, 95%CI 3.041–13.455, p < 0.001) or preeclampsia (OR 12.434, 95%CI 5.166–29.928, p < 0.001) had increased risks of AFOs compared to controls. CONCLUSIONS: Severe ICP and preeclampsia are associated with a higher incidence of AFOs. Frontiers Media S.A. 2023-06-30 /pmc/articles/PMC10349544/ /pubmed/37456565 http://dx.doi.org/10.3389/fped.2023.1136244 Text en © 2023 Kong, Zhu and Mei. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pediatrics Kong, Chengcai Zhu, Zonghao Mei, Fenglin Risk factors associated with cesarean section and adverse fetal outcomes in intrahepatic cholestasis of pregnancy |
title | Risk factors associated with cesarean section and adverse fetal outcomes in intrahepatic cholestasis of pregnancy |
title_full | Risk factors associated with cesarean section and adverse fetal outcomes in intrahepatic cholestasis of pregnancy |
title_fullStr | Risk factors associated with cesarean section and adverse fetal outcomes in intrahepatic cholestasis of pregnancy |
title_full_unstemmed | Risk factors associated with cesarean section and adverse fetal outcomes in intrahepatic cholestasis of pregnancy |
title_short | Risk factors associated with cesarean section and adverse fetal outcomes in intrahepatic cholestasis of pregnancy |
title_sort | risk factors associated with cesarean section and adverse fetal outcomes in intrahepatic cholestasis of pregnancy |
topic | Pediatrics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349544/ https://www.ncbi.nlm.nih.gov/pubmed/37456565 http://dx.doi.org/10.3389/fped.2023.1136244 |
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