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Hyperammonemia: A Report of Maternal Biliary Cirrhosis and Neonatal Outcome

Although uncommon during pregnancy, cirrhosis results in multiple medical complications impacting both mother and fetus. Previous reports suggest liver dysfunction in pregnancy causes accumulation of neurotoxins within the maternal compartment that increases neonatal morbidity through placental tran...

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Autores principales: Hussamy, Deana J., Nelson, David B., Shivvers, Stephan A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4010006/
https://www.ncbi.nlm.nih.gov/pubmed/24829827
http://dx.doi.org/10.1155/2013/507169
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author Hussamy, Deana J.
Nelson, David B.
Shivvers, Stephan A.
author_facet Hussamy, Deana J.
Nelson, David B.
Shivvers, Stephan A.
author_sort Hussamy, Deana J.
collection PubMed
description Although uncommon during pregnancy, cirrhosis results in multiple medical complications impacting both mother and fetus. Previous reports suggest liver dysfunction in pregnancy causes accumulation of neurotoxins within the maternal compartment that increases neonatal morbidity through placental transfer. We present a case of a 36-year-old G(2)P(1) female with history of biliary cirrhosis presenting at 32-weeks' gestation with hepatic congestion progressing to hepatic encephalopathy prompting delivery. Umbilical cord sampling and postnatal infant testing demonstrated elevated ammonia levels which resolved by 12 hours of life without intervention. At discharge, the infant did not demonstrate evidence of neurologic deficit. We conclude that acute maternal hepatic encephalopathy and hyperammonemia due to chronic liver disease do not portend adverse neonatal outcomes, notably encephalopathy.
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spelling pubmed-40100062014-05-14 Hyperammonemia: A Report of Maternal Biliary Cirrhosis and Neonatal Outcome Hussamy, Deana J. Nelson, David B. Shivvers, Stephan A. Case Rep Crit Care Case Report Although uncommon during pregnancy, cirrhosis results in multiple medical complications impacting both mother and fetus. Previous reports suggest liver dysfunction in pregnancy causes accumulation of neurotoxins within the maternal compartment that increases neonatal morbidity through placental transfer. We present a case of a 36-year-old G(2)P(1) female with history of biliary cirrhosis presenting at 32-weeks' gestation with hepatic congestion progressing to hepatic encephalopathy prompting delivery. Umbilical cord sampling and postnatal infant testing demonstrated elevated ammonia levels which resolved by 12 hours of life without intervention. At discharge, the infant did not demonstrate evidence of neurologic deficit. We conclude that acute maternal hepatic encephalopathy and hyperammonemia due to chronic liver disease do not portend adverse neonatal outcomes, notably encephalopathy. Hindawi Publishing Corporation 2013 2013-02-12 /pmc/articles/PMC4010006/ /pubmed/24829827 http://dx.doi.org/10.1155/2013/507169 Text en Copyright © 2013 Deana J. Hussamy et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Hussamy, Deana J.
Nelson, David B.
Shivvers, Stephan A.
Hyperammonemia: A Report of Maternal Biliary Cirrhosis and Neonatal Outcome
title Hyperammonemia: A Report of Maternal Biliary Cirrhosis and Neonatal Outcome
title_full Hyperammonemia: A Report of Maternal Biliary Cirrhosis and Neonatal Outcome
title_fullStr Hyperammonemia: A Report of Maternal Biliary Cirrhosis and Neonatal Outcome
title_full_unstemmed Hyperammonemia: A Report of Maternal Biliary Cirrhosis and Neonatal Outcome
title_short Hyperammonemia: A Report of Maternal Biliary Cirrhosis and Neonatal Outcome
title_sort hyperammonemia: a report of maternal biliary cirrhosis and neonatal outcome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4010006/
https://www.ncbi.nlm.nih.gov/pubmed/24829827
http://dx.doi.org/10.1155/2013/507169
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