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Severe Cholestatic Drug-Induced Liver Injury With Cephalosporin Use
Drug-induced liver injury (DILI) is a phenomenon that occurs with nearly all classes of medications. Cholestatic DILI represents a fraction of these cases and can present as bland cholestasis, cholestatic hepatitis, secondary sclerosis cholangitis, and vanishing bile duct syndrome. Risk factors have...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9815788/ https://www.ncbi.nlm.nih.gov/pubmed/36620795 http://dx.doi.org/10.7759/cureus.32262 |
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author | Yang, Kevin Moga, Tiberiu Nallapeta, Naren S Duve, Robert Miranda, Clive J Ismail, Mayada Mahl, Thomas |
author_facet | Yang, Kevin Moga, Tiberiu Nallapeta, Naren S Duve, Robert Miranda, Clive J Ismail, Mayada Mahl, Thomas |
author_sort | Yang, Kevin |
collection | PubMed |
description | Drug-induced liver injury (DILI) is a phenomenon that occurs with nearly all classes of medications. Cholestatic DILI represents a fraction of these cases and can present as bland cholestasis, cholestatic hepatitis, secondary sclerosis cholangitis, and vanishing bile duct syndrome. Risk factors have been identified for cholestatic DILI, including older age, genetic determinants, and certain medications such as amoxicillin-clavulanate. Here, we describe a complicated case of severe cholestatic DILI secondary to cephalosporin use. A 27-year-old female presented to the hospital initially with fever and abdominal pain for four weeks after an emergency C-section for pre-eclampsia and hemolysis, elevated liver enzymes, lowered platelets (HELLP) syndrome. She was found to have a retroperitoneal abscess and underwent bilateral drain placement. She was initially started on cefazolin, and then coverage was broadened to cefepime. Shortly after, alkaline phosphatase (ALP) rose and peaked at 3498 IU/L, with aspartate aminotransferase (AST) and alanine transaminase (ALT) elevated at 274 IU/L and 122 IU/L, respectively. Extensive testing for secondary causes and a liver biopsy were consistent with DILI. Liver enzymes down-trended with the cessation of cefepime. This case report highlights that prompt recognition of the culprit medication is paramount to recovering normal liver function. |
format | Online Article Text |
id | pubmed-9815788 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-98157882023-01-06 Severe Cholestatic Drug-Induced Liver Injury With Cephalosporin Use Yang, Kevin Moga, Tiberiu Nallapeta, Naren S Duve, Robert Miranda, Clive J Ismail, Mayada Mahl, Thomas Cureus Gastroenterology Drug-induced liver injury (DILI) is a phenomenon that occurs with nearly all classes of medications. Cholestatic DILI represents a fraction of these cases and can present as bland cholestasis, cholestatic hepatitis, secondary sclerosis cholangitis, and vanishing bile duct syndrome. Risk factors have been identified for cholestatic DILI, including older age, genetic determinants, and certain medications such as amoxicillin-clavulanate. Here, we describe a complicated case of severe cholestatic DILI secondary to cephalosporin use. A 27-year-old female presented to the hospital initially with fever and abdominal pain for four weeks after an emergency C-section for pre-eclampsia and hemolysis, elevated liver enzymes, lowered platelets (HELLP) syndrome. She was found to have a retroperitoneal abscess and underwent bilateral drain placement. She was initially started on cefazolin, and then coverage was broadened to cefepime. Shortly after, alkaline phosphatase (ALP) rose and peaked at 3498 IU/L, with aspartate aminotransferase (AST) and alanine transaminase (ALT) elevated at 274 IU/L and 122 IU/L, respectively. Extensive testing for secondary causes and a liver biopsy were consistent with DILI. Liver enzymes down-trended with the cessation of cefepime. This case report highlights that prompt recognition of the culprit medication is paramount to recovering normal liver function. Cureus 2022-12-06 /pmc/articles/PMC9815788/ /pubmed/36620795 http://dx.doi.org/10.7759/cureus.32262 Text en Copyright © 2022, Yang et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Gastroenterology Yang, Kevin Moga, Tiberiu Nallapeta, Naren S Duve, Robert Miranda, Clive J Ismail, Mayada Mahl, Thomas Severe Cholestatic Drug-Induced Liver Injury With Cephalosporin Use |
title | Severe Cholestatic Drug-Induced Liver Injury With Cephalosporin Use |
title_full | Severe Cholestatic Drug-Induced Liver Injury With Cephalosporin Use |
title_fullStr | Severe Cholestatic Drug-Induced Liver Injury With Cephalosporin Use |
title_full_unstemmed | Severe Cholestatic Drug-Induced Liver Injury With Cephalosporin Use |
title_short | Severe Cholestatic Drug-Induced Liver Injury With Cephalosporin Use |
title_sort | severe cholestatic drug-induced liver injury with cephalosporin use |
topic | Gastroenterology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9815788/ https://www.ncbi.nlm.nih.gov/pubmed/36620795 http://dx.doi.org/10.7759/cureus.32262 |
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