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Drug‐induced cholestasis

Cholestatic drug‐induced liver injury (DILI) can be a diagnostic challenge due to a large differential diagnosis, variability in clinical presentation, and lack of serologic biomarkers associated with this condition. The clinical presentation of drug‐induced cholestasis includes bland cholestasis, c...

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Detalles Bibliográficos
Autores principales: Sundaram, Vinay, Björnsson, Einar S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678916/
https://www.ncbi.nlm.nih.gov/pubmed/29404489
http://dx.doi.org/10.1002/hep4.1088
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author Sundaram, Vinay
Björnsson, Einar S.
author_facet Sundaram, Vinay
Björnsson, Einar S.
author_sort Sundaram, Vinay
collection PubMed
description Cholestatic drug‐induced liver injury (DILI) can be a diagnostic challenge due to a large differential diagnosis, variability in clinical presentation, and lack of serologic biomarkers associated with this condition. The clinical presentation of drug‐induced cholestasis includes bland cholestasis, cholestatic hepatitis, secondary sclerosing cholangitis, and vanishing bile duct syndrome. The associate mortality of cholestatic DILI can be as high as 10%, and thus prompt recognition and removal of the offending agent is of critical importance. Several risk factors have been identified for drug‐induced cholestasis, including older age, genetic determinants, and properties of certain medications. Antibiotics, particularly amoxicillin/clavulanate, remain the predominant cause of cholestatic DILI, although a variety of other medications associated with this condition have been identified. In this review, we summarize the presentation, clinical approach, risk factors, implicated medications, and management of drug‐induced cholestatic liver injury. (Hepatology Communications 2017;1:726–735)
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spelling pubmed-56789162018-02-05 Drug‐induced cholestasis Sundaram, Vinay Björnsson, Einar S. Hepatol Commun Review Article Cholestatic drug‐induced liver injury (DILI) can be a diagnostic challenge due to a large differential diagnosis, variability in clinical presentation, and lack of serologic biomarkers associated with this condition. The clinical presentation of drug‐induced cholestasis includes bland cholestasis, cholestatic hepatitis, secondary sclerosing cholangitis, and vanishing bile duct syndrome. The associate mortality of cholestatic DILI can be as high as 10%, and thus prompt recognition and removal of the offending agent is of critical importance. Several risk factors have been identified for drug‐induced cholestasis, including older age, genetic determinants, and properties of certain medications. Antibiotics, particularly amoxicillin/clavulanate, remain the predominant cause of cholestatic DILI, although a variety of other medications associated with this condition have been identified. In this review, we summarize the presentation, clinical approach, risk factors, implicated medications, and management of drug‐induced cholestatic liver injury. (Hepatology Communications 2017;1:726–735) John Wiley and Sons Inc. 2017-09-11 /pmc/articles/PMC5678916/ /pubmed/29404489 http://dx.doi.org/10.1002/hep4.1088 Text en © 2017 The Authors. Hepatology Communications published by Wiley Periodicals, Inc., on behalf of the American Association for the Study of Liver Diseases. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Review Article
Sundaram, Vinay
Björnsson, Einar S.
Drug‐induced cholestasis
title Drug‐induced cholestasis
title_full Drug‐induced cholestasis
title_fullStr Drug‐induced cholestasis
title_full_unstemmed Drug‐induced cholestasis
title_short Drug‐induced cholestasis
title_sort drug‐induced cholestasis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678916/
https://www.ncbi.nlm.nih.gov/pubmed/29404489
http://dx.doi.org/10.1002/hep4.1088
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