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Drug-induced cholestasis: causative agents and challenges in diagnosis and management

Authors :
Jose M. Pinazo-Bandera
Juan Pedro Toro-Ortiz
Raúl J. Andrade
Miren García-Cortés
Source :
Exploration of Digestive Diseases, Vol 2, Iss 5, Pp 202-222 (2023)
Publication Year :
2023
Publisher :
Open Exploration Publishing Inc., 2023.

Abstract

Drug-induced liver injury (DILI) is an adverse reaction to drugs and other xenobiotics that can have serious consequences and jeopardise progress in pharmacological therapy. While DILI is predominantly hepatocellular, a non-negligible percentage of patients who present with cholestatic damage. Mixed damage is typically lumped together with cholestatic damage in the literature. Drug-induced cholestasis is often caused by the use of some non-steroidal anti-inflammatory drugs (NSAIDs), antibiotics (i.e., amoxicillin-clavulanic acid), statins, and anabolic agents, among others. Drug-associated cholestasis tends to have a more chronic course and mostly affects older population. There is also a genetic predisposition to toxic cholestasis caused by some drugs (amoxicillin-clavulanic acid, statins, etc.). Recently, anatomical alterations of the biliary tract induced by drugs (especially immunotherapy drugs) have been described. Bile duct injury is one of the histopathological findings that have prognostic significance in DILI. A correct differential diagnosis with other causes of cholestasis is mandatory to reach an accurate diagnosis. Ursodexycholic acid, corticosteroids, and replacement therapies have been used as a therapeutic arsenal, although more evidence is needed to establish them as a routine therapeutic management in clinical practice. The breakthrough and validation of biomarkers of cholestasis and bile duct injury is an urgent need for drug development and post-marketing phase.

Details

Language :
English
ISSN :
28336321
Volume :
2
Issue :
5
Database :
Directory of Open Access Journals
Journal :
Exploration of Digestive Diseases
Publication Type :
Academic Journal
Accession number :
edsdoj.8913248e32124acc9bfefeead2afcb91
Document Type :
article
Full Text :
https://doi.org/10.37349/edd.2023.00027