Critical Review of Gaps in the Diagnosis and Management of Drug-Induced Liver Injury Associated with Severe Cutaneous Adverse Reactions
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Date
2021-11-01
Authors
Villanueva-Paz, Marina
Niu, Hao
Segovia-Zafra, Antonio
Medina-Caliz, Inmaculada
Sanabria-Cabrera, Judith
Lucena, M. Isabel
Andrade, Raul J.
Alvarez-Alvarez, Ismael
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Mdpi
Abstract
Drug-induced liver injury (DILI) encompasses the unexpected damage that drugs can cause to the liver. DILI may develop in the context of an immunoallergic syndrome with cutaneous manifestations, which are sometimes severe (SCARs). Nevirapine, allopurinol, anti-epileptics, sulfonamides, and antibiotics are the most frequent culprit drugs for DILI associated with SCARs. Interestingly, alleles HLA-B*58:01 and HLA-A*31:01 are associated with both adverse reactions. However, there is no consensus about the criteria used for the characterization of liver injury in this context, and the different thresholds for DILI definition make it difficult to gain insight into this complex disorder. Moreover, current limitations when evaluating causality in patients with DILI associated with SCARs are related to the plethora of causality assessment methods and the lack of consensual complementary tools. Finally, the management of this condition encompasses the treatment of liver and skin injury. Although the use of immunomodulant agents is accepted for SCARs, their role in treating liver injury remains controversial. Further randomized clinical trials are needed to test their efficacy and safety to address this complex entity. Therefore, this review aims to identify the current gaps in the definition, diagnosis, prognosis, and management of DILI associated with SCARs, proposing different strategies to fill in these gaps.
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Keywords
drug-induced liver injury, severe cutaneous adverse reactions, hypersensitivity, gaps, causality assessment, diagnosis, management, clinical trial, immune response, Toxic epidermal necrolysis, Stevens-johnson syndrome, Systemic symptoms dress, Induced hypersensitivity reactions, Lymphocyte-transformation test, Causality assessment methods, Clinical-features, Idiosyncratic hepatotoxicity, Intravenous immunoglobulin, Immunomodulating therapies