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Critical Review of Gaps in the Diagnosis and Management of Drug-Induced Liver Injury Associated with Severe Cutaneous Adverse Reactions

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 antibioti...

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Autores principales: Villanueva-Paz, Marina, Niu, Hao, Segovia-Zafra, Antonio, Medina-Caliz, Inmaculada, Sanabria-Cabrera, Judith, Lucena, M. Isabel, Andrade, Raúl J., Alvarez-Alvarez, Ismael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8618381/
https://www.ncbi.nlm.nih.gov/pubmed/34830594
http://dx.doi.org/10.3390/jcm10225317
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author Villanueva-Paz, Marina
Niu, Hao
Segovia-Zafra, Antonio
Medina-Caliz, Inmaculada
Sanabria-Cabrera, Judith
Lucena, M. Isabel
Andrade, Raúl J.
Alvarez-Alvarez, Ismael
author_facet Villanueva-Paz, Marina
Niu, Hao
Segovia-Zafra, Antonio
Medina-Caliz, Inmaculada
Sanabria-Cabrera, Judith
Lucena, M. Isabel
Andrade, Raúl J.
Alvarez-Alvarez, Ismael
author_sort Villanueva-Paz, Marina
collection PubMed
description 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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spelling pubmed-86183812021-11-27 Critical Review of Gaps in the Diagnosis and Management of Drug-Induced Liver Injury Associated with Severe Cutaneous Adverse Reactions Villanueva-Paz, Marina Niu, Hao Segovia-Zafra, Antonio Medina-Caliz, Inmaculada Sanabria-Cabrera, Judith Lucena, M. Isabel Andrade, Raúl J. Alvarez-Alvarez, Ismael J Clin Med Review 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. MDPI 2021-11-15 /pmc/articles/PMC8618381/ /pubmed/34830594 http://dx.doi.org/10.3390/jcm10225317 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Villanueva-Paz, Marina
Niu, Hao
Segovia-Zafra, Antonio
Medina-Caliz, Inmaculada
Sanabria-Cabrera, Judith
Lucena, M. Isabel
Andrade, Raúl J.
Alvarez-Alvarez, Ismael
Critical Review of Gaps in the Diagnosis and Management of Drug-Induced Liver Injury Associated with Severe Cutaneous Adverse Reactions
title Critical Review of Gaps in the Diagnosis and Management of Drug-Induced Liver Injury Associated with Severe Cutaneous Adverse Reactions
title_full Critical Review of Gaps in the Diagnosis and Management of Drug-Induced Liver Injury Associated with Severe Cutaneous Adverse Reactions
title_fullStr Critical Review of Gaps in the Diagnosis and Management of Drug-Induced Liver Injury Associated with Severe Cutaneous Adverse Reactions
title_full_unstemmed Critical Review of Gaps in the Diagnosis and Management of Drug-Induced Liver Injury Associated with Severe Cutaneous Adverse Reactions
title_short Critical Review of Gaps in the Diagnosis and Management of Drug-Induced Liver Injury Associated with Severe Cutaneous Adverse Reactions
title_sort critical review of gaps in the diagnosis and management of drug-induced liver injury associated with severe cutaneous adverse reactions
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8618381/
https://www.ncbi.nlm.nih.gov/pubmed/34830594
http://dx.doi.org/10.3390/jcm10225317
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