Assessment of Serious Acute and Chronic Idiosyncratic Drug-Induced Liver Injury in Clinical Practice.
Biomarkers
/ blood
Blood Coagulation Disorders
/ etiology
Chemical and Drug Induced Liver Injury
/ blood
Chemical and Drug Induced Liver Injury, Chronic
/ blood
Drug Eruptions
/ etiology
Fatty Liver
/ etiology
Hepatic Encephalopathy
/ etiology
Humans
Liver Failure, Acute
/ etiology
Phenotype
Risk Factors
Severity of Illness Index
Journal
Seminars in liver disease
ISSN: 1098-8971
Titre abrégé: Semin Liver Dis
Pays: United States
ID NLM: 8110297
Informations de publication
Date de publication:
07 2019
07 2019
Historique:
pubmed:
3
5
2019
medline:
30
4
2020
entrez:
4
5
2019
Statut:
ppublish
Résumé
Drug-induced liver injury (DILI) is the leading cause of acute liver failure (ALF) in developed countries. The extremely variable phenotype of DILI, both in presentation and in severity, is one of the distinctive characteristics of the disease and one of the major challenges that hepatologists face when assessing hepatotoxicity cases. A new Hy's law that more accurately predicts the risk of ALF related to DILI has been proposed and validated. Other prognostic scoring algorithms for the early identification of DILI patients who may go on to develop ALF have been developed as it is of most clinical relevance to stratify patients for closer monitoring. Recent data indicate that acute DILI often presents a more prolonged resolution or evolves into chronicity at a higher frequency than other forms of acute liver injury. Risk factors for chronicity, specific phenotypes, and histological features are discussed in this study. Biomarkers to predict DILI outcome are in need.
Identifiants
pubmed: 31049898
doi: 10.1055/s-0039-1685519
doi:
Substances chimiques
Biomarkers
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
381-394Informations de copyright
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.
Déclaration de conflit d'intérêts
None.