Liver Injury Associated with Metamizole Exposure: Features of an Underestimated Adverse Event
Autor: | Andreas Benesic, Jens Neumann, Alexander L. Gerbes, Sabine Weber |
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Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
Male
medicine.medical_specialty Necrosis Antinuclear antibody positivity Dipyrone Toxicology Gastroenterology Internal medicine medicine Humans Pharmacology (medical) Original Research Article Prospective Studies Adverse effect Prospective cohort study Pharmacology Liver injury business.industry Jaundice Liver Failure Acute Metamizole medicine.disease Cohort Female medicine.symptom Chemical and Drug Induced Liver Injury business medicine.drug |
Zdroj: | Drug Safety |
ISSN: | 1179-1942 0114-5916 |
Popis: | Introduction and Objective The potential of metamizole to cause drug-induced liver injury (DILI) has received increasing attention. We investigated the distinguishing features of a case series comprising 32 patients with suspected metamizole-induced DILI. Methods For the current analysis, 32 of 238 patients with DILI included in our prospective study on drugs potentially causing DILI were included. Diagnosis of DILI was based on expert opinion and RUCAM (Roussel Uclaf Causality Assessment Method) score and supported by an in vitro test using monocyte-derived hepatocyte-like cells. Results Suspected metamizole-DILI was characterised by a female predominance, hepatocellular pattern of injury, high proportion of antinuclear antibody positivity, and predominance of eosinophilic cell infiltration and necrosis in the histopathological analysis. With 22%, a high proportion of these metamizole-associated liver injury cases developed acute liver failure, which was characterised by a longer latency of metamizole use and more pronounced liver biochemistry abnormalities at onset and peak levels. Furthermore, jaundice was a common finding in the metamizole-associated liver injury cases with 66% presenting with peak bilirubin levels of 3 mg/dL or higher, which was associated with a worse outcome and a higher frequency of acute liver failure. Conclusions Our analysis of a well-characterised DILI cohort further supports the potential of metamizole causing DILI and provides important features for the establishment of a signature pattern of liver injury observed in patients treated with metamizole. Clinical Trial Registration ClinicalTrials.gov: NCT 02353455. Supplementary Information The online version contains supplementary material available at 10.1007/s40264-021-01049-z. |
Databáze: | OpenAIRE |
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