Hepatotoxicity due to antitubercular drugs in multidrug-resistant tuberculosis patients

Authors

  • Teodoro Julio Oscanoa Espinoza Centro de Investigación de Seguridad del Medicamento. Facultad de Medicina Humana, Universidad de San Martin de Porres https://orcid.org/0000-0001-9379-4767
  • Saul Moscol Universidad Nacional Mayor de San Marcos, Facultad de Medicina. Lima, Perú. Hospital Nacional Guillermo Almenara Irigoyen, Servicio de Neumología, EsSalud. Lima, Perú. Médico Especialista en Neumología. https://orcid.org/0000-0002-6096-5571
  • Julio Luque Universidad de San Martin de Porres, Facultad de Medicina Humana, Centro de Investigación de Seguridad del Medicamento. Lima, Perú Médico internista, Doctor en Medicina. https://orcid.org/0000-0001-8868-2883
  • Silvia Leon-Curiñaupa Universidad de San Martin de Porres, Facultad de Medicina Humana, Centro de Investigación de Seguridad del Medicamento. Lima, Perú. Estudiante de Medicina. https://orcid.org/0000-0003-1336-9846
  • Jose Amado-Tineo Universidad Nacional Mayor de San Marcos, Facultad de Medicina. Lima, Perú. Médico internista, Doctor en Medicina. https://orcid.org/0000-0002-3286-4650

DOI:

https://doi.org/10.24265/horizmed.2022.v22n1.05

Keywords:

Tuberculosis, Multidrug-Resistant, Chemical and Drug Induced Liver Injury, Antitubercular Agents, Tuberculosis

Abstract

Objective: To describe the clinical characteristics of drug-induced liver injury (DILI) in multidrug-resistant tuberculosis (MDR-TB) patients.
Materials and methods: A retrospective study conducted in hospitalized patients with MDR-TB and DILI. The criteria of the DILI Expert Working Group were used for the diagnosis of DILI, and the RUCAM (Roussel Uclaf Causality Assessment
Method) for the causality analysis. The specific association between DILI and antitubercular drugs was established by drug rechallenge or discontinuation and recovery. Results: Seven cases of MDR-TB and DILI are described in this research. The mean age (standard deviation) was 39.10 (3.30) years.
Mean DILI occurred 30.40 (27.70) days after starting the treatment. Three (43.00 %) patients presented jaundice. Regarding the type of injury, four (57.00 %) had hepatocellular injury and three (43.00 %) cholestatic injury. Four patients showed mild DILI and
three moderate DILI. All the patients had taken pyrazinamide (pyrazinamide alone: four patients; pyrazinamide and ethionamide: one patient; pyrazinamide, rifampin and isoniazid: one patient; pyrazinamide and rifampicin: one patient). The mean hospital stay was 48.10 (48.70) days. The mean serum alkaline phosphatase (AP), alanine aminotransferase (ALT) and gamma-glutamyltranspeptidase (GGT) were 2.40 (1.10), 7.90 (7.10) and 5.60 (3.70) times the upper limit of normal (ULN), respectively. The mean
total bilirubin was 2.30 (2.00), with a range of 0.50 to 6.40 mg/dl. As part of the discharge plan, quinolones were given to seven patients (levofloxacin: six patients; ofloxacin: one patient) and amoxicillin/clavulanic acid was added to one patient. Conclusions: MDR-TB patients may develop DILI after the first month of treatment. Hepatocellular injury was the most
common type of liver injury, and pyrazinamide was the most frequently used antimycobacterial.

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Published

2022-03-30

How to Cite

1.
Oscanoa Espinoza TJ, Moscol S, Luque J, Leon-Curiñaupa S, Amado-Tineo J. Hepatotoxicity due to antitubercular drugs in multidrug-resistant tuberculosis patients. Horiz Med [Internet]. 2022Mar.30 [cited 2025May1];22(1):e1715. Available from: https://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/1715

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