Hepatotoxicity due to antitubercular drugs in multidrug-resistant tuberculosis patients
Descripción del Articulo
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...
Autores: | , , , , |
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Formato: | artículo |
Fecha de Publicación: | 2022 |
Institución: | Universidad de San Martín de Porres |
Repositorio: | Horizonte médico |
Lenguaje: | español |
OAI Identifier: | oai:horizontemedico.usmp.edu.pe:article/1715 |
Enlace del recurso: | https://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/1715 |
Nivel de acceso: | acceso abierto |
Materia: | Tuberculosis Resistente a Multidrogas Daño Hepático Inducido por Droga Fármacos Antituberculosos Tuberculosis Tuberculosis, Multidrug-Resistant Chemical and Drug Induced Liver Injury Antitubercular Agents |
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dc.title.none.fl_str_mv |
Hepatotoxicity due to antitubercular drugs in multidrug-resistant tuberculosis patients Hepatotoxicidad por antituberculosos en pacientes con tuberculosis multidrogorresistente |
title |
Hepatotoxicity due to antitubercular drugs in multidrug-resistant tuberculosis patients |
spellingShingle |
Hepatotoxicity due to antitubercular drugs in multidrug-resistant tuberculosis patients Oscanoa Espinoza, Teodoro Julio Tuberculosis Resistente a Multidrogas Daño Hepático Inducido por Droga Fármacos Antituberculosos Tuberculosis Tuberculosis, Multidrug-Resistant Chemical and Drug Induced Liver Injury Antitubercular Agents Tuberculosis |
title_short |
Hepatotoxicity due to antitubercular drugs in multidrug-resistant tuberculosis patients |
title_full |
Hepatotoxicity due to antitubercular drugs in multidrug-resistant tuberculosis patients |
title_fullStr |
Hepatotoxicity due to antitubercular drugs in multidrug-resistant tuberculosis patients |
title_full_unstemmed |
Hepatotoxicity due to antitubercular drugs in multidrug-resistant tuberculosis patients |
title_sort |
Hepatotoxicity due to antitubercular drugs in multidrug-resistant tuberculosis patients |
dc.creator.none.fl_str_mv |
Oscanoa Espinoza, Teodoro Julio Moscol, Saul Luque, Julio Leon-Curiñaupa, Silvia Amado-Tineo, Jose |
author |
Oscanoa Espinoza, Teodoro Julio |
author_facet |
Oscanoa Espinoza, Teodoro Julio Moscol, Saul Luque, Julio Leon-Curiñaupa, Silvia Amado-Tineo, Jose |
author_role |
author |
author2 |
Moscol, Saul Luque, Julio Leon-Curiñaupa, Silvia Amado-Tineo, Jose |
author2_role |
author author author author |
dc.subject.none.fl_str_mv |
Tuberculosis Resistente a Multidrogas Daño Hepático Inducido por Droga Fármacos Antituberculosos Tuberculosis Tuberculosis, Multidrug-Resistant Chemical and Drug Induced Liver Injury Antitubercular Agents Tuberculosis |
topic |
Tuberculosis Resistente a Multidrogas Daño Hepático Inducido por Droga Fármacos Antituberculosos Tuberculosis Tuberculosis, Multidrug-Resistant Chemical and Drug Induced Liver Injury Antitubercular Agents Tuberculosis |
description |
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 AssessmentMethod) 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 andthree 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 meantotal 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 mostcommon type of liver injury, and pyrazinamide was the most frequently used antimycobacterial. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-03-30 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
https://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/1715 10.24265/horizmed.2022.v22n1.05 |
url |
https://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/1715 |
identifier_str_mv |
10.24265/horizmed.2022.v22n1.05 |
dc.language.none.fl_str_mv |
spa |
language |
spa |
dc.relation.none.fl_str_mv |
https://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/1715/1057 https://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/1715/1171 https://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/1715/1139 |
dc.rights.none.fl_str_mv |
Derechos de autor 2022 Horizonte Médico (Lima) https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Derechos de autor 2022 Horizonte Médico (Lima) https://creativecommons.org/licenses/by/4.0 |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf text/xml text/html |
dc.publisher.none.fl_str_mv |
Universidad de San Martín de Porres. Facultad de Medicina Humana |
publisher.none.fl_str_mv |
Universidad de San Martín de Porres. Facultad de Medicina Humana |
dc.source.none.fl_str_mv |
Horizonte Médico (Lima); Vol. 22 No. 1 (2022): January - March; e1715 Horizonte Médico (Lima); Vol. 22 Núm. 1 (2022): Enero - Marzo; e1715 Horizonte Médico (Lima); v. 22 n. 1 (2022): Enero - Marzo; e1715 2227-3530 1727-558X reponame:Horizonte médico instname:Universidad de San Martín de Porres instacron:USMP |
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Universidad de San Martín de Porres |
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Horizonte médico |
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Horizonte médico |
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spelling |
Hepatotoxicity due to antitubercular drugs in multidrug-resistant tuberculosis patientsHepatotoxicidad por antituberculosos en pacientes con tuberculosis multidrogorresistenteOscanoa Espinoza, Teodoro Julio Moscol, SaulLuque, Julio Leon-Curiñaupa, Silvia Amado-Tineo, Jose Tuberculosis Resistente a MultidrogasDaño Hepático Inducido por DrogaFármacos AntituberculososTuberculosisTuberculosis, Multidrug-ResistantChemical and Drug Induced Liver InjuryAntitubercular Agents TuberculosisObjective: 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 AssessmentMethod) 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 andthree 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 meantotal 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 mostcommon type of liver injury, and pyrazinamide was the most frequently used antimycobacterial.Objetivo: Describir las características clínicas de la injuria hepática inducida por antituberculosos (IHIA) en pacientes con tuberculosis multirresistente (MDR-TB).Materiales y métodos: Estudio retrospectivo de pacientes hospitalizados con TB-MDR e IHIA. Se utilizó los criterios de laDILI-Expert Working Group, y el instrumento de análisis de causalidad fue el RUCAM (Roussel Uclaf Causality AssessmentMethod). La asociación específica de la IHIA con un antituberculoso fue por un proceso de reexposición o suspensión y recuperación. Resultados: Reportamos 7 casos de MDR-TB e IHIA; la edad media (desviación estándar) fue de 39,1 (3,3) años. La media de la IHIAapareció después de 30,4 (27,70) días de iniciar el tratamiento. Tres (43,00 %) pacientes presentaron ictericia. En cuanto al patrón, en 4 (57,00 %) fue hepatocelular y en 3 (43,00 %), colestásico. En 4 pacientes, la IHIA fue leve, y moderada en 3. En todos los casos estuvo involucrada la pirazinamida (pirazinamida sola, 4; pirazinamida y etionamida, 1; pirazinamida, rifampicina e isoniazida, 1;pirazinamida y rifampicina, 1). La estancia hospitalaria media fue de 48,10 (48,70) días. Los promedios de fosfatasa alcalina (FA), alanina aminotransferasa (ALT) y gamma-glutamiltranspeptidasa (GGT) sérica fueron 2,40 (1,10), 7,9 (7,10) y 5,60 (3,70) veces el límite superior normal (NUL), respectivamente. La bilirrubina total media fue 2,30 (2,10), rango de 0,50 a 6,40 mg/dl. Como parte del esquema de alta del paciente, se administraron quinolonas a 7 pacientes (levofloxacino, 6; ofloxacino,1), y en un paciente se agregó ácido amoxicilina/ácido clavulánico.Conclusiones: La IHIA en pacientes con TB-MDR puede aparecer después del primer mes de tratamiento. El patrón de lesión común fue hepatocelular, y la pirazinamida fue el antimicobacteriano involucrado con mayor frecuencia.Universidad de San Martín de Porres. Facultad de Medicina Humana2022-03-30info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdftext/xmltext/htmlhttps://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/171510.24265/horizmed.2022.v22n1.05Horizonte Médico (Lima); Vol. 22 No. 1 (2022): January - March; e1715Horizonte Médico (Lima); Vol. 22 Núm. 1 (2022): Enero - Marzo; e1715Horizonte Médico (Lima); v. 22 n. 1 (2022): Enero - Marzo; e17152227-35301727-558Xreponame:Horizonte médicoinstname:Universidad de San Martín de Porresinstacron:USMPspahttps://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/1715/1057https://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/1715/1171https://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/1715/1139Derechos de autor 2022 Horizonte Médico (Lima)https://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessoai:horizontemedico.usmp.edu.pe:article/17152022-06-22T17:14:58Z |
score |
13.754011 |
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La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).