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Serious hepatotoxicity following use of isoniazid preventive therapy in HIV patients in Eritrea

WHO information note indicates that isoniazid preventive therapy (IPT) is generally safe with little risk of hepatotoxicity. However, when the policy of IPT for HIV patients was introduced in Eritrea, frequent IPT‐associated hepatotoxicity and fatality have been reported to the Pharmacovigilance Cen...

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Autores principales: Russom, Mulugeta, Debesai, Merhawi, Zeregabr, Mehari, Berhane, Araia, Tekeste, Theodros, Teklesenbet, Teklezghi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6066797/
https://www.ncbi.nlm.nih.gov/pubmed/30073087
http://dx.doi.org/10.1002/prp2.423
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author Russom, Mulugeta
Debesai, Merhawi
Zeregabr, Mehari
Berhane, Araia
Tekeste, Theodros
Teklesenbet, Teklezghi
author_facet Russom, Mulugeta
Debesai, Merhawi
Zeregabr, Mehari
Berhane, Araia
Tekeste, Theodros
Teklesenbet, Teklezghi
author_sort Russom, Mulugeta
collection PubMed
description WHO information note indicates that isoniazid preventive therapy (IPT) is generally safe with little risk of hepatotoxicity. However, when the policy of IPT for HIV patients was introduced in Eritrea, frequent IPT‐associated hepatotoxicity and fatality have been reported to the Pharmacovigilance Centre. The aim of the study is to assess the causal association of IPT and hepatotoxicity and identify possible risk factors in patients on Highly Active Anti‐retroviral Therapy (HAART). This is a case series assessment of spontaneously reported cases to the Eritrean Pharmacovigilance Centre. Data extracted from VigiFlow (reported between 2014 and 2016) were exported to excel spread sheet for descriptive and qualitative analysis. Naranjo probability scale and Austin Bradford‐Hill criteria were used to assess causality. The P‐Method was used to assess preventability. A total of 31 of cases of hepatotoxicity related to IPT were retrieved. Majority (80.6%) of the cases were marked as “serious” due to life‐threatening situation (n = 15), hospitalization (n = 6), and death (n = 4). Baseline liver function test was normal in 61.3% and hepatitis B and C infections were ruled out in 77.4%. IPT was discontinued in 26 cases and reaction abated in 22 of them. Causality assessment using Austin Bradford‐Hill criteria found that the association was strong, consistent and specific with a plausible temporal relationship and biological mechanism. IPT‐associated hepatotoxicity that led to treatment interruption and death was observed in patients on HAART in Eritrea. Hence, close laboratory monitoring of patients is recommended to minimize the risk.
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spelling pubmed-60667972018-08-02 Serious hepatotoxicity following use of isoniazid preventive therapy in HIV patients in Eritrea Russom, Mulugeta Debesai, Merhawi Zeregabr, Mehari Berhane, Araia Tekeste, Theodros Teklesenbet, Teklezghi Pharmacol Res Perspect Original Articles WHO information note indicates that isoniazid preventive therapy (IPT) is generally safe with little risk of hepatotoxicity. However, when the policy of IPT for HIV patients was introduced in Eritrea, frequent IPT‐associated hepatotoxicity and fatality have been reported to the Pharmacovigilance Centre. The aim of the study is to assess the causal association of IPT and hepatotoxicity and identify possible risk factors in patients on Highly Active Anti‐retroviral Therapy (HAART). This is a case series assessment of spontaneously reported cases to the Eritrean Pharmacovigilance Centre. Data extracted from VigiFlow (reported between 2014 and 2016) were exported to excel spread sheet for descriptive and qualitative analysis. Naranjo probability scale and Austin Bradford‐Hill criteria were used to assess causality. The P‐Method was used to assess preventability. A total of 31 of cases of hepatotoxicity related to IPT were retrieved. Majority (80.6%) of the cases were marked as “serious” due to life‐threatening situation (n = 15), hospitalization (n = 6), and death (n = 4). Baseline liver function test was normal in 61.3% and hepatitis B and C infections were ruled out in 77.4%. IPT was discontinued in 26 cases and reaction abated in 22 of them. Causality assessment using Austin Bradford‐Hill criteria found that the association was strong, consistent and specific with a plausible temporal relationship and biological mechanism. IPT‐associated hepatotoxicity that led to treatment interruption and death was observed in patients on HAART in Eritrea. Hence, close laboratory monitoring of patients is recommended to minimize the risk. John Wiley and Sons Inc. 2018-07-31 /pmc/articles/PMC6066797/ /pubmed/30073087 http://dx.doi.org/10.1002/prp2.423 Text en © 2018 The Authors. Pharmacology Research & Perspectives published by John Wiley & Sons Ltd, British Pharmacological Society and American Society for Pharmacology and Experimental Therapeutics. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Russom, Mulugeta
Debesai, Merhawi
Zeregabr, Mehari
Berhane, Araia
Tekeste, Theodros
Teklesenbet, Teklezghi
Serious hepatotoxicity following use of isoniazid preventive therapy in HIV patients in Eritrea
title Serious hepatotoxicity following use of isoniazid preventive therapy in HIV patients in Eritrea
title_full Serious hepatotoxicity following use of isoniazid preventive therapy in HIV patients in Eritrea
title_fullStr Serious hepatotoxicity following use of isoniazid preventive therapy in HIV patients in Eritrea
title_full_unstemmed Serious hepatotoxicity following use of isoniazid preventive therapy in HIV patients in Eritrea
title_short Serious hepatotoxicity following use of isoniazid preventive therapy in HIV patients in Eritrea
title_sort serious hepatotoxicity following use of isoniazid preventive therapy in hiv patients in eritrea
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6066797/
https://www.ncbi.nlm.nih.gov/pubmed/30073087
http://dx.doi.org/10.1002/prp2.423
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