Effectiveness and potential drug interactions in antiviral therapy for the treatment of chronic hepatitis C: real-life data from a specialized center in southern Brazil

Detalhes bibliográficos
Autor(a) principal: Hepp Schwambachi, Karin
Data de Publicação: 2022
Outros Autores: Raquel Blatt, Carine
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Pharmaceutical Sciences
Texto Completo: https://www.revistas.usp.br/bjps/article/view/201155
Resumo: Direct-acting antivirals used in the treatment of hepatitis C have demonstrated high rates of efficacy, are well tolerated and considered safe. However, they are not free of drug interactions. To describe the effectiveness of hepatitis C treatment and the incidence and severity of potential drug interactions between drugs used during this treatment. A cross-sectional study with 148 patients who began treatment for hepatitis C between April and June 2016 in a specialized center in Brazil. Drug interactions were identified in the Truven Health Analytic/DynaMed Plus and Hep-C Interactions databases. Regarding treatment outcome, 93.9% of patients achieved SVR, 2.7% relapsed and 3.4% did not return after the end of the follow-up period. A total of 328 chronic diseases were identified (71 different diseases), and 88.5% of the patients had at least one chronic disease. The patients reported the use of 474 drugs (121 different drugs), with 3.2 drugs per patient on average. We identified 265 potential drug interactions, classified as important (6.0%), with clinical significance (20.7%) and without clinical significance or with insufficient data (69.4%). Cirrhotic patients had a higher average number of potential drug interactions than non-cirrhotic patients (2.51 x 0.79, p = 0.000). Hepatitis C treatment with direct-acting antivirals are effective and safe for most of patients.
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spelling Effectiveness and potential drug interactions in antiviral therapy for the treatment of chronic hepatitis C: real-life data from a specialized center in southern BrazilHepatitis C; Drug interactions; Direct-acting antivirals; Safety; Real-world dataDirect-acting antivirals used in the treatment of hepatitis C have demonstrated high rates of efficacy, are well tolerated and considered safe. However, they are not free of drug interactions. To describe the effectiveness of hepatitis C treatment and the incidence and severity of potential drug interactions between drugs used during this treatment. A cross-sectional study with 148 patients who began treatment for hepatitis C between April and June 2016 in a specialized center in Brazil. Drug interactions were identified in the Truven Health Analytic/DynaMed Plus and Hep-C Interactions databases. Regarding treatment outcome, 93.9% of patients achieved SVR, 2.7% relapsed and 3.4% did not return after the end of the follow-up period. A total of 328 chronic diseases were identified (71 different diseases), and 88.5% of the patients had at least one chronic disease. The patients reported the use of 474 drugs (121 different drugs), with 3.2 drugs per patient on average. We identified 265 potential drug interactions, classified as important (6.0%), with clinical significance (20.7%) and without clinical significance or with insufficient data (69.4%). Cirrhotic patients had a higher average number of potential drug interactions than non-cirrhotic patients (2.51 x 0.79, p = 0.000). Hepatitis C treatment with direct-acting antivirals are effective and safe for most of patients.Universidade de São Paulo. Faculdade de Ciências Farmacêuticas2022-11-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/bjps/article/view/20115510.1590/s2175-9790201900041874Brazilian Journal of Pharmaceutical Sciences; Vol. 57 (2021)Brazilian Journal of Pharmaceutical Sciences; v. 57 (2021)Brazilian Journal of Pharmaceutical Sciences; Vol. 57 (2021)2175-97901984-8250reponame:Brazilian Journal of Pharmaceutical Sciencesinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/bjps/article/view/201155/185296https://www.revistas.usp.br/bjps/article/view/201155/185297Copyright (c) 2022 Brazilian Journal of Pharmaceutical Scienceshttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessHepp Schwambachi, KarinRaquel Blatt, Carine2022-11-09T17:40:50Zoai:revistas.usp.br:article/201155Revistahttps://www.revistas.usp.br/bjps/indexPUBhttps://old.scielo.br/oai/scielo-oai.phpbjps@usp.br||elizabeth.igne@gmail.com2175-97901984-8250opendoar:2022-11-09T17:40:50Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Effectiveness and potential drug interactions in antiviral therapy for the treatment of chronic hepatitis C: real-life data from a specialized center in southern Brazil
title Effectiveness and potential drug interactions in antiviral therapy for the treatment of chronic hepatitis C: real-life data from a specialized center in southern Brazil
spellingShingle Effectiveness and potential drug interactions in antiviral therapy for the treatment of chronic hepatitis C: real-life data from a specialized center in southern Brazil
Hepp Schwambachi, Karin
Hepatitis C; Drug interactions; Direct-acting antivirals; Safety; Real-world data
title_short Effectiveness and potential drug interactions in antiviral therapy for the treatment of chronic hepatitis C: real-life data from a specialized center in southern Brazil
title_full Effectiveness and potential drug interactions in antiviral therapy for the treatment of chronic hepatitis C: real-life data from a specialized center in southern Brazil
title_fullStr Effectiveness and potential drug interactions in antiviral therapy for the treatment of chronic hepatitis C: real-life data from a specialized center in southern Brazil
title_full_unstemmed Effectiveness and potential drug interactions in antiviral therapy for the treatment of chronic hepatitis C: real-life data from a specialized center in southern Brazil
title_sort Effectiveness and potential drug interactions in antiviral therapy for the treatment of chronic hepatitis C: real-life data from a specialized center in southern Brazil
author Hepp Schwambachi, Karin
author_facet Hepp Schwambachi, Karin
Raquel Blatt, Carine
author_role author
author2 Raquel Blatt, Carine
author2_role author
dc.contributor.author.fl_str_mv Hepp Schwambachi, Karin
Raquel Blatt, Carine
dc.subject.por.fl_str_mv Hepatitis C; Drug interactions; Direct-acting antivirals; Safety; Real-world data
topic Hepatitis C; Drug interactions; Direct-acting antivirals; Safety; Real-world data
description Direct-acting antivirals used in the treatment of hepatitis C have demonstrated high rates of efficacy, are well tolerated and considered safe. However, they are not free of drug interactions. To describe the effectiveness of hepatitis C treatment and the incidence and severity of potential drug interactions between drugs used during this treatment. A cross-sectional study with 148 patients who began treatment for hepatitis C between April and June 2016 in a specialized center in Brazil. Drug interactions were identified in the Truven Health Analytic/DynaMed Plus and Hep-C Interactions databases. Regarding treatment outcome, 93.9% of patients achieved SVR, 2.7% relapsed and 3.4% did not return after the end of the follow-up period. A total of 328 chronic diseases were identified (71 different diseases), and 88.5% of the patients had at least one chronic disease. The patients reported the use of 474 drugs (121 different drugs), with 3.2 drugs per patient on average. We identified 265 potential drug interactions, classified as important (6.0%), with clinical significance (20.7%) and without clinical significance or with insufficient data (69.4%). Cirrhotic patients had a higher average number of potential drug interactions than non-cirrhotic patients (2.51 x 0.79, p = 0.000). Hepatitis C treatment with direct-acting antivirals are effective and safe for most of patients.
publishDate 2022
dc.date.none.fl_str_mv 2022-11-09
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/bjps/article/view/201155
10.1590/s2175-9790201900041874
url https://www.revistas.usp.br/bjps/article/view/201155
identifier_str_mv 10.1590/s2175-9790201900041874
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/bjps/article/view/201155/185296
https://www.revistas.usp.br/bjps/article/view/201155/185297
dc.rights.driver.fl_str_mv Copyright (c) 2022 Brazilian Journal of Pharmaceutical Sciences
https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2022 Brazilian Journal of Pharmaceutical Sciences
https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade de São Paulo. Faculdade de Ciências Farmacêuticas
publisher.none.fl_str_mv Universidade de São Paulo. Faculdade de Ciências Farmacêuticas
dc.source.none.fl_str_mv Brazilian Journal of Pharmaceutical Sciences; Vol. 57 (2021)
Brazilian Journal of Pharmaceutical Sciences; v. 57 (2021)
Brazilian Journal of Pharmaceutical Sciences; Vol. 57 (2021)
2175-9790
1984-8250
reponame:Brazilian Journal of Pharmaceutical Sciences
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Brazilian Journal of Pharmaceutical Sciences
collection Brazilian Journal of Pharmaceutical Sciences
repository.name.fl_str_mv Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)
repository.mail.fl_str_mv bjps@usp.br||elizabeth.igne@gmail.com
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