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dc.creatorGonzález-Serna Martín, Manuel Alejandroes
dc.creatorMacías Sánchez, Juanes
dc.creatorCorma Gómez, Anaïses
dc.creatorTellez, Franciscoes
dc.creatorCucurull, Josepes
dc.creatorReal Navarrete, Luis Migueles
dc.creatorGranados, Rafaeles
dc.creatorRivero Juárez, Antonioes
dc.creatorHernández Quero, Josées
dc.creatorMerino, Doloreses
dc.creatorPalacios, Rosarioes
dc.creatorRíos-Villegas, María Josées
dc.creatorCollado, Antonioes
dc.creatorPineda Vergara, Juan Antonioes
dc.date.accessioned2024-04-05T10:31:59Z
dc.date.available2024-04-05T10:31:59Z
dc.date.issued2022-09
dc.identifier.citationGonzález-Serna Martín, M.A., Macías Sánchez, J., Corma Gómez, A., Tellez, F., Cucurull, J., Real Navarrete, L.M.,...,Pineda Vergara, J.A. (2022). High efficacy of glecaprevir/pibrentasvir for HCV-infected individuals with active drug use. Journal of Infection, 85 (3), 322-326. https://doi.org/10.1016/j.jinf.2022.06.005.
dc.identifier.issn0163-4453es
dc.identifier.issn1532-2742es
dc.identifier.urihttps://hdl.handle.net/11441/156690
dc.description.abstractObjectives Real world data on glecaprevir/pibrentasvir (G/P) among active drug users are scarce. We evaluated the sustained virological response (SVR) rates of G/P among individuals with and without active drug use in routine clinical practice. Methods Two ongoing prospective multicenter cohorts of individuals starting G/P were analyzed. Overall SVR intention-to-treat (ITT), discontinuations due to adverse effects and dropouts were evaluated. Results in patients with active, past and without active drug use were compared. Results Overall, 644 individuals started G/P and have reached the date of SVR evaluation. Of them, 613 (95.2%) individuals achieved SVR. There were two (0.3%) relapses, one (0.2%) discontinuation due to side effects and 35 (5.4%) dropouts. SVR rates for patients with active drug use, past drug use and those who never used drugs were 85.4%(n/N = 70/82), 96.1%(n/N = 320/333) and 97.4%(n/N = 223/229) respectively (p < 0.001). After adjustment by sex, age, HCV genotype and opioid agonist therapy, active drug use was the only factor independently associated with SVR (ITT) [adjusted OR (95%confidence interval): 0.29(0.09–0.99),p = 0.048]. Conclusions Active drug use was independently associated with lower SVR rates to G/P, mainly due to voluntary dropout. G/P could be particularly beneficial in this scenario but specific strategies designed to increase the retention in care are needed.es
dc.description.sponsorshipInstituto de Salud Carlos III PI018/00606 (Co-funded by European Regional Development Fund/European Social Fund)es
dc.description.sponsorshipMinistry of Science, Innovation and Universities of Spain CP18/00146 and CP18/00111es
dc.description.sponsorshipInstituto de Salud Carlos III (CM19/00251)es
dc.description.sponsorshipServicio Andaluz de Salud B-0061-2021 and A1-0060-2021es
dc.formatapplication/pdfes
dc.format.extent5 p.es
dc.language.isoenges
dc.publisherElsevieres
dc.relation.ispartofJournal of Infection, 85 (3), 322-326.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectGlecaprevir/pibrentasvires
dc.subjectHCV therapyes
dc.subjectDrug usees
dc.subjectOpiate agonist therapyes
dc.subjectPWIDes
dc.titleHigh efficacy of glecaprevir/pibrentasvir for HCV-infected individuals with active drug usees
dc.typeinfo:eu-repo/semantics/articlees
dc.type.versioninfo:eu-repo/semantics/acceptedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Fisiologíaes
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Medicinaes
dc.relation.projectIDPI018/00606es
dc.relation.projectIDCP18/00146es
dc.relation.projectIDCP18/00111es
dc.relation.projectIDCM19/00251es
dc.relation.projectIDB-0061-2021es
dc.relation.projectIDA1-0060-2021es
dc.relation.publisherversionhttps://dx.doi.org/10.1016/j.jinf.2022.06.005es
dc.identifier.doi10.1016/j.jinf.2022.06.005es
dc.journaltitleJournal of Infectiones
dc.publication.volumen85es
dc.publication.issue3es
dc.publication.initialPage322es
dc.publication.endPage326es
dc.contributor.funderInstituto de Salud Carlos IIIes
dc.contributor.funderEuropean Commission (EC). Fondo Europeo de Desarrollo Regional (FEDER)es
dc.contributor.funderMinisterio de Ciencia, Innovación y Universidades (MICINN). Españaes
dc.contributor.funderServicio Andaluz de Saludes
dc.description.awardwinningPremio Trimestral Publicación Científica Destacada de la US. Facultad de Farmacia

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