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dc.contributor.authorFranco, Antonioes_ES
dc.contributor.authorMoreso, Francesces_ES
dc.contributor.authorSolà-Porta, Eulàliaes_ES
dc.contributor.authorBeneyto, Isabeles_ES
dc.contributor.authorEsforzado, Núriaes_ES
dc.contributor.authorGonzalez-Roncero, Franciscoes_ES
dc.contributor.authorSancho, Asunciónes_ES
dc.contributor.authorMelilli, Edoardoes_ES
dc.contributor.authorRuiz San Millán, Juan Carlos es_ES
dc.contributor.authorGaleano, Cristinaes_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2023-09-13T16:36:48Z
dc.date.available2023-09-13T16:36:48Z
dc.date.issued2023es_ES
dc.identifier.issn2077-0383es_ES
dc.identifier.urihttps://hdl.handle.net/10902/29911
dc.description.abstractHistorically, donor infection with hepatitis-C virus (HCV) has been a barrier to kidney transplantation. However, in recent years, it has been reported that HCV positive kidney donors transplanted into HCV negative recipients offer acceptable mid-term results. However, acceptance of HCV donors, especially viremic, has not broadened in the clinical practice. This is an observational, multicenter, retrospective study including kidney transplants from HCV positive donors into negative recipients reported to the Spanish group from 2013 to 2021. Recipients from viremic donors received peri-transplant treatment with direct antiviral agents (DAA) for 8-12 weeks. We included 75 recipients from 44 HCV non-viremic donors and 41 from 25 HCV viremic donors. Primary non function, delayed graft function, acute rejection rate, renal function at the end of follow up, and patient and graft survival were not different between groups. Viral replication was not detected in recipients from non-viremic donors. Recipient treatment with DAA started pre-transplant avoids (n = 21) or attenuates (n = 5) viral replication but leads to non-different outcomes to post-transplant treatment with DAA (n = 15). HCV seroconversion was more frequent in recipients from viremic donors (73% vs. 16%, p < 0.001). One recipient of a viremic donor died due to hepatocellular carcinoma at 38 months. Donor HCV viremia seems not to be a risk factor for kidney transplant recipients receiving peri-transplant DAA, but continuous surveillance should be advisedes_ES
dc.format.extent11 p.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceJournal of Clinical Medicine, 2023, 12(5), 1773es_ES
dc.subject.otherKidney transplantationes_ES
dc.subject.otherHepatitis C viruses_ES
dc.subject.otherViremic donores_ES
dc.subject.otherGraft outcomees_ES
dc.subject.otherHepatocelulares_ES
dc.subject.otherCarcinomaes_ES
dc.titleOutcome of kidney transplants from viremic and non-viremic hepatitis C virus positive donors into negative recipients: Results of the spanish registryes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.3390/jcm12051773es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.3390/jcm12051773es_ES
dc.type.versionpublishedVersiones_ES


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Attribution 4.0 InternationalExcepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International