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dc.contributor.authorCorma Gómez, Anaís
dc.contributor.authorMorano, Luis
dc.contributor.authorTéllez, Francisco
dc.contributor.authorRivero Juárez, Antonio
dc.contributor.authorReal, Luis M.
dc.contributor.authorAlados, Juan Carlos
dc.contributor.authorRíos Villegas, María José
dc.contributor.authorVera Méndez, Francisco Jesús
dc.contributor.authorPalacios Muñoz, Rosario
dc.contributor.authorGreijo, Paloma
dc.contributor.authorMacías, Juan
dc.contributor.authorPineda, Juan A.
dc.date.accessioned2025-01-31T12:56:04Z
dc.date.available2025-01-31T12:56:04Z
dc.date.issued2019
dc.identifier.citationCorma-Gómez A, Morano L, Téllez F, Rivero-Juárez A, Real LM, Alados JC, Ríos-Villegas MJ, Vera-Méndez FJ, Muñoz RP, Geijo P, Macías J, Pineda JA; RIS-HEP13 and GEHEP 011 study groups. HIV infection does not increase the risk of liver complications in hepatitis C virus-infected patient with advanced fibrosis, after sustained virological response with direct-acting antivirals. AIDS. 2019 Jun 1;33(7):1167-1174. doi: 10.1097/QAD.0000000000002186es
dc.identifier.urihttp://hdl.handle.net/10952/9062
dc.description.abstractObjective: To assess the impact of HIV coinfection on the risk of developing liver-related complications in HCV-infected patients with advanced fibrosis treated with direct-acting antivirals (DAA) after sustained virological response (SVR). Design: Prospective cohort study. Setting: Multicenter. Subjects: Patients from the GEHEP and HEPAVIR cohorts were selected if they fulfilled the following criteria: treatment against HCV with all oral DAA combination; SVR achievement, defined as undetectable plasma HCV RNA 12 weeks after the end of therapy; pretreatment liver stiffness equal to or higher than 9.5 kPa; liver stiffness measurement at the time of SVR. Main outcome measure(s): The primary variable was the time until the development of a liver complication or requiring liver transplant. Results: Seven hundred and seventeen patients were included and 507 (71%) were coinfected with HIV. After a median follow-up time of 21 (14-25) months, 15 (2.1%) patients developed a liver complication and/or underwent a liver transplant and 15 (2.0%) died. The probability of remaining free of hepatic complications or transplant at 1 and 2 was, respectively, 99 and 96% in HCV-monoinfected patients and 99 and 98% in coinfected patients (P = 0.648). In a multivariate analysis, in which nonliver-related death was considered as a competing event, HIV coinfection was not associated with the appearance of hepatic complications or requiring liver transplant [hazard ratio = 0.24; 95% CI (0.03-1.93), P = 0.181]. Having presented hepatic decompensation prior to SVR [hazard ratio = 29.06; 95% CI (3.91-216.16), P < 0.001] and the value of liver stiffness at the SVR time-point (hazard ratio = 1.12; 95% CI (1.07-1.18), P < 0.001] were associated with a higher probability of development of liver events. Conclusion: HIV coinfection is not associated with a higher probability of developing liver complications in HCV-infected patients with advanced fibrosis, who achieved SVR with interferon-free regimens.es
dc.language.isoenes
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleHIV infection does not increase the risk of liver complications in HCV- infected patients with advanced fibrosis treated with direct-acting antiviralses
dc.typejournal articlees
dc.rights.accessRightsopen accesses
dc.journal.titleAIDSes
dc.volume.number33es
dc.issue.number4es
dc.description.disciplineMedicinaes
dc.identifier.doi10.1097/QAD.0000000000002186es
dc.description.facultyMedicinaes


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