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Successful Treatment of Hepatitis C with Simeprevir, Sofosbuvir, and Ribavirin in an HIV Coinfected Liver Transplant Patient with Advanced Chronic Kidney Disease.
Maruyama, Anna; Hussaini, Trana; Partovi, Nilufar; Erb, Siegfried R; Azalgara, Vladimir Marquez; Zalunardo, Nadia; Pick, Neora; Hull, Mark; Yoshida, Eric M.
Afiliação
  • Maruyama A; Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, BC, Canada.
  • Hussaini T; Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, BC, Canada.
  • Partovi N; Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, BC, Canada.
  • Erb SR; Division of Gastroenterology, University of British Columbia, Vancouver, BC, Canada.
  • Azalgara VM; Division of Gastroenterology, University of British Columbia, Vancouver, BC, Canada.
  • Zalunardo N; Division of Nephrology, University of British Columbia, Vancouver, BC, Canada.
  • Pick N; Division of AIDS, University of British Columbia, Vancouver, BC, Canada.
  • Hull M; Division of AIDS, University of British Columbia, Vancouver, BC, Canada.
  • Yoshida EM; Division of Gastroenterology, University of British Columbia, Vancouver, BC, Canada.
Can J Infect Dis Med Microbiol ; 2016: 8372835, 2016.
Article em En | MEDLINE | ID: mdl-27366182
ABSTRACT
Although major advances have occurred in treating patients with hepatitis C virus (HCV) with the development of new direct-acting antivirals (DAAs), treatment of liver transplant recipients with HCV, human immunodeficiency virus (HIV) coinfection, and renal disease is challenging due to the lack of efficacy and safety data in this population. We report a case of successful HCV therapy in a postliver transplant HIV coinfected patient, with stage 4 chronic kidney disease, using an all-oral regimen of simeprevir, sofosbuvir, and ribavirin. The 51-year-old male achieved SVR24, and no specific HIV-related or transplant-related adverse events were documented during the treatment period. The new DAAs show promise for HIV coinfected patients and those with severe to end-stage renal disease (ESRD); however, robust clinical trials or large cohort studies will need to be conducted to confirm the efficacy and safety of these newer agents in this setting.

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Observational_studies Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Observational_studies Idioma: En Ano de publicação: 2016 Tipo de documento: Article