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      Efficacy and safety of sofosbuvir in the treatment of hep C among patients on hemodialysis: a systematic review and meta-analysis

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          Abstract

          Hepatitis C virus (HCV) infection among maintenance hemodialysis patients is implicated in increased morbidity and mortality compared to uninfected patients. Sofosbuvir (SOF)-based regimens may not be optimal among patients requiring hemodialysis. Several studies, however, provide evidence that use of SOF among HCV-positive patients with renal impairment, is effective and safe. We searched Pubmed and Embase to identify studies reporting the efficacy and safety of SOF-based regimens for the treatment of HCV-positive patients on maintenance hemodialysis and performed a random effects meta-analysis. The overall pooled estimate of the efficacy of SOF-based therapy was 95% (95% CI 91–98%). The efficacy of the SOF-based regimen was 92% (95% CI 80–99%), 98% (95% CI 96–100%), and 100% (95% CI 95–100%) for the following doses: 400 mg on alternate days, 400 mg daily, and 200 mg daily, respectively. The most frequent adverse event was fatigue with a pooled prevalence of 16% (95% CI 5–29%), followed by anemia 15% (95% CI 3–31%), and nausea or vomiting 14% (95% CI 4–27%). Anemia was more prevalent in treatment regimens containing ribavirin (46%, 95% CI 33–59%) compared to ribavirin-free regimens (3%, 95% CI 0–9%). This study suggests that SOF-based regimens in the treatment of HCV infection among hemodialysis patients are both effective and safe.

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          Mortality, Hospitalization, and Quality of Life among Patients with Hepatitis C Infection on Hemodialysis.

          Hepatitis C virus (HCV) infection is widely prevalent among patients on hemodialysis (HD), but very rarely treated. The aim of our study is to evaluate the burdens of HCV suffered by patients on HD.
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            Pharmacokinetics, safety and efficacy of a full dose sofosbuvir-based regimen given daily in hemodialysis patients with chronic hepatitis C.

            Hepatitis C virus (HCV) infection is an independent risk factor for chronic kidney disease and leads to faster liver disease progression in patients requiring hemodialysis than in those with normal renal function. Little is known about the use of a sofosbuvir-containing regimen for infected patients on hemodialysis. We aimed to describe the pharmacokinetics, safety and efficacy of sofosbuvir in 2 dosing regimens and associated antiviral agents in HCV-infected patients requiring hemodialysis.
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              Safety and Efficacy of Current DAA Regimens in Kidney and Liver Transplant Recipients with Hepatitis C: Results from the HCV-TARGET Study.

              Data outside of clinical trials with direct acting antiviral (DAA) regimens with or without ribavirin as treatment of chronic HCV in solid organ transplant recipients is limited.
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                Author and article information

                Contributors
                fanti_sechante@brown.edu
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                31 August 2020
                31 August 2020
                2020
                : 10
                : 14332
                Affiliations
                [1 ]GRID grid.40263.33, ISNI 0000 0004 1936 9094, Infectious Diseases Division, , Warren Alpert Medical School of Brown University, Rhode Island Hospital, ; 593 Eddy Street, POB 328, Providence, RI USA
                [2 ]GRID grid.40263.33, ISNI 0000 0004 1936 9094, Kidney Disease Division, , Warren Alpert Medical School of Brown University, Rhode Island Hospital, ; Providence, RI USA
                [3 ]GRID grid.26790.3a, ISNI 0000 0004 1936 8606, Division of Digestive Health and Liver Disease, Miller School of Medicine, , University of Miami, ; Miami, FL USA
                Article
                71205
                10.1038/s41598-020-71205-5
                7459301
                32868869
                abcaaadd-2bdd-405c-b9b1-bea76096a9cf
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 25 January 2020
                : 10 August 2020
                Funding
                Funded by: National Institute of Allergy and Infectious Diseases
                Award ID: K24 AI119158
                Award Recipient :
                Categories
                Article
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                © The Author(s) 2020

                Uncategorized
                hepatology,infectious diseases
                Uncategorized
                hepatology, infectious diseases

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