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Management of hepatitis C viral infection in chronic kidney disease patients on hemodialysis in the era of direct-acting antivirals
Article in English | WPRIM (Western Pacific) | ID: wpr-718639
Responsible library: WPRO
ABSTRACT
The advent of novel, direct-acting antiviral (DAA) regimens for hepatitis C virus (HCV) infection has revolutionized its treatment by producing a sustained virologic response of more than 95% with few side effects and no comorbidities in the general population. Until recently, ideal DAA regimens have not been available to patients with severe renal impairment and end-stage renal disease because there are limited data on the pharmacokinetics, safety, and efficacy of treatment in this unique population. In a hemodialysis context, identifying patients in need of treatment and preventing HCV transmission may also be a matter of concern. Recently published studies suggest that a combination of paritaprevir/ritonavir/ombitasvir and dasabuvir, elbasvir/grazoprevir, or glecaprevir/pibrentasvir successfully treats HCV infection in chronic kidney disease stage 4 or 5 patients with or without hemodialysis.
Subject(s)

Full text: Available Health context: SDG3 - Health and Well-Being Health problem: Target 3.3: End transmission of communicable diseases Database: WPRIM (Western Pacific) Main subject: Antiviral Agents / Pharmacokinetics / Comorbidity / Renal Dialysis / Hepatitis C / Hepacivirus / Hepatitis C, Chronic / Renal Insufficiency, Chronic / Hepatitis / Kidney Failure, Chronic Limits: Humans Language: English Journal: Clinical and Molecular Hepatology Year: 2018 Document type: Article
Full text: Available Health context: SDG3 - Health and Well-Being Health problem: Target 3.3: End transmission of communicable diseases Database: WPRIM (Western Pacific) Main subject: Antiviral Agents / Pharmacokinetics / Comorbidity / Renal Dialysis / Hepatitis C / Hepacivirus / Hepatitis C, Chronic / Renal Insufficiency, Chronic / Hepatitis / Kidney Failure, Chronic Limits: Humans Language: English Journal: Clinical and Molecular Hepatology Year: 2018 Document type: Article
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