The landscape of therapeutic options for HCV infection has dramatically changed with the approval of all-oral direct-acting antiviral (DAA) regimens. DAAs target important steps in the HCV viral life cycle, resulting in higher response rates and fewer adverse events than were afforded with interferon and ribavirin, the prior standard of care. The achievement of sustained virologic response (SVR) rates in excess of 90% with use of DAA regimens has not only translated into HCV eradication for the hundreds of thousands treated but is also anticipated to decrease the incidence of major complications associated with chronic HCV infection. Additionally, the favorable side effect profile of DAAs has made HCV therapy feasible in difficult-to-treat populations, including those with previous exposure to interferon and ribavirin, cirrhosis, decompensated liver disease, HIV and HCV co-infection, and severe renal dysfunction/end stage renal disease. Given this tremendous progress, all patients infected with HCV infection should be treated.
Keyphrases
- hepatitis c virus
- human immunodeficiency virus
- end stage renal disease
- chronic kidney disease
- peritoneal dialysis
- newly diagnosed
- healthcare
- risk factors
- ejection fraction
- antiretroviral therapy
- palliative care
- dendritic cells
- stem cells
- hiv positive
- hepatitis b virus
- immune response
- atrial fibrillation
- prognostic factors
- early onset
- quality improvement