Pegylated interferon for the treatment of hepatitis C virus in haemodialysis patients
Author(s) -
Daniel Teta,
Brigitte Landtwing Lüscher,
JeanJacques Gonvers,
P Francioli,
Olivier Phan,
Michel Burnier
Publication year - 2005
Publication title -
nephrology dialysis transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.654
H-Index - 168
eISSN - 1460-2385
pISSN - 0931-0509
DOI - 10.1093/ndt/gfh747
Subject(s) - medicine , ribavirin , cirrhosis , hepatocellular carcinoma , gastroenterology , pegylated interferon , hepatitis c , dialysis , hepatitis c virus , interferon , hemodialysis , liver disease , kidney disease , transplantation , liver transplantation , immunology , virus
In patients undergoing maintenance haemodialysis, hepatitis C virus (HCV) infection is common and may lead to severe complications such as chronic hepatitis, cirrhosis and hepatocellular carcinoma. It is recommended to eradicate HCV infection in dialysis patients awaiting renal transplantation and those with acute hepatitis C or significant chronic liver disease. Interferon-a-2a in monotherapy thrice weekly, which is the standard treatment for HCV infection in this setting, has many drawbacks such as poor tolerance and marginal response [1]. The addition of ribavirin is generally contra-indicated in these patients due to a risk of haemolytic anaemia. Pegylated interferon was developed by attaching a large polyethylene glycol (PEG) moiety (40 kDa) to interferon in order to confer greater stability and prolonged systemic exposure to allow once-weekly administration [2]. In two randomized controlled trials, PEG–interferon-a-2a in monotherapy was more efficient than conventional interferon for the treatment of HCV infection associated with chronic liver disease [3,4]. Currently, there is no published experience concerning the use of this compound in patients with end-stage renal disease (ESRD).
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