American Journal of Kidney Diseases
Volume 51, Issue 2 , Pages 263-277, February 2008

Interferon Treatment in Hemodialysis Patients With Chronic Hepatitis C Virus Infection: A Systematic Review of the Literature and Meta-analysis of Treatment Efficacy and Harms

  • Craig E. Gordon, MD, MS

      Affiliations

    • Division of Nephrology, Institute for Clinical Research and Health Policy Studies, Tufts-New England Medical Center, Boston MA
    • Corresponding Author InformationAddress correspondence to Craig E. Gordon, MD, MS, Tufts-New England Medical Center, 750 Washington St, Box 391, Boston, MA 02111.
  • ,
  • Katrin Uhlig, MD, MS

      Affiliations

    • Division of Nephrology, Institute for Clinical Research and Health Policy Studies, Tufts-New England Medical Center, Boston MA
  • ,
  • Joseph Lau, MD

      Affiliations

    • Division of Clinical Care Research, Institute for Clinical Research and Health Policy Studies, Tufts-New England Medical Center, Boston MA
  • ,
  • Christopher H. Schmid, PhD

      Affiliations

    • Biostatistics Research Center, Institute for Clinical Research and Health Policy Studies, Boston MA
  • ,
  • Andrew S. Levey, MD

      Affiliations

    • Division of Nephrology, Institute for Clinical Research and Health Policy Studies, Tufts-New England Medical Center, Boston MA
  • ,
  • John B. Wong, MD

      Affiliations

    • Clinical Decision Making, Department of Medicine, Tufts-New England Medical Center, Boston MA.

Received 6 June 2007; accepted 9 November 2007.

Background

Hepatitis C virus (HCV) infection is prevalent in patients undergoing hemodialysis and is associated with greater mortality. We determined the efficacy and harms of interferon (IFN) and pegylated IFN (PEG-IFN) treatment of hemodialysis patients with chronic HCV infection and identified factors associated with these outcomes.

Study Design

Meta-analysis and meta-regression of randomized controlled trials, uncontrolled trials, and prospective observational studies.

Setting & Population

Hemodialysis patients with chronic HCV infection.

Selection Criteria for Studies

MEDLINE indexed studies since 1966, sample size greater than 10.

Intervention

IFN-based treatment, including PEG-IFN with and without ribavirin.

Outcomes

Sustained virological response (SVR) 6 months after treatment, rate of treatment discontinuation caused by adverse events, and factors associated with these outcomes.

Results

20 studies of 459 IFN-treated patients, 3 studies of 38 PEG-IFN–treated patients, and 2 studies of 49 PEG-IFN and ribavirin-treated patients met inclusion criteria. The overall SVR rate was 41% (95% confidence interval [CI], 33 to 49) for IFN and 37% (95% CI, 9 to 77) for PEG-IFN. Treatment discontinuation rates were 26% (95% CI, 20 to 34) for IFN and 28% (95% CI, 12 to 53) for PEG-IFN. SVR was higher with 3 million units (MU) or higher of IFN 3 times weekly, with lower mean HCV RNA, and with lower rates of cirrhosis, HCV genotype 1 or elevated transaminase, but these findings were not statistically significant. Treatment discontinuation rates were greater in studies using larger doses.

Limitations

Publication bias, few randomized controlled trials, and limitations in generalizability to all hemodialysis patients.

Conclusion

IFN treatment of hemodialysis patients results in an SVR rate of 41%. Higher dose, lower mean HCV RNA level, and lower rates of cirrhosis, transaminase level increase, and HCV genotype 1 may be associated with greater SVR rates, but additional studies using individual patient data are needed.

Index Words: Hepatitis C virus, interferon, hemodialysis, sustained virological response, meta-analysis

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 Because an author of this manuscript is an editor for AJKD, the peer-review and decision-making processes were handled entirely by an Associate Editor (Beth M. Piraino, MD, University of Pittsburgh School of Medicine) who served as Acting Editor-in-Chief. Details of the journal’s procedures for potential editor conflicts are given in the Editorial Policies section of the AJKD website.

PII: S0272-6386(07)01482-5

doi:10.1053/j.ajkd.2007.11.003

American Journal of Kidney Diseases
Volume 51, Issue 2 , Pages 263-277, February 2008