Recurrent hepatitis C virus (HCV) in liver transplant patients is a major cause of graft loss, liver failure, and need for retransplantation. The results available to date with the use of interferon alfa (IFN-alpha) in the treatment of recurrent HCV in liver transplant patients have been disappointi
A randomized study comparing ribavirin and interferon alfa monotherapy for hepatitis C recurrence after liver transplantation
β Scribed by Edward J. Gane; Su-Kong Lo; Stephen M. Riordan; Bernard C. Portmann; Johnson Y. Lau; Nikolai V. Naoumov; Professor Roger Williams
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 120 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0270-9139
No coin nor oath required. For personal study only.
β¦ Synopsis
Hepatitis C virus (HCV) infection usually recurs after orthotopic liver transplantation (OLT), and most patients develop graft damage. This study compared the efficacy of interferon alfa (IFN-β£) and ribavirin monotherapies in liver transplant recipients with chronic hepatitis C in the graft. Thirty OLT recipients with chronic hepatitis C were randomized to receive either IFN-β£ (3 MU three times a week) or ribavirin (up to 1.2 g daily) for 24 weeks. Virological, biochemical, and histological responses to treatment were assessed. Twenty-eight patients completed the treatment regimen, two ribavirin-treated patients being withdrawn because of severe hemolysis. Normalization of serum aspartate aminotransferase was achieved in 13 of 14 patients receiving ribavirin (93%) and 6 of 14 patients receiving IFN-β£ (43%; P β«Ψβ¬ .01). Lobular inflammation was reduced in 9/14 ribavirin-treated (64%) and 3 of 14 IFN-β£-treated patients (21%; P β«Ψβ¬ .05), each of whom had a biochemical response. However, the total histological activity index did not improve in either the interferon (P β«Ψβ¬ .43) or the ribavirin (P β«Ψβ¬ .96) group. Posttreatment viremia levels were significantly reduced in IFN-β£-treated (P β«Ψβ¬ .05) but not in ribavirin-treated (P β«Ψβ¬ .88) patients. Hemolysis occurred in all ribavirin-treated patients, with serum hemoglobin decreasing to F10 g/dL in 50%. Total leukocyte and lymphocyte counts decreased significantly during ribavirin treatment (P β«Ψβ¬ .02 and P β«Ψβ¬ .004, respectively). We concluded that in patients with chronic hepatitis C after OLT, IFN-β£ retains an antiviral effect whereas ribavirin is superior in achieving normalization of serum aspartate aminotransferase levels and reducing lobular inflammation, but not the total histological activity index. These findings provide a rationale for combination therapy in the post-OLT setting, although patients must be carefully monitored for hemoly-
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