Brazilian Journal of Medical and Biological Research (Feb 2002)

Lamivudine therapy for hepatitis B in renal transplantation

  • F.R.L. Santos,
  • A.R. Haiashi,
  • M.R.T. Araújo,
  • H. Abensur,
  • J.E. Romão Junior,
  • I.L. Noronha

DOI
https://doi.org/10.1590/S0100-879X2002000200008
Journal volume & issue
Vol. 35, no. 2
pp. 199 – 203

Abstract

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Antiviral therapies are associated with an increased risk of acute rejection in transplant patients. The aim of the present study was to evaluate the efficacy and safety of lamivudine therapy for hepatitis B virus (HBV) infection in renal transplant patients. Six patients were included in this study. They received 150 mg/day of lamivudine during a follow-up period of 24 months. The laboratory tests monitored were HBV DNA, HBsAg, HBeAg, ALT, gamma-GT, serum creatinine and blood cyclosporine levels. The HBV DNA became undetectable in four patients as early as in the third month of treatment. After six months, the viral load was also negative in the other two patients, and remained so until 18 months of follow-up. The medication was well tolerated with no major side effects. Lamivudine was safe and effective in blocking HBV replication in renal transplant patients without any apparent increase in the risk of graft failure for the 24-month period of study.

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