Results of
liver transplantation (LT) for
hepatitis B have improved significantly with the use of
hepatitis B immune globulin (
HBIG) and/or
lamivudine. The aim of this study is to review the long-term outcome of patients who underwent LT for
hepatitis B. Records of 41 patients who underwent LT for
hepatitis B and survived 3 months or longer post-LT were reviewed. Twenty patients were administered no immunoprophylaxis or short-term intramuscular
HBIG, whereas 21 patients were administered high-dose intravenous (IV)
HBIG. Median post-LT follow-up in these 2 groups was 76 months (range, 4 to 155 months) and 25 months (range, 4 to 68 months), respectively.
Hepatitis B recurred in 15 (75%) and 4 patients (19%) who underwent LT in the pre-
HBIG and post-
HBIG eras, respectively. Cumulative rates of recurrent
hepatitis B at 1 and 3 years post-LT in these 2 groups were 66% and 77% and 20% and 20%, respectively (P <.001). Recurrent
hepatitis B in the post-
HBIG era correlated with antibody to
hepatitis B surface antigen titer less than 100 IU/L. Nine patients with recurrent
hepatitis B were administered
lamivudine for 13 to 49 months (median, 28 months); 6 patients continued to have stable or improved
liver disease, whereas 3 patients developed virological breakthrough with slow deterioration of
liver disease. Long-term IV
HBIG is effective in preventing recurrent
hepatitis B. The risk for recurrent
hepatitis B is negligible after the first year post-LT. Among patients with no virological breakthrough,
lamivudine can stabilize or improve
liver disease for up to 4 years in patients with recurrent
hepatitis B post-LT.