The growing disparity between available organs for liver transplantation an
d the number of waiting recipients has prompted significant debate over org
an allocation and distribution. In light of this debate, recipient selectio
n and prediction of factors relating to outcome have become increasingly im
portant. Current immunosuppressive regimens provide excellent short- and lo
ng-term survival for patients and grafts. Increasingly, efforts are being m
ade to decrease or withdraw immunosuppression late after transplantation to
minimize long-term side effects. Viral disease, particularly cytomegalovir
us infection, results in significant morbidity and mortality in patients, H
owever, strategies for targeting high-risk patients with prophylactic antiv
iral therapy have been successful in reducing the incidence of cytomegalovi
rus disease. Recurrent viral hepatitis following liver transplantation may
limit long-term graft success. Lamivudine appears to limit recurrent infect
ion with hepatitis B virus in a significant number of patients who develop
this condition following liver transplantation and may represent a cost sav
ings over hepatitis B immunoglobulin. Although the overall survival of pati
ents with chronic hepatitis C virus infection after orthotopic liver transp
lantation is excellent, significant morbidity and mortality occur in the su
bset of patients with severe recurrent disease. Interferon may delay the on
set of disease in patients infected with hepatitis C virus following orthot
opic liver transplantation, and investigation continues into antiviral ther
apy in this group of patients. (C) 1999 Lippincott Williams & Wilkins, Inc.