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Box 157, Department of Medicine, University of Cambridge School of Clinical
Medicine, Addenbrooke's Hospital, Cambridge CB2 2QQ, UK
Correspondence to: Dr Alexander gja1000{at}cam.ac.uk
Submitted 8 February
2000;
Accepted 4 September 2000
Many recent and significant advances in the field of chronic
viral hepatitis, including therapy, suggest that an update on chronic
hepatitis is timely.
Chronic hepatitis B virus infection remains a significant worldwide
cause of liver cirrhosis and hepatocellular carcinoma, despite the wide
availability of a long established and effective vaccine. Transmission
occurs via perinatal, sexual, and parenteral routes (particularly
intravenous drug abuse and although blood products still carry a risk,
this is now extremely low in Western countries). Only a minority of
infected adult cases develop chronic hepatitis but in children under 1 year, 90% develop chronic hepatitis. The clinical spectrum of chronic
liver injury ranges from mild inflammation to end stage liver
cirrhosis. Interferon alfa has been the mainstay of treatment for
patients with active disease but nucleoside analogues (lamivudine and
adefovir) are now available with similar efficacy. Patients with end
stage liver disease and hepatocellular carcinoma can be offered
transplantation but infection in the graft is commonplace. The
combination of hepatitis B immunoglobulin and newer antiviral drugs
reduce the incidence and severity of graft infection significantly.
The hepatitis C virus epidemic of the latter half of the 20th century
now affects more than 1% of populations worldwide. This RNA virus is
spread parenterally and is becoming the leading indication for liver
transplantation. The majority of patients develop chronic hepatitis,
which may be progressive, evolving to significant liver disease
(cirrhosis or hepatocellular carcinoma) in about 20% cases after
decades. Treatment with the combination of interferon alfa and
ribavirin is successful in up to 40% cases. Liver transplantation is a
therapeutic option for some but graft infection is universal and often
complicated by progressive liver fibrosis. A vaccine remains a remote
prospect so that prevention is crucial.
Hepatitis D virus infection occurs on a background of hepatitis B virus
infection and can also cause liver damage. The response to antiviral
therapy is poor.
The newer "hepatitis" viruses G and TT do not cause significant
liver injury.
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