Fatal Hepatic Decompensation in a Patient with Hepatitis B Cirrhosis Following Famciclovir Withdrawal

Hepatitis B virus (HBV) infection is a major cause of chronic liver disease worldwide. Famciclovir is a nucleoside analogue with potent antiviral activity that appears promising in the management of patients with HBV infection. No data exist regarding the safety of nucleoside analogue withdrawal in...

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Main Authors: Robert P Myers, Rabindra Chaudhary, Kevin Fonseca, Samuel S Lee
Format: Article
Language:English
Published: Hindawi Limited 2000-01-01
Series:Canadian Journal of Gastroenterology
Online Access:http://dx.doi.org/10.1155/2000/142782
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spelling doaj-6aaca725d1ab4792b12f5b51a3ece4622020-11-24T21:17:59ZengHindawi LimitedCanadian Journal of Gastroenterology0835-79002000-01-0114872572710.1155/2000/142782Fatal Hepatic Decompensation in a Patient with Hepatitis B Cirrhosis Following Famciclovir WithdrawalRobert P Myers0Rabindra Chaudhary1Kevin Fonseca2Samuel S Lee3Division of Gastroenterology and Hepatology, University of Calgary, Calgary, Alberta, CanadaDivision of Gastroenterology and Hepatology, University of Calgary, Calgary, Alberta, CanadaDivision of Gastroenterology and Hepatology, University of Calgary, Calgary, Alberta, CanadaDivision of Gastroenterology and Hepatology, University of Calgary, Calgary, Alberta, CanadaHepatitis B virus (HBV) infection is a major cause of chronic liver disease worldwide. Famciclovir is a nucleoside analogue with potent antiviral activity that appears promising in the management of patients with HBV infection. No data exist regarding the safety of nucleoside analogue withdrawal in patients treated for HBV cirrhosis. The authors describe a 41-year-old man with compensated HBV cirrhosis who developed fatal hepatic decompensation due to a rebound in viral replication within six weeks of discontinuing famciclovir therapy. Although several mutations in the HBV DNA polymerase gene have been documented, none has been associated with famciclovir resistance or adverse clinical outcomes. Clinicians should consider the risk of inducing serious flares in hepatic inflammation as a result of abrupt nucleoside analogue withdrawal. Until further data are available regarding the safety of withdrawal of these agents, indefinite treatment may be required in patients with established cirrhosis.http://dx.doi.org/10.1155/2000/142782
collection DOAJ
language English
format Article
sources DOAJ
author Robert P Myers
Rabindra Chaudhary
Kevin Fonseca
Samuel S Lee
spellingShingle Robert P Myers
Rabindra Chaudhary
Kevin Fonseca
Samuel S Lee
Fatal Hepatic Decompensation in a Patient with Hepatitis B Cirrhosis Following Famciclovir Withdrawal
Canadian Journal of Gastroenterology
author_facet Robert P Myers
Rabindra Chaudhary
Kevin Fonseca
Samuel S Lee
author_sort Robert P Myers
title Fatal Hepatic Decompensation in a Patient with Hepatitis B Cirrhosis Following Famciclovir Withdrawal
title_short Fatal Hepatic Decompensation in a Patient with Hepatitis B Cirrhosis Following Famciclovir Withdrawal
title_full Fatal Hepatic Decompensation in a Patient with Hepatitis B Cirrhosis Following Famciclovir Withdrawal
title_fullStr Fatal Hepatic Decompensation in a Patient with Hepatitis B Cirrhosis Following Famciclovir Withdrawal
title_full_unstemmed Fatal Hepatic Decompensation in a Patient with Hepatitis B Cirrhosis Following Famciclovir Withdrawal
title_sort fatal hepatic decompensation in a patient with hepatitis b cirrhosis following famciclovir withdrawal
publisher Hindawi Limited
series Canadian Journal of Gastroenterology
issn 0835-7900
publishDate 2000-01-01
description Hepatitis B virus (HBV) infection is a major cause of chronic liver disease worldwide. Famciclovir is a nucleoside analogue with potent antiviral activity that appears promising in the management of patients with HBV infection. No data exist regarding the safety of nucleoside analogue withdrawal in patients treated for HBV cirrhosis. The authors describe a 41-year-old man with compensated HBV cirrhosis who developed fatal hepatic decompensation due to a rebound in viral replication within six weeks of discontinuing famciclovir therapy. Although several mutations in the HBV DNA polymerase gene have been documented, none has been associated with famciclovir resistance or adverse clinical outcomes. Clinicians should consider the risk of inducing serious flares in hepatic inflammation as a result of abrupt nucleoside analogue withdrawal. Until further data are available regarding the safety of withdrawal of these agents, indefinite treatment may be required in patients with established cirrhosis.
url http://dx.doi.org/10.1155/2000/142782
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