Timing of lamivudine administration according to Child class in patients with decompensated cirrhosis
Version of Record online: 13 JUL 2005
Journal of Gastroenterology and Hepatology
Volume 20, Issue 10, pages 1527–1532, October 2005
How to Cite
BAE, S. H., YOON, S. K., CHOI, J. Y., JANG, J. W., CHO, S. H., YANG, J. M., HAN, N. I., AHN, B. M., CHUNG, K. W. and SUN, H. S. (2005), Timing of lamivudine administration according to Child class in patients with decompensated cirrhosis. Journal of Gastroenterology and Hepatology, 20: 1527–1532. doi: 10.1111/j.1440-1746.2005.03886.x
- Issue online: 31 AUG 2005
- Version of Record online: 13 JUL 2005
- Accepted for publication 10 November 2004.
- chronic hepatitis B;
- liver cirrhosis
Background: Few clinical trials have investigated the use of lamivudine (LAM) in patients with decompensated cirrhosis related to chronic hepatitis B. The aim of the present study was to evaluate the efficacy of extended LAM treatment and to determine the timing of LAM administration in patients with decompensated cirrhosis.
Methods: A total of 17 patients were treated with LAM 100 mg/day. The mean duration of follow up was 28 ± 8.4 months (range: 14–42 months). All patients were evaluated for evidence of clinical, biochemical and serologic replication of hepatitis B virus (HBV) infection. There were 12 patients with Child class B and five with Child class C.
Results: Ten of 17 patients (58.2%) responded to LAM treatment. Of the breakthrough patients, six (86%) had YMDD motif variants. Clinical improvement was observed in nine out of 10 responders (90%), six of the seven breakthrough patients (86%) and five of six patients with YMDD variant DNA. Mean time to achieve a 2-point reduction in Child–Pugh–Turcotte score was 14 months in patients with Child class C, compared with 5.9 months in those with Child class B (P < 0.001). Mean time required to gain a 0.5 g/dL increment in albumin was 14 months in Child class C and 5.8 months in Child class B. Hepatitis B e antigen (HBeAg) seroconversion was achieved in five of 13 HBeAg-positive patients at the last follow up and during the follow-up period.
Conclusion: Long-term administration of LAM for patients with decompensated cirrhosis is effective. Earlier LAM administration in Child class B patients led to improved clinical outcomes.
© 2005 Blackwell Publishing Asia Pty Ltd