Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2009 Apr 7;15(13):1650-2.
doi: 10.3748/wjg.15.1650.

A combination treatment of entecavir and early-phase corticosteroid in severe exacerbation of chronic hepatitis B

Affiliations
Case Reports

A combination treatment of entecavir and early-phase corticosteroid in severe exacerbation of chronic hepatitis B

Kazuyuki Matsumoto et al. World J Gastroenterol. .

Abstract

Of patients with severe exacerbation of chronic hepatitis B accompanied by jaundice and coagulopathy, 20%-30% have a fatal outcome. In this report, we describe 2 cases of severe exacerbation of chronic hepatitis B with jaundice and coagulopathy who were successfully treated with a combination of entecavir and corticosteroid. In both cases, rapid reductions in serum hepatitis B virus (HBV)-DNA levels were observed, and corticosteroid was stopped after serum HBV-DNA levels became undetectable. Entecavir treatment was continued. Generally, entecavir treatment reduced serum HBV-DNA levels rapidly, although the improvement in liver function was delayed by a few weeks. During this time lag, liver cell injury continued and the disease progressed. Corticosteroid suppressed the excessive host immune response and was useful for stopping progressive deterioration. A combination of entecavir and early-phase corticosteroid may be a useful treatment in severe exacerbation of chronic hepatitis B.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Patient clinical course. ALT: Alanine aminotransferase; PT: Prothrombin activity; T. Bil: Total bilirubin; HBV DNA: Hepatitis B virus DNA. At 6 wk, his serum transaminase level was normalized. At 12 wk, his serum HBV-DNA level became 3.3 LGE/mL and prednisolone was stopped.
Figure 2
Figure 2
Patient clinical course. ALT: Alanine aminotransferase; PT: Prothrombin activity; T. Bil: Total bilirubin; HBV DNA: Hepatitis B virus DNA. At 8 wk, her serum transaminase level was normalized. At 15 wk, her serum HBV-DNA level became undetectable and the prednisolone was stopped.

Similar articles

Cited by

References

    1. Papatheodoridis GV, Manolakopoulos S, Dusheiko G, Archimandritis AJ. Therapeutic strategies in the management of patients with chronic hepatitis B virus infection. Lancet Infect Dis. 2008;8:167–178. - PubMed
    1. Perrillo RP. Acute flares in chronic hepatitis B: the natural and unnatural history of an immunologically mediated liver disease. Gastroenterology. 2001;120:1009–1022. - PubMed
    1. Seeff LB, Koff RS. Evolving concepts of the clinical and serologic consequences of hepatitis B virus infection. Semin Liver Dis. 1986;6:11–22. - PubMed
    1. Yuen MF, Yuan HJ, Hui CK, Wong DK, Wong WM, Chan AO, Wong BC, Lai CL. A large population study of spontaneous HBeAg seroconversion and acute exacerbation of chronic hepatitis B infection: implications for antiviral therapy. Gut. 2003;52:416–419. - PMC - PubMed
    1. Tsubota A, Arase Y, Suzuki Y, Suzuki F, Sezaki H, Hosaka T, Akuta N, Someya T, Kobayashi M, Saitoh S, et al. Lamivudine monotherapy for spontaneous severe acute exacerbation of chronic hepatitis B. J Gastroenterol Hepatol. 2005;20:426–432. - PubMed

Publication types