Literature DB >> 15476146

Treatment of chronic hepatitis B: who to treat, what to use, and for how long?

Scott K Fung1, Anna S F Lok.   

Abstract

Chronic hepatitis B infection continues to be a major public health concern worldwide. The natural history of the disease can be divided into 4 different phases: immune tolerance, immune clearance, inactive carrier, and reactivation. The goals of treatment are sustained viral suppression, normalization of ALT, and improvement in liver histology. Antiviral agents in current use include standard interferon-alpha, lamivudine, and adefovir. With an improved understanding of the natural history of the disease and a growing repertoire of antiviral drugs, the important questions are: who should receive treatment, what is the best agent to use, and what is the optimal duration of therapy? Treatment is indicated for patients in the immune clearance and reactivation phases. Patients with high pretreatment ALT level, detectable HBV DNA in the serum, and active inflammation on liver biopsy are predicted to have the highest chance of response to treatment. The choice of a particular agent must balance long-term benefits such as the likelihood of a sustained response against long-term risks such as drug resistance. Interferon treatment leads to a more durable response but is associated with unpleasant side effects. Lamivudine is effective and well tolerated but requires long-term therapy and is associated with drug resistance. Adefovir has proven efficacy and a very low rate of drug resistance but is associated with a small risk of reversible nephrotoxicity. For HBeAG-positive chronic hepatitis B and HBeAG-negative chronic hepatitis B, the duration of interferon therapy is 4-6 months and 12 months, respectively. Duration of treatment is at least 1 year with lamivudine and adefovir; longer duration of treatment is needed in most patients, but the optimal duration of treatment and the criteria for stopping treatment have not been established.

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Year:  2004        PMID: 15476146     DOI: 10.1016/s1542-3565(04)00386-6

Source DB:  PubMed          Journal:  Clin Gastroenterol Hepatol        ISSN: 1542-3565            Impact factor:   11.382


  6 in total

1.  He Jie Tang in the treatment of chronic hepatitis B patients.

Authors:  Ze-Xiong Chen; Shi-Jun Zhang; Shao-Xian Lao; Hong-Tao Hu; Cui-Yi Zhang; Shi-He Guan; Yan-Li Gu
Journal:  World J Gastroenterol       Date:  2005-11-14       Impact factor: 5.742

Review 2.  The "return" of hepatitis B.

Authors:  Zahariy-A Krastev
Journal:  World J Gastroenterol       Date:  2006-11-28       Impact factor: 5.742

3.  Lamivudine resistance mutations in patients infected with hepatitis B virus genotype D.

Authors:  Orhan Yıldız; Bilgehan Aygen; Nese Demirtürk; Tuna Demirdal; Dilara Inan; Taner Yıldırmak; Arzu Kantürk; Ediz Tütüncü
Journal:  World J Gastroenterol       Date:  2011-12-07       Impact factor: 5.742

4.  Using a population-based approach to prevent hepatocellular cancer in New South Wales, Australia: effects on health services utilisation.

Authors:  Monica C Robotin; Melanie Q Kansil; Jacob George; Kirsten Howard; Steven Tipper; Miriam Levy; Nghi Phung; Andrew G Penman
Journal:  BMC Health Serv Res       Date:  2010-07-21       Impact factor: 2.655

5.  Molecular epidemical characteristics of Lamivudine resistance mutations of HBV in southern China.

Authors:  Si-Yue Li; Li Qin; Lei Zhang; Xing-Bo Song; Yi Zhou; Juan Zhou; Xiao-Jun Lu; Ju Cao; Lan-Lan Wang; Jun Wang; Bin-Wu Ying
Journal:  Med Sci Monit       Date:  2011-10

6.  The impact of vaccination and antiviral therapy on hepatitis B and hepatitis D epidemiology.

Authors:  Ashish Goyal; John M Murray
Journal:  PLoS One       Date:  2014-10-14       Impact factor: 3.240

  6 in total

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