Asian-Pacific consensus statement on the management of chronic hepatitis B: A 2012 update
Journal
Hepatology International
Journal Volume
6
Journal Issue
3
Pages
531-561
Date Issued
2012
Author(s)
Liaw Y.-F.
Piratvisuth T.
Chan H.L.Y.
Chien R.-N.
Gane E.
Locarnini S.
Lim S.-G.
Han K.-H.
Amarapurkar D.
Cooksley G.
Jafri W.
Mohamed R.
Hou J.-L.
Chuang W.-L.
Lesmana L.A.
Sollano J.D.
Suh D.-J.
Omata M.
Abstract
Large volume of new data on the natural history and treatment of chronic hepatitis B virus (HBV) infection have become available since 2008. These include further studies in asymptomatic subjects with chronic HBV infection and community-based cohorts, the role of HBV genotype/naturally occurring HBV mutations, the application of non-invasive assessment of hepatic fibrosis and quantitation of HBV surface antigen and new drug or new strategies towards more effective therapy. To update HBV management guidelines, relevant new data were reviewed and assessed by experts from the region, and the significance of the reported findings was discussed and debated. The earlier "Asian-Pacific consensus statement on the management of chronic hepatitis B" was revised accordingly. The key terms used in the statement were also defined. The new guidelines include general management, indications for fibrosis assessment, time to start or stop drug therapy, choice of drug to initiate therapy, when and how to monitor the patients during and after stopping drug therapy. Recommendations on the therapy of patients in special circumstances, including women in childbearing age, patients with antiviral drug resistance, concurrent viral infection, hepatic decompensation, patients receiving immune suppression or chemotherapy and patients in the setting of liver transplantation and hepatocellular carcinoma, are also included. ? Asian Pacific Association for the Study of the Liver 2012.
SDGs
Other Subjects
adefovir dipivoxil; alanine aminotransferase; alpha interferon; antivirus agent; biological marker; clevudine; emtricitabine; emtricitabine plus tenofovir disoproxil; entecavir; hepatitis antibody; hepatitis B surface antibody; hepatitis B surface antigen; interferon; lamivudine; lb 80830; peginterferon; peginterferon alpha; peginterferon alpha2a; peginterferon alpha2b; placebo; ribavirin; telbivudine; tenofovir disoproxil; thymosin alpha1; unclassified drug; virus DNA; alopecia; amino acid substitution; antigen detection; antiviral resistance; article; bleeding; bone density; bone marrow suppression; chemoembolization; clinical assessment; combination chemotherapy; consensus development; creatinine blood level; delta agent hepatitis; dose response; drug contraindication; drug cost; drug dose comparison; drug dose sequence; drug indication; drug induced headache; drug megadose; drug monitoring; drug safety; drug substitution; drug tolerability; drug withdrawal; fatigue; flu like syndrome; genotype; hepatitis B; Hepatitis B virus; hepatitis C; human; Human immunodeficiency virus infection; immunomodulation; immunosuppressive treatment; infection; injection site reaction; lactic acidosis; liver cell carcinoma; liver cirrhosis; liver failure; liver fibrosis; liver necrosis; liver transplantation; low drug dose; mixed infection; monotherapy; muscle necrosis; musculoskeletal disease; myalgia; myopathy; nephrotoxicity; neutropenia; nonhuman; optimal drug dose; osteomalacia; outcome assessment; pharmacogenetics; practice guideline; pregnancy; priority journal; recommended drug dose; recurrent infection; rhabdomyolysis; seroconversion; side effect; survival time; thrombocytopenia; unspecified side effect; viral clearance; virus mutation; virus pathogenesis; virus reactivation
Publisher
Springer New York LLC
Type
journal article