单位:[1]Natl Cheng Kung Univ Hosp, Dept Med, Tainan 70428, Taiwan[2]Peking Univ, Hlth Sci Ctr, Dept Microbiol, Beijing 100083, Peoples R China[3]Capital Univ Med Sci, Beijing Friendship Hosp, Liver Res Ctr, Beijing 100050, Peoples R China临床科室国家中心肝病分中心首都医科大学附属北京友谊医院[4]Alice Ho Miu Ling Nethersole Hosp, Dept Med, Hong Kong, Hong Kong, Peoples R China[5]Natl Univ Singapore Hosp, Mt Elizabeth Med Ctr, Singapore 228510, Singapore[6]Aga Khan Univ, Karachi 3500, Pakistan[7]Univ Indonesia, Jakarta Dept Med, Jakarta 10350, Indonesia[8]Chang Gung Mem Hosp & Univ, Liver Res Unit, Taipei 105, Taiwan[9]Victorian Infect Dis Reference Lab, Melbourne, Vic 3051, Australia[10]Univ Tokyo, Dept Gastroenterol, Bunkyo Ku, Tokyo 1138655, Japan[11]Univ Santo Tomas Hosp, Manila 100864, Philippines[12]Asan Med Ctr, Seoul 138376, South Korea[13]Chulalongkorn Univ, GI Unit, Dept Med, Bangkok 10330, Thailand[14]Univ Med & Pharm, Dept Immunol & Physiopathol, Ho Chi Minh City, Vietnam[15]Catholic Univ Korea, Div Hepatogastroenterol, Div Internal Med, Kangnam St Marys Hosp, Seoul 137040, South Korea[16]Shanghai Jing An Qu Cent Hosp, Clin Immun Res Ctr, Shanghai 200040, Peoples R China[17]Univ Delhi, GB Pant Hosp, New Delhi 110002, India[*1]Natl Cheng Kung Univ Hosp, Dept Med, 138 Sheng Li Rd, Tainan 70428, Taiwan
Chronic hepatitis B (CHB) is a serious global health concern, particularly in the Asia-Pacific region. New information on the clinical management of CHB is emerging rapidly, requiring that physicians be alerted to updated treatment recommendations. The ACT-HBV Asia-Pacific Steering Committee members, composed of experts in hepatitis B from throughout the Asia-Pacific region, reviewed and discussed new clinical data as reported in the literature or presented at recent international congresses, and recommended that physicians be alerted to updated treatment recommendations. Hepatitis B e antigen (HBeAg)-positive patients with HBV DNA levels of >= 20 000 IU/ml (>= 10(5) copies/ml) and elevated alanine aminotransferase levels should be considered for treatment. It is suggested that HBV DNA >= 2000 IU/ml (>= 10(4) copies/ml) is the more appropriate threshold for the treatment of HBeAg-negative patients. Lamivudine, adefovir dipivoxil, interferon alpha-2b, thymosin alpha-1, and, most recently, entecavir, and pegylated interferon alpha-2a are licensed for the management of CHB. The treatment recommendations from the 2005 Asian-Pacific Consensus Statement on the Management of Chronic Hepatitis B have been updated to incorporate these new therapeutic options. A summary of treatment recommendations for special patient populations is also included.