Guidelines for the treatment of chronic hepatitis and cirrhosis due to hepatitis B virus infection for the fiscal year 2008 in Japan

被引:46
作者
Kumada, Hiromitsu [16 ]
Okanoue, Takeshi [1 ]
Onji, Morikazu [2 ]
Moriwaki, Hisataka [3 ]
Izumi, Namiki [4 ]
Tanaka, Eiji [5 ]
Chayama, Kazuaki [6 ]
Sakisaka, Shotaro [7 ]
Takehara, Tetsuo [8 ]
Oketani, Makoto [9 ]
Suzuki, Fumitaka [16 ]
Toyota, Joji [10 ]
Nomura, Hideyuki [11 ]
Yoshioka, Kentaro [12 ]
Seike, Masataka [13 ]
Yotsuyanagi, Hiroshi [14 ]
Ueno, Yoshiyuki [15 ]
机构
[1] Saiseikai Suita Hosp, Dept Gastroenterol & Hepatol, Suita, Osaka, Japan
[2] Ehime Univ, Dept Gastroenterol & Metabol, Grad Sch Med, Matsuyama, Ehime 790, Japan
[3] Gifu Univ, Dept Internal Med, Gifu, Japan
[4] Musashino Red Cross Hosp, Dept Gastroenterol & Hepatol, Musashino, Tokyo, Japan
[5] Shinshu Univ, Dept Internal Med, Matsumoto, Nagano 390, Japan
[6] Hiroshima Univ, Dept Med & Mol Sci, Div Frontier Med Sci, Programs Biomed Res,Grad Sch Biomed Sci, Hiroshima, Japan
[7] Fukuoka Univ, Sch Med, Dept Gastroenterol & Hepatol, Fukuoka 81401, Japan
[8] Osaka Univ, Dept Gastroenterol & Hepatol, Osaka, Japan
[9] Hlth Res Human & Environm Sci, Dept Digest & Lifestyle Related Dis, Kagoshima, Japan
[10] Sapporo Kosei Gen Hosp, Dept Gastroenterol, Sapporo, Hokkaido, Japan
[11] Shin Kokura Hosp, Ctr Liver Dis, Kitakyusyu City, Japan
[12] Fujita Hlth Univ, Div Liver Biliary Tract & Pancreas Dis, Dept Internal Med, Aichi, Japan
[13] Oita Univ, Dept Internal Med, Fac Med, Oita 87011, Japan
[14] Univ Tokyo, Dept Infect Dis, Tokyo, Japan
[15] Tohoku Univ, Div Gastroenterol, Grad Sch Med, Sendai, Miyagi 980, Japan
[16] Toranomon Gen Hosp, Dept Hepatol, Tokyo, Japan
关键词
chronic hepatitis; cirrhosis; hepatitis B virus; hepatocellular carcinoma; interferon; liver supportive therapies; nucleos(t)ide analogs; VIROLOGICAL RESPONSE; COMBINATION THERAPY; LAMIVUDINE; RESISTANCE; ENTECAVIR; EFFICACY; TRIAL; RISK; ACID;
D O I
10.1111/j.1872-034X.2009.00633.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
In the 2008 guidelines for the treatment of patients with cirrhosis, who are infected with hepatitis B virus (HBV), the main goal is to normalize levels of alanine and aspartate aminotransferases by eliminating HBV or reducing viral loads. In patients with compensated cirrhosis, the clearance of HBV from serum is aimed for by entecavir, as the main resort, for histological improvement toward the prevention of hepatocellular carcinoma (HCC). In patients with decompensated cirrhosis, by contrast, meticulous therapeutic strategies are adopted for the reversal to compensation, toward the eventual goal of decreasing the risk of HCC. For maintaining liver function and preventing HCC, branched chain amino acids and nutrient supplements are applied, in addition to conventional liver supportive therapies. For patients with chronic hepatitis B, separate guidelines are applied to those younger than 35 years and those aged 35 years or older. Even for patients with chronic hepatitis who are negative for hepatitis e antigen (HBeAg), but who harbor HBV DNA in titers of 7 log copies/mL or more, a "drug-free state" is aimed for by sequential treatment with interferon (IFN) plus entecavir as the first line. For patients with chronic hepatitis B aged 35 years or older, who are HBeAg-negative and carry HBV DNA in titers of less than 7 log copies/mL, long-term IFN for 24-48 weeks is adopted anew. To HBeAg-negative patients who have either or both platelet counts of less than 150 x 10(3)/mm(3) and less than 7 log copies of HBV DNA, also, long-term IFN for 24-48 weeks is indicated.
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页数:7
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