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Clinical effect of Adefovir Dipivoxil combined with Rougan Huaxian Granules on chronic hepatitis B cirrhosis |
LYU Yanhang1 WU Shanshan1 WANG Zhenchang2 |
1.Graduate School, Guangxi University of Chinese Medicine, Guangxi Zhuang Autonomous Region, Nanning 530222, China;
2.Department of Spleen, Stomach and Liver Diseases, Guangxi International Zhuang Medical Hospital, Guangxi Zhuang Autonomous Region, Nanning 530201, China |
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Abstract Objective To observe the clinical efficacy of Adefovir Dipivoxil combined with Rougan Huaxian Granules in the treatment of patients with chronic hepatitis B virus (HBV) cirrhosis. Methods From March 2017 to March 2019, 100 patients with chronic hepatitis B cirrhosis diagnosed by The First Affiliated Hospital of Guangxi University of Chinese Medicine were selected. According to the random number table method, they were divided into the control group and the treatment group, with 50 patients in each group. The control group was treated with Adefovir Dipivoxil alone, and the treatment group was treated with Rougan Huaxian Granules on the basis of the control group for a total of 6 months. The clinical symptoms, liver function, liver fibrosis 4 items, liver B-mode ultrasound, the content of HBV-DNA, hepatitis B e antigen (HBeAg) and hepatitis B e antibody (HBeAb) in the two groups were observed before and after treatment. Results The traditional Chinese medicine syndrome scores of patients in both groups after treatment were better than those before treatment, and the treatment group was better than the control group at the same period (P < 0.05). In the two groups after treatment liver function index [aspartic transaminase (AST), alanine transaminase (ALT), total bilirubin (HBIL)], liver fibrosis index [serum hyaluronic acid (HA), laminin (LN), type Ⅲ procollagen (PCⅢ), type Ⅳ collagen (Ⅳ-C)], portal vein diameter, the thickness of the spleen decreased significantly before the treatment (all P < 0.05), and compared with the control group, the degree of the treatment group decreased more significantly (P < 0.05). After treatment, HBV-DNA negative conversion rate, HBeAg negative conversion rate and HBeAg/HBeAb serum conversion in the treatment group were all higher than those in the con
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