Clinical efficacy of Biejiaruangan compound tablets in treatment of primary biliary cirrhosis
ObjectiveTo evaluate the clinical efficacy of Biejiaruangan compound tablets in the treatment of primary biliary cirrhosis (PBC). MethodsIn a randomized, double-blind, placebo-controlled study, 56 patients with PBC were collected and equally divided into treatment group and control group. The treatm...
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Format: | Article |
Language: | zho |
Published: |
Editorial Department of Journal of Clinical Hepatology
2015-02-01
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Series: | Linchuang Gandanbing Zazhi |
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Online Access: | http://www.lcgdbzz.org/qk_content.asp?id=6266&ClassID=11415055 |
Summary: | ObjectiveTo evaluate the clinical efficacy of Biejiaruangan compound tablets in the treatment of primary biliary cirrhosis (PBC). MethodsIn a randomized, double-blind, placebo-controlled study, 56 patients with PBC were collected and equally divided into treatment group and control group. The treatment group was given Biejiaruangan compound tablets (4 pills per dose, 3 doses per day, oral administration) combined with ursodeoxycholic acid (UDCA) tablets (50 mg/pill, 10-15 mg per kg per day). The control group was given placebo (4 pills per dose, 3 doses per day, oral administration) combined with UDCA tablets (50 mg/pill, 10-15 mg per kg per day). All patients were treated for 12 months. Clinical symptoms, PBC-40 scales, liver function [alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), γ-glutamyl transpeptidase (GGT), and total bilirubin (TBil)], and liver stiffness values in the two groups were evaluated before and after treatment. Comparison of continuous data between the two groups was made by t test, and comparison of categorical data was made by chi-square test. ResultsThe levels of ALT, AST, GGT, ALP, and TBil in the treatment group significantly decreased after 12 months of treatment (t=3.2019, P<0.01; t=3.0953, P<0.01; t=3.0279, P<0.01; t=2.4420, P<0.05; t=2.1621, P<0.05). In the control group, only the level of GGT significantly decreased after treatment (t=19981, P<0.01). The levels of GGT and ALP were significantly lower in the treatment group than in the control group (t=2.0061, P<0.05; t=2.3106, P<0.05). The liver stiffness value in the treatment group significantly decreased after treatment (14.37±10.58 vs 1002±5.96 kPa, t=2.1134, P<0.05). The PBC-40 scales of skin itch, fatigue, and social dimension in the treatment group significantly decreased after treatment for 12 months (t=2.5158, P<0.05; t=2.1409, P<0.05; t=3.2441, P<0.05). There were significant differences in scales of fatigue and social dimension between the two groups after 12 months of treatment (t=3.1491, P<0.05; t=26287, P<0.05). ConclusionBiejiaruangan compound tablets can significantly improve liver function, reduce the liver stiffness value, and improve PBC-40 scales of skin itch and fatigue in patients with PBC. This therapy holds promise for widespread clinical application. |
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ISSN: | 1001-5256 1001-5256 |