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Multicenter clinical study on Fuzhenghuayu capsule against liver fibrosis due to chronic hepatitis B

机译:扶正化瘀胶囊抗慢性乙型肝炎肝纤维化的多中心临床研究

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AIM: To study the efficacy and safety of Fuzhenghuayu capsule (FZHY capsule, a capsule for strengthening body resistance to remove blood stasis) against liver fibrosis due to chronic hepatitis B. METHODS: Multicenter, randomized, double blinded and parallel control experiment was conducted in patients (aged from 18 to 65 years) with liver fibrosis due to chronic hepatitis B. Hepatic histologic changes and HBV markers were examined at wk 0 and 24 during treatment. Serologic parameters (HA, LM, P-III-P, IV-C) were determined and B ultrasound examination of the spleen and liver was performed at wk 0,12 and 24. Liver function (liver function and serologic parameters for liver fibrosis) was observed at wk 0, 6, 12, 18 and 24. Blood and urine routine test, renal function and ECG were examined before and after treatment. RESULTS: There was no significant difference between experimental group (110 cases) and control group (106 cases) in demographic features, vital signs, course of illness, history for drug anaphylaxis and previous therapy, liver function, serologic parameters for liver fibrosis, liver histologic examination (99 cases in experimental group, 96 cases in control group), HBV markers, and renal function. According to the criteria for liver fibrosis staging, mean score of fibrotic stage(s) in experimental group after treatment (1.80) decreased significantly compared to the previous treatment (2.33, P < 0.05), but there was no significant difference in mean score of fibrotic stage(s) (2.11 and 2.14 respectively). There was a significant difference in reverse rate between experimental group (52%) and control group (23.3%) in liver biopsy. With marked effect on decreasing the mean value of inflammatory activity and score of inflammation (P < 0.05), Fuzhenghuayu capsule had rather good effects on inhibiting inflammatory activity and was superior to that of Heluoshugan capsule. Compared to that of pretreatment, there was a significant decrease in HA, LM, P-III-P and IV-C content in experimental group after 12 and 24 wk of treatment. The difference in HA, LM, P-III-P and IV-C content between 12 and 24 wk of treatment and pretreatment in experimental group was significantly greater than that in control group (P < 0.01-0.05). The effect, defined as two of four parameters lowering more than 30% of the baseline, was 72.7% in experimental group and 27.4% in control group (P < 0.01). Obvious improvement in serum Alb, ALT, AST and GGT was seen in two groups. Compared to that of control group, marked improvement in GGT and Alb was seen in experimental group (P < 0.05). The effective rate of improvement in serum ALT was 72.7% in experimental group and 59.4% in control group. No significant difference was seen in blood and urine routine and ECG before and after treatment. There was also no significant difference in stable rate in ALT and serologic parameters for liver fibrosis between experimental group and control group after 12 wk of withdrawal. CONCLUSION: Fuzhenghuayu capsule has good therapeutic effects on alleviating liver fibrosis due to chronic hepatitis B without any adverse effect and is superior to that of Heluoshugan capsule.
机译:目的:研究扶正化瘀胶囊(FZHY胶囊,增强机体抵抗血瘀的胶囊)对慢性乙型肝炎肝纤维化的疗效和安全性。方法:进行多中心,随机,双盲和平行对照实验。慢性乙型肝炎引起的肝纤维化患者(年龄在18至65岁之间)。在治疗期间第0周和第24周检查了肝组织学变化和HBV标志物。测定血清学参数(HA,LM,P-III-P,IV-C),并在第0、12和24周进行脾脏和肝脏的B超检查。肝功能(肝纤维化的肝功能和血清学参数)在第0、6、12、18和24周观察到。在治疗前后检查血液和尿液常规测试,肾功能和心电图。结果:实验组(110例)和对照组(106例)在人口统计学特征,生命体征,病程,药物过敏和既往治疗史,肝功能,肝纤维化血清学指标,肝功能方面无显着差异。组织学检查(实验组99例,对照组96例),HBV标志物和肾功能。根据肝纤维化分期的标准,实验组治疗后纤维化分期的平均得分(1.80)较之前治疗显着降低(2.33,P <0.05),但治疗前的平均得分无明显差异。纤维化阶段(分别为2.11和2.14)。肝活检中,实验组(52%)和对照组(23.3%)的逆转率有显着差异。扶正化瘀胶囊对降低炎症活性的平均值和降低炎症评分有显着效果(P <0.05),对炎症活性的抑制作用较好,优于黑螺舒肝胶囊。与预处理相比,在治疗12周和24周后,实验组的HA,LM,P-III-P和IV-C含量显着降低。实验组与治疗组在12至24周之间HA,LM,P-III-P和IV-C含量的差异明显大于对照组(P <0.01-0.05)。定义为四个参数中的两个参数降低了基线以上30%的效果,实验组为72.7%,对照组为27.4%(P <0.01)。两组患者的血清Alb,ALT,AST和GGT均有明显改善。与对照组相比,实验组GGT和Alb明显改善(P <0.05)。实验组血清ALT改善有效率为72.7%,对照组为59.4%。治疗前后血常规,尿常规和心电图无明显差异。停药12周后,实验组与对照组的肝纤维化ALT稳定率和血清学指标之间也无显着差异。结论:扶正化瘀胶囊对慢性乙型肝炎肝纤维化有较好的缓解作用,且无不良反应,优于合络舒肝胶囊。

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