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作 者:宋建新[1] 田德英[1] 齐俊英[1] 魏镜龙[1]
机构地区:[1]同济医科大学附属同济医院传染科,武汉430030
出 处:《中西医结合肝病杂志》1999年第6期14-16,共3页Chinese Journal of Integrated Traditional and Western Medicine on Liver Diseases
摘 要:目的:观察罗扰不剂治疗慢性乙型和丙型肝炎的疗效。方法:常规治疗组以罗扰素水剂3×10^6U,隔日1次,持续3个月;调整治疗组以罗扰素水剂4.5×10^6U,隔日1次,持续3~6个月;于治疗前、中、结果时及结束后3~6个月时检测HCV、HBV感染标志物及肝功能,并定量检测HCV-RNA、HBV-DNA及扰素抗体。结果:常规治疗组HCV-RNA转阴率为50%,HBeAg和HBV-DNA转阴率为46.Aim: To evaluate the clinical effect of Roferon-A in the treatment of patients with hepatitis B and C. Method: Group 1 : 44 patients were given only Roferon-A 3×106U every two days for 3 months. Group 2:some patients with no effect in Group 1 were given Roferon-A 4. 5×106U every two days for another 3 to 6 months. HCV-Ab. HBV markers and ALT were detected before, during and at the end of the treatment and 3 to 6 months after the treatment. And at the same time the concentration of HCV-RNA. HBV-DNA in serum and antibody to Roferon-A were detected quantitatively. Results: In Group 1. HCV-RNA in 50% patients with hepatitis C became negative. HBeAg and HBV-DNA in 46. 2% patients with hepatitis B became negative. And the copies of HCV-RNA and HBV-DNA and the level of antibody to Roferon-A were negatively correlated with the effect of Roferon-A. Conclusion: The results showed that Ro-feron-A's eliminating rates of HCV-RNA、 HBV-DNA and the remission of ALT were close to that of Roferon. and were in dose-dependent manner.
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