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首页|期刊导航|河北医学|前列地尔联合替比夫定对乙肝肝硬化患者疗效和血清炎性因子的影响

前列地尔联合替比夫定对乙肝肝硬化患者疗效和血清炎性因子的影响

陈逊 刘海滨

河北医学2017,Vol.23Issue(12):1963-1966,4.
河北医学2017,Vol.23Issue(12):1963-1966,4.DOI:10.3969/j.issn.1006-6233.2017.12.008

前列地尔联合替比夫定对乙肝肝硬化患者疗效和血清炎性因子的影响

Effects of Alprostadil Combined with Telbivudine on Clinical Efficacy and Serum Inflammatory Factor in Patients of Hepatitis B Virus-related Cirrhosis

陈逊 1刘海滨1

作者信息

  • 1. 湖南省邵阳市中心医院消化内科,湖南 邵阳 422000
  • 折叠

摘要

Abstract

Objective:To explore clinical efficacy and serum inflammatory factor use of alprostadil combined with telbivudine in treatment of hepatitis B virus-related cirrhosis,providing a theoretical basis for clinical treatment.Methods:98 patients with hepatitis B cirrhosis admitted in our hospital from June 2014 to June 2016,were selected.According to the random number table,patients were divided into telbivudine group (49 cases) and combined group (49 cases).On the basis of routine treatment,telbivudine group was given telbivudine,combined group was given telbivudine and alprostadil for 12 weeks.To observe and analyze the changes of serum HBV DNA levels,liver function and serum inflammatory factor.Results:After treatment,overall efficacy of combined group was significantly higher than that of telbivudine group (89.30% VS.63.89%,P< 0.05).After treatment,the serum HBV and DNA levels of the two groups were significant lower than those before treatment,but there was no significant difference (P>0.05) between two groups.After treatment,serum AST,ALT,Tbil,IL-6,IL-22 and hs-CRP levels of combined group were significantly lower than those of telbivudine group (P<0.05).Conclusion:Alprostadil combined with telbivudine could reduce serum HBV DNA levels,improve liver function,and alleviate the inflammatory condition of patients with ghepatitis B virus-related cirrhosis.

关键词

前列地尔/替比夫定/乙型肝炎肝硬化/炎性因子

Key words

Alprostadil/Telbivudine/Hepatitis B virus-related cirrhosis/Inflammatory factor

引用本文复制引用

陈逊,刘海滨..前列地尔联合替比夫定对乙肝肝硬化患者疗效和血清炎性因子的影响[J].河北医学,2017,23(12):1963-1966,4.

河北医学

OACSTPCD

1006-6233

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