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恩替卡韦和阿德福韦酯治疗慢性乙型肝炎的真实世界效果评价

王莹 林畅琪 李伟南 郜艳晖 贾卫东 李粤平 杨翌 周舒冬

广东药科大学学报2017,Vol.33Issue(5):671-676,6.
广东药科大学学报2017,Vol.33Issue(5):671-676,6.DOI:10.16809/j.cnki.2096-3653.2017061401

恩替卡韦和阿德福韦酯治疗慢性乙型肝炎的真实世界效果评价

Evaluation of the efficacy of entecavir and adefovir dipivoxil in the treatment of chronic hepatitis B based the real world study

王莹 1林畅琪 1李伟南 1郜艳晖 1贾卫东 2李粤平 2杨翌 1周舒冬1

作者信息

  • 1. 广东药科大学 公共卫生学院,广东 广州 510006
  • 2. 广州市第八人民医院,广东 广州510060
  • 折叠

摘要

Abstract

Objective To study the efficacy of entecavir ( ETV ) and adefovir dipivoxil ( ADV ) in the treatment of chronic hepatitis B based on the real world study. Methods A total of 427 patients with chronic hepatitis B treated with ETV or ADV were retrospectively collected from January 2008 to December 2015 at Guangzhou Eighth People's Hospital. HBV DNA, HBeAg and ALT in patients were measured before and after ADV or ETV treatment. Meantime, HBV DNA negative conversion rate, HBeAg seroconversion rate and ALT normal rate were analyzed. The survival analysis method was used to compare the efficacy of ADV and ETV treatment. Results Both in HBeAg positive and negative groups, the HBV DNA negative conversion rate in patients was higher in the ETV group than that in the ADV group. In HBeAg (+) subgroup, the HBeAg seroconversion rate was also higher in the ETV group. The ALT normalization rate in the ETV group was different from that in the ADV group at the 3rd and 18th months. In HBeAg (-) subgroup, there was no significant difference in ALT normalization rate between two treatment groups. The HBV DNA response rates in both HBeAg positive and negative patients were different between two treatment groups by COX multivariate analysis. Conclusion ETV is superior to ADV in the treatment of chronic hepatitis B patients with HBeAg positive or negative condition.

关键词

慢性乙型肝炎/真实世界/ETV/ADV

Key words

chronic hepatitis B/real world/ETV/ADV

分类

医药卫生

引用本文复制引用

王莹,林畅琪,李伟南,郜艳晖,贾卫东,李粤平,杨翌,周舒冬..恩替卡韦和阿德福韦酯治疗慢性乙型肝炎的真实世界效果评价[J].广东药科大学学报,2017,33(5):671-676,6.

基金项目

国家自然科学基金资助(No.71573059) (No.71573059)

广东省公益研究与能力建设项目资助(2014A020212302) (2014A020212302)

广东药科大学学报

OACSTPCD

1006-8783

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