摘要
目的:回顾性分析替比夫定治疗HBeAg阳性慢性乙型肝炎(CHB)患者两年的临床疗效和安全性。方法:纳入HBeAg阳性CHB患者,随机分为两组,分别使用替比夫定、阿德福韦酯治疗两年,每3~6个月进行HBVDNA、ALT及HbeAg检测,并进行安全性评估。结果:共纳入67例HBeAg阳性CHB患者(替比夫定组33例、阿德福韦酯34例),治疗12和24个月范围,其HBVDNA不可测,ALT复常以及12个月范围HBeAg血清转换两组患者比较无显著性差异,而治疗24个月范围替比夫定组患者HBeAg血清转换为42.4%(14/33)高于阿德福韦酯组17.6%(6/34)(P<0.05),且两组安全性良好。结论:替比夫定较阿德福韦酯具有更显著抗病毒疗效。两组均具有良好的安全性和耐受性。
Objective:To retrospective analyze on the clinical efficacy and safety of patients with HBeAg-positive chronic hepatitis B treated with telbivudine for two years. Methods:We divided patients with HBeAg-positive chronic hepatitis B into two groups by random grouping, One group was treated with telbivudine for two years, while the other with adefovir dipivoxil for two years. We tested their HBV-DNA, ALT, and HbeAg level for every 3-6 months. And then we evaluated the drug safety. Results:There were 67 patients (33 in group one and 34 in group two). There were no significant difference in the change of the level of HBV-DNA,ALT and HBeAg during treatment months of 12 and 24. The serum HBeAg conversion rate in group treated with telbivudine (42.4%) was higher than the group treated with adefovir dipivoxi(l17.6%)during the 24 treatment months(P0.05). Both of the groups had good drug safety. Conclusion:Telbivudine had better antiviral effects than adefovir dipivoxil. Both groups had good safety and tolerability.
出处
《甘肃医药》
2013年第7期491-493,共3页
Gansu Medical Journal