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干扰素联合阿德福韦酯治疗HBeAg(+)慢性乙型肝炎疗效观察
引用本文:彭福江,张天晓,袁美蓉,陈福生. 干扰素联合阿德福韦酯治疗HBeAg(+)慢性乙型肝炎疗效观察[J]. 中国药师, 2014, 0(6): 984-986
作者姓名:彭福江  张天晓  袁美蓉  陈福生
作者单位:东莞市长安医院内科 广东东莞 523850;东莞市长安医院内科 广东东莞 523850;东莞市长安医院内科 广东东莞 523850;东莞市长安医院内科 广东东莞 523850
基金项目:东莞市科技计划项目(编号:201210515000148)
摘    要:目的:观察普通干扰素(IFN)和阿德福韦酯(ADV)联合治疗HBeAg(+)慢性乙型肝炎(CHB)的疗效.方法:100名HBeAg(+)的CHB患者随机分为联合治疗组(IFN+ ADV组)及单药治疗组(IFN组).IFN组予500MU普通IFNα-2b隔日1次皮下注射,IFN+ ADV组在IFN组治疗基础上加服ADV 10 mg·d-1;所有患者均治疗48周,随访24周.治疗前筛查、治疗后每4周血常规、每12周检测HBV DNA,乙肝两对半定量、肝功能、肾功能、甲状腺功能.记录不良反应.结果:治疗24周,IFN+ ADV组与IFN组HBV DNA水平分别下降(3.67±0.96)log10IU·ml-1和(2.85±1.14)log10IU·ml-1,较基线均显著降低(P =0.000),两组比较,IFN+ ADV组优于IFN组(P=0.000);两组HBV DNA低于检测下线比例分别为46.0%vs24.0%(P=0.021),ALT复常率分别为76.0% vs 56.0% (P =0.035),IFN+ ADV组均高于IFN组;两组HBeAg转阴率及HBeAg血清转换率分别为30.0% vs 28.05% (P=0.826),21.2% vs 17.6% (P =0.653),差异无统计学意义.IFN+ ADV组脱落2例,IFN组脱落4例,两组不良反应相似,均无严重不良事件发生,未影响治疗.结论:干扰素联合阿德福韦酯或干扰素单用治疗对HBeAg(+)的CHB患者均有效,安全性良好;治疗24周,联合治疗可提高患者病毒学应答率及生化学应答率,未能提高患者HBeAg血清转换率及联合应答率.

关 键 词:普通干扰素  阿德福韦酯  慢性乙型肝炎
收稿时间:2013-11-17
修稿时间:2014-03-20

Clinical Observation of Interferon Combined with Adefovir Dipivoxil in the Treatment of Patients with HBeAg(+) Chronic Hepatitis B
Peng Fujiang,Zhang Tianxiao,Yuan Meirong and Chen Fusheng. Clinical Observation of Interferon Combined with Adefovir Dipivoxil in the Treatment of Patients with HBeAg(+) Chronic Hepatitis B[J]. China Pharmacist, 2014, 0(6): 984-986
Authors:Peng Fujiang  Zhang Tianxiao  Yuan Meirong  Chen Fusheng
Affiliation:Department of Internal Medicine of Changan Hospital, Guangdong Dongguan 523850, China;Department of Internal Medicine of Changan Hospital, Guangdong Dongguan 523850, China;Department of Internal Medicine of Changan Hospital, Guangdong Dongguan 523850, China;Department of Internal Medicine of Changan Hospital, Guangdong Dongguan 523850, China
Abstract:Objective:To observe the clinical effect of standard interferon (IFN) and adefovir dipivoxil (ADV) in the treatment of patients with HBeAg(+) chronic hepatitis B (CHB).Methods:Totally 100 patients were randomly divided into the IFN and ADV group (IFN + ADV group,50 cases) and the IFN group (IFN group,50 cases).The IFN group was injected with IFNα-2b subcutaneously,qod,and the IFN + ADV group was treated with ADV 10 mg · d-1 additionally.The treatment course was 48 weeks and the follow-up course was 24 weeks.Blood routine examination was determined every 4 weeks,HBV DNA was determined every 12 weeks,two pairs of semi-hepatitis B,liver function,renal function and thyroid function were determined before and after the treatment.The adverse reactions were compared.Results:In the 24th week,the HBV DNA level of IFN + ADV group and IFN group was decreased with (3.67 ± 0.96) log10 IU · ml-1 and (2.85 ± 1.14) log10 IU · ml-1,respectively,both were lower than that of the base level (P =0.000),and that of IFN + ADV group was the lowest (P =0.000) ; the ratio of HBV DNA level lower than the detection line was 46.0% and 24.0%,respectively (P =0.021) ; the normalization rate of ALT were 76.0% and 56.0%,respectively (P =0.035),and there were significant differences between the two groups.The negative conversion rate of HBeAg and the seroconversion rate of HBeAg was 30.0% and 28.05% (P =0.826),21.2% and 17.6%,respectively(P =0.653),while there were no significant differences between the two groups.Two cases lost in the IFN + ADV group and 4 cases lost in the IFN group.The incidence of adverse reactions between the two groups was similar,and there was no serious adversereaction occurred.Conclusion:Interferon with adefovir dipivoxil or interferon alone is effective and safe in the treatment of patients with HBeAg(+) chronic hepatitis B.After the 24-week treatment,the combination therapy can increase the rate of virological response and biochemical response,while the seroconversion rate of HBeAg and the combined response are unchanged.
Keywords:Interferon   Adefovir dipivoxil   Chronic hepatitis B
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