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经拉米夫定联合阿德福韦酯治疗失败的慢性乙型肝炎患者的挽救治疗
作者:李忠斌 1   邵清 1   李冰 1   李梵 1   夏晶 2   陈松海 1   王春艳 1   陈国凤 1  
单位:1.解放军第302医院 肝硬化诊疗二中心 北京 100039 2.新疆军区第23医院 感染科 乌鲁木齐 830000 
关键词:恩替卡韦 替诺福韦酯 肝炎 乙型 慢性 耐药 疗效 
分类号:
出版年,卷(期):页码:2017,9(4):54-58
摘要:

摘要:目的 探讨拉米夫定(LAM)联合阿德福韦酯(ADV)治疗失败的慢性乙型肝炎(CHB)患
者的挽救治疗方法。方法 选取解放军第302医院2013年3月至2014年3月LAM联合ADV挽救治疗失
败的CHB患者100例为研究对象,依据患者的经济情况和意愿分为对照组和挽救组,每组50例。对
照组继续给予LAM (100 mg/d)联合ADV(10 mg/d)治疗;挽救组患者每日给予300 mg替诺福韦
酯(TDF)联合0.5 mg恩替卡韦(ETV),所有患者均连续治疗48周。治疗基线、12周、24周和48
周时分别进行病毒学、生物化学和血清学检测。回顾性分析比较两组患者上述治疗时间点的HBV
DNA低于检测下限率、肝功能复常率、病毒学突破率、HBeAg血清学转换率及药物的不良反应。结
果 挽救组患者治疗48周后HBV DNA低于检测下限率、肝功能复常率和病毒学突破率分别为94.0%
(47/50)、89.2%(33/37)和0.0%(0/50),对照组分别为34.0%(17/50)、25.7%(9/35)和14.0%
(7/50),差异有统计学意义(P均< 0.05)。治疗48周后,挽救组和对照组患者HBeAg血清学转换
率分别为15.4%(4/26)和16.7%(4/24),差异无统计学意义(χ 2 = 0.023,P = 0.769)。两组患者的
耐受性均良好,未出现因严重不良反应而导致停药的病例。结论 对于LAM联合ADV治疗后疗效欠佳
或发生病毒学突破的CHB患者,TDF联合ETV是一种效果理想且安全的挽救治疗方案。

Abstract: Objective To explore the retreatment of chronic hepatitis B patients with failure of lamivudine
and adefovir combination therapy. Methods Total of 100 chronic hepatitis B (CHB) patients with treatment
failure by LAM and ADV combined therapy were selected and divided into control group and remedy group
according to financial condition and the will of the patients, 50 cases in each group. Patients in control group
were continually given LAM (100 mg/d) and ADV (10 mg/d) treatment. Patients in remedy group were treated
with TDF (300 mg/d) joint ETV (0.5 mg/d). All patients were treated for 48 weeks. Virology, biochemistry,
serology tests were implemented at treatment baseline, 12 weeks, 24 weeks and 48 weeks after treatment.
The serum HBV DNA negative conversion rate, liver function recovery rate, virological breakthrough rate,
HBeAg seroconversion rate and adverse effects were retrospectively evaluated. Results After 48 weeks, the
HBV DNA negative conversion rate, liver function recovery rate, virological breakthrough rate were 94.0%
(47/50), 89.2% (33/37) and 0.0% (0/50) in remedy group; in control group, the above indicators were 34.0%
(17/50), 25.7% (9/35) and 14.0% (7/50), the differences were statistically significant (P < 0.05). After 48
weeks, the seroconversion rate (from HBeAg to HBeAb) was 15.4% (4/26) in remedy group and 16.7% (4/24)
in control group, the differences had no statistical significance (χ 2 = 0.023, P = 0.769). Patients in both groups
were well tolerated, without any case of drug withdrawal caused by severe adverse effects. Conclusions

The therapy of TDF combined with ETV is an effective and safe therapeutic strategy for CHB patients with
treatment failure by LAM combined with ADV therapy.

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