中华实验和临床感染病杂志(电子版)
中華實驗和臨床感染病雜誌(電子版)
중화실험화림상감염병잡지(전자판)
CHINESE JOURNAL OF EXPERIMENTAL AND CLINICAL INFECTIOUS DISEASES(ELECTRONIC VERSION)
2014年
5期
639-641
,共3页
陈常云%马丽%牟君%李艳婷%邵红雨%谷雨明%徐云生%崔云竹%尹常健
陳常雲%馬麗%牟君%李豔婷%邵紅雨%穀雨明%徐雲生%崔雲竹%尹常健
진상운%마려%모군%리염정%소홍우%곡우명%서운생%최운죽%윤상건
肝炎,乙型,慢性%恩替卡韦%阿德福韦酯
肝炎,乙型,慢性%恩替卡韋%阿德福韋酯
간염,을형,만성%은체잡위%아덕복위지
Chronic hepatitis B%Entecavir%Adefovir dipivoxil
目的:观察恩替卡韦(ETV)治疗慢性乙型肝炎的临床疗效。方法36例慢性乙型肝炎患者包括初治治疗组(20例)和阿德福韦酯(ADV)耐药组(16例),两组患者分别给予ETV 0.5 mg口服,1次/d,治疗96周。结果 ETV初治组和ADV耐药组患者治疗96周后,ALT复常率分别为100%和93.75%,差异无统计学意义(χ2=4.553,P>0.05);HBV DNA低于检测下限的比率均为100%;HBeAg阴转率分别为42.8%和40.0%,差异无统计学意义(χ2=0.422,P >0.05);HBeAg血清学转换率分别为21.4%和20.0%,差异无统计学意义(χ2=0.059,P>0.05)。两组患者耐受性均良好,无明显不良反应。结论 ETV治疗慢性乙型肝炎,对初治及阿德福韦耐药患者均能有效地控制病毒复制,改善肝功能,促使HBeAg血清学转换,长期服药安全性好。
目的:觀察恩替卡韋(ETV)治療慢性乙型肝炎的臨床療效。方法36例慢性乙型肝炎患者包括初治治療組(20例)和阿德福韋酯(ADV)耐藥組(16例),兩組患者分彆給予ETV 0.5 mg口服,1次/d,治療96週。結果 ETV初治組和ADV耐藥組患者治療96週後,ALT複常率分彆為100%和93.75%,差異無統計學意義(χ2=4.553,P>0.05);HBV DNA低于檢測下限的比率均為100%;HBeAg陰轉率分彆為42.8%和40.0%,差異無統計學意義(χ2=0.422,P >0.05);HBeAg血清學轉換率分彆為21.4%和20.0%,差異無統計學意義(χ2=0.059,P>0.05)。兩組患者耐受性均良好,無明顯不良反應。結論 ETV治療慢性乙型肝炎,對初治及阿德福韋耐藥患者均能有效地控製病毒複製,改善肝功能,促使HBeAg血清學轉換,長期服藥安全性好。
목적:관찰은체잡위(ETV)치료만성을형간염적림상료효。방법36례만성을형간염환자포괄초치치료조(20례)화아덕복위지(ADV)내약조(16례),량조환자분별급여ETV 0.5 mg구복,1차/d,치료96주。결과 ETV초치조화ADV내약조환자치료96주후,ALT복상솔분별위100%화93.75%,차이무통계학의의(χ2=4.553,P>0.05);HBV DNA저우검측하한적비솔균위100%;HBeAg음전솔분별위42.8%화40.0%,차이무통계학의의(χ2=0.422,P >0.05);HBeAg혈청학전환솔분별위21.4%화20.0%,차이무통계학의의(χ2=0.059,P>0.05)。량조환자내수성균량호,무명현불량반응。결론 ETV치료만성을형간염,대초치급아덕복위내약환자균능유효지공제병독복제,개선간공능,촉사HBeAg혈청학전환,장기복약안전성호。
Objective To analyze the antiviral effects of enticavir in patients with hepatitis B. Methods Total of 36 patients with chronic hepatitis B including 20 na?ve patients and 16 patients with adefovir dipivoxil (ADV)-resistant, were treated with enticavir 0.5 mg daily. The efficacy was evaluated at 4th , 12th, 24th, 48th and 96th month, respectively. Results At 96th month after treatment, the rates of ALT becoming normal were 100%and 93.75%in na?ve and in ADV-resistant patients, respectively, with no signiifcant difference (χ2=4.553, P>0.05). The negative rats of HBV DNA of the two groups were all 100%. Negative rates of HBeAg of the two groups were 42.8%and 40.0%, with no signiifcant difference (χ2=0.422, P>0.05). The HBeAg seroconversion rate of the two groups were 21.4%and 20.0%, respectively, with no significant difference (χ2= 0.059,P > 0.05). The two groups were all well tolerated and had no obvious adverse reactions. Conclusions Entecavir could effectively inhibit the replication of HBV, normalize of ALT and enhance conversion from anti-HBe to HBeAg for cases with na?ve patients and patients with ADV-resistant. It is safey for long-term medication.