中国医学创新
中國醫學創新
중국의학창신
Medical Innovation of China
2015年
29期
45-48
,共4页
范敏%涂德幸%孙文峰%金丽红
範敏%塗德倖%孫文峰%金麗紅
범민%도덕행%손문봉%금려홍
慢性乙型肝炎%干扰素α-2a%阿德福韦酯%抗病毒%联合
慢性乙型肝炎%榦擾素α-2a%阿德福韋酯%抗病毒%聯閤
만성을형간염%간우소α-2a%아덕복위지%항병독%연합
Chronic hepatitis B%Peginterferon α-2a%Adefovir dipivioxil%Anti-virus%Combined
目的:探讨低水平转氨酶慢性乙型肝炎的抗病毒疗效。方法:156例低水平转氨酶慢性乙型肝炎患者,随机分为e抗原阳性治疗组42例(A组)及对照组40例(B组),e抗原阴性治疗组36例(C组)及对照组38例(D组),治疗组给予派罗欣180μg皮下注射1次/周,24周后联合阿德福韦酯10 mg 1次/d,48周后停用派罗欣单用阿德福韦酯;对照组给予阿德福韦酯10 mg 1次/d。两组均按2005年版《慢性乙型肝炎防治指南》标准停药。结果:e抗原阳性治疗组与对照组在治疗48、72周时HBV-DNA阴转率、e抗原血清学转换率、停药24周复发率比较差异均有统计学意义(P<0.05);e抗原阴性治疗组与对照组在治疗24、48、72周时HBV-DNA阴转率比较差异均无统计学意义(P>0.05),停药24周复发率比较差异有统计学意义(P<0.05)。结论:长效干扰素联合阿德福韦酯治疗低水平转氨酶慢性乙型肝炎对于e抗原阳性患者能够提高疗效及降低复发率,对于e抗原阴性患者能够降低复发率。
目的:探討低水平轉氨酶慢性乙型肝炎的抗病毒療效。方法:156例低水平轉氨酶慢性乙型肝炎患者,隨機分為e抗原暘性治療組42例(A組)及對照組40例(B組),e抗原陰性治療組36例(C組)及對照組38例(D組),治療組給予派囉訢180μg皮下註射1次/週,24週後聯閤阿德福韋酯10 mg 1次/d,48週後停用派囉訢單用阿德福韋酯;對照組給予阿德福韋酯10 mg 1次/d。兩組均按2005年版《慢性乙型肝炎防治指南》標準停藥。結果:e抗原暘性治療組與對照組在治療48、72週時HBV-DNA陰轉率、e抗原血清學轉換率、停藥24週複髮率比較差異均有統計學意義(P<0.05);e抗原陰性治療組與對照組在治療24、48、72週時HBV-DNA陰轉率比較差異均無統計學意義(P>0.05),停藥24週複髮率比較差異有統計學意義(P<0.05)。結論:長效榦擾素聯閤阿德福韋酯治療低水平轉氨酶慢性乙型肝炎對于e抗原暘性患者能夠提高療效及降低複髮率,對于e抗原陰性患者能夠降低複髮率。
목적:탐토저수평전안매만성을형간염적항병독료효。방법:156례저수평전안매만성을형간염환자,수궤분위e항원양성치료조42례(A조)급대조조40례(B조),e항원음성치료조36례(C조)급대조조38례(D조),치료조급여파라흔180μg피하주사1차/주,24주후연합아덕복위지10 mg 1차/d,48주후정용파라흔단용아덕복위지;대조조급여아덕복위지10 mg 1차/d。량조균안2005년판《만성을형간염방치지남》표준정약。결과:e항원양성치료조여대조조재치료48、72주시HBV-DNA음전솔、e항원혈청학전환솔、정약24주복발솔비교차이균유통계학의의(P<0.05);e항원음성치료조여대조조재치료24、48、72주시HBV-DNA음전솔비교차이균무통계학의의(P>0.05),정약24주복발솔비교차이유통계학의의(P<0.05)。결론:장효간우소연합아덕복위지치료저수평전안매만성을형간염대우e항원양성환자능구제고료효급강저복발솔,대우e항원음성환자능구강저복발솔。
Objective: To investigate the effect of antivirus treatment in chronic hepatitis B (CHB) patients with low ALT level.Method: 156 CHB patients with low ALT level were equally randomly divided into 4 groups: the HBeAg (+) treatment group (group A)for 42 cases and the control group (group B)for 40 cases; the HBeAg(-) treatment group (group C)for 36 cases and the corresponding control group (group D)for 38 cases. The patients in the HBeAg(+) or HBeAg(-) treatment group were respectively given peginterferon α-2a(180 μg) once a week,after 24 weeks, these patients were added with Adefovir dipivioxil(10 mg) once a day ,after 48 weeks,Peginterferon α-2a was stoped and Adefovir dipivioxil was given continually to the patients.Two control groups were respectively given Adefovir dipivioxil (10 mg, once a day), the stopping standand of antiviral drugs was according to the guideline of prevention and treatment for CHB in 2005,China.Result: The HBV-DNA conversion rates ,HBeAg conversion rates and the relapsing rate after stop of antivirus drugs for 24 weeks in group A were all significantly different from the group B(P<0.05); the HBV-DNA conversion rates after treatment for 24,48 and 72 weeks were not different between group C and group D(P>0.05), however, the relapsing rate after stop of antivirus drugs for 24 weeks in group C was significantly different from the group D (P<0.05).Conclusion:Peginterferon α-2a combined with Adefovir dipivioxil treatment may enhance therapeutic effect and lower relapsing rate in HBeAg(+) CHB patients with low ALT level, furthermore, it can decrease relapsing rate for HBeAg(-) CHB patients.