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首页> 外文期刊>American Journal of Health Research >Changes in serum liver enzymes level after switching from stavudine/lamivudine to zidovudine/lamivudine in NNRTIs based anti-retroviral regimens in Hawassa, Southern Ethiopia
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Changes in serum liver enzymes level after switching from stavudine/lamivudine to zidovudine/lamivudine in NNRTIs based anti-retroviral regimens in Hawassa, Southern Ethiopia

机译:在埃塞俄比亚南部哈瓦萨市基于NNRTIs的抗逆转录病毒疗法中,从司他夫定/拉米夫定改为齐多夫定/拉米夫定后血清肝酶水平的变化

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Background: During stavudine phase-out in a resource limited countries, Zidovudine or Tenofovir is used to substitute stavudine. However, data concerning any difference in liver enzymes level after therapy change (switching) in Ethiopia is very limited. Methods: This prospective cohort study was carried out from May 2013 to July 2014 at ART clinic of Hawassa University teaching hospital. Of hundred fifty HIV-infected; immunologically stable adults receiving triple antiretroviral therapy: 120 were patients receiving stavudine based regimen with either of efavirenz or nevirapine during ART initiation (switch group); and the rest 30 patients were receiving zidovudine based regimen with either of efavirenz or nevirapine and also never switched (control group). Lamivudine is common for both groups. Levels of serum liver enzymes were determined and hepatotoxicity assessed according to World Health Organization ART guideline. Statistical analysis was done using Statistical Package for Social Sciences (SPSS) Version 20. Results: Serum mean AST and ALT level in the switch group decreased significantly over the time observed (p=<0.0001 for both enzymes); however ALP level was significantly increased (p=<0.0001). Hepatotoxicity in the switch group was significantly decreased (AST grade > 1 from 35.8% to15.8%; and ALT from 20.8% to 3.3%) after 12 month of therapy change. Conclusion: Significantly a decreased hepatotoxicity was observed at the 12 month of post switch and this indicated that a substitution of stavudine to Zidovudine could have a potential to reverse hepatotoxicity. However, significantly decreased white blood cells count and abnormally increased level of ALP enzyme should require periodic monitoring and further investigations.
机译:背景:在资源有限的国家逐步淘汰司他夫定期间,齐多夫定或替诺福韦用于替代司他夫定。但是,关于埃塞俄比亚治疗改变(转换)后肝酶水平差异的数据非常有限。方法:这项前瞻性队列研究于2013年5月至2014年7月在Hawassa大学教学医院的ART诊所进行。在一百五十个艾滋病毒感染者中;免疫学稳定的成年人接受三联抗逆转录病毒疗法:120例接受抗逆转录病毒疗法的患者在开始抗逆转录病毒治疗时接受依伐他定联合依非韦伦或奈韦拉平治疗(开关组);其余30例患者接受基于齐多夫定的依非韦伦或奈韦拉平治疗,也从未切换(对照组)。拉米夫定在两组中都很常见。根据世界卫生组织ART指南确定血清肝酶水平并评估肝毒性。使用社会科学统计软件包(SPSS)版本20进行统计分析。结果:转换组的血清AST和ALT平均水平在观察到的时间内显着下降(两种酶的p = <0.0001);但是,ALP水平显着增加(p = <0.0001)。更换治疗12个月后,转换组的肝毒性显着降低(AST级> 1从35.8%至15.8%; ALT从20.8%至3.3%)。结论:转换后12个月观察到肝毒性显着降低,这表明用司他夫定替代齐多夫定可能具有逆转肝毒性的潜力。但是,白细胞计数显着下降和ALP酶水平异常升高应要求定期监测和进一步研究。

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