首页> 外文期刊>International Journal of Basic & Clinical Pharmacology >Comparative study of adverse effect profile of first line drugs Zidovudine (ZDV) + Lamivudine (3TC) + Nevirapine (NVP) Vs Tenofovir (TDF) + Lamivudine (3TC) + Atazanavir (ATV) + Ritonovir (RTV) in HIV/AIDS patients
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Comparative study of adverse effect profile of first line drugs Zidovudine (ZDV) + Lamivudine (3TC) + Nevirapine (NVP) Vs Tenofovir (TDF) + Lamivudine (3TC) + Atazanavir (ATV) + Ritonovir (RTV) in HIV/AIDS patients

机译:一线药物齐多夫定(ZDV)+拉米夫定(3TC)+奈韦拉平(NVP)与替诺福韦(TDF)+拉米夫定(3TC)+阿扎那韦(ATV)+利托诺韦(RTV)不良反应概况的比较研究

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Background: The biggest threat to mankind from the health perspective is probably the virus Human Immunodeficiency Virus (HIV) responsible for a serious disease known as Acquired Immune Deficiency Syndrome (AIDS). To compare the adverse effect profile of two antiretroviral regimens i.e, Zidovudine (ZDV) + Lamivudine (3TC) + Nevirapine (NVP) [regimen A] Vs Tenofovir (TDF) + Lamivudine (3TC) + Atazanavir(ATV) + Ritonavir (RTV) [regimen B] by clinical and biochemical methods. Methods: This prospective, observational study was carried out in 200 HIV positive patients receiving first line and second-line antiretroviral therapy (ART) at ART centre, GGH, Vijayawada. Out of 200 patients, 100 patients received regimen A [(ZDV) + (3TC) + (NVP)] and 100 patients were treated with regimen B [(TDF) + (3TC) + (ATV) + (RTV)]. The collected data has been analysed and presented. Results: Out of 200 patients, 110 patients developed ADRs. In this 110, 38 patients received regimen A and 18 patients received regimen B and had CD4 + count 250 cells/ mm 3 . Conclusions: The ADRs were most common in those patients whose CD4+ count is less than 250cells/cu mm. Though the patients on second line showed significant increase in CD4+count, number of patients with ADRs were also more with regimen B. Though atazanavir containing regimen is more efficacious than zidovudine containing regimen, but regimen B produces more serious adverse effects. So, second line drugs are reserved for treatment failures to first line, drug resistance and for those not tolerating first line drugs.
机译:背景:从健康角度来看,对人类最大的威胁可能是人类免疫缺陷病毒(HIV)病毒,它是一种严重的疾病,称为后天免疫机能丧失综合症(AIDS)。为了比较两种抗逆转录病毒疗法的不良反应,齐多夫定(ZDV)+拉米夫定(3TC)+奈韦拉平(NVP)[方案A]与Tenofovir(TDF)+拉米夫定(3TC)+ Atazanavir(ATV)+利托那韦(RTV) [方案B]通过临床和生化方法。方法:这项前瞻性观察研究是在维杰亚瓦达州GGH的ART中心对200例接受一线和二线抗逆转录病毒治疗(ART)的HIV阳性患者进行的。在200名患者中,有100名患者接受了方案A [(ZDV)+(3TC)+(NVP)],而100名患者接受了方案B [(TDF)+(3TC)+(ATV)+(RTV)]治疗。收集的数据已经过分析和展示。结果:在200名患者中,有110名患者出现了ADR。在这110名患者中,有38位患者接受了方案A,有18位患者接受了方案B,并且CD4 +计数为250细胞/ mm 3。结论:ADR在CD4 +计数小于250细胞/立方毫米的患者中最为常见。尽管二线患者显示CD4 +计数显着增加,但方案B的ADR患者人数也更多。尽管含阿扎那韦的方案比齐多夫定方案更有效,但方案B会产生更严重的不良反应。因此,保留二线药物用于一线药物治疗失败,耐药性以及不耐受一线药物的药物。

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