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首页> 外文期刊>BMC Infectious Diseases >Nevirapine- versus Efavirenz-based antiretroviral therapy regimens in antiretroviral-naive patients with HIV and Tuberculosis infections in India: a multi-centre study
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Nevirapine- versus Efavirenz-based antiretroviral therapy regimens in antiretroviral-naive patients with HIV and Tuberculosis infections in India: a multi-centre study

机译:在印度患有HIV和结核病感染的抗逆转录病毒初治患者中,基于奈韦拉平和依法韦仑的抗逆转录病毒疗法方案:一项多中心研究

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According to World Health Organization (WHO) guidelines, which have also been adopted by the National AIDS Control Organization (NACO), India, Efavirenz-based Anti-Retroviral Therapy (ART) is better in Human-Immunodeficiency-Virus (HIV)-infected patients who are also being treated with Rifampicin-based Anti-Tuberculous Therapy (ATT). However, Efavirenz is much more expensive. We hypothesize that Nevirapine is a cheaper alternative that possesses equal efficacy as Efavirenz in HIV-Tuberculosis (TB) co-infected patients. A parallel open-label randomized clinical trial was conducted at All India Institute of Medical Sciences (AIIMS), New Delhi and National AIDS Research Institute (NARI), Pune. Those who were ART-na?ve and co-infected with TB were randomized to receive either Nevirapine (Group 1)- or Efavirenz (Group 2)-based ART along with Rifampicin-based ATT. ATT was begun first in ART-na?ve patients according to the NACO guidelines, with a median of 27?days between ATT and ART in both groups. The primary endpoint was a composite unfavourable outcome (death and/or ART failure) at 96?weeks, and the secondary outcome was successful TB treatment at 48?weeks. A total of 284 patients (mean age 36.7?±?8.1?years) were randomized in a 1:1 ratio to receive either Nevirapine (n?=?144)- or Efavirenz (n?=?140)-based ART after a median ATT-ART gap of 27?days. The median CD4 count was 105 cells/μl, with a median viral load of 820,200 copies/μl and no significant difference between the groups. Composite unfavourable outcomes were reported in 49 patients in the Nevirapine group and 51 patients in the Efavirenz group (35.3% vs. 36.9%; hazard ratio, 0.95, 95% confidence interval (CI), 0.63,1.43, adjusted). There was no difference in successful TB treatment outcome between the groups (71.5% vs. 65.6%, 95% CI -3.8,17.9, adjusted). The results were similar, showing no difference between the groups in the two centres of the study after adjusting for disease stage. Composite unfavourable outcome in HIV-TB co-infected patients who were ART-na?ve showed no statistically significant difference in the Nevirapine or Efavirenz groups.. Therefore, Nevirapine-based ART is a reasonable alternative to Efavirenz in resource-limited settings. However, multi-centric studies with larger sample sizes are required to confirm these findings. NCT01805258 (Retrospectively registered on March 6, 2013) Date of registration: March 2013.
机译:根据世界卫生组织(WHO)的指导方针,印度国家艾滋病控制组织(NACO)也已采用该指导原则,基于依凡韦伦的抗逆转录病毒疗法(ART)在感染人类免疫缺陷病毒(HIV)方面效果更好还接受以利福平为基础的抗结核疗法(ATT)进行治疗的患者。但是,依法韦仑价格昂贵得多。我们假设奈韦拉平是一种更便宜的替代品,在HIV-结核病(TB)合并感染的患者中具有与依非韦伦同等的疗效。在新德里的全印度医学科学研究所(AIIMS)和浦那的国家艾滋病研究所(NARI)进行了一项平行的开放标签随机临床试验。那些未接受过ART治疗并与TB共同感染的患者被随机分配接受基于奈韦拉平(第1组)或依法韦伦(第2组)的ART以及基于利福平的ATT。根据NACO指南,初次接触ART的患者首先开始ATT,两组之间ATT和ART之间的中位数为27天。主要终点是96周时的复合不良预后(死亡和/或ART失败),次要终点是48周时成功的TB治疗。总共284例患者(平均年龄36.7±8.1年)以1:1的比例随机分配,接受基于奈韦拉平(n = 144)或依法韦伦(n = 140)的ART。 ATT-ART差距中位数为27天。 CD4的中位数为105个细胞/μl,病毒载量为820,200拷贝/μl,两组之间无显着差异。奈韦拉平组和依法韦仑组分别有49例和51例患者报告了综合不良结果(35.3%vs. 36.9%;危险比为0.95、95%置信区间(CI),0.63、1.43,调整后)。两组之间成功的结核治疗结果无差异(71.5%vs. 65.6%,95%CI -3.8,17.9,调整后)。结果相似,表明在调整疾病阶段后,两个研究中心的组之间没有差异。初次接受抗病毒治疗的HIV-TB合并感染患者的综合不利结果在奈韦拉平或依非韦伦组中无统计学差异。因此,在资源有限的情况下,基于奈韦拉平的抗逆转录病毒治疗可以替代依法韦伦。但是,需要更大样本量的多中心研究来确认这些发现。 NCT01805258(追溯注册于2013年3月6日)注册日期:2013年3月。

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