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首页> 外文期刊>Journal of the International Association of Physicians in AIDS Care: JIAPAC >Efavirenz Outperforms Boosted Atazanavir among Treatment-Naive HIV-1-Infected Persons in Routine Clinical Care
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Efavirenz Outperforms Boosted Atazanavir among Treatment-Naive HIV-1-Infected Persons in Routine Clinical Care

机译:在常规治疗中,未经治疗的HIV-1感染者中依法韦仑的效果优于增强的阿扎那韦

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摘要

Background: Effectiveness of antiretroviral therapy (ART) in a routine clinical care may result different from the clinical trials. We assessed the virologic outcomes in treatment-naive persons who received either efavirenz (EFV) or atazanavir/ritonavir (ATV/r) with a backbone of tenofovir/emtricitabine (TDF/FTC) as their combination ART (cART). Methods: This was a retrospective cohort study conducted at the Washington University HIV Outpatient Clinic from January 2004 to June 2009. Predictors of virologic suppression (HIV RNA level <400 copies/mL) by week 48 were assessed by multivariate Cox proportional hazards regression models. Results: Of 324 persons, 221(68%) received EFV and 103 (32%) received ATV/r. Persons on EFV had 1.4-fold increased likelihood of virologic suppression (95% confidence interval, 1.0-1.8) when compared to ATV/r after adjustment with primary drug resistance, pre-cART opportunistic infection, HIV RNA levels, and timing to start cART. Conclusions: In routine clinical care settings, EFV had higher likelihood of achieving virologic suppression than ATV/r with backbone of TDF/FTC.
机译:背景:抗逆转录病毒疗法(ART)在常规临床护理中的有效性可能与临床试验有所不同。我们评估了以替诺福韦/恩曲他滨(TDF / FTC)为骨架的依法韦仑(EFV)或阿扎那韦/利托那韦(ATV / r)(初治)的复合治疗(ART)的病毒学结局。方法:这是一项回顾性队列研究,于2004年1月至2009年6月在华盛顿大学HIV门诊诊所进行。通过多变量Cox比例风险回归模型评估了第48周的病毒学抑制因子(HIV RNA水平<400拷贝/ mL)。结果:在324人中,有221人(68%)接受了EFV,有103人(32%)接受了ATV / r。调整原发性耐药性,cART前机会性感染,HIV RNA水平和开始cART的时间后,与ATV / r相比,使用EFV的人被病毒抑制的可能性增加1.4倍(95%置信区间,1.0-1.8)。 。结论:在常规的临床护理环境中,EFV比具有TDF / FTC骨架的ATV / r获得病毒抑制的可能性更高。

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