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拉替拉韦或依非韦伦为基础的 HIV 治疗方案起始后病毒学抑制和 CD4+ 细胞计数恢复。

Virologic suppression and CD4+ cell count recovery after initiation of raltegravir or efavirenz-containing HIV treatment regimens.

机构信息

Department of Epidemiology, University of North Carolina, Chapel Hill, North Carolina.

Division of HIV/AIDS Prevention, Centers for Disease Control and Prevention, Atlanta, Georgia.

出版信息

AIDS. 2018 Jan 14;32(2):261-266. doi: 10.1097/QAD.0000000000001668.

Abstract

OBJECTIVE

To explore the effectiveness of raltegravir-based antiretroviral therapy (ART) on treatment response among ART-naive patients seeking routine clinical care.

DESIGN

Cohort study of adults enrolled in HIV care in the United States.

METHODS

We compared virologic suppression and CD4 cell count recovery over a 2.5 year period after initiation of an ART regimen containing raltegravir or efavirenz using observational data from a US clinical cohort, generalized to the US population of people with diagnosed HIV. We accounted for nonrandom treatment assignment, informative censoring, and nonrandom selection from the US target population using inverse probability weights.

RESULTS

Of the 2843 patients included in the study, 2476 initiated the efavirenz-containing regimen and 367 initiated the raltegravir-containing regimen. In the weighted intent-to-treat analysis, patients spent an average of 74 (95% confidence interval: 41, 106) additional days alive with a suppressed viral load on the raltegravir regimen than on the efavirenz regimen over the 2.5-year study period. CD4 cell count recovery was also superior under the raltegravir regimen.

CONCLUSION

Patients receiving raltegravir spent more time alive and suppressed than patients receiving efavirenz, but the probability of viral suppression by 2.5 years after treatment was similar between groups. Optimizing the amount of time spent in a state of viral suppression is important to improve survival among people living with HIV and to reduce onward transmission.

摘要

目的

探索在接受常规临床护理的初治患者中,基于拉替拉韦的抗逆转录病毒疗法(ART)对治疗反应的效果。

设计

在美国接受 HIV 护理的成年人队列研究。

方法

我们使用来自美国临床队列的观察数据,比较了在开始包含拉替拉韦或依非韦伦的 ART 方案后 2.5 年内病毒学抑制和 CD4 细胞计数恢复情况,该队列数据推广至美国所有确诊 HIV 人群。我们使用逆概率加权法考虑了非随机治疗分配、信息性删失和从美国目标人群中进行的非随机选择。

结果

在纳入的 2843 例患者中,2476 例患者开始接受依非韦伦方案,367 例患者开始接受拉替拉韦方案。在加权意向治疗分析中,与依非韦伦方案相比,在 2.5 年的研究期间,接受拉替拉韦方案的患者平均多存活 74 天(95%置信区间:41,106),且病毒载量得到抑制。拉替拉韦方案也能更好地恢复 CD4 细胞计数。

结论

与接受依非韦伦的患者相比,接受拉替拉韦的患者存活时间更长且病毒得到抑制,但治疗后 2.5 年病毒抑制的概率在两组间相似。优化病毒抑制状态的持续时间对于改善 HIV 感染者的生存和减少病毒传播至关重要。

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