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Impact of choice of NRTI in first-line antiretroviral therapy: A cohort analysis of stavudine vs. tenofovir

机译:一线抗逆转录病毒疗法中选择NRTI的影响:司他夫定与替诺福韦的队列分析

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Objective: In April 2010, South Africa replaced stavudine with tenofovir in first-line antiretroviral therapy (ART) despite tenofovir's higher cost. We examined treatment outcomes over 24 months amongst patients initiated on tenofovir-based vs. stavudine-based first-line regimens. Methods: Prospective cohort analysis of 3940 patients newly initiating either stavudine-based (April 2009 to March 2010) or tenofovir-based (April 2010 to March 2011) ART in Johannesburg, South Africa. Cox proportional hazards models and Fine and Gray's competing risk regression accounting for death were used to model mortality and loss to follow-up, respectively. Linear and log-binomial regression were used to evaluate associations with immunologic response and unsuppressed virus (≥400 copies/ml), respectively. Results: About 1878 patients prescribed tenofovir and 2062 patients prescribed stavudine were included. One hundred and sixty-six (8.8%) tenofovir and 244 (11.8%) stavudine patients died. Three hundred and fifty (18.6%) tenofovir and 379 (18.4%) stavudine patients were lost to follow-up over 24 months on ART. Adjusted regression models showed tenofovir and stavudine were comparable regarding death, loss to follow-up, immunologic response and virologic status. Conclusions: We found no difference in mortality, loss to follow-up, immunological and virologic outcomes over the first 24-months on ART associated with tenofovir compared with stavudine.
机译:目的:尽管替诺福韦的费用较高,但南非在一线抗逆转录病毒疗法(ART)中用替诺福韦替代司他夫定。我们检查了基于替诺福韦和司他夫定一线方案开始治疗的患者在24个月内的治疗效果。方法:对南非约翰内斯堡新开始使用司他夫定(2009年4月至2010年3月)或使用替诺福韦(2010年4月至2011年3月)ART的3940例患者进行前瞻性队列分析。使用Cox比例风险模型以及考虑死亡的Fine和Gray的竞争风险回归分别对死亡率和后续损失进行建模。线性回归和对数二项式回归分别用于评估与免疫反应和未抑制病毒(≥400拷贝/ ml)的相关性。结果:包括约1878例处方替诺福韦的患者和2062例处方司他夫定的患者。 166名(8.8%)替诺福韦和244名(11.8%)司他夫定患者死亡。在24个月的ART期间,失去了三百五十(18.6%)替诺福韦和379(18.4%)司他夫定患者失访。调整后的回归模型显示替诺福韦和司他夫定在死亡,随访失败,免疫应答和病毒学状况方面具有可比性。结论:与司他夫定相比,与替诺福韦相关的ART的前24个月的死亡率,随访失败,免疫学和病毒学结果均无差异。

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