Treatment outcomes of tenofovir versus zidovudine-based first-line antiretroviral therapy regimens at Zewditu Memorial Hospital: A retrospective cohort study

Abel Terefe, Mamo Feyissa, W. Shibeshi
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引用次数: 1

Abstract

Tenofovir-based regimen is the preferred first line treatment in Ethiopia despite limited local data on its effectiveness and tolerability over zidovudine-based regimen. Therefore, this study compared the outcomes of tenofovir and zidovudine-based regimens focusing on toxicity driven regimen substitution and mortality. A retrospective cohort study was conducted in Zewditu Memorial Hospital. All ART naive patients who started ART between August 31, 2010, and August 31, 2013, were included. Data were collected by reviewing of patient’s medical records. Kaplan-Meier test and Cox regression analysis were used to compare survival for toxicity driven substitution and mortality, and to identify the independent predictors respectively. A total of 223 patients were included in this study, among which 164 (73.5%) TDF and 59 (26.6%) AZT-based regimens. A total of 71 (31.8%) primary outcomes such as toxicity driven regimen substitution, mortality, and lost to follow-up were observed, 48(29.3%) among TDF and 23(39.0%) in AZT-based regimens. The risk of toxicity driven regimen substitution was more than five times higher in AZT than TDF group (AHR=5.07, p=0.013). The estimated cumulative mortality at 6, 12, 18 and 24 months was 6, 9, 9 and 9% in TDF group whereas it was 9, 13, 13, and 13% in AZT group. There was no statistically significant difference in mortality and regimen failure between TDF and AZT groups. TDF-based regimen has superior outcome and better survival for toxicity driven regimen change than AZT-based regimen. This study finding supports recommendation of TDF-based regimen as preferred first-line ART. Key words: antiretroviral therapy (ART), Tenofovir (TDF), Zidovudine (AZT), toxicity driven regimen substitution, Survival.
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Zewditu纪念医院替诺福韦与齐多夫定一线抗逆转录病毒治疗方案的治疗结果:一项回顾性队列研究
基于替诺福韦的方案是埃塞俄比亚首选的一线治疗方案,尽管当地关于其有效性和耐受性的数据有限。因此,本研究比较了以替诺福韦和齐多夫定为基础的方案的结果,重点关注毒性驱动的方案替代和死亡率。在泽迪图纪念医院进行了一项回顾性队列研究。纳入2010年8月31日至2013年8月30日期间开始接受抗逆转录病毒疗法的所有未接受抗逆转录疫苗疗法的患者。通过查阅患者的医疗记录来收集数据。Kaplan-Meier检验和Cox回归分析用于比较毒性驱动的替代的存活率和死亡率,并分别确定独立的预测因素。本研究共纳入223名患者,其中164名(73.5%)采用TDF治疗,59名(26.6%)采用AZT治疗。共观察到71个(31.8%)主要结果,如毒性驱动的方案替代、死亡率和随访失败,TDF中48个(29.3%),基于AZT的方案中23个(39.0%)。AZT的毒性驱动方案替代风险是TDF组的五倍多(AHR=5.07,p=0.013)。TDF组在6、12、18和24个月时的估计累积死亡率分别为6%、9%、9%和9%,而AZT组为9%、13%、13%和13%。TDF组和AZT组之间的死亡率和方案失败率没有统计学上的显著差异。与基于AZT的方案相比,基于TDF的方案在毒性驱动的方案改变方面具有更好的结果和更好的生存率。这项研究结果支持以TDF为基础的方案作为首选一线ART的建议。关键词:抗逆转录病毒疗法(ART)、替诺福韦(TDF)、齐多夫定(AZT)、毒性驱动的方案替代、生存。
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