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Rates of switching to second-line antiretroviral therapy and impact of delayed switching on immunologic, virologic, and mortality outcomes among HIV-infected adults with virologic failure in Rakai, Uganda

机译:乌干达拉凯市二线抗逆转录病毒疗法的转换率以及延迟转换对HIV感染的具有病毒学衰竭的成年人的免疫,病毒学和死亡率的影响

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Background Switch from first to second-line ART is recommended by WHO for patients with virologic failure. Delays in switching may contribute to accumulated drug resistance, advanced immunosuppression, increased morbidity and mortality. The 3rd 90′ of UNAIDS 90:90:90 targets 90% viral suppression for persons on ART. We evaluated the rate of switching to second-line antiretroviral therapy (ART), and the impact of delayed switching on immunologic, virologic, and mortality outcomes in the Rakai Health Sciences Program (RHSP) Clinical Cohort Study which started providing ART in 2004 and implemented 6 monthly routine virologic monitoring beginning in 2005. Methods Retrospective cohort study of HIV-infected adults on first-line ART who had two consecutive viral loads (VLs) >1000 copies/ml after 6?months on ART between June 2004 and June 2011 was studied for switching to second-line ART. Immunologic decline after virologic failure was defined as decrease in CD4 count of ≥50 cells/ul and virologic increase was defined as increase of 0.5 log 10 copies/ml. Competing risk models were used to summarize rates of switching to second-line ART while cox proportional hazard marginal structural models were used to assess the risk of virologic increase or immunologic decline associated with delay to switch first line ART failing patients. Results The cumulative incidence of switching at 6, 12, and 24?months following virologic failure were 30.2%, 44.6%, and 65.0%, respectively. The switching rate was increased with higher VL at the time of virologic failure; compared to those with VLs?≤?5000 copies/ml, patients with VLs?=?5001–10,000 copies/ml had an aHR?=?1.81 (95% CI?=?0.9–3.6), and patients with VLs?>?10,000 copies/ml had an aHR?=?3.38 (95%CI?=?1.9–6.2). The switching rate was also increased with CD4 p =?0.009). Patients switched after 12?months of of virologic failure were more likely to experience CD4 decline and/or further VL increases. Conclusions Intervention strategies that aid clinicians to promptly switch patients to second-line ART as soon as virologic failure on 1st line ART is confirmed should be prioritized.
机译:背景世界卫生组织建议对于病毒学衰竭的患者从一线抗病毒治疗转为二线抗病毒治疗。转换延迟可能导致累积的耐药性,高级免疫抑制,发病率和死亡率增加。联合国艾滋病规划署90:90:90的第3个90'目标是对接受ART治疗的人进行90%的病毒抑制。我们在Rakai健康科学计划(RHSP)临床队列研究中评估了二线抗逆转录病毒疗法(ART)的转换率以及延迟转换对免疫,病毒学和死亡率结果的影响,该研究于2004年开始提供ART并已实施从2005年开始,每月进行6次常规病毒学监测。方法回顾性队列研究是对2004年6月至2011年6月在ART进行6个月后连续两次连续病毒载量(VLs)> 1000拷贝/ ml的一线抗病毒治疗的成年人进行的回顾性队列研究。研究了切换到二线ART。病毒性衰竭后的免疫学下降被定义为CD4计数≥50细胞/ ul的减少,病毒学的增加被定义为0.5 log 10个拷贝/ ml的增加。竞争风险模型用于总结转用二线抗病毒治疗的比率,而考克斯比例风险边缘结构模型用于评估与一线抗病毒治疗失败的患者延误相关的病毒学增加或免疫学下降的风险。结果病毒学衰竭后6、12和24个月的转换累积发生率分别为30.2%,44.6%和65.0%。病毒学失败时,较高的VL会增加转换率。与VLs≤≤5000拷贝/ ml的患者相比,VLs≥= 5001–10,000拷贝/ ml的患者的aHR≥1.81(95%CI≤0.9-3.6),VLs≥ 10,000拷贝/ ml的aHR等于3.38(95%CI等于1.9-6.2)。切换速率也随着CD4 p = 0.009而增加。病毒学衰竭12个月后转诊的患者更有可能经历CD4下降和/或VL进一步升高。结论一旦确定一线抗病毒治疗失败,应优先考虑可帮助临床医生立即将患者转至二线抗病毒治疗的干预策略。

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