HIV Epidemiology & Biostatistics Group, Research Department of Infection & Population Health, UCL Medical School, London, UK.
HIV Med. 2010 Mar;11(3):216-24. doi: 10.1111/j.1468-1293.2009.00771.x. Epub 2009 Dec 3.
OBJECTIVE: The aim of the study was to assess whether a simple, routinely available measure of antiretroviral therapy (ART) adherence predicts viral rebound at the next HIV viral load (VL) measurement in virally suppressed patients. METHODS: The analysis was performed on the Royal Free HIV Cohort, London, UK. Each 'drug coverage-viral load episode' (DCVL episode) was defined as a 6-month period immediately prior to a VL < or =50 HIV-1 RNA copies/mL (time-zero), during which the patient had been continuously on HAART, with all measured VLs < or =50 copies/mL. The next VL after time-zero was used to assess whether VL rebound (defined as >200 copies/mL) had occurred. Drug coverage, our measure of adherence, was calculated as the proportion of days in the 6-month period covered by a valid prescription for at least three antiretroviral drugs. RESULTS: A total of 376 (2.4%) VL rebounds occurred in 15 660 DCVL episodes among 1632 patients. Drug coverage was 100% for 32% of episodes, 95-99% for 16% of episodes and < or =60% for 10% of episodes. The risk ratio of rebound associated with a 10% increase in drug coverage, adjusted for potential confounding variables, was 0.93 (95% confidence interval 0.88-0.98). CONCLUSIONS: Antiretroviral drug coverage assessed at the time of VL measurement in patients with undetectable VL is potentially clinically useful for predicting VL rebound at the next VL measurement.
目的:本研究旨在评估一种简单的、常规可用的抗逆转录病毒治疗(ART)依从性测量方法是否能预测病毒载量(VL)抑制患者下一次 VL 测量时病毒反弹。
方法:本分析基于英国伦敦皇家自由 HIV 队列进行。每个“药物覆盖率-VL 发作”(DCVL 发作)定义为 VL<或=50 HIV-1 RNA 拷贝/mL(时间零)之前的 6 个月期间,在此期间患者持续接受高效抗逆转录病毒治疗(HAART),所有测量的 VL<或=50 拷贝/mL。时间零后下一次 VL 用于评估是否发生 VL 反弹(定义为>200 拷贝/mL)。药物覆盖率是依从性的衡量标准,计算方法为 6 个月期间至少有三种抗逆转录病毒药物的有效处方覆盖的天数比例。
结果:在 1632 名患者的 15660 个 DCVL 发作中,共发生了 376 次(2.4%)VL 反弹。发作的药物覆盖率为 100%占 32%,95%-99%占 16%,<或=60%占 10%。药物覆盖率每增加 10%,与反弹相关的风险比为 0.93(95%置信区间 0.88-0.98),调整了潜在混杂变量后。
结论:在 VL 不可检测的患者中,在测量 VL 时评估抗逆转录病毒药物覆盖率,对于预测下一次 VL 测量时的 VL 反弹具有潜在的临床意义。
HIV Med. 2009-5-6
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