Philadelphia FIGHT Community Health Centers, Philadelphia, PA.
AIDS Activities Coordinating Office, Philadelphia Department of Public Health, Philadelphia, PA.
J Acquir Immune Defic Syndr. 2018 Oct 1;79(2):173-178. doi: 10.1097/QAI.0000000000001772.
Pre-exposure prophylaxis (PrEP) for HIV prevention with daily tenofovir and emtricitabine is effective when taken consistently. Currently, there is no objective way to monitor PrEP adherence. Urine has been shown to be highly correlated with plasma tenofovir levels, with urine tenofovir levels >1000 ng/mL demonstrating recent (1-2 days) adherence to PrEP.
This study was conducted at an urban community health center in Philadelphia, Pennsylvania.
PrEP was administered to 50 young men who have sex with men and transgender women of color using weekly, biweekly, and/or monthly dispensation schedules. Primary objectives were retention at 48 weeks (in care at week 48 and completing ≥50% of medication pickups) and adherence assessed by urine tenofovir levels. Risk behaviors and sexually transmitted infection diagnoses were also collected.
Seventy percent of participants were retained in care at 48 weeks. The proportion of subjects with urine tenofovir consistent with recent adherence was 80, 74.4, 82.4, 82.4, and 69.7% at weeks 4, 12, 24, 36, and 48, respectively. Sixty-one sexually transmitted infections were diagnosed over 231 screenings throughout 48 weeks, with no significant change between the first and second 24-week periods (P = 0.43; 0 seroconversions). At week 48, more than half of subjects reported an increase or no change in condom use, an increase in their ability to discuss HIV with partners, and no change in number of sexual partners from baseline.
These data demonstrate PrEP can be successfully delivered to a high-risk population with high program retention and medication adherence measured by urine tenofovir levels.
每日服用替诺福韦和恩曲他滨进行 HIV 暴露前预防(PrEP)在持续服用时是有效的。目前,还没有客观监测 PrEP 依从性的方法。尿液与血浆替诺福韦水平高度相关,尿液替诺福韦水平 >1000ng/ml 表明最近(1-2 天)有 PrEP 服用依从性。
这项研究在宾夕法尼亚州费城的一家城市社区卫生中心进行。
为 50 名男男性行为者和跨性别女性提供 PrEP,采用每周、每两周和/或每月的配药方案。主要目标是在 48 周时保持(第 48 周在治疗中并完成 ≥50%的药物取药)和通过尿液替诺福韦水平评估依从性。还收集了风险行为和性传播感染的诊断。
70%的参与者在第 48 周时仍在接受治疗。尿液替诺福韦水平提示最近有依从性的参与者比例分别为第 4、12、24、36 和 48 周时的 80%、74.4%、82.4%、82.4%和 69.7%。在 48 周内进行了 231 次筛查,共诊断出 61 例性传播感染,第一和第二 24 周期间没有显著变化(P = 0.43;无 0 例血清转换)。在第 48 周时,超过一半的受试者报告说,他们使用避孕套的情况有所增加或没有变化,与伴侣讨论 HIV 的能力有所提高,与基线相比性伴侣数量没有变化。
这些数据表明,替诺福韦可以成功地用于高危人群,通过尿液替诺福韦水平来衡量,该方案具有较高的保留率和药物依从性。