Department of Medicine, University of California San Diego, San Diego, California, USA.
Department of Medicine, Ronald Reagan UCLA Medical Center, University of California Los Angeles, Los Angeles, California, USA.
AIDS Patient Care STDS. 2021 Dec;35(12):481-487. doi: 10.1089/apc.2021.0114.
Little information is known about the cisgender women who seek and initiate pre-exposure prophylaxis (PrEP) for HIV prevention in the United States. Adherence Enhancement Guided by Individualized Texting and Drug Levels was a 48-week single-arm open-label demonstration study of daily oral tenofovir disoproxil fumaratel emtricitabine (TDF/FTC) in cisgender women ≥ 18 years old at risk for HIV. Participants were surveyed at screening and enrollment about sociodemographics, HIV risk perception and behaviors, and PrEP perspectives and aggregated into three risk groups according to HIV sexual risk behavior: being in a serodiscordant partnership (SD), engaging in sex work (SW), and having partners with unknown HIV status at risk for HIV (UP). One hundred sixty-seven women presented for screening with = 31 screen failures. Of the 162 women completing enrollment, mean age was 40 (standard deviation 11), with 41% non-Hispanic Black, 22% non-Hispanic White, and 19% Latina. Compared with those who screened ineligible, enrolled participants were more likely to have heard of PrEP, had higher HIV risk perception, and reported higher perceived PrEP efficacy. Sixty-four women (47%) were categorized as SD, 21 (15%) as SW, and 51 (38%) as UP. The SW were more likely to report higher levels of drinking and drug use ( = 0.002) and history of intimate partner violence in the past year ( < 0.001) compared with SD and UP. Among cisgender women enrolled, there were significant differences between the three risk groups by demographics, HIV risk behavior, and PrEP perspectives, suggesting that interventions to successfully implement PrEP in US women may need to be tailored by HIV risk group. Clinical Trial Registration number: NCT02584140.
关于在美国寻求并开始接受 HIV 预防的顺性别女性,我们知之甚少。《基于个体短信和药物水平的依从性增强指导》是一项为期 48 周的单臂开放性标签研究,研究对象为≥18 岁有 HIV 感染风险的顺性别女性,每日口服替诺福韦二吡呋酯富马酸丙酚替诺福韦片(TDF/FTC)。参与者在筛查和入组时接受了社会人口统计学、HIV 风险感知和行为以及 PrEP 观点的调查,并根据 HIV 性风险行为分为三个风险组:处于性伴侣不一致(SD)关系中、从事性工作(SW)和与 HIV 状况未知的高危伴侣(UP)。共有 167 名女性接受了筛查,其中有 31 名女性筛查不合格。在完成入组的 162 名女性中,平均年龄为 40 岁(标准差 11),41%是非西班牙裔黑人,22%是非西班牙裔白人,19%是拉丁裔。与那些筛查不合格的女性相比,入组的参与者更有可能听说过 PrEP,对 HIV 风险感知更高,并且报告了更高的 PrEP 效果感知。64 名女性(47%)被归类为 SD,21 名(15%)为 SW,51 名(38%)为 UP。SW 更有可能报告更高水平的饮酒和吸毒(=0.002)以及过去一年中亲密伴侣暴力史( < 0.001),与 SD 和 UP 相比。在入组的顺性别女性中,三个风险组在人口统计学、HIV 风险行为和 PrEP 观点方面存在显著差异,这表明为了在美国女性中成功实施 PrEP,可能需要根据 HIV 风险组量身定制干预措施。临床试验注册号:NCT02584140。
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