Liu Albert Y, Cohen Stephanie E, Vittinghoff Eric, Anderson Peter L, Doblecki-Lewis Susanne, Bacon Oliver, Chege Wairimu, Postle Brian S, Matheson Tim, Amico K Rivet, Liegler Teri, Rawlings M Keith, Trainor Nikole, Blue Robert Wilder, Estrada Yannine, Coleman Megan E, Cardenas Gabriel, Feaster Daniel J, Grant Robert, Philip Susan S, Elion Richard, Buchbinder Susan, Kolber Michael A
San Francisco Department of Public Health, San Francisco, California2Department of Medicine, University of California, San Francisco.
Department of Epidemiology and Biostatistics, University of California, San Francisco.
JAMA Intern Med. 2016 Jan;176(1):75-84. doi: 10.1001/jamainternmed.2015.4683.
Several randomized clinical trials have demonstrated the efficacy of preexposure prophylaxis (PrEP) in preventing human immunodeficiency virus (HIV) acquisition. Little is known about adherence to the regimen, sexual practices, and overall effectiveness when PrEP is implemented in clinics that treat sexually transmitted infections (STIs) and community-based clinics serving men who have sex with men (MSM).
To assess PrEP adherence, sexual behaviors, and the incidence of STIs and HIV infection in a cohort of MSM and transgender women initiating PrEP in the United States.
DESIGN, SETTING, AND PARTICIPANTS: Demonstration project conducted from October 1, 2012, through February 10, 2015 (last date of follow-up), among 557 MSM and transgender women in 2 STI clinics in San Francisco, California, and Miami, Florida, and a community health center in Washington, DC. Data were analyzed from December 18, 2014, through August 8, 2015.
A combination of daily, oral tenofovir disoproxil fumarate and emtricitabine was provided free of charge for 48 weeks. All participants received HIV testing, brief client-centered counseling, and clinical monitoring.
Concentrations of tenofovir diphosphate in dried blood spot samples, self-reported numbers of anal sex partners and episodes of condomless receptive anal sex, and incidence of STI and HIV acquisition.
Overall, 557 participants initiated PrEP, and 437 of these (78.5%) were retained through 48 weeks. Based on the findings from the 294 participants who underwent measurement of tenofovir diphosphate levels, 80.0% to 85.6% had protective levels (consistent with ≥4 doses/wk) at follow-up visits. African American participants (56.8% of visits; P = .003) and those from the Miami site (65.1% of visits; P < .001) were less likely to have protective levels, whereas those with stable housing (86.8%; P = .02) and those reporting at least 2 condomless anal sex partners in the past 3 months (88.6%; P = .01) were more likely to have protective levels. The mean number of anal sex partners declined during follow-up from 10.9 to 9.3, whereas the proportion engaging in condomless receptive anal sex remained stable at 65.5% to 65.6%. Overall STI incidence was high (90 per 100 person-years) but did not increase over time. Two individuals became HIV infected during follow-up (HIV incidence, 0.43 [95% CI, 0.05-1.54] infections per 100 person-years); both had tenofovir diphosphate levels consistent with fewer than 2 doses/wk at seroconversion.
The incidence of HIV acquisition was extremely low despite a high incidence of STIs in a large US PrEP demonstration project. Adherence was higher among those participants who reported more risk behaviors. Interventions that address racial and geographic disparities and housing instability may increase the impact of PrEP.
多项随机临床试验已证明暴露前预防(PrEP)在预防人类免疫缺陷病毒(HIV)感染方面的有效性。对于在治疗性传播感染(STIs)的诊所以及为男男性行为者(MSM)服务的社区诊所实施PrEP时的服药依从性、性行为及总体效果,人们了解甚少。
评估美国开始PrEP治疗的一组男男性行为者和跨性别女性中的PrEP服药依从性、性行为以及性传播感染和HIV感染的发生率。
设计、地点和参与者:2012年10月1日至2015年2月10日(最后随访日期)在加利福尼亚州旧金山和佛罗里达州迈阿密的2家性传播感染诊所以及华盛顿特区的1家社区健康中心对557名男男性行为者和跨性别女性开展的示范项目。数据于2014年12月18日至2015年8月8日进行分析。
免费提供每日口服替诺福韦酯富马酸盐和恩曲他滨联合用药,为期48周。所有参与者均接受HIV检测、以服务对象为中心的简短咨询以及临床监测。
干血斑样本中替诺福韦二磷酸盐的浓度、自我报告的肛交性伴侣数量和无保护被动肛交次数,以及性传播感染和HIV感染的发生率。
总体而言,557名参与者开始PrEP治疗,其中437名(78.5%)持续治疗48周。根据对294名接受替诺福韦二磷酸盐水平检测的参与者的研究结果,80.0%至85.6%的参与者在随访时达到了保护水平(相当于每周≥4剂)。非裔美国参与者(56.8%的随访;P = 0.003)以及迈阿密诊所的参与者(65.1%的随访;P < 0.001)达到保护水平的可能性较小,而有稳定住房的参与者(86.8%;P = 0.02)以及在过去3个月内报告至少有2名无保护肛交性伴侣的参与者(88.6%;P = 0.01)达到保护水平的可能性较大。随访期间,肛交性伴侣的平均数量从10.9降至9.3,而进行无保护被动肛交的比例保持稳定,为65.5%至65.6%。总体性传播感染发生率较高(每100人年90例),但未随时间增加。随访期间有2人感染HIV(HIV感染率,每100人年0.43例[95%CI,0.05 - 1.54例]);两人在血清转化时替诺福韦二磷酸盐水平均相当于每周少于2剂。
在美国一项大型PrEP示范项目中,尽管性传播感染发生率较高,但HIV感染率极低。报告更多危险行为的参与者服药依从性更高。解决种族和地域差异以及住房不稳定问题的干预措施可能会增强PrEP的效果。