Ayieko James, Balzer Laura B, Aoko Colette, Sunday Helen, Kakande Elijah, Kabami Jane, Koss Catherine, Chamie Gabriel, Kamya Moses R, Petersen Maya L, Havlir Diane V
Center for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Department of Biostatistics, University of California, Berkeley, California, USA.
J Int AIDS Soc. 2025 Jun;28 Suppl 1:e26450. doi: 10.1002/jia2.26450.
Post-exposure prophylaxis (PEP) remains underutilized despite being the only prevention option currently available that covers risk after an exposure. We sought to evaluate uptake and patterns of use of PEP among men and women in rural Uganda and Kenya.
We analysed PEP uptake from three randomized trials enrolling persons aged ≥15 years with HIV risk from antenatal clinics, outpatient departments and community settings from April through August 2021 (NCT04810650). In each trial, participants were randomized to a person-centred, dynamic choice HIV prevention (DCP) model or standard-of-care (SoC) arm. DCP offered choice of biomedical product (oral pre-exposure prophylaxis [PrEP] or PEP) with an option to switch over time; service location (clinic vs. out-of-clinic); testing option (rapid blood-based test or oral HIV self-test). The SoC offered HIV prevention services as per in-country guidelines. In both arms, PEP comprised a 28-day oral Tenofovir/Lamivudine/Dolutegravir course with HIV testing at start and end of the 28-day period. We described patterns of and predictors of self-reported PEP use over the 12 months of follow-up.
A total of 1232 participants were enrolled, balanced by arm and country. Of the 1147 (93%) who completed at least one survey on self-reported use of biomedical prevention, the median follow-up time was 12 months [IQR: 11, 12]. Overall, a total of 104 courses of PEP were dispensed to 59 participants. PEP use was significantly higher among persons enrolled in the DCP arm (relative risk [RR] = 3.30; 95% CI: 1.58-6.91), from Uganda (RR = 3.17; 95% CI: 1.53-6.59), reporting alcohol use (RR = 2.20; 95% CI: 1.30-3.72) and men (RR = 2.08; 95% CI: 1.11-3.91). Of the 59 PEP users, 14 (24%) transitioned to PrEP and 28(47%) used PEP on more than one occasion. Multiple uses of PEP were more common among persons from Uganda versus Kenya (RR = 4.43; 95% CI: 1.10-17.80) and persons enrolled from the community (RR = 4.45; 95% CI: 1.89-10.45) versus clinic. There were no seroconversions reported among PEP users. No serious adverse events were reported.
PEP reaches groups such as men and those who use alcohol who are more likely to benefit from this short-term prevention modality than PrEP. There is a need to make PEP accessible within a context of person-centred delivery to optimize its benefits.
暴露后预防(PEP)尽管是目前唯一一种涵盖暴露后风险的预防选择,但仍未得到充分利用。我们试图评估乌干达和肯尼亚农村地区男性和女性对PEP的接受情况及使用模式。
我们分析了2021年4月至8月期间在三个随机试验中≥15岁有感染艾滋病毒风险的参与者从产前诊所、门诊部和社区环境中接受PEP的情况(NCT04810650)。在每个试验中,参与者被随机分配到以人为主的动态选择艾滋病毒预防(DCP)模式组或标准护理(SoC)组。DCP提供生物医学产品(口服暴露前预防[PrEP]或PEP)的选择,并可随时间切换;服务地点(诊所与诊所外);检测选项(基于血液的快速检测或口服艾滋病毒自我检测)。SoC根据国内指南提供艾滋病毒预防服务。在两组中,PEP均包括为期28天的口服替诺福韦/拉米夫定/多替拉韦疗程,并在28天疗程开始和结束时进行艾滋病毒检测。我们描述了在12个月随访期间自我报告的PEP使用模式和预测因素。
共招募了1232名参与者,两组和两个国家的情况均衡。在1147名(93%)完成至少一项关于自我报告使用生物医学预防措施调查的参与者中,中位随访时间为12个月[四分位间距:11,12]。总体而言,共向59名参与者发放了104个PEP疗程。DCP组参与者中PEP的使用显著更高(相对风险[RR]=3.30;95%置信区间:1.58-6.91),来自乌干达的参与者(RR=3.17;95%置信区间:1.53-6.59),报告饮酒的参与者(RR=2.20;95%置信区间:1.30-3.72)以及男性参与者(RR=2.08;95%置信区间:1.11-3.91)。在59名PEP使用者中,14名(24%)转为使用PrEP,28名(47%)不止一次使用PEP。与肯尼亚相比,乌干达参与者多次使用PEP的情况更为常见(RR=4.43;95%置信区间:1.10-17.80),与从诊所招募的参与者相比,从社区招募的参与者多次使用PEP的情况更为常见(RR=4.45;95%置信区间:1.89-10.45)。PEP使用者中未报告血清转化情况。未报告严重不良事件。
PEP惠及了男性和饮酒者等群体,这些群体比PrEP更有可能从这种短期预防方式中受益。有必要在以人为主的服务提供背景下使PEP易于获得,以优化其益处。