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An analysis of baseline data from the PROUD study: an open-label randomised trial of pre-exposure prophylaxis

机译:PROUD研究的基线数据分析:暴露前预防的开放标签随机试验

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Background Pre-exposure prophylaxis (PrEP) has proven biological efficacy to reduce the sexual acquisition of the human immunodeficiency virus (HIV). The PROUD study found that PrEP conferred higher protection than in placebo-controlled trials, reducing HIV incidence by 86?% in a population with seven-fold higher HIV incidence than expected. We present the baseline characteristics of the PROUD study population and place the findings in the context of national sexual health clinic data. Methods The PROUD study was designed to explore the real-world effectiveness of PrEP (tenofovir-emtricitabine) by randomising HIV-negative gay and other men who have sex with men (GMSM) to receive open-label PrEP immediately or after a deferral period of 12?months. At enrolment, participants self-completed two baseline questionnaires collecting information on demographics, sexual behaviour and lifestyle in the last 30 and 90?days. These data were compared to data from HIV-negative GMSM attending sexual health clinics in 2013, collated by Public Health England using the genitourinary medicine clinic activity database (GUMCAD). Results The median age of participants was 35 (IQR: 29–43). Typically participants were white (81?%), educated at a university level (61?%) and in full-time employment (72?%). Of all participants, 217 (40?%) were born outside the UK. A sexually transmitted infection (STI) was reported to have been diagnosed in the previous 12?months in 330/515 (64?%) and 473/544 (87?%) participants reported ever having being diagnosed with an STI. At enrolment, 47/280 (17?%) participants were diagnosed with an STI. Participants reported a median (IQR) of 10 (5–20) partners in the last 90?days, a median (IQR) of 2 (1–5) were condomless sex acts where the participant was receptive and 2 (1–6) were condomless where the participant was insertive. Post-exposure prophylaxis had been prescribed to 184 (34?%) participants in the past 12?months. The number of STI diagnoses was high compared to those reported in GUMCAD attendees. Conclusions The PROUD study population are at substantially higher risk of acquiring HIV infection sexually than the overall population of GMSM attending sexual health clinics in England. These findings contribute to explaining the extraordinary HIV incidence rate during follow-up and demonstrate that, despite broad eligibility criteria, the population interested in PrEP was highly selective. Trial registration Current Controlled Trials ISRCTN94465371 . Date of registration: 28 February 2013.
机译:背景技术暴露前预防(PrEP)已被证明具有生物功效,可减少人类免疫缺陷病毒(HIV)的性获得。 PROUD研究发现PrEP给予的保护作用高于安慰剂对照试验,使HIV感染率比预期高7倍,从而使HIV感染率降低了86%。我们介绍了PROUD研究人群的基线特征,并将研究结果置于全国性健康诊所数据的背景下。方法PROUD研究旨在通过将HIV阴性的男同性恋者和其他与男性发生性关系的男性(GMSM)随机接受立即开放标签PrEP来探索PrEP(替诺福韦-恩曲他滨)在现实世界中的有效性。 12个月。入学时,参与者自行填写了两个基线问卷,以收集有关过去30天和90天的人口统计学,性行为和生活方式的信息。将这些数据与2013年就诊于性健康诊所的HIV阴性GMSM数据进行了比较,该数据由英国公共卫生使用泌尿生殖医学诊所活动数据库(GUMCAD)进行了整理。结果参与者的中位年龄为35岁(IQR:29–43)。通常,参与者为白人(81%),大学学历(61%)和全职工作(72%)。在所有参与者中,有217名(40%)在英国以外出生。据报道,在过去的12个月中,有330/515(64%)和473/544(87%)的参与者被诊断出患有性传播疾病(STI)。入学时,47/280(17%)的参与者被诊断出患有性病。参与者报告在过去90天内,中位(IQR)为10(5-20​​)个伴侣,中位(IQR)为2(1-5)是参与者接受的无避孕套性行为,其中2(1-6)参与者插入时没有避孕套。在过去的12个月中,已对184名(34%)的参与者进行了暴露后预防。与GUMCAD参加者报告的STI诊断相比,其诊断数量很高。结论PROUD研究人群的性感染HIV风险要比英格兰性健康诊所的GMSM总人群高。这些发现有助于解释随访期间异常的HIV发生率,并表明尽管有广泛的资格标准,但对PrEP感兴趣的人群具有很高的选择性。试用注册电流控制试验ISRCTN94465371。注册日期:2013年2月28日。

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