Witzel T Charles, Wright Talen, McCabe Leanne, Gabriel Michelle M, Wolton Aedan, Gafos Mitzy, Ward Denise, Lampe Fiona C, Phillips Andrew N, Trevelion Roy, Collaco-Moraes Yolanda, Harbottle Justin, Speakman Andrew, Bonell Chris, Dunn David D, McCormack Sheena, Burns Fiona M, Weatherburn Peter, Rodger Alison J
Department of Public Health, Environments and Society, London School of Hygiene and Tropical Medicine, 15-17 Tavistock Place, London WC1H 9SH, United Kingdom.
Medical Research Council Clinical Trials Unit at University College London, 90 High Holborn, London WC1V 6LJ, United Kingdom.
EClinicalMedicine. 2021 Feb 11;32:100700. doi: 10.1016/j.eclinm.2020.100700. eCollection 2021 Feb.
Globally, trans people are disproportionately affected by HIV, but research on strategies to increase testing are limited. SELPHI is a randomised-controlled-trial (RCT) of 10,135 men, trans men, and trans women reporting lifetime anal intercourse with male partners ( or trans), evaluating whether the offer of free HIV self-testing (HIVST) increases diagnosis. This subgroup analysis from the SELPHI RCT aims to describe key HIVST outcomes and HIVST acceptability for trans people.
SELPHI recruited using social networking and trans focused social media. Participants were randomised 60/40 to baseline HIVST (Biosure™) (BT) vs no baseline HIVST (nBT); and at 3-months (if completed the survey and reported recent CAI) 50/50 to 3-monthly HIVST (RT) vs no repeat HIVST (nRT). Outcomes were self-reported through online surveys. We conducted a qualitative study of semi-structured peer-led participant interviews ( = 20) exploring HIVST motivations and experiences. These were analysed using a framework approach.
SELPHI recruited and randomised 118 trans men and trans women (94 trans men, 24 trans women), of whom 20 (16 trans men, 4 trans women) underwent the second randomisation. Median age at baseline was 29 (IQR: 22, 37), 79% were white, 79% were UK born, 37% had degree level education, and 31% had never tested for HIV. 62% ( = 59) of trans men completed the 3-month survey, but survey completion by trans women in nBT was too low (1/11) for randomised comparison. In trans men HIV testing uptake by 3 months was significantly higher in BT (95% 36/38) vs nBT (29%, 6/21) (RR=3.32 (1.68, 6.55) <0.001). Trans people randomised to RT reported 3 times higher rate of HIV testing compared to nRT during the two-year follow-up (IRR 3.66 (1.86, 8.01) <0.0001). STI testing frequency (mean number of tests during each 13 week period/ 2-year follow-up) was not significantly different across interventions: RT (0.03) and nRT (0.01) (IRR=1.86 95%CI; 0.77, 5.15; = 0.15). Social harms were rare. Acceptability was very high in BT: 97% (38/39) found instructions easy to understand, 97% (37/38) found the HIVST simple to use and 100% (39/39) reported good overall experience. In interviews, reported HIVST benefits included increased autonomy, privacy, convenience and avoidance of health care providers perceived to be discriminatory and services that increased dysphoria. Minor lancet and test processing issues were reported.
HIVST significantly increased testing uptake and frequency in trans men and trans people overall, although recruitment and retention of trans women was low. HIVST acceptability was high and indicates easy access to this novel technology may increase HIV testing access for this key population.
在全球范围内,跨性别者受艾滋病毒影响的比例过高,但关于增加检测策略的研究有限。SELPHI是一项针对10135名有与男性伴侣(或跨性别者)终生肛交史的男性、跨性别男性和跨性别女性的随机对照试验(RCT),评估免费艾滋病毒自我检测(HIVST)的提供是否能增加诊断率。这项来自SELPHI RCT的亚组分析旨在描述跨性别者的关键HIVST结果和HIVST可接受性。
SELPHI通过社交网络和专注于跨性别的社交媒体进行招募。参与者以60/40的比例随机分为接受基线HIVST(Biosure™)(BT)组和不接受基线HIVST(nBT)组;在3个月时(如果完成调查并报告近期肛交插入),以50/50的比例随机分为每3个月进行一次HIVST(RT)组和不进行重复HIVST(nRT)组。结果通过在线调查进行自我报告。我们对由同伴主导的半结构化参与者访谈(n = 20)进行了定性研究,探讨HIVST的动机和体验。采用框架方法对这些访谈进行分析。
SELPHI招募并随机分配了118名跨性别男性和跨性别女性(94名跨性别男性,24名跨性别女性),其中20名(16名跨性别男性,4名跨性别女性)进行了第二次随机分组。基线时的中位年龄为29岁(四分位间距:22,37),79%为白人,79%在英国出生,37%拥有学位水平的教育,31%从未进行过艾滋病毒检测。62%(n = 59)的跨性别男性完成了3个月的调查,但nBT组中跨性别女性的调查完成率过低(1/11),无法进行随机比较。在跨性别男性中,3个月时BT组的艾滋病毒检测率(95%,36/38)显著高于nBT组(29%,6/21)(相对风险 = 3.32(1.68,6.55)<0.001)。在两年的随访中随机分配到RT组的跨性别者报告的艾滋病毒检测率是nRT组的3倍(发病率比3.66(1.86,8.01)<0.0001)。性传播感染检测频率(每13周期间/两年随访期间的平均检测次数)在各干预组之间无显著差异:RT组(0.0