在津巴布韦哈拉雷进行的抗体介导预防 HVTN703/HPTN081 试验中,接受艾滋病毒抗体的易感染艾滋病毒妇女接受暴露前预防的普遍程度和相关因素:一项横断面研究

B. Siziba, N. Mgodi, B. Ngara, T. D. Chawana, Miria Chitukuta, P. Mukwekwerere, Muchaneta Bhondai-Mhuri, Z. M. Chirenje, Felix Godwin Sivukile Mhlanga
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摘要

关于易感染艾滋病的女性在参与试验后采取暴露前预防措施(PrEP)的证据很有限。本研究调查了参与艾滋病预防试验后接受 PrEP 的流行率和相关因素。前抗体介导预防(AMP)研究的参与者在退出研究至少一年后,被邀请到津巴布韦的三个 AMP 临床研究点进行研究。AMP 研究评估了疫苗研究中心 01 广谱中和单克隆抗体在减少撒哈拉以南非洲妇女感染 HIV-1 方面的安全性和有效性。易感染艾滋病毒的参与者被纳入研究,并在参与研究的整个过程中接受降低风险咨询。在横断面研究中,完成了半结构化访谈问卷。从 2022 年 2 月到 2022 年 8 月,在加入 AMP 研究的 434 名参与者中,共有 298 人受邀,225 人参与了研究;28% 的人在参与研究后尝试获得 PrEP,20% 的人在参与研究后的某个阶段使用了 PrEP,15% 的人在发放问卷时正在使用 PrEP。接受 PrEP 与参与研究后有新的性伴侣以及前一个月的平均性接触次数较多有关。获得 PrEP 所面临的挑战包括与医疗机构、交通问题和耻辱感有关的问题。大多数(85%)前 AMP 参与者在接受问卷调查时未服用 PrEP。我们观察到,在研究期间接受过降低风险咨询的参与者在研究结束后对 PrEP 的接受度很低。对于退出艾滋病预防试验的易感人群,应考虑采取措施提高 PrEP 的吸收率。
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Prevalence and factors associated with uptake of pre-exposure prophylaxis amongst women vulnerable to HIV who received HIV antibodies in Antibody Mediated Prevention HVTN703/HPTN081 trial in Harare, Zimbabwe: a cross-sectional study
There is limited evidence on pre-exposure prophylaxis (PrEP) uptake post-trial participation for women vulnerable to HIV. This study investigates the prevalence and factors associated with PrEP uptake post-participation in an HIV prevention trial.Former Antibody Mediated Prevention (AMP) study participants were invited to the three AMP clinical research sites in Zimbabwe after at least a year of exiting the study. The AMP study evaluated the safety and efficacy of Vaccine Research Center 01 broadly neutralising monoclonal antibody in reducing acquisition of HIV-1 infection in women in sub-Saharan Africa. Participants vulnerable to HIV were enrolled and risk reduction counselling was done throughout study participation. In a cross-sectional study, semi-structured interview administered questionnaires were completed. The primary outcome was uptake of PrEP after the study exit.From February 2022 to August 2022, out of 434 participants enrolled in the AMP study, a total of 298 were invited and 225 participated in the study; 28% made an attempt to access PrEP after study participation, 20% used PrEP at some point after study participation and 15% were on PrEP at the time of questionnaire administration. PrEP uptake was associated with new sexual partners after study participation and higher average number of sexual encounters in the previous month. Challenges faced in accessing PrEP included those related to the health facility, transport problems and stigma.The majority (85%) of former AMP participants were not on PrEP at the time of questionnaire administration. We observed poor uptake of PrEP post-study exit among participants who had received risk reduction counselling through study duration. Measures to improve PrEP uptake should be considered on participants vulnerable to HIV when exiting HIV prevention trials.
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