Exploring the Use of Oral Pre-exposure Prophylaxis (PrEP) Among Women from Durban, South Africa as Part of the HIV Prevention Package in a Clinical Trial

被引:23
|
作者
Beesham, Ivana [1 ]
Heffron, Renee [2 ]
Evans, Shannon [1 ]
Baeten, Jared M. [3 ]
Smit, Jenni [1 ]
Beksinska, Mags [1 ]
Mansoor, Leila E. [4 ]
机构
[1] Univ Witwatersrand, Dept Obstet & Gynaecol, MatCH Res Unit MRU, Fac Hlth Sci, Durban, South Africa
[2] Univ Washington, Dept Epidemiol, Dept Global Hlth, Seattle, WA 98195 USA
[3] Univ Washington, Dept Med, Dept Epidemiol, Dept Global Hlth, Seattle, WA USA
[4] Univ KwaZulu Natal, Ctr AIDS Programme Res South Africa CAPRISA, Durban, South Africa
基金
比尔及梅琳达.盖茨基金会; 英国医学研究理事会;
关键词
Oral pre-exposure prophylaxis; Clinical trials; HIV prevention; Women; INFECTION;
D O I
10.1007/s10461-020-03072-0
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
HIV endpoint-driven clinical trials in Africa enroll women who are at heightened risk of acquiring HIV. In 2017, the South African Medical Research Council recommended the provision of oral pre-exposure prophylaxis (PrEP) in HIV prevention trials, at which time the Evidence for Contraceptive Options and HIV Outcomes trial was ongoing and began to provide PrEP on-site at some trial sites. We interviewed 132 women who initiated PrEP on-site at the Durban, South Africa trial site to explore PrEP use, and conducted phone-based interviews 4-6 months post-trial exit to explore post-trial PrEP access. PrEP uptake was high (42.6%). Among women initiating PrEP on-site, 87.9% felt at risk of acquiring HIV. Most women (> 90%) heard of PrEP for the first time from study staff and three-quarters who initiated PrEP on-site continued at trial-exit. PrEP use declined post-trial exit with more than 50% of women discontinuing PrEP, and barriers relating to access emerged.
引用
收藏
页码:1112 / 1119
页数:8
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