Acceptability and use of a dapivirine vaginal ring in a phase III trial

被引:106
|
作者
Montgomery, Elizabeth T. [1 ]
van der Straten, Ariane [1 ,2 ]
Chitukuta, Miria [3 ]
Reddy, Krishnaveni [4 ]
Woeber, Kubashni [5 ]
Atujuna, Millicent [6 ]
Bekker, Linda-Gail [6 ]
Etima, Juliane [7 ]
Nakyanzi, Teopista [7 ]
Mayo, Ashley J. [8 ]
Katz, Ariana [1 ]
Laborde, Nicole [1 ]
Grossman, Cynthia I. [9 ]
Soto-Torres, Lydia [10 ]
Palanee-Phillips, Thesla [4 ]
Baeten, Jared M. [11 ]
机构
[1] UCSF, RTI Int, Womens Global Hlth Imperat, San Francisco, CA USA
[2] UCSF, Ctr AIDS Prevent Studies, Dept Med, San Francisco, CA USA
[3] UZ UCSF Collaborat Res Programme, Harare, Zimbabwe
[4] Wits Reprod Hlth & HIV Inst WRHI, Johannesburg, South Africa
[5] South Africa Med Res Council, HIV Prevent Res Unit, Durban, South Africa
[6] Desmond Tutu HIV Res Ctr, Cape Town, South Africa
[7] Makerere Univ, Johns Hopkins Univ, Res Unit, Kampala, Uganda
[8] FHI360, Durham, NC USA
[9] NIMH, Bethesda, MD 20892 USA
[10] NIH, Div Aids, Bldg 10, Bethesda, MD 20892 USA
[11] Univ Washington, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
Africa; dapivirine; HIV prevention; qualitative; vaginal ring; women; HIV PREVENTION; PREEXPOSURE PROPHYLAXIS; AFRICAN WOMEN; ANTIRETROVIRAL PROPHYLAXIS; MICROBICIDE; INFECTION; ADHERENCE; TENOFOVIR; ZIMBABWE; GEL;
D O I
10.1097/QAD.0000000000001452
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: The MTN-020/ASPIRE trial evaluated the safety and effectiveness of the dapivirine vaginal ring for prevention of HIV-1 infection among African women. A nested qualitative component was conducted at six of 15 study sites in Uganda, Malawi, Zimbabwe and South Africa to evaluate acceptability of and adherence to the ring. Method: Qualitative study participants (n = 214) were interviewed with one of three modalities: single in-depth interview, up to three serial interviews or an exit Focus Group Discussion. Using semistructured guides administered in local languages, 280 interviews were audio-recorded, transcribed, translated, coded and analyzed. Results: We identified three key findings: first, despite initial fears about the ring's appearance and potential side effects, participants grew to like it and developed a sense of ownership of the ring once they had used it. Second, uptake and sustained adherence challenges were generally overcome with staff and peer support. Participants developed gradual familiarity with ring use through trial progression, and most reported that it was easy to use and integrate into their lives. Using the ring in ASPIRE was akin to joining a team and contributing to a broader, communal good. Third, the actual or perceived dynamics of participants' male partner relationship(s) were the most consistently described influence (which ranged from positive to negative) on participants' acceptability and use of the ring. Conclusion: It is critical that demonstration projects address challenges during the early adoption stages of ring diffusion to help achieve its potential public health impact as an effective, long-acting, female-initiated HIV prevention option addressing women's disproportionate HIV burden. Copyright (C) 2017 Wolters Kluwer Health, Inc. All rights reserved.
引用
收藏
页码:1159 / 1167
页数:9
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