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“我绝对需要知道我的伴侣仍将受到保护”:美国不同 HIV 血清学异性伴侣对 HIV 治愈相关研究的看法。

"I Would Absolutely Need to Know That My Partner Is Still Going to be Protected": Perceptions of HIV Cure-Related Research Among Diverse HIV Serodifferent Couples in the United States.

机构信息

Health Policy and Management, UNC Gillings School of Global Public Health, Chapel Hill, North Carolina USA.

Division of Infectious Diseases and Global Public Health, Department of Medicine, University of California, San Diego (UCSD), San Diego, California, USA.

出版信息

AIDS Res Hum Retroviruses. 2023 Aug;39(8):400-413. doi: 10.1089/AID.2022.0036. Epub 2022 Sep 8.

Abstract

Most HIV cure studies remain in the early stage of investigation and may carry clinical risks to the participants and, in some cases, their partners. Surprisingly little sociobehavioral research has investigated the perceptions of couples-including HIV serodifferent couples-around HIV cure research, including factors that would influence recruitment and retention in trials. We conducted a qualitative study to explore perceptions of diverse HIV serodifferent partners in the United States. We recruited 10 diverse HIV serodifferent couples (20 participants). We found participants had learned to cope with the reality of HIV, including protections during sex, and ascribed both positive and negative meanings to an HIV cure. Partners expressed concern about each other's health and potentially caring for a sick partner and emphasized the importance of safety when participating in an HIV cure trial. They identified the need for partner protection measures during analytical treatment interruptions (ATIs) as an ethical imperative. Participants recounted experiences of HIV stigma due to being in HIV serodifferent relationships and viewed ATIs as leading to a detectable viral load, which could limit sexual expression, complicate disclosure decision making, and worsen HIV-related stigma. Our study's main contribution is to inform efforts to meaningfully engage diverse HIV serodifferent partners in HIV cure research in the United States. Our data suggest people with HIV make decisions to participate in research based on close ones in their life and underscore the critical importance of acknowledging relationship dynamics in decisions to participate in research.

摘要

大多数 HIV 治愈研究仍处于研究的早期阶段,可能会给参与者带来临床风险,在某些情况下,也会给他们的伴侣带来风险。令人惊讶的是,很少有社会行为研究调查了包括 HIV 血清学不同的夫妇在内的夫妇对 HIV 治愈研究的看法,包括影响试验招募和保留的因素。我们进行了一项定性研究,以探索美国不同 HIV 血清学不同伴侣的看法。我们招募了 10 对不同 HIV 血清学不同的夫妇(20 名参与者)。我们发现参与者已经学会了应对 HIV 的现实,包括性行为期间的保护措施,并赋予 HIV 治愈积极和消极的意义。伴侣们对彼此的健康表示担忧,并可能照顾生病的伴侣,并强调在参与 HIV 治愈试验时安全的重要性。他们认为,在分析性治疗中断 (ATI) 期间采取保护伴侣的措施是一种道德义务。参与者讲述了由于处于 HIV 血清学不同的关系而遭受 HIV 耻辱的经历,并认为 ATI 会导致可检测的病毒载量,这可能会限制性行为表达,使披露决策复杂化,并加剧与 HIV 相关的耻辱。我们研究的主要贡献是为在美国有意义地让不同 HIV 血清学不同的伴侣参与 HIV 治愈研究提供信息。我们的数据表明,HIV 感染者根据生活中的亲密关系做出参与研究的决定,并强调在参与研究的决策中承认关系动态的至关重要性。

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