Centering autonomy and choice to support oral PrEP utilization among people who inject drugs: qualitative lessons from HPTN 094 INTEGRA.

IF 3.7 2区 医学 Q1 SUBSTANCE ABUSE Addiction Science & Clinical Practice Pub Date : 2024-12-18 DOI:10.1186/s13722-024-00520-3
Amaya Perez-Brumer, Rose Schmidt, Rebecca Kennedy, Jordan E Lake, Yolanda R Villarreal, Sydney Bornstein, Irene Kuo, Omar Nieto, Julie Franks, Cecile Denis, Nabila El-Bassel, Steve Shoptaw, Peter Davidson, Laramie R Smith
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Abstract

Background: Oral Pre-exposure prophylaxis (PrEP) is effective in preventing HIV transmission. However, despite high rates of HIV risk behaviors among people who inject drugs (PWID), this population remains underserved by current HIV prevention efforts in the United States. To address this challenge, we conducted an in-depth exploration of perspectives on using oral PrEP among PWID engaged in the HIV Prevention Trials Network (HPTN) 094 INTEGRA Study.

Methods: Guided by the Practical, Robust, Implementation, and Sustainability Model (PRISM), our qualitative study drew on semi-structured interviews conducted as part of the embedded implementation science evaluation of HPTN 094 INTEGRA. Seventy-seven PWID participants from five sites across New York City, Houston, Los Angeles, Philadelphia, and Washington DC were interviewed to assess intervention delivery, care access, and engagement sustainability. Audio files were transcribed verbatim and analyzed via an inductive and deductive thematic approach.

Results: Most participants (n = 46, 59.7%) discussed oral PrEP during their interview, though not directly prompted. Participants discussing PrEP had a mean age of 41.6 years and were predominantly white (54.3%) and cisgender men (60.9%). Among these, 15 participants described using PrEP. All participants had facilitated access to oral PrEP. Yet, the choice to use PrEP was influenced by personal risk perceptions, (mis)information about PrEP, and external factors (i.e. housing, financial security), which, for some, limited the autonomy to use PrEP. Two key themes emerged among participants using PrEP: ease of access and perceptions of high HIV risk. Those not using PrEP described two themes: low risk perception and prioritizing more urgent needs. Among participants not using PrEP a subgroup commonly described ambivalent interest, PrEP knowledge gaps, and PrEP readiness (i.e., contemplation).

Conclusions: Qualitative findings highlight that facilitated PrEP access was insufficient to motivate use for many participants. Rather, PrEP decision-making process (i.e., choice) was linked to risk perception and individuals' capability to leverage PrEP as a resource based on their circumstances (i.e., autonomy). Participants' descriptions of the centrality of choice and autonomy for PrEP use underscore that ease of access is a necessary pre-condition, but person-centered interventions should also address housing, financial stability, and urgent medical conditions to promote PrEP utilization among PWID.

Clinical trial registration: NCT04804027.

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以自主和选择为中心,支持注射吸毒者口服PrEP的使用:来自HPTN 094 INTEGRA的定性教训。
背景:口服暴露前预防(PrEP)是预防HIV传播的有效方法。然而,尽管注射吸毒者(PWID)的艾滋病毒风险行为率很高,但这一人群在美国目前的艾滋病毒预防工作中仍然得不到充分的服务。为了应对这一挑战,我们深入探讨了参与HIV预防试验网络(HPTN) 094 INTEGRA研究的PWID患者使用口服PrEP的观点。方法:在实用、稳健、实施和可持续性模型(PRISM)的指导下,我们的定性研究利用了半结构化访谈,作为HPTN 094 INTEGRA嵌入式实施科学评估的一部分。来自纽约市、休斯顿、洛杉矶、费城和华盛顿特区五个地点的77名PWID参与者接受了采访,以评估干预措施的提供、护理获取和参与的可持续性。音频文件逐字转录,并通过归纳和演绎的主题方法进行分析。结果:大多数参与者(n = 46, 59.7%)在访谈中讨论了口服PrEP,尽管没有直接提示。讨论PrEP的参与者平均年龄为41.6岁,主要是白人(54.3%)和顺性男性(60.9%)。其中,15名参与者描述了使用PrEP的情况。所有参与者都促进了口服PrEP的获取。然而,使用PrEP的选择受到个人风险认知、有关PrEP的(错误)信息和外部因素(即住房、财务安全)的影响,这些因素限制了一些人使用PrEP的自主权。使用PrEP的参与者中出现了两个关键主题:获取的便利性和对艾滋病毒高风险的认知。那些没有使用PrEP的人描述了两个主题:低风险认知和优先考虑更紧迫的需求。在不使用PrEP的参与者中,一个亚组通常描述了矛盾的兴趣,PrEP知识差距和PrEP准备(即沉思)。结论:定性研究结果强调,便利的PrEP获取不足以激励许多参与者使用。相反,PrEP决策过程(即选择)与风险感知和个人根据其环境(即自主性)利用PrEP作为资源的能力有关。参与者对PrEP使用的选择和自主权的中心地位的描述强调了易于获取是必要的先决条件,但以人为本的干预措施还应解决住房、金融稳定和紧急医疗条件问题,以促进PWID中PrEP的利用。临床试验注册:NCT04804027。
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来源期刊
Addiction Science & Clinical Practice
Addiction Science & Clinical Practice Psychology-Clinical Psychology
CiteScore
3.90
自引率
10.80%
发文量
64
审稿时长
28 weeks
期刊介绍: Addiction Science & Clinical Practice provides a forum for clinically relevant research and perspectives that contribute to improving the quality of care for people with unhealthy alcohol, tobacco, or other drug use and addictive behaviours across a spectrum of clinical settings. Addiction Science & Clinical Practice accepts articles of clinical relevance related to the prevention and treatment of unhealthy alcohol, tobacco, and other drug use across the spectrum of clinical settings. Topics of interest address issues related to the following: the spectrum of unhealthy use of alcohol, tobacco, and other drugs among the range of affected persons (e.g., not limited by age, race/ethnicity, gender, or sexual orientation); the array of clinical prevention and treatment practices (from health messages, to identification and early intervention, to more extensive interventions including counseling and pharmacotherapy and other management strategies); and identification and management of medical, psychiatric, social, and other health consequences of substance use. Addiction Science & Clinical Practice is particularly interested in articles that address how to improve the quality of care for people with unhealthy substance use and related conditions as described in the (US) Institute of Medicine report, Improving the Quality of Healthcare for Mental Health and Substance Use Conditions (Washington, DC: National Academies Press, 2006). Such articles address the quality of care and of health services. Although the journal also welcomes submissions that address these conditions in addiction speciality-treatment settings, the journal is particularly interested in including articles that address unhealthy use outside these settings, including experience with novel models of care and outcomes, and outcomes of research-practice collaborations. Although Addiction Science & Clinical Practice is generally not an outlet for basic science research, we will accept basic science research manuscripts that have clearly described potential clinical relevance and are accessible to audiences outside a narrow laboratory research field.
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