Understanding the lived experience research priorities for improving health-related quality of life in people living with HIV with cognitive impairment.

IF 1.7 4区 医学 Q3 INFECTIOUS DISEASES
HIV Research & Clinical Practice Pub Date : 2024-12-01 Epub Date: 2024-06-03
Kate Alford, Jaime H Vera, John Hammond, Stephanie Daley
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Abstract

Background: People living with HIV experience higher rates of cognitive impairment (CI), and at younger ages, than the general population. These individuals report poor health-related quality of life (HRQL), however, interventions aimed at assisting people living with HIV to live well with CI do not currently exist and represent an important un-met need in this population.

Objective: This study aimed to identify the lived experience research priorities for improving HRQL and identify interventions to support priority areas.

Methods: A Research Advisory Group was established with 15 lived experience, academic, healthcare, and third sector professionals. Additionally, two semi-structured focus groups were undertaken, with health and third sector professionals and people living with HIV with CI. Participants were asked to rank factors impacting HRQL, identified in prior research, in terms of priority and intervention development. Findings were analysed using a combination of conventional and summative content analysis. Study findings were feedback to our Research Advisory Group.

Results: Five people living with HIV with CI, recruited through third sector agencies [Male 80%; median age 59 (range 56-78); White British 60%; homosexual 60%], and three healthcare and third sector participants (66% third sector professionals from two local HIV charities; 33% HIV-specific clinical psychologist) took part in two focus groups and ranked interventions targeting improvement in physical function, social connectedness, cognition and perceived control over cognitive health as priority areas. Findings were then fed back to the Research Advisory Group who recommended the development of an illness-specific cognitive rehabilitation programme and improved information provision as important avenues for intervention development.

Conclusion: Given the absence of meaningful patient and public involvement, intervention, and support guidelines for people living with HIV with CI, this provides a roadmap for future research in this important and growing area of HIV clinical care.

了解认知障碍艾滋病病毒感染者的生活经历,改善其与健康相关的生活质量的研究重点。
背景:与普通人群相比,艾滋病病毒感染者的认知障碍(CI)发生率更高,年龄也更小。这些人报告的健康相关生活质量(HRQL)很差,然而,目前还没有旨在帮助艾滋病病毒感染者与认知障碍患者和谐相处的干预措施,这也是这一人群尚未满足的重要需求:本研究旨在确定改善 HRQL 的生活体验研究重点,并确定支持重点领域的干预措施:方法:成立了一个由 15 名生活经验、学术、医疗保健和第三部门专业人士组成的研究咨询小组。此外,还与医疗保健和第三部门的专业人士以及感染了 CI 的 HIV 感染者开展了两次半结构化焦点小组讨论。参与者被要求对先前研究中确定的影响 HRQL 的因素进行优先排序和干预发展。研究结果采用传统分析和总结性内容分析相结合的方法进行分析。研究结果已反馈给我们的研究顾问小组:通过第三部门机构招募的五名患有认知障碍的艾滋病病毒感染者[男性占 80%;年龄中位数为 59 岁(56-78 岁不等);英国白人占 60%;同性恋占 60%],以及三名医疗保健和第三部门参与者(66% 为来自当地两家艾滋病慈善机构的第三部门专业人士;33% 为专门从事艾滋病临床工作的心理学家)参加了两个焦点小组,并将旨在改善身体功能、社会联系、认知和认知健康控制感知的干预措施列为优先领域。研究结果随后反馈给了研究顾问小组,该小组建议制定一项针对特定疾病的认知康复计划,并将改善信息提供作为制定干预措施的重要途径:鉴于目前还没有针对患有认知障碍的艾滋病病毒感染者的有意义的患者和公众参与、干预和支持指南,本研究为今后在这一重要且不断发展的艾滋病临床护理领域开展研究提供了路线图。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.90
自引率
6.20%
发文量
15
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