An (un)restricted living: a qualitative exploration of the mental health and well-being of people living with HIV in England

IF 4.9 2区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Vasiliki Papageorgiou , Lucy Cullen , T Charles Witzel , Alex Sparrowhawk , Flavien Coukan , Janey Sewell , Alison Rodger , Carl May , Fiona Burns
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引用次数: 0

Abstract

People living with HIV, who have access to treatment, now have normal life expectancy. However, stigma and discrimination continue to affect health and well-being. We conducted focus groups with people living with HIV (n = 37), and key informant interviews (n = 20) with clinical and non-clinical workers who support people with HIV between May and November 2023. We aimed to explore the ongoing challenges and concerns faced by people living with HIV in England to inform a new model of person-centred HIV care. Participants discussed living well in relation to: 1) an unrestricted living; 2) emotional sexual health and intimacy well-being; and 3) autonomy of health and healthcare. Aspirations for an unrestricted living revolved around experiencing life in the same way as others, rather than having to compromise a sense of self or negotiate experiences differently due to their HIV status. Participants also shared a desire to live fulfilled sex lives without fear of being stigmatised due to living with HIV, and of feeling deserving of a satisfying sex life and sexual intimacy. There was also a particular anxiety about sharing an HIV status with new sexual partners. Conversations around sex and intimacy needed to be opened up to cover topics including pleasure and sexual wellness. A compromised autonomy of health referred to physical health; for example, the need for daily medication. Autonomy of healthcare referred to the challenges of negotiating an often fragmented and fractured healthcare service. Some shared experiences of discrimination by non-HIV healthcare workers and a requirement to advocate for their needs which is a specific challenge for marginalised groups. Person-centred care, which uses an intersectional approach to delivering HIV care, would respond to the needs and aspirations of people with HIV and their whole self. This offers the potential to address HIV-related stigma which continues to hinder progress.
(非)限制生活:对英格兰艾滋病毒感染者的心理健康和福祉的定性探索
获得治疗的艾滋病毒感染者现在有了正常的预期寿命。然而,耻辱和歧视继续影响健康和福祉。我们在2023年5月至11月期间对艾滋病毒感染者进行了焦点小组(n = 37),并对支持艾滋病毒感染者的临床和非临床工作人员进行了关键信息提供者访谈(n = 20)。我们的目的是探索英国艾滋病毒感染者面临的持续挑战和关注,为以人为本的艾滋病毒护理新模式提供信息。与会者讨论了生活的方方面面:1)不受限制的生活;2)情感性健康与亲密关系幸福感;3)健康和保健的自主权。对不受限制的生活的渴望围绕着以与他人相同的方式体验生活,而不是因为他们的艾滋病毒状况而不得不妥协自我意识或谈判不同的经历。参与者也都渴望过着充实的性生活,而不用担心因感染艾滋病毒而被污名化,并且觉得自己应该拥有令人满意的性生活和性亲密。与新的性伴侣分享艾滋病毒感染状况也是一种特别的焦虑。关于性和亲密关系的对话需要开放,以涵盖包括快乐和性健康在内的话题。健康自主权受损指的是身体健康;例如,需要每天服药。医疗保健自治指的是谈判往往是分散和断裂的医疗保健服务的挑战。非艾滋病毒保健工作者有一些共同的歧视经历,需要倡导他们的需求,这对边缘化群体来说是一个具体的挑战。以人为本的护理采用交叉方法提供艾滋病毒护理,将满足艾滋病毒感染者及其整个自我的需求和愿望。这提供了解决与艾滋病毒有关的耻辱的潜力,这种耻辱继续阻碍进展。
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来源期刊
Social Science & Medicine
Social Science & Medicine PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH-
CiteScore
9.10
自引率
5.60%
发文量
762
审稿时长
38 days
期刊介绍: Social Science & Medicine provides an international and interdisciplinary forum for the dissemination of social science research on health. We publish original research articles (both empirical and theoretical), reviews, position papers and commentaries on health issues, to inform current research, policy and practice in all areas of common interest to social scientists, health practitioners, and policy makers. The journal publishes material relevant to any aspect of health from a wide range of social science disciplines (anthropology, economics, epidemiology, geography, policy, psychology, and sociology), and material relevant to the social sciences from any of the professions concerned with physical and mental health, health care, clinical practice, and health policy and organization. We encourage material which is of general interest to an international readership.
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