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首页> 外文期刊>AIDS care. >'He was no longer listening to me': A qualitative study in six Sub-Saharan African countries exploring next-of-kin perspectives on caring following the death of a relative from AIDS
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'He was no longer listening to me': A qualitative study in six Sub-Saharan African countries exploring next-of-kin perspectives on caring following the death of a relative from AIDS

机译:“他不再倾听我”:六个撒哈拉以南非洲国家的定性研究探讨了在艾滋病联合死亡之后关心的关心视角

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In the era of widespread antiretroviral therapy, few studies have explored the perspectives of the relatives involved in caring for people living with HIV (PLHIV) during periods of ill-health leading up to their demise. In this analysis, we explore the process of care for PLHIV as their death approached, from their relatives' perspective. We apply Tronto's care ethics framework that distinguishes between care-receiving among PLHIV on the one hand, and caring about, caring for and care-giving by their relatives on the other. We draw on 44 in-depth interviews conducted with caregivers following the death of their relatives, in seven rural settings in Eastern and Southern Africa. Relatives suggested that prior to the onset of poor health, few of the deceased had disclosed their HIV status and fewer still were relying on anyone for help. This lack of disclosure meant that some caregivers spoke of enduring a long period of worry, and feelings of helplessness as they were unable to translate their concern and "caring about" into "caring for". This transition often occurred when the deceased became in need of physical, emotional or financial care. The responsibility was often culturally prescribed, rarely questioned and usually fell to women. The move to "care-giving" was characterised by physical acts of providing care for their relative, which lasted until death. Tronto's conceptualisation of caring relationships highlights how the burden of caring often intensifies as family members' caring evolves from "caring about", to "caring for", and eventually to "giving care" to their relatives. This progression can lead to caregivers experiencing frustration, provoking tensions with their relatives and highlighting the need for interventions to support family members caring for PLHIV. Interventions should also encourage PLHIV to disclose their HIV status and seek early access to HIV care and treatment services.
机译:在广泛的抗逆转录病毒治疗的时代,很少有研究已经探讨了在不健康的卫生期间患有艾滋病毒(Plhiv)的关注人民参与的亲属的观点,导致他们的消亡。在这种分析中,我们从亲戚的角度探讨了他们的死亡,我们探讨了Plhiv的照顾过程。我们申请Tronto的护理道德框架,一方面关心Plhiv之间的护理,并关心和照顾他们的亲戚在另一方面。在南部非洲的七个农村环境中,我们在亲戚死亡之后汲取了44次与护理人员进行的观众进行过44次进行。亲戚建议,在健康状况不佳之前,未经死者的少数人披露了他们的艾滋病毒状态,仍然依赖于任何人帮助。这种缺乏披露意味着一些护理人员谈到了持久的担忧,并且无助的感觉,因为他们无法翻译他们的关注和“关心”关心“关心”。当死者因需要身体,情感或经济护理时经常发生这种过渡。责任往往是在文化上方的规定,很少受到质疑,通常落在妇女上。 “照顾”的举动是通过为其亲戚提供护理的物理行为的特点,持续到死亡。 Tronto对关怀关系的概念化凸显了照顾的负担如何常被为家庭成员的关怀从“关心”演变而来,以“照顾”,最终“为他们的亲戚”照顾“。这一进展可以导致护理人员遭受挫折,引发与他们的亲属的紧张局势,并突出需要干预措施,以支持为Plhiv提供关怀的家庭成员。干预措施还应鼓励PLHIV披露其艾滋病毒状况,并寻求早期获得艾滋病毒护理和治疗服务。

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