“我有希望,但我很担心”:对感染围产期获得性艾滋病毒的青少年和年轻成年人的养育观点。

Cynthia D. Fair, Ashley Jutras
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引用次数: 0

摘要

患有围产期获得性艾滋病毒(PHIV)的青少年可以很好地进入青年期。关于艾滋病毒对青少年和年轻人(AYA)的社会影响已经有了广泛的研究。然而,很少有研究考察他们更广泛的家庭体系。本研究为质性探索专案,检视照顾者抚养aids患者的观点。方法18名照顾14岁以上感染艾滋病毒的青少年和年轻人的护理人员完成了半结构化的录音访谈。问题集中在青少年发展的突出方面,以及孩子一生中为人父母的经历。脚本是针对突发主题进行编码的。结果过去和现在的护理经历与HIV的污名化本质一致。与药物依从性和性行为相关的日常担忧很常见。面向未来的期望标志着希望,以及对继续斗争的承认。讨论卫生保健系统的负面经历强调了对艾滋病毒相关污名进行持续教育的必要性。研究结果表明,像其他正常发育青少年的父母一样,照顾者可能需要在性问题上得到支持。此外,护理人员对提供AYA的适当监督水平表示担忧,因为他们对自己的健康承担了更多的责任。社会心理和卫生保健专业人员之间的合作,以确定支持战略,将使护理人员和艾滋病毒感染者都受益。(PsycInfo Database Record (c) 2022 APA,版权所有)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
"I have hope, but I'm worried": Perspectives on parenting adolescents and young adults living with perinatally-acquired HIV.
INTRODUCTION Youth with perinatally-acquired HIV (PHIV) are living well into young adulthood. There has been extensive research on the social impacts of PHIV on adolescents and young adults (AYA). However, little research has examined their broader family system. This qualitative exploratory project examined the perspectives of caregivers raising AYA with PHIV. METHOD Eighteen caregivers who cared for adolescents and young adults with PHIV over the age of 14 completed semistructured audio-recorded interviews. Questions focused on salient aspects of adolescent development and parenting experiences over the course of their child's life. Transcripts were coded for emergent themes. RESULTS Past and present caregiving experiences were consistently contextualized by the stigmatized nature of HIV. Daily concerns related to medication adherence and sexual behavior were common. Future-oriented expectations were marked by hope, as well as an acknowledgment of continued struggle. DISCUSSION Negative experiences with the health care system underscore the need for ongoing education about HIV-related stigma. Findings suggest that caregivers, like other parents of typically developing youth, may need support addressing sexuality. Additionally, caregivers expressed concerns over the appropriate levels of supervision to offer their AYA as they assumed more responsibility for their own health. Collaboration among psychosocial and health care professionals to identify support strategies will benefit both caregivers and AYA living with PHIV. (PsycInfo Database Record (c) 2022 APA, all rights reserved).
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