Tarwireyi F
University of Zimbabwe, College of Health Sciences, Department of Paediatrics and Child Health, P.O. Box A 178, Avondale, Harare, Zimbabwe.
Cent Afr J Med. 2005 Jul-Aug;51(7-8):71-6.
To assess how people living with HIV and AIDS reacted to the knowledge of the infection and how they are coping with stigma and discrimination.
The study was conducted in the two high density urban suburbs of Mabvuku and Tafara in Harare, Zimbabwe.
The study was a descriptive cross sectional survey.
A total of 600 participants (160 men and 440 women) who had received their HIV results after Voluntary Counselling and Testing for HIV at the Zimbabwe AIDS Prevention and Support Organization (ZAPSO) Mabvuku/Tafara Voluntary Counselling and Testing Centre were interviewed.
Reactions to the diagnosis of HIV, disclosure of sero-status, experiences of self, family and community induced stigma and discrimination, coping mechanisms and desired interventions to reduce stigma.
The majority, 61.7%, had been diagnosed HIV positive less than two years at the time of the study. While 33.3% felt hurt, 41% were immediately depressed when they discovered they were HIV positive. Eighty five percent had not disclosed their sero-status to anyone. While 55% experience self induced stigma, 56.7% experienced family induced and 38.3% experienced community induced stigma. People living with HIV and AIDS were coping with stigma through withdrawal (60%); joining support groups (83.3%); seeking counselling (95%) and praying (86.7%). Encouraging community counselling and HIV testing with disclosure of status was perceived by 98.3% of the respondents as an effective method to reduce HIV and AIDS related stigma and discrimination.
While non disclosure of sero status is still high, self, family and community induced stigma pose a big challenge. Withdrawal (used mostly by men), seeking counselling and joining support groups (used mostly by older women) are the common coping behaviours being used by HIV positive clients. There is need to improve counselling capacities so as to meet the demands from a stigma reduction perspective as well as from a coping perspective.
评估艾滋病毒感染者和艾滋病患者对感染情况的知晓反应,以及他们如何应对耻辱感和歧视。
该研究在津巴布韦哈拉雷的马布武库和塔法拉这两个高密度城市郊区开展。
该研究为描述性横断面调查。
对在津巴布韦艾滋病预防与支持组织(ZAPSO)马布武库/塔法拉自愿咨询检测中心接受自愿咨询检测后得知艾滋病毒检测结果的600名参与者(160名男性和440名女性)进行了访谈。
对艾滋病毒诊断的反应、血清学状态的披露、自我、家庭和社区引发的耻辱感和歧视经历、应对机制以及减少耻辱感所需的干预措施。
在研究时,大多数人(61.7%)被诊断为艾滋病毒阳性不到两年。发现自己艾滋病毒呈阳性时,33.3%的人感到受伤,41%的人立即情绪低落。85%的人未向任何人透露其血清学状态。55%的人有自我引发的耻辱感,56.7%的人有家庭引发的耻辱感,38.3%的人有社区引发的耻辱感。艾滋病毒感染者和艾滋病患者通过回避(60%)、加入支持小组(83.3%)、寻求咨询(95%)和祈祷(86.7%)来应对耻辱感。98.3%的受访者认为鼓励社区咨询和艾滋病毒检测并披露检测结果是减少与艾滋病毒和艾滋病相关的耻辱感和歧视的有效方法。
虽然血清学状态的未披露率仍然很高,但自我、家庭和社区引发的耻辱感构成了巨大挑战。回避(主要为男性采用)、寻求咨询和加入支持小组(主要为老年女性采用)是艾滋病毒阳性患者常用的应对行为。有必要提高咨询能力,以便从减少耻辱感以及应对的角度满足需求。