North-West University, Potchefstroom Campus, South Africa.
Int J Nurs Stud. 2010 Apr;47(4):475-86. doi: 10.1016/j.ijnurstu.2009.09.008. Epub 2009 Oct 24.
Descriptive literature exists on the effects of HIV-related stigma on the lives of people living with HIV infection but few empirical studies have measured perceived HIV stigma nor explored its potential relationship to quality of life (QoL) over time in people living with HIV infection.
A cohort study of a purposive convenient sample of 1457 HIV-positive persons was followed for one year in a longitudinal design that examined the effects of stigma and the life satisfaction dimension of the HIV/AIDS Targeted Quality of Life Instrument (HAT-QOL) over time, as well as the influence of other demographic and assessed social variables. Data were collected three times about six months apart from December 2005 to March 2007.
The average age in this sample was 36.8 years (SD=8.78, n=1454) and 72.7% (n=1056) were female. The initial sample of participants was balanced among the five countries: Lesotho, Malawi, South Africa, Swaziland, and Tanzania. An attrition analysis demonstrated few demographic differences between those who remained in the study 12 months later compared with those at baseline. However, those who completed the study and who answered the QoL questions had significantly higher life satisfaction scores at baseline than those who left the study. There was a general increase in the report of life satisfaction QoL in all countries over the one-year period. However, as stigma scores increased over time there was a significant decrease in life satisfaction with differing rates of change by country. Certain factors had a positive influence on life satisfaction QoL: positive HIV media reports, taking antiretrovirals, reduced symptom intensity, and disclosure to a friend.
This cohort study is the first to document empirically in a longitudinal sample, that perceived HIV stigma has a significantly negative and constant impact upon life satisfaction QoL for people with HIV infection. In the absence of any intervention to address and reduce stigmatization, individuals will continue to report poorer life satisfaction evidenced by reduced living enjoyment, loss of control in life, decreased social interactivity, and decreased perceived health status.
现有的描述性文献探讨了艾滋病相关耻辱感对艾滋病病毒感染者生活的影响,但很少有实证研究测量过艾滋病感染者的感知艾滋病耻辱感,也没有探讨其随时间推移与艾滋病病毒感染者生活质量(QoL)之间的潜在关系。
本研究采用纵向设计,对 1457 名艾滋病病毒阳性者进行了一项基于目的的方便样本队列研究,在 1 年的随访期内,考察了耻辱感和艾滋病/艾滋病针对性生活质量工具(HAT-QOL)的生活满意度维度随时间的变化情况,以及其他人口统计学和评估的社会变量的影响。数据于 2005 年 12 月至 2007 年 3 月间,每隔六个月收集三次。
该样本的平均年龄为 36.8 岁(SD=8.78,n=1454),72.7%(n=1056)为女性。最初的参与者样本在莱索托、马拉维、南非、斯威士兰和坦桑尼亚这五个国家之间保持平衡。一项损耗分析表明,与基线相比,12 个月后仍留在研究中的参与者在人口统计学方面差异不大。然而,完成研究并回答生活质量问题的参与者,其基线生活满意度评分明显高于离开研究的参与者。在一年的时间里,所有国家的生活满意度 QoL 报告都普遍有所提高。然而,随着耻辱感评分随时间的推移而增加,生活满意度呈显著下降趋势,且各国的变化率不同。某些因素对生活满意度 QoL 有积极影响:积极的艾滋病媒体报道、服用抗逆转录病毒药物、症状强度降低以及向朋友透露病情。
本队列研究首次在纵向样本中实证记录,感知艾滋病耻辱感对艾滋病病毒感染者的生活满意度 QoL 具有显著的负面影响和持续影响。在没有任何干预措施来解决和减少污名化的情况下,个体将继续报告较差的生活满意度,表现为生活享受减少、生活失去控制、社交互动减少和健康感知下降。