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非洲盘尾丝虫病皮肤病中的性别与耻辱感

Gender and the stigma of onchocercal skin disease in Africa.

作者信息

Vlassoff C, Weiss M, Ovuga E B, Eneanya C, Nwel P T, Babalola S S, Awedoba A K, Theophilus B, Cofie P, Shetabi P

机构信息

Policy Branch, Canadian International Development Agency, Hull, Que.

出版信息

Soc Sci Med. 2000 May;50(10):1353-68. doi: 10.1016/s0277-9536(99)00389-5.

Abstract

This paper reports results from a multicenter study of gender differences in the stigma associated with onchocercal skin disease (OSD) in five African sites: Cameroon, Ghana, Nigeria (Awka and Ibadan) and Uganda. The studies used a common protocol to compare affected and unaffected respondents, that is, men and women with onchodermatitis in highly endemic areas and respondents from communities with low endemicity or no onchocerciasis. The methods were both quantitative and qualitative, allowing for the comparison of stigma scores and people's verbal descriptions of their experiences and attitudes. Questions to the unaffected were asked after providing them with photographs and short descriptions (vignettes) depicting typical cases. We found that stigma was expressed more openly by the unaffected, who perceived OSD as something foreign or removed from themselves, whereas the affected tended to deny that they experienced stigma as a result of the condition. Gender differences in stigma scores were not significantly different for men and women, but qualitative data revealed that stigma was experienced differently by men and women, and that men and women were affected by it in distinctive ways. Men were more concerned about the impact of the disease on sexual performance and economic prospects, whereas women expressed more concern about physical appearance and life chances, especially marriage. Similar trends were found in the different sites in the responses of affected and unaffected respondents, and differences between them, despite geographical and cultural variations.

摘要

本文报告了一项多中心研究的结果,该研究针对喀麦隆、加纳、尼日利亚(阿库和伊巴丹)和乌干达这五个非洲地区盘尾丝虫性皮肤病(OSD)相关耻辱感的性别差异展开。这些研究采用了通用方案,对受影响和未受影响的受访者进行比较,即高流行地区患有盘尾丝虫性皮炎的男性和女性,以及来自低流行或无盘尾丝虫病社区的受访者。研究方法包括定量和定性两种,以便比较耻辱感得分以及人们对自身经历和态度的口头描述。在向未受影响的受访者提供描绘典型病例的照片和简短描述(案例 vignettes)后,向他们提问。我们发现,未受影响者更公开地表达耻辱感,他们将盘尾丝虫性皮肤病视为外来的或与自己无关的事物,而受影响者则倾向于否认他们因该病而遭受耻辱感。耻辱感得分的性别差异在男性和女性之间并无显著差异,但定性数据显示,男性和女性对耻辱感的体验不同,且受到耻辱感影响的方式也各有特点。男性更关注疾病对性功能和经济前景的影响,而女性则更关注外貌和生活机会,尤其是婚姻。在不同地区,受影响和未受影响的受访者的回答中都发现了类似趋势,以及他们之间的差异,尽管存在地理和文化差异。

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