银屑病的社会心理影响：身体严重程度、生活质量和污名化。

The psychosocial impact of psoriasis: physical severity, quality of life, and stigmatization.

作者信息

Perrott S B, Murray A H, Lowe J, Mathieson C M

机构信息

Department of Psychology, Mount Saint Vincent University, 166 Bedford Highway, Halifax, Nova Scotia, Canada, B3M 2J6.

出版信息

Physiol Behav. 2000 Sep 15;70(5):567-71. doi: 10.1016/s0031-9384(00)00290-0.

DOI:10.1016/s0031-9384(00)00290-0

PMID:11111012

Abstract

Men (N=58) and women (N=43) living with psoriasis completed questionnaires assessing quality of life and feelings of stigmatization. Physician ratings of disease severity were used in conjunction with these variables to account for psychosocial impact. Results showed that ratings of severity were poor predictors of quality of life and stigmatization. Demographic variables (e.g., sex and education) were also generally poor predictors of psychosocial outcome. It is concluded that attempts to understand the psychological impact of psoriasis in terms of current measures of disease severity and demographic characteristics will be limited.

摘要

患有银屑病的男性（N = 58）和女性（N = 43）完成了评估生活质量和耻辱感的问卷调查。医生对疾病严重程度的评分与这些变量一起用于考量心理社会影响。结果显示，严重程度评分对生活质量和耻辱感的预测性较差。人口统计学变量（如性别和教育程度）通常对心理社会结果的预测性也较差。研究得出结论，试图根据当前疾病严重程度的测量指标和人口统计学特征来理解银屑病的心理影响是有限的。