Suppr超能文献

银屑病患者的皮肤病特异性和通用心理测量方法

Skin-Disease Specific and Generic Psychometric Measures in Patients with Psoriasis.

作者信息

Kowalewska Beata, Jankowiak Barbara, Krajewska-Kułak Elżbieta, Milewski Rafał, Sobolewski Marek

机构信息

The Department of Integrated Medical Care, Medical University in Białystok, 7A MC Skłodowskiej Str., 15-096, Białystok, Poland.

Doctoral Studies at Faculty of Health Sciences, Department of Primary Healthcare, Medical University of Bialystok, Białystok, Poland.

出版信息

Dermatol Ther (Heidelb). 2021 Dec;11(6):1999-2015. doi: 10.1007/s13555-021-00609-6. Epub 2021 Sep 28.

Abstract

INTRODUCTION

Psychosocial problems of patients with chronic dermatoses, such as psoriasis, add to their somatic ailments, which results in the lack of illness acceptance, lowered self-esteem, deteriorated quality of life, and an array of somatic comorbidities. The aim of this study was to analyze the effect of psoriasis on the quality of life, sense of stigmatization, self-esteem, and satisfaction with life in patients with psoriasis.

METHODS

The study was based on a short survey prepared by the authors and five validated scales: Dermatology Life Quality Index (DLQI), 6-Item Stigmatization Scale, 33-Item Feelings of Stigmatization Questionnaire, Rosenberg Self-Esteem Scale (SES), and Satisfaction With Life Scale (SWLS). The study included 111 patients with psoriasis (46.8% women and 53.2% men). The inclusion criteria of the study were the diagnosis of plaque psoriasis and written informed consent to participate.

RESULTS

DLQI scores ranged between 0 and 28 points (pts) (mean 10.8 pts). Mean stigmatization scores determined with the 33- and 6-Item Stigmatization Scale were 81.6 pts and 7.5 pts, respectively. The mean SWLS score for the study group (18.5 pts) was slightly below the average. The mean score SES of 27 pts implies that the study respondents' self-esteem level was slightly above the average.

CONCLUSIONS

Satisfaction with life turned out to be significantly modulated by overall stigmatization level on the 33-Item Stigmatization Scale (the stronger the sense of stigmatization, the lower the satisfaction with life) and education (respondents with higher education presented with higher satisfaction with life than those with non-higher education).

摘要

引言

慢性皮肤病患者,如银屑病患者,存在心理社会问题,这会加重他们的躯体疾病,进而导致患者不接受疾病、自尊降低、生活质量恶化以及一系列躯体合并症。本研究的目的是分析银屑病对银屑病患者生活质量、耻辱感、自尊和生活满意度的影响。

方法

本研究基于作者编制的一份简短调查问卷以及五个经过验证的量表:皮肤病生活质量指数(DLQI)、6项耻辱感量表、33项耻辱感问卷、罗森伯格自尊量表(SES)和生活满意度量表(SWLS)。该研究纳入了111例银屑病患者(女性占46.8%,男性占53.2%)。研究的纳入标准为斑块状银屑病的诊断以及参与研究的书面知情同意书。

结果

DLQI评分在0至28分之间(平均10.8分)。用33项和6项耻辱感量表测定的平均耻辱感评分分别为81.6分和7.5分。研究组的平均SWLS评分为18.5分,略低于平均水平。平均SES评分为27分,这意味着研究受访者的自尊水平略高于平均水平。

结论

结果表明,33项耻辱感量表上的总体耻辱感水平(耻辱感越强,生活满意度越低)和教育程度(受过高等教育的受访者比未受过高等教育的受访者生活满意度更高)对生活满意度有显著调节作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e414/8611141/de3e58bf7249/13555_2021_609_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验