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希腊银屑病患者的生活质量和心理社会状况:一项横断面研究。

Quality of life and psychosocial aspects in Greek patients with psoriasis: a cross-sectional study.

作者信息

Kouris Anargyros, Christodoulou Christos, Stefanaki Christina, Livaditis Miltiadis, Tsatovidou Revekka, Kouskoukis Constantinos, Petridis Athanasios, Kontochristopoulos George

机构信息

"Andreas Sygros" Skin Hospital, Athens, Greece.

"Attikon" University Hospital, Athens, Greece.

出版信息

An Bras Dermatol. 2015 Nov-Dec;90(6):841-5. doi: 10.1590/abd1806-4841.20154147.

Abstract

BACKGROUND

Psoriasis is a common, long-term skin disease associated with high levels of psychological distress and a considerable adverse impact on life. The effects of psoriasis, beyond skin affliction, are seldom recognized and often undertreated.

OBJECTIVE

The aim of the study is to evaluate the quality of life, anxiety and depression, self-esteem and loneliness in patients with psoriasis.

METHODS

Eighty-four patients with psoriasis were enrolled in the study. The quality of life, depression and anxiety, loneliness and self-esteem of the patient were assessed using the Dermatology Life Quality Index, Hospital Anxiety and Depression Scale, the UCLA loneliness Scale (UCLA-Version 3) and Rosenberg's Self-esteem Scale, respectively.

RESULTS

The Dermatology Quality of Life Index score among psoriasis patients was 12.61 ± 4.88. They had statistically significantly higher scores according to the Hospital Anxiety and Depression Scale -anxiety subscale (p=0.032)-compared with healthy volunteers. Moreover, a statistically significant difference was found between the two groups concerning the UCLA-scale (p=0.033) and RSES-scale (p<0.0001). Female patients presented with lower self-esteem than male patients.

CONCLUSION

Psoriasis is a distressing, recurrent disorder that significantly impairs quality of life. Therefore, the recognition and future management of psoriasis may require the involvement of multi-disciplinary teams to manage the physical, psychological and social aspects of the condition, as is the case for systemic, long-term conditions.

摘要

背景

银屑病是一种常见的慢性皮肤病,与高水平的心理困扰相关,对生活有相当大的负面影响。银屑病的影响除了皮肤病变外,很少被认识到,而且常常治疗不足。

目的

本研究旨在评估银屑病患者的生活质量、焦虑和抑郁、自尊和孤独感。

方法

84例银屑病患者纳入本研究。分别使用皮肤病生活质量指数、医院焦虑抑郁量表、加州大学洛杉矶分校孤独量表(第3版)和罗森伯格自尊量表评估患者的生活质量、抑郁和焦虑、孤独感和自尊。

结果

银屑病患者的皮肤病生活质量指数评分为12.61±4.88。与健康志愿者相比,他们在医院焦虑抑郁量表焦虑分量表上的得分在统计学上显著更高(p=0.032)。此外,两组在加州大学洛杉矶分校孤独量表(p=0.033)和罗森伯格自尊量表(p<0.0001)上存在统计学显著差异。女性患者的自尊低于男性患者。

结论

银屑病是一种令人痛苦的复发性疾病,严重损害生活质量。因此,银屑病的识别和未来管理可能需要多学科团队的参与,以管理该疾病的身体、心理和社会方面,系统性长期疾病的情况也是如此。

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本文引用的文献

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Patients with psoriasis feel stigmatized.银屑病患者感到被歧视。
Acta Derm Venereol. 2012 Jan;92(1):67-72. doi: 10.2340/00015555-1193.
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Effect of daily stressors on psoriasis: a prospective study.日常应激源对银屑病的影响:一项前瞻性研究。
J Invest Dermatol. 2009 Aug;129(8):2075-7. doi: 10.1038/jid.2008.460. Epub 2009 Feb 5.
7
Quality of life in patients with psoriasis.银屑病患者的生活质量
Health Qual Life Outcomes. 2006 Jun 6;4:35. doi: 10.1186/1477-7525-4-35.
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Psychiatric morbidity in psoriasis: a review.银屑病中的精神疾病:综述
Australas J Dermatol. 2004 Aug;45(3):155-9; quiz 160-1. doi: 10.1111/j.1440-0960.2004.00078.x.

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