The Psychosocial Impact of Atopic Dermatitis

被引：28

作者：

Gochnauer, Heather ^{[1
,2
]}

Valdes-Rodriguez, Rodrigo ^{[1
,2
]}

Cardwell, Leah ^{[3
]}

Anolik, Rachel B. ^{[1
]}

机构：

[1] Reading Hlth Phys Network, Dermatol Sect, Wyomissing, PA 19610 USA

[2] Temple Univ, Dept Dermatol, Lewis Katz Sch Med, Philadelphia, PA 19122 USA

[3] Wake Forest Univ, Bowman Gray Sch Med, Dept Dermatol, Winston Salem, NC 27103 USA

来源：

MANAGEMENT OF ATOPIC DERMATITIS: METHODS AND CHALLENGES | 2017年 / 1027卷

关键词：

Atopic dermatitis; Quality of life index; Psychosocial impact atopic dermatitis; QUALITY-OF-LIFE; SKIN-DISEASE; INITIAL VALIDATION; CHILDHOOD ECZEMA; YOUNG-CHILDREN; TIME SPENT; SEVERITY; FAMILIES; HEALTH; SLEEP;

D O I：

10.1007/978-3-319-64804-0_6

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

Atopic dermatitis is a chronic skin condition which has significant psychosocial and quality of life impact. The condition causes physical discomfort, emotional distress, embarrassment, social stigma and daily activity limitation. In an effort to assess these aspects of disease burden, quality of life measurement tools were developed. Through use of these tools, we have expanded our knowledge of the psychosocial and quality of life burden of this condition. A variety of quality of life assessment tools exist, yet there is no consensus on which tool is best suited to assess the quality of life impact of atopic dermatitis. Research studies assessing quality of life in atopic dermatitis patients utilize a variety of quality of life measurement tools; this complicates comparisons across research studies. Though comparison across studies is difficult, the data echoes tremendous overall burden of disease, especially pertaining to psychosocial status and life quality.

引用

页码：57 / 69

页数：13

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