The Hidradenitis Suppurativa Quality of Life (HiSQOL) score: development and validation of a measure for clinical trials

被引:87
作者
Kirby, J. S. [1 ]
Thorlacius, L. [2 ,3 ]
Villumsen, B. [4 ]
Ingram, J. R. [5 ]
Garg, A. [6 ]
Christensen, K. B. [2 ,3 ]
Butt, M. [1 ]
Esmann, S. [2 ,3 ]
Tan, J. [7 ]
Jemec, G. B. E. [2 ,3 ]
机构
[1] Penn State Hlth Milton S Hershey Med Ctr, Dept Dermatol, Hershey, PA USA
[2] Zealand Univ Hosp, Dept Dermatol, Roskilde, Denmark
[3] Univ Copenhagen, Fac Hlth Sci, Copenhagen, Denmark
[4] Patients Assoc HS Denmark, Copenhagen, Denmark
[5] Cardiff Univ, Univ Wales Hosp, Div Infect & Immun, Heath Pk, Cardiff CF14 4XN, S Glam, Wales
[6] Donald & Barbara Zucker Sch Med Hofstra Northwell, Dept Dermatol, New Hyde Pk, NY USA
[7] Univ Western Ontario, Dept Med, Windsor, ON, Canada
基金
美国医疗保健研究与质量局;
关键词
CONCEPTUAL-MODEL; HEALTH; PATHOGENESIS; VALIDITY; SCALES; IMPACT;
D O I
10.1111/bjd.18692
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background Hidradenitis suppurativa (HS) is a chronic, inflammatory condition that can have a large negative impact on health-related quality of life (HRQOL). A reliable and validated measure of HS-specific HRQOL in clinical studies is needed. Objectives To develop and validate the Hidradenitis Suppurativa Quality Of Life (HiSQOL (c)) scale, for clinical trial measurement of HS-specific HRQOL. Methods In stage 1, qualitative concept elicitation interviews were conducted with patients with HS in Denmark (n = 21) and the U.S.A. (n = 21). In stage 2, cognitive debriefing interviews were performed with U.S. (n = 30) and Danish patients with HS (n = 30). In stage 3 an observational study of 222 patients with HS in the U.S.A. was conducted for item reduction, measure validation and assessment of psychometric properties. In stage 4, an observational study of 215 patients with HS in Denmark was conducted to confirm the psychometric structure derived in stage 3. In both studies the Dermatology Life Quality Index, Hospital Anxiety and Depression Scale and numerical rating scale for pain were also included. Results In concept elicitation, 99 items were generated, which were reduced to 41 after removing duplicates. In cognitive debriefing, two items were added and one item removed. A 42-item instrument was psychometrically assessed. Based on psychometric analyses and patient input, the instrument was reduced to 17 items that had strong psychometric properties in both the U.S. and Danish samples. Conclusions The HiSQOL is a reliable and valid instrument to measure HS-specific HRQOL in clinical trials.
引用
收藏
页码:340 / 348
页数:9
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