特应性皮炎瘙痒的评估:瘙痒严重程度量表(SPS)的验证

G. Yosipovitch, E. Simpson, A. Bushmakin, J. Cappelleri, T. Luger, S. Ständer, W. Tom, K. Benjamin, W. Ports, A. Tallman, H. Tan, R. Gerber
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引用次数: 8

摘要

简介:瘙痒是特应性皮炎(AD)的主要特征,也是最令人烦恼的症状。瘙痒严重程度量表(SPS)是一个4分的评分量表,改编自特应性皮炎严重程度指数,以提供24小时回忆期内瘙痒严重程度的测量。本分析的目的是评估SPS在AD中的定性和定量有效性。方法:对美国AD患者的SPS内容效度进行定性评价。SPS的心理测量特性评估使用了两项研究crisaborole治疗轻中度AD的3期试验的数据(研究AD-301: NCT02118766;研究AD-302: NCT02118792)。结果:14例患者被纳入定性分析,由于SPS的单项目、单概念性质,被认为是足够的。瘙痒是最常见的症状,美国英语(n=9)和美国西班牙语(n=5)的SPS易于理解和完成。心理测量分析使用了来自1344名患者的数据。重测信度分析表明,单次SPS观测的类内相关系数为0.54,至少2次SPS观测的类内相关系数为0.70。SPS评分与研究者静态全局评估(ISGA)评分、生活质量测量和AD 5个体征中的4个相关(Pearson相关性,第29天≥0.40)。无病/清组(ISGA 0)与重病组(ISGA 4)的评分差异为0.80。临床重要差异估计为0.20,临床重要反应估计至少比基线降低0.19点。讨论:SPS是一种评估AD患者瘙痒的合适工具,也是一种有效可靠的瘙痒严重程度测量方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessment of pruritus in atopic dermatitis: validation of the Severity of Pruritus Scale (SPS)
Introduction: Pruritus, or itch, is a central feature of atopic dermatitis (AD) and is often cited as the most bothersome symptom. The Severity of Pruritus Scale (SPS) is a 4-point rating scale adapted from the Atopic Dermatitis Severity Index to provide a measure of pruritus severity within a 24-hour recall period. The objective of this analysis was to assess the qualitative and quantitative validity of the SPS in AD. Methods: Content validity of the SPS was evaluated qualitatively in US patients with AD. Psychometric properties of the SPS were evaluated using data from 2 phase 3 trials conducted to investigate crisaborole in mild to moderate AD (study AD-301: NCT02118766; study AD-302: NCT02118792). Results: Fourteen patients were included in the qualitative analysis, considered adequate because of the single-item, single-concept nature of the SPS. Itch was the most prevalent symptom, and the SPS was easily understood and completed in US English (n=9) and US Spanish (n=5). The psychometric analysis used data from 1344 patients. Test-retest reliability analysis identified an intraclass correlation coefficient of 0.54 for a single SPS observation, and at least 0.70 when at least 2 SPS observations were averaged. SPS scores correlated with Investigator’s Static Global Assessment (ISGA) scores, measures of quality of life, and 4 of 5 signs of AD (Pearson correlations, ≥0.40 at day 29). The difference in score between the no disease group/clear (ISGA 0) and the severe disease group (ISGA 4) was 0.80. The clinically important difference was estimated to be 0.20 and the clinically important response was estimated to be at least a 0.19-point reduction from baseline. Discussion: The SPS is an appropriate tool to assess itch in patients with AD and is a valid and reliable measure of pruritus severity.
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