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验证斑块状银屑病患者的瘙痒峰值数字评分量表:一项 2 期研究的结果。

Validation of the Peak Pruritus-Numerical Rating Scale in patients with chronic plaque psoriasis: results from a phase 2 study.

机构信息

Dermatology Consulting Services, PLLC, High Point, NC, USA.

Pfizer Inc, Groton, CT, USA.

出版信息

Int J Dermatol. 2024 Dec;63(12):e375-e382. doi: 10.1111/ijd.17428. Epub 2024 Aug 19.

DOI:10.1111/ijd.17428
PMID:39160651
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11588994/
Abstract

BACKGROUND

Pruritus is a common, bothersome symptom for patients with mild-to-moderate plaque psoriasis (PsO), yet no validated scale assesses it in this patient population. We aimed to validate the Peak Pruritus-Numerical Rating Scale (PP-NRS) using data from a Phase 2b study investigating the efficacy of brepocitinib in patients with mild-to-moderate chronic PsO.

METHODS

Patients completed the PP-NRS daily from baseline for the first 2 weeks after the dose administration and subsequently only on visit days. Test-retest reliability (intraclass correlation coefficient [ICC]), construct validity (known group validity and convergent validity), ability to detect change, and meaningful within-patient change (MWPC) were evaluated using correlation and regression analyses.

RESULTS

The PP-NRS demonstrated acceptable test-retest reliability (ICC: 0.86-0.89). Known-group evidence demonstrated that PP-NRS scores could discriminate between different degrees of disease severity. Convergent validity was supported by significant correlation coefficients between the PP-NRS and Patient Global Assessment (PtGA), Dermatology Life Quality Index, and Psoriasis Symptom Inventory, which generally exceeded 0.50. The ability to detect change was evidenced by an approximately linear relationship between changes in PP-NRS and Physician Global Assessment or PtGA of psoriasis scores. The value of 2.8 was determined as the MWPC for the PP-NRS.

CONCLUSIONS

PP-NRS is a reliable, practical test for assessing pruritus in mild-to-moderate PsO clinical trials.

GOV IDENTIFIER

NCT03850483.

摘要

背景

瘙痒是轻度至中度斑块状银屑病(PsO)患者常见且令人困扰的症状,但没有经过验证的量表能够评估此类患者的瘙痒程度。我们旨在使用评估 Brepocitinib 治疗轻度至中度慢性 PsO 患者疗效的 2b 期研究数据,对瘙痒峰值数字评分量表(PP-NRS)进行验证。

方法

患者在给药后前 2 周的每天和随后的就诊日完成 PP-NRS 评估。采用相关性分析和回归分析评估重测信度(组内相关系数 [ICC])、结构效度(已知组有效性和收敛效度)、识别变化的能力和患者的有意义变化(MWPC)。

结果

PP-NRS 显示出可接受的重测信度(ICC:0.86-0.89)。已知组证据表明,PP-NRS 评分可区分不同严重程度的疾病。PP-NRS 与医生整体评估(PGA)、皮肤病生活质量指数和银屑病症状量表之间具有显著的相关性,通常超过 0.50,这支持了收敛效度。PP-NRS 能够识别变化,其评分变化与 PGA 或 PtGA 评分的变化之间呈近似线性关系。PP-NRS 的 MWPC 值确定为 2.8。

结论

PP-NRS 是一种可靠、实用的工具,可用于评估轻度至中度斑块状银屑病临床试验中的瘙痒。

GOV IDENTIFIER

NCT03850483

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6474/11588994/cc22e81a6d4e/IJD-63-e375-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6474/11588994/7dd663bce942/IJD-63-e375-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6474/11588994/cc22e81a6d4e/IJD-63-e375-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6474/11588994/7dd663bce942/IJD-63-e375-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6474/11588994/cc22e81a6d4e/IJD-63-e375-g001.jpg

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Efficacy and safety of topical brepocitinib cream for mild-to-moderate chronic plaque psoriasis: a phase IIb randomized double-blind vehicle-controlled parallel-group study.外用巴瑞替尼乳膏治疗轻度至中度慢性斑块状银屑病的疗效和安全性:一项IIb期随机双盲赋形剂对照平行组研究。
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