评价慢性瘙痒症的新型“瘙痒影响量表”(PIS)的构建与验证。

IF 1.9 Q3 DERMATOLOGY
Indian Dermatology Online Journal Pub Date : 2025-02-27 eCollection Date: 2025-03-01 DOI:10.4103/idoj.idoj_835_23
Dileep Saugat, Asit Mittal, Kapil Vyas, Pratap Bhan Kaushik, Lalit Gupta, Kriti Maheshwari
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引用次数: 0

摘要

背景:目前可用的瘙痒评估工具可能并不总是满足印度人口和具有相似社会文化背景的人口的需求。为了克服这一局限性,我们构建并验证了一种新的评估工具“瘙痒影响量表(PIS)”。目的和目标:主要目的是构建和验证新的PIS。次要目的是评估PIS对症状变化的反应性。患者和方法:本研究设计主要目的为横断面,次要目的为纵向。本研究招募了435例不同病因的慢性瘙痒患者,用于构建PIS量表。要求患者填写四种不同的瘙痒测量工具,即数字评定量表(NRS)、皮肤病生活质量指数(DLQI)、12项瘙痒严重程度评分(PSS)和新构建的PIS。PIS是由现有的标准评估工具衍生而来,经过某些修改,以保持量表的心理测量特性和人口的社会文化需求之间的平衡。评估量表的效度和信度。为了检测PIS对瘙痒强度变化的反应,我们对276名患者进行了随访,并指示他们在基线后6周重新填写所有四个量表。通过比较基线时所有量表的平均得分与6周时的平均得分来判断反应性。并对4个量表的得分变化进行相关性比较。结果:PIS与NRS (ρ = 0.938, P < 0.0001)、DLQI (ρ = 0.914, P < 0.01)、12- PSS (ρ = 0.913, P < 0.001)呈正相关(Cronbach α = 0.882)。PIS在间隔3小时的重现性令人满意(Cronbach α = 0.994)。6周重评估时PIS测量的瘙痒变化的反应性与NRS (ρ = 0.689, P值< 0.0001)、DLQI (ρ = 0.586, P值< 0.0001)和12-PSS (ρ = 0.928, P值)的变化具有良好的相关性。局限性:本研究的一个值得注意的局限性是缺乏对不同工具组成的不同项目(在一个结构内)进行比较。结论:新建立的PIS在研究人群中是一种有效的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Construction and Validation of a Novel "Pruritus Impact Scale" (PIS) for Assessment of Chronic Pruritus.

Background: Currently available pruritus assessment tools may not always fulfill the needs of the Indian population and populations who share similar sociocultural backgrounds. To overcome this limitation, a new assessment tool "Pruritus Impact Scale (PIS)" was constructed and validated.

Aims and objectives: The primary objective is to construct and validate the novel PIS. The secondary objective is to evaluate the responsiveness of PIS to changes in symptoms.

Patients and methods: This study design was cross-sectional for the primary objective and longitudinal for the secondary objective. The study recruited 435 patients of chronic pruritus of different etiologies for the construction of the PIS scale. Patients were asked to fill out four different pruritus measuring tools i.e., Numerical Rating Scale (NRS), Dermatology Life Quality Index (DLQI), 12-item Pruritus Severity Score (PSS), and newly constructed PIS. The PIS was derived from existing standard assessment tools with certain modifications to keep a balance of psychometric properties of the scale and the sociocultural needs of the population. The validity and reliability of the scale was assessed. For detecting the response of PIS to change in pruritus intensity, 276 patients were followed and were instructed to refill all four scales at 6 weeks from the baseline. The responsiveness was judged by comparing the mean score of all scales at baseline with the mean score at 6 weeks. In addition, the changes in the scores among all 4 scales were correlated and compared.

Results: PIS showed strong internal consistency (Cronbach α = 0.882) and positively correlated with other validated pruritic tools such as NRS (ρ = 0.938, P < 0.0001), DLQI (ρ = 0.914, P < 0.01) and 12- PSS (ρ = 0.913, P < 0.001) at baseline. PIS showed satisfactory reproducibility at 3-hour intervals (Cronbach α = 0.994). Responsiveness to change in pruritus as measured by PIS at 6 weeks reassessment was correlated well with the changes in NRS (ρ = 0.689, P value < 0.0001), DLQI (ρ = 0.586, P value < 0.0001) and 12-PSS (ρ = 0.928, P value <0.0001).

Limitations: A noteworthy limitation of the present study is the lack of comparison of different items (within a construct) comprised in different tools used for comparison.

Conclusions: The newly constructed PIS is a valid tool in the studied population.

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来源期刊
CiteScore
2.00
自引率
11.80%
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审稿时长
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