用于评估慢性瘙痒患者瘙痒强度的标记数量级量表的验证

C. Zeidler, M. Röchter, S. Ständer, M. Pereira
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摘要

简介:常用视觉模拟量表(VAS)、数值评定量表(NRS)和言语评定量表(VRS)评估瘙痒强度。然而,这些量表存在局限性,特别是线性量表(VAS、NRS)的天花板效应和对VRS变化的敏感性降低。在标记震级量表(LMS)中,由一条垂直线组成,口头锚点呈准对数分布,天花板效应被降低,从而允许在量表的高端进行更高的判别性评估。方法:172例患者在30-60分钟内完成两次LMS量表,评估量表的信度,并采用NRS和VAS进行收敛效度分析。对LMS变化的敏感性是通过分析每天两次使用含有薄荷基丙二醇的润肤剂14天后LMS评分的变化来研究的。结果:LMS评估24 h内平均(Cronbach α: 0.955)和最差(Cronbach α: 0.945)瘙痒强度的重测信度极好,LMS与NRS评估最差(r=0.783)和平均(r=0.808)瘙痒强度的相关性强至极强。润肤剂治疗后LMS评分显著降低(P<0.01)。在基线时患有严重瘙痒(VRS≥3)的患者中,我们记录到使用LMS的平均瘙痒强度改善了30.2%,而使用NRS的改善了25.0%;使用LMS的最差瘙痒强度改善了27.8%,而使用NRS的改善了11.1%。大多数患者认为LMS是评估瘙痒强度的合适工具(89.6%),并会再次使用LMS(91.9%)。讨论:LMS是一种被广泛接受的评估CP的合适工具。它对检测严重CP患者瘙痒强度的变化特别有用。
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Validation of the labeled magnitude scale for the assessment of itch intensity in patients with chronic pruritus
Introduction: The visual analogue scale (VAS), the numerical rating scale (NRS), and the verbal rating scale (VRS) are routinely used to assess pruritus intensity. However, these scales have limitations, especially the ceiling effect of linear scales (VAS, NRS) and the reduced sensitivity to change of the VRS. In the labeled magnitude scale (LMS) consisting of a vertical line with verbal anchors distributed quasi-logarithmically, the ceiling effect is reduced, allowing a higher discriminative assessment at the higher end of the scale. Methods: A total of 172 patients completed the LMS twice within 30–60 minutes to assess the reliability of the scale, as well as the NRS and VAS for analyses of convergent validity. Sensitivity to change of the LMS was investigated by analyzing changes in scores after a twice-daily application of an emollient containing menthoxypropanediol for 14 days. Results: Test-retest reliability was excellent for the LMS assessing average (Cronbach α: 0.955) and worst (Cronbach α: 0.945) pruritus intensity in the last 24 hours, while strong to very strong correlations were observed between the LMS and NRS assessing the worst (r=0.783) and average (r=0.808) pruritus intensity, respectively. Treatment with an emollient lead to a significant decrease in LMS scores (P<0.01). In patients with severe pruritus at baseline (VRS ≥3), we recorded a 30.2% improvement of average pruritus intensity using the LMS compared with a 25.0% improvement using the NRS and a 27.8% improvement of worst pruritus intensity using the LMS compared with an 11.1% improvement with the NRS. Most patients considered the LMS an appropriate instrument to assess pruritus intensity (89.6%) and would use it again (91.9%). Discussion: The LMS is an appropriate well-accepted instrument to assess CP. It is especially useful to detect variations in pruritus intensity in patients with severe CP.
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