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慢性特应性瘙痒中的患者需求与治疗目标:湿疹有影响吗?

Patient Needs and Treatment Goals in Chronic Atopic Pruritus: Does Eczema Make a Difference?

作者信息

Müller Svenja, Zeidler Claudia, Mess Christian, Kahnert Stefan M, Löwe Bernd, Weigel Angelika, Witte Felix, Huck Volker, Nguyen Lynhda, Augustin Matthias, Frank Gina, Agelopoulos Konstantin, Wiegmann Henning, Köchel Ansgar, Conrad Rupert, Schneider Gudrun, Schneider Stefan W, Ständer Sonja, Hansen-Abeck Inga, Abeck Finn

机构信息

Department of Dermatology and Center for Chronic Pruritus (KCP), University Hospital Münster, Münster, Germany.

Department of Dermatology and Venereology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

出版信息

Acta Derm Venereol. 2025 Mar 12;105:adv42773. doi: 10.2340/actadv.v105.42773.

Abstract

Chronic pruritus (≥ 6 weeks) is a frequent symptom in atopic diseases, with phenotypes ranging from non-lesional skin to inflammatory diseases like atopic dermatitis. Data on patients' needs and treatment goals depending on the skin phenotype and disease burden are limited. This study aimed to analyse the impact of distinct phenotypes of chronic atopic pruritus on disease burden and treatment goals. Another objective was to investigate whether the disease burden influences the treatment goals. Patient-reported outcomes of 1,086 adult patients (n = 529 with atopic dermatitis, n = 557 with chronic pruritus on non-lesional skin with atopic skin diathesis) were analysed age- and gender-matched (mean age 49.7 ± 19.0 years; n = 605 female [55.7%]), comparing pruritus intensity (Numeric Rating Scale), quality of life (Dermatology Life Quality Index, ItchyQol), anxiety and depression (Hospital Anxiety and Depression Scale), and patient needs (Patient Needs Questionnaire of the Patient Benefit Index-Pruritus). Although the disease burden was significantly higher in patients with atopic dermatitis (prolonged disease duration, increased quality of life impairment, higher pruritus intensity), the treat-ment goals of both phenotypes matched in 92.6%. The most important needs were to no longer experience itching, find a clear diagnosis and therapy, and have confidence in the therapy.

摘要

慢性瘙痒(≥6周)是特应性疾病中的常见症状,其表型范围从无皮损皮肤到特应性皮炎等炎症性疾病。关于患者需求及取决于皮肤表型和疾病负担的治疗目标的数据有限。本研究旨在分析慢性特应性瘙痒的不同表型对疾病负担和治疗目标的影响。另一个目标是调查疾病负担是否会影响治疗目标。分析了1086例成年患者(n = 529例特应性皮炎患者,n = 557例有特应性皮肤素质的无皮损皮肤慢性瘙痒患者)的患者报告结局,进行了年龄和性别匹配(平均年龄49.7±19.0岁;n = 605例女性[55.7%]),比较瘙痒强度(数字评定量表)、生活质量(皮肤病生活质量指数、ItchyQol)、焦虑和抑郁(医院焦虑抑郁量表)以及患者需求(患者受益指数-瘙痒患者需求问卷)。尽管特应性皮炎患者的疾病负担显著更高(病程延长、生活质量损害加重、瘙痒强度更高),但两种表型的治疗目标在92.6%的方面相匹配。最重要的需求是不再经历瘙痒、找到明确的诊断和治疗方法以及对治疗有信心。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fca8/11926422/55b7d418fc90/ActaDV-105-42773-g001.jpg

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