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斑秃患者的健康相关生活质量:一项基于常模比较的日本调查结果

Health-related quality of life in patients with alopecia areata: Results of a Japanese survey with norm-based comparisons.

作者信息

Ito Taisuke, Kamei Kazumasa, Yuasa Akira, Matsumoto Fumihiro, Hoshi Yayoi, Okada Masafumi, Noto Shinichi

机构信息

Department of Dermatology, Hamamatsu University School of Medicine, Hamamatsu, Japan.

Inflammation and Immunology Medical Affairs, Pfizer Japan Inc., Tokyo, Japan.

出版信息

J Dermatol. 2022 Jun;49(6):584-593. doi: 10.1111/1346-8138.16364. Epub 2022 Mar 28.

Abstract

Alopecia areata (AA) is a non-scarring hair loss disorder affecting approximately 2% of the global population. AA is reported to have a significant negative impact on the emotional and psychological well-being of the patients. This study aimed to evaluate the health-related quality of life (HRQoL) of Japanese patients with AA in comparison to the Japanese population norms (national standard values for Japanese) using Short Form Health Survey 36 Item Version 2.0 (SF-36v2). The study also aimed to access the negative effect of AA on patients' daily lives and the proportion of patients having anxiety and/or depression. This cross-sectional, non-interventional web-based survey study included 400 participants aged 17-84 years currently suffering from medically diagnosed AA. The assessment tools integrated in the online questionnaire included SF-36v2, the Dermatology Life Quality Index (DLQI), and the Hospital Anxiety and Depression Scale (HADS). All outcome measures from the tools were evaluated across the study population. SF-36v2 subscale scores for patients with AA revealed lower scores specifically for mental health (45.7 ± 10.1 points), social functioning (45.8 ± 10.9 points), vitality (46.2 ± 9.8 points), and role emotional (46.9 ± 11.6 points) as compared to the Japanese population norms of 50 ± 10 points each. The DLQI questionnaire-based analysis indicated that 32.1% of respondents showed a moderate to extremely large effect on their lives; and HADS-A (anxiety) and HADS-D (depression) scores categorized 46.0% and 41.8% respondents as doubtful-to-definite cases, respectively. Multivariate linear regression revealed that hair loss range, age, comorbidities, and depression significantly worsened DLQI scores. In conclusion, the results of this survey demonstrated that a significant decrease in the HRQoL scores was observed in Japanese patients with AA in comparison with the national norms. Hence, emphasis on mental health is crucial for AA management.

摘要

斑秃(AA)是一种非瘢痕性脱发疾病,影响着全球约2%的人口。据报道,AA对患者的情绪和心理健康有重大负面影响。本研究旨在使用简明健康调查问卷第2.0版(SF-36v2),评估日本斑秃患者与日本人群规范(日本人的国家标准值)相比的健康相关生活质量(HRQoL)。该研究还旨在了解AA对患者日常生活的负面影响以及患有焦虑和/或抑郁的患者比例。这项横断面、非干预性的基于网络的调查研究纳入了400名年龄在17至84岁之间、目前患有医学诊断斑秃的参与者。在线问卷中整合的评估工具包括SF-36v2、皮肤病生活质量指数(DLQI)和医院焦虑抑郁量表(HADS)。对工具中的所有结果指标在研究人群中进行了评估。与日本人群规范中每项均为50±10分相比,AA患者的SF-36v2子量表得分显示,在心理健康(45.7±10.1分)、社会功能(45.8±10.9分)、活力(46.2±9.8分)和角色情感(46.9±11.6分)方面得分较低。基于DLQI问卷的分析表明,32.1%的受访者对其生活有中度至极大影响;HADS-A(焦虑)和HADS-D(抑郁)得分分别将46.0%和41.8%的受访者归类为可疑至确诊病例。多变量线性回归显示,脱发范围、年龄、合并症和抑郁显著恶化了DLQI得分。总之,这项调查结果表明,与国家标准相比,日本斑秃患者的HRQoL得分显著下降。因此,重视心理健康对斑秃的管理至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6592/9314875/83955603b07a/JDE-49-584-g001.jpg

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