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本文引用的文献

1
Methods of outcomes measurement in nail psoriasis.甲银屑病的结局测量方法。
Dermatology. 2010;221 Suppl 1:23-8. doi: 10.1159/000316177. Epub 2010 Aug 9.
2
The burden of nail psoriasis: an introduction.指甲银屑病的负担:引言。
Dermatology. 2010;221 Suppl 1:1-5. doi: 10.1159/000316169. Epub 2010 Aug 9.
3
Nail psoriasis in Germany: epidemiology and burden of disease.德国甲银屑病的流行病学和疾病负担。
Br J Dermatol. 2010 Sep;163(3):580-5. doi: 10.1111/j.1365-2133.2010.09831.x. Epub 2010 Apr 28.
4
Co-morbidity and age-related prevalence of psoriasis: Analysis of health insurance data in Germany.共病和与年龄相关的银屑病患病率:德国健康保险数据的分析。
Acta Derm Venereol. 2010 Mar;90(2):147-51. doi: 10.2340/00015555-0770.
5
Development and validation of nail psoriasis quality of life scale (NPQ10).指甲银屑病生活质量量表(NPQ10)的制定与验证。
J Eur Acad Dermatol Venereol. 2010 Jan;24(1):22-7. doi: 10.1111/j.1468-3083.2009.03344.x.
6
Psoriatic nail disease: quality of life and treatment.银屑病甲病:生活质量与治疗。
J Cutan Med Surg. 2009 Sep-Oct;13 Suppl 2:S102-6. doi: 10.2310/7750.2009.00027.
7
Work-related lost productivity and its economic impact on Canadian patients with moderate to severe psoriasis.与工作相关的生产力损失及其对加拿大中重度银屑病患者的经济影响。
J Cutan Med Surg. 2009 Jul-Aug;13(4):192-7. doi: 10.2310/7750.2009.08068.
8
Approach to managing patients with nail psoriasis.指甲银屑病患者的管理方法。
J Eur Acad Dermatol Venereol. 2009 Sep;23 Suppl 1:15-21. doi: 10.1111/j.1468-3083.2009.03364.x.
9
Economic burden of psoriasis compared to the general population and stratified by disease severity.与普通人群相比,银屑病的经济负担及按疾病严重程度分层的情况。
Curr Med Res Opin. 2009 Oct;25(10):2429-38. doi: 10.1185/03007990903185557.
10
Sustained improvement in joint pain and nail symptoms with etanercept therapy in patients with moderate-to-severe psoriasis.中重度银屑病患者使用依那西普治疗后关节疼痛和指甲症状持续改善。
J Eur Acad Dermatol Venereol. 2009 Aug;23(8):896-904. doi: 10.1111/j.1468-3083.2009.03211.x. Epub 2009 May 3.

指甲银屑病作为一种严重程度指标:来自PsoReal研究的结果。

Nail psoriasis as a severity indicator: results from the PsoReal study.

作者信息

Radtke Marc A, Langenbruch Anna K, Schäfer Ines, Herberger Katharina, Reich Kristian, Augustin Matthias

机构信息

Institute for Health Services Research in Dermatology and Nursing, University Medical Center of Hamburg-Eppendorf, Hamburg;

出版信息

Patient Relat Outcome Meas. 2011 Jul;2:1-6. doi: 10.2147/PROM.S14861. Epub 2010 Dec 22.

DOI:10.2147/PROM.S14861
PMID:22915964
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3417918/
Abstract

BACKGROUND

Although nail psoriasis affects a substantial proportion of psoriasis patients and causes significant psychologic distress, few epidemiologic data characterizing patients with nail involvement are available. The aim of this research was to elucidate differences between patients with nail psoriasis and those without any nail involvement, taking quality indicators of health care from the patient's perspective into account.

METHODS

In total, 2449 patient members of the Deutscher Psoriasis Bund, the largest patient organization for psoriasis in Germany, were interviewed in this nationwide, noninterventional, cross-sectional study. Patients with nail psoriasis were compared with patients without any nail involvement with regard to gender, age, disease duration, affected body surface area, health-related quality of life (Dermatology Life Quality Index [DLQI] ED-5D), patient-defined treatment benefit, amount of inpatient treatments, disease duration, and numbers of work days lost.

RESULTS

Data from 2449 patients with psoriasis were analyzed. Overall, 44.8% (1078) of patients were female, mean age was 57.0 ± 11.7 years, and 72.8% had nail involvement and showed higher values for affected body surface area than those without nail involvement (8.3% versus 5.6%, respectively; P < 0.004). Health-related quality of life was significantly lower in patients with nail psoriasis (DLQI 7.2 versus 5.3; ED-5D 60.1 versus 67.3), who had more days off work (9.8 versus 3.3).

CONCLUSION

Nail involvement is an important symptom of psoriasis and is associated with greater disease severity and quality of life impairment. Accordingly, management of psoriasis should include a special focus on nail involvement.

摘要

背景

尽管甲银屑病影响了相当一部分银屑病患者,并导致严重的心理困扰,但关于甲受累患者特征的流行病学数据却很少。本研究的目的是从患者角度考虑医疗保健质量指标,阐明甲银屑病患者与无甲受累患者之间的差异。

方法

在这项全国性、非干预性横断面研究中,对德国最大的银屑病患者组织——德国银屑病联盟的2449名患者成员进行了访谈。将甲银屑病患者与无甲受累患者在性别、年龄、病程、体表面积受累情况、健康相关生活质量(皮肤病生活质量指数[DLQI]、欧洲五维健康量表[ED-5D])、患者定义的治疗获益、住院治疗次数、病程以及误工天数等方面进行比较。

结果

对2449例银屑病患者的数据进行了分析。总体而言,44.8%(1078例)的患者为女性,平均年龄为57.0±11.7岁,72.8%的患者有甲受累,其体表面积受累值高于无甲受累患者(分别为8.3%和5.6%;P<0.004)。甲银屑病患者的健康相关生活质量显著较低(DLQI为7.2对5.3;ED-5D为60.1对67.3),误工天数更多(9.8天对3.3天)。

结论

甲受累是银屑病的一个重要症状,与更严重的疾病程度和生活质量受损相关。因此,银屑病的管理应特别关注甲受累情况。