Quality of life and stigmatization in people with skin diseases in Europe: A large survey from the ‘burden of skin diseases’ EADV project

Author:

Gisondi Paolo1ORCID,Puig Luis2ORCID,Richard Marie Aleth3ORCID,Paul Carle4,Nijsten Tamar5,Taieb Charles6ORCID,Stratigos Alex7,Trakatelli Myrto8,Salavastru Carmen9,

Affiliation:

1. Section of Dermatology and Venereology, Department of Medicine University of Verona Verona Italy

2. Department of Dermatology, Hospital de la Santa Creu i Sant Pau Universitat Autònoma de Barcelona Barcelona Spain

3. CEReSS‐EA 3279, Research Centre in Health Services and Quality of Life Aix Marseille University, Dermatology Department University Hospital Timone, Assistance Publique Hôpitaux de Marseille, APHM Marseille France

4. INSERM Infinity U1291 Université de Toulouse et CHU Toulouse France

5. Department of Dermatology Erasmus MC Rotterdam The Netherlands

6. Patients Priority EMMA Fontenay Sous‐Bois France

7. Department of Dermatology, Andreas Syggros Hospital, Medical School National and Kapodistrian University of Athens Athens Greece

8. Second Department of Dermatology and Venerology of Aristotle School of Medicine Papageorgiou Hospital Thessaloniki Greece

9. Department of Pediatric Dermatology Carol Davila University of Medicine and Pharmacy, Colentina Clinical Hospital Bucharest Romania

Abstract

AbstractBackgroundSeveral large studies on the burden of skin diseases have been performed in patients recruited in hospitals or clinical centres, thus missing people with skin diseases who do not undergo a clinical consultation.ObjectivesTo evaluate the burden of the most common dermatological diseases in adult patients across Europe, in terms of quality of life, work life, and stigmatization.MethodsPopulation‐based survey on a representative sample of the European general population aged 18 years or older. Participants who declared to have had one or more skin problem or disease during the previous 12 months completed the Dermatology Life Quality Index questionnaire, and answered questions regarding the impact of their skin disease on daily and work life, anxiety/depression, and stigmatization.ResultsThe study population included 19,915 individuals, 44.7% of whom were men. Quality of life was particularly impaired in people with hidradenitis suppurativa (HS), and sexually transmitted diseases. About a half of participants with acne, alopecia, or chronic urticaria, and about 40% of those with atopic dermatitis (AD), skin cancers, or psoriasis reported a modest to extremely large effect of the disease on their quality of life. Overall, 88.1% of participants considered their skin disease as embarrassing in personal life and 83% in work life. About half of the respondents reported sleeping difficulty, feeling tired, and impact of the disease on taking care of themselves. Concerning stigmatization, 14.5% felt to have been rejected by others because of the skin disease, and 19.2% to have been looked at with disgust. Anxiety and depression were frequently reported by patients with all the diseases.ConclusionsSkin diseases may heavily affect patients' daily and work life, and cause feelings of stigmatization. An early intervention is needed to avoid consequences on the patients' life course.

Publisher

Wiley

Subject

Infectious Diseases,Dermatology

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. The Role of the Gut Microbiome and Microbial Dysbiosis in Common Skin Diseases;International Journal of Molecular Sciences;2024-02-06

2. Learning lessons for the battle against disease burden and stigmatization in chronic skin diseases: Call for action needed?;Journal of the European Academy of Dermatology and Venereology;2023-10

3. The burden of skin disease in Europe;Journal of the European Academy of Dermatology and Venereology;2023-10

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