alexa European patient perspectives on the impact of psoriasis: the EUROPSO patient membership survey.


Dermatology Case Reports

Author(s): Dubertret L, Mrowietz U, Ranki A, van de Kerkhof PC, Chimenti S,

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Abstract BACKGROUND: EUROPSO (European Federation of Psoriasis Patient Associations) undertook a Europe-wide survey examining quality of life and patients' perspectives on treatment and their disease. OBJECTIVES: To explore patients' perspectives of psoriasis on their lifestyle and well-being and to gain insight into the effectiveness of and satisfaction with currently available therapies for psoriasis. METHODS: Self-administered questionnaires (n = 50,500) were mailed to members of psoriasis patient associations in Belgium, the Czech Republic, Finland, France, Germany, Italy and the Netherlands. RESULTS: Responses were received from 18,386 patients (36\%), of whom 17,990 had psoriasis. Mean age at onset of psoriasis was 30.5 years, 59\% of respondents had self-reported moderate to severe psoriasis (3\% or greater body surface area involvement) and 30\% had been diagnosed with psoriatic arthritis. The mean Psoriasis Disability Index score was 12.2 (25\% of the maximum score), increasing to 21 (44\%) in patients with more than 10\% body surface area involvement. The greatest impact was on activities of daily living, especially affecting clothing choice, bathing routine and sporting activities. Overall, 77\% replied that psoriasis was a problem or a significant problem. While patients were satisfied with the information and care from their dermatologist (40\% highly satisfied), available treatment options were less satisfactory, with over 70\% reporting only low to moderate satisfaction. CONCLUSIONS: This is the largest survey of people with psoriasis in Europe and shows that psoriasis has a profound impact on quality of life. This article was published in Br J Dermatol and referenced in Dermatology Case Reports

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