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A survey of the social and psychological effects of psoriasis

RAMSAY, B., O'REAGAN, MYRA·1988·British Journal of Dermatology

Abstract

One hundred and four consecutive patients with psoriasis who were being treated in two Dublin dermatology hospital units answered a questionnaire. Social and emotional morbidity was present for many patients despite access to modern treatment facilities. Fifty five percent of patients had never experienced a complete remission from their psoriasis. A large percentage of patients avoided common social activities, for example swimming and sports; 50% felt that psoriasis had inhibited their sexual relationships and 11% of patients said they would avoid having children in case their offspring should develop the condition. Thirty-six per cent felt the hospital doctor spent most of the consultation time writing prescriptions and 59% of patients had never been given an explanatory pamphlet or book about psoriasis. To help patients to come to terms with what is for many a lifelong condition, greater efforts should be made to improve the communication at consultation, and provide more patient education.

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Metadata

Authors
RAMSAY, B., & O'REAGAN, M.
Venue
British Journal of Dermatology
Published
1988-02
Volume
118
Issue
2
Pages
195-201
ISSN
  • 0007-0963 (ISSN-L)
  • 1365-2133
OpenAlex
W1971292080
Cited by
216
References
0
FWCI
0.29
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: A survey of the social and psychological effects of psoriasis. https://app.cochat.ai/papers/10.1111/j.1365-2133.1988.tb01774.x
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RAMSAY, B., & O'REAGAN, M. (1988). A survey of the social and psychological effects of psoriasis. British Journal of Dermatology. https://doi.org/10.1111/j.1365-2133.1988.tb01774.x

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.