Literature DB >> 25827464

Extent of misconceptions, negative prejudices and discriminatory behaviour to psoriasis patients in France.

B Halioua1, D Sid-Mohand2, M E Roussel3, A Maury-le-Breton3, A de Fontaubert3, J F Stalder4.   

Abstract

BACKGROUND: The perception of stigmatization of patients with psoriasis is largely due to misconceptions and negative prejudice about this skin disease. 'Uneducated' judgments can give rise to discriminatory behaviours.
OBJECTIVE: Evaluate the prevalence, in France, of misconceptions, negative prejudice and discriminatory behaviour towards psoriasis patients.
METHODS: Online survey conducted in June 2011, aimed at 1005 persons aged 16-64 years, representative of the French population. The representativeness of the sample was ensured by quota methodology (gender, age, occupation of the interviewed person) after stratification by region and location category. The respondents were asked to respond to a questionnaire on their knowledge of psoriasis, their attitude and main feelings/perceptions towards psoriasis patients.
RESULTS: About 62.4% of respondents recognize a lack of information about psoriasis and 19.7% have misconceptions about this disease. About 16.5% believe that psoriasis is contagious, 6.8% believe this skin disease is related to personal hygiene and 3.2% believe that it affects more people with low personal hygiene. About 50.0% of respondents show discriminatory behaviour towards psoriasis patients, reflected by reluctance to maintain friendship ties/a relationship of friendliness (7.6%), to have lunch or dinner with a person with visible manifestations (17.9%), to give a kiss on the cheek in greeting (29.7%), to shake hands (28.8%) and to have sexual relations/intercourse (44.1%). Patients with negative prejudice about the psoriasis frequently have misconceptions towards psoriasis patients. About 52.8% of respondents do not know anyone with psoriasis. Socio-demographic indicators such as gender, education level and rural or urban way of life are not associated with an increased prevalence of misconceptions and/or discriminatory behaviour.
CONCLUSION: The lack of knowledge about psoriasis in France is important. There is an urgent need to strengthen information campaigns about psoriasis intended for the General Public.
© 2015 European Academy of Dermatology and Venereology.

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Mesh:

Year:  2015        PMID: 25827464     DOI: 10.1111/jdv.13095

Source DB:  PubMed          Journal:  J Eur Acad Dermatol Venereol        ISSN: 0926-9959            Impact factor:   6.166


  3 in total

1.  Stigmatisation and body image impairment in dermatological patients: protocol for an observational multicentre study in 16 European countries.

Authors:  Florence J Dalgard; Anthony Bewley; Andrea W Evers; Uwe Gieler; Lars Lien; Francesca Sampogna; Sonja Ständer; Lucia Tomas-Aragones; Ninke Vulink; Jörg Kupfer
Journal:  BMJ Open       Date:  2018-12-22       Impact factor: 2.692

2.  The Lived Experience of Psoriasis Patients from Social Stigma and Rejection: A Qualitative Study.

Authors:  Alireza Ghorbanibirgani; Masoud Fallahi-Khoshknab; Kourosh Zarea; Heidarali Abedi
Journal:  Iran Red Crescent Med J       Date:  2016-05-21       Impact factor: 0.611

3.  Psychopathological Variables and Sleep Quality in Psoriatic Patients.

Authors:  Maria Luca; Antonina Luca; Maria Letizia Musumeci; Federica Fiorentini; Giuseppe Micali; Carmela Calandra
Journal:  Int J Mol Sci       Date:  2016-07-21       Impact factor: 5.923

  3 in total

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