Literature DB >> 24814298

Psoriasis: snapshots of the unspoken: using novel methods to explore patients' personal models of psoriasis and the impact on well-being.

C Bundy1, M Borthwick, H McAteer, L Cordingley, L Howells, P Bristow, S McBride.   

Abstract

BACKGROUND: People with psoriasis report high levels of undermanaged distress. This is compounded by the problem that some patients find it difficult to discuss their emotions. Distress prevents optimal self-management, which may exacerbate psoriasis flares, thereby creating a vicious cycle.
OBJECTIVES: To offer people with psoriasis a novel way of expressing their personal models of psoriasis in order to gain a better understanding of their experiences of living with the condition.
METHODS: We used a qualitative technique - asking people with psoriasis to complete a postcard entitled 'Dear Psoriasis...' - to collect survey data on their personal models of psoriasis.
RESULTS: One hundred and four returned postcards provided new insights into the extent of and reasons for distress in psoriasis. Seven dominant themes emerged: identity and relationships; battleground; control; emotional consequences; hypervigilance; coping; treatment burden.
CONCLUSIONS: Reports of distress were common, and for many it was long-standing. Some reported low self-esteem and self-denigration bordering on self-loathing, and described being hypervigilant and in a constant battle with their skin. Many people did not expect to have intimate relationships, resulting in reduced social support for patients in the future. This research underscores the need for patient support and psychological treatment to be made available as part of routine care.
© 2014 British Association of Dermatologists.

Entities:  

Mesh:

Year:  2014        PMID: 24814298     DOI: 10.1111/bjd.13101

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN: 0007-0963            Impact factor:   9.302


  5 in total

1.  How important is subjective well-being for patients? A qualitative interview study of people with psoriasis.

Authors:  Antonia-Luise Newi; Athanasios Tsianakas; Sophia von Martial; Rachel Sommer; Christine Blome
Journal:  Qual Life Res       Date:  2022-08-10       Impact factor: 3.440

2.  A multicenter, non-interventional study to evaluate patient-reported experiences of living with psoriasis.

Authors:  David Pariser; Brad Schenkel; Chureen Carter; Kamyar Farahi; T Michelle Brown; Charles N Ellis
Journal:  J Dermatolog Treat       Date:  2015-07-03       Impact factor: 3.359

3.  Associations between site of skin lesions and depression, social anxiety, body-related emotions and feelings of stigmatization in psoriasis patients.

Authors:  Patryk Łakuta; Kamil Marcinkiewicz; Beata Bergler-Czop; Ligia Brzezińska-Wcisło; Anna Słomian
Journal:  Postepy Dermatol Alergol       Date:  2018-02-20       Impact factor: 1.837

4.  Comparative effectiveness of biological therapies on improvements in quality of life in patients with psoriasis.

Authors:  I Y K Iskandar; D M Ashcroft; R B Warren; M Lunt; K McElhone; C H Smith; N J Reynolds; C E M Griffiths
Journal:  Br J Dermatol       Date:  2017-10-19       Impact factor: 9.302

5.  Effect of cognitive behavioral therapy on anxiety and depression in patients with psoriasis: A protocol for systematic review and meta-analysis.

Authors:  Chuan Tan; Jianmei Jiang; Xiaoling Deng; Wei Xiang; Tingting Hu
Journal:  Medicine (Baltimore)       Date:  2021-11-19       Impact factor: 1.889

  5 in total

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