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Views and experiences of managing eczema: systematic review and thematic synthesis of qualitative studies.

  • Teasdale, E1
  • Muller, I1
  • Sivyer, K2
  • Ghio, D1
  • Greenwell, K2
  • Wilczynska, S1
  • Roberts, A3
  • Ridd, M J4
  • Francis, N1
  • Yardley, L2, 5
  • Thomas, K S6
  • Santer, M1
  • 1 Department of Primary Care, Population Science and Medical Education, Faculty of Medicine, University of Southampton, Southampton, UK.
  • 2 Centre for Clinical and Community Applications of Health Psychology, University of Southampton, Southampton, UK.
  • 3 Patient and Public Contributor, Nottingham, UK.
  • 4 Department of Population Health Sciences, University of Bristol, Bristol, UK.
  • 5 School of Experimental Psychology, University of Bristol, Bristol, UK.
  • 6 Centre for Evidence Based Dermatology, University of Nottingham, Nottingham, UK.
Published Article
British Journal of Dermatology
Wiley (Blackwell Publishing)
Publication Date
Apr 01, 2021
DOI: 10.1111/bjd.19299
PMID: 32531800


The number of qualitative studies on eczema has increased rapidly in recent years. Systematically reviewing these can provide greater understandings of people's perceptions of eczema and eczema treatments. We sought to systematically review and thematically synthesize qualitative studies exploring views and experiences of people with eczema and parents/carers of children with eczema. We searched MEDLINE, EMBASE, PsycINFO and CINAHL from the earliest date available to February 2019. We selected papers focusing on views and experiences of eczema and eczema treatments, and barriers/facilitators to eczema self-management. We excluded papers focusing on health service provision models or health professionals' views. We synthesized 39 papers (reporting 32 studies) from 13 countries. We developed four analytical themes: (1) Eczema not viewed as a long-term condition; (2) Significant psychosocial impact not acknowledged by others; (3) Hesitancy (patient/carer uncertainty) about eczema treatments; and (4) Insufficient information and advice. Our findings suggest that people with eczema and their carers experience frustration at having to manage a condition that is often seen by others as mundane but has significant psychosocial impact and is difficult to manage due to concerns about, and burden of, treatment. This frustration can be exacerbated by experiences of conflicting and/or insufficient information and advice from health professionals, family and others. Effective self-management of eczema could be supported by addressing beliefs and concerns about treatments; seeking positive ways to promote a 'control not cure' message; acknowledging psychosocial impacts of eczema and treatment burden; and providing clear consistent advice or signposting towards reliable information. © 2020 The Authors. British Journal of Dermatology published by John Wiley & Sons Ltd on behalf of British Association of Dermatologists.

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