P A Nelson1, C A Chew-Graham, C E M Griffiths, L Cordingley. 1. Dermatology Research Centre, Institute Inflammation and Repair, The University of Manchester, Manchester, Academic Health Science Centre, Manchester, UK. pauline.nelson@manchester.ac.uk
Abstract
BACKGROUND: Psoriasis is a life-long inflammatory condition that can impact on quality of life, psychological and social functioning. Previous literature suggests patient dissatisfaction with psoriasis management; however, little is known about people's specific experiences of health care consultations. OBJECTIVES: The study aimed to explore in depth the perspectives of people living with psoriasis including coping responses, self-care strategies and how consultations with health care professionals in both primary and secondary care are experienced. METHODS: Qualitative semistructured interviews were carried out with a diverse sample of 29 people with psoriasis generated purposively and recruited from community sources in North West England. Interviews were coded using Framework Analysis to produce a thematic framework incorporating key emerging issues and concepts. RESULTS: Participants experienced psoriasis as a complex condition involving physical, psychological and social challenges, as well as issues of control, but perceived that these were largely unacknowledged by practitioners in health care consultations. Practitioners were perceived as lacking knowledge and expertise in the management of psoriasis, lacking empathy with the effects of psoriasis and failing to manage it as a long-term condition. This perceived lack of support resulted in some participants withdrawing from conventional health service providers and seeking alternative sources of help. CONCLUSIONS: Psoriasis needs to be recognized and managed as a complex long-term condition with emotional and social needs that are addressed alongside appropriate diagnosis and regular reviews of treatments which may involve referrals to specialist care.
BACKGROUND:Psoriasis is a life-long inflammatory condition that can impact on quality of life, psychological and social functioning. Previous literature suggests patient dissatisfaction with psoriasis management; however, little is known about people's specific experiences of health care consultations. OBJECTIVES: The study aimed to explore in depth the perspectives of people living with psoriasis including coping responses, self-care strategies and how consultations with health care professionals in both primary and secondary care are experienced. METHODS: Qualitative semistructured interviews were carried out with a diverse sample of 29 people with psoriasis generated purposively and recruited from community sources in North West England. Interviews were coded using Framework Analysis to produce a thematic framework incorporating key emerging issues and concepts. RESULTS:Participants experienced psoriasis as a complex condition involving physical, psychological and social challenges, as well as issues of control, but perceived that these were largely unacknowledged by practitioners in health care consultations. Practitioners were perceived as lacking knowledge and expertise in the management of psoriasis, lacking empathy with the effects of psoriasis and failing to manage it as a long-term condition. This perceived lack of support resulted in some participants withdrawing from conventional health service providers and seeking alternative sources of help. CONCLUSIONS:Psoriasis needs to be recognized and managed as a complex long-term condition with emotional and social needs that are addressed alongside appropriate diagnosis and regular reviews of treatments which may involve referrals to specialist care.
Authors: Rachael J Thorneloe; Christopher E M Griffiths; Darren M Ashcroft; Lis Cordingley Journal: BMC Health Serv Res Date: 2017-02-07 Impact factor: 2.655
Authors: Rachael J Thorneloe; Christopher E M Griffiths; Richard Emsley; Darren M Ashcroft; Lis Cordingley Journal: J Invest Dermatol Date: 2017-11-26 Impact factor: 8.551
Authors: Pauline A Nelson; Zoë Barker; Christopher E M Griffiths; Lis Cordingley; Carolyn A Chew-Graham Journal: BMC Fam Pract Date: 2013-10-20 Impact factor: 2.497
Authors: Pauline A Nelson; Karen Kane; Anna Chisholm; Christina J Pearce; Christopher Keyworth; Martin K Rutter; Carolyn A Chew-Graham; Christopher E M Griffiths; Lis Cordingley Journal: Health Expect Date: 2015-09-04 Impact factor: 3.377
Authors: Emma Teasdale; Ingrid Muller; Amirah Abdullah Sani; Kim S Thomas; Beth Stuart; Miriam Santer Journal: BMJ Open Date: 2018-01-11 Impact factor: 2.692