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Barriers to healthcare access and experiences of stigma: Findings from a coproduced Long Covid case-finding study.
Clutterbuck, Donna; Ramasawmy, Mel; Pantelic, Marija; Hayer, Jasmine; Begum, Fauzia; Faghy, Mark; Nasir, Nayab; Causer, Barry; Heightman, Melissa; Allsopp, Gail; Wootton, Dan; Khan, M Asad; Hastie, Claire; Jackson, Monique; Rayner, Clare; Brown, Darren; Parrett, Emily; Jones, Geraint; Clarke, Rowan; Mcfarland, Sammie; Gabbay, Mark; Banerjee, Amitava; Alwan, Nisreen A.
Afiliação
  • Clutterbuck D; School of Primary Care, Population Sciences and Medical Education, University of Southampton, Southampton, UK.
  • Ramasawmy M; Institute of Health Informatics, University College London, London, UK.
  • Pantelic M; Brighton and Sussex Medical School, University of Sussex, Falmer, UK.
  • Hayer J; Department of Social Policy and Intervention, University of Oxford, Oxford, UK.
  • Begum F; PPIE Co-applicant for STIMULATE-ICP, London, UK.
  • Faghy M; Member of the Community Advisory Board as person with lived experience of Long Covid, Southampton, UK.
  • Nasir N; University Hospitals of Derby and Burton NHS Foundation Trust, Derbyshire, UK.
  • Causer B; Clinical Exercise and Rehabilitation Research Centre, University of Derby, Derby, UK.
  • Heightman M; Department of Health and Social Care, Office for Health Improvement and Disparities, UK.
  • Allsopp G; Merton Public Health, Merton Council, London, UK.
  • Wootton D; University College London Hospitals NHS Trust, London, UK.
  • Khan MA; Royal College of General Practitioners, London, UK.
  • Hastie C; Clinical Infection Microbiology and Immunology, University of Liverpool, Liverpool, UK.
  • Jackson M; Liverpool University Hospitals NHS Foundation Trust, Liverpool, UK.
  • Rayner C; Member of the Community Advisory Board as person with lived experience of Long Covid, Southampton, UK.
  • Brown D; Manchester University Hospitals NHS Foundation Trust, Manchester, UK.
  • Parrett E; Member of the Community Advisory Board as person with lived experience of Long Covid, Southampton, UK.
  • Jones G; Long Covid Support Charity, London, UK.
  • Clarke R; Member of the Community Advisory Board as person with lived experience of Long Covid, Southampton, UK.
  • Mcfarland S; Member of the Community Advisory Board as person with lived experience of Long Covid, Southampton, UK.
  • Gabbay M; Member of the Community Advisory Board as person with lived experience of Long Covid, Southampton, UK.
  • Banerjee A; Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.
  • Alwan NA; Member of the Community Advisory Board as person with lived experience of Long Covid, Southampton, UK.
Health Expect ; 27(2): e14037, 2024 04.
Article em En | MEDLINE | ID: mdl-38634418
ABSTRACT
BACKGROUND AND

AIM:

Long Covid is often stigmatised, particularly in people who are disadvantaged within society. This may prevent them from seeking help and could lead to widening health inequalities. This coproduced study with a Community Advisory Board (CAB) of people with Long Covid aimed to understand healthcare and wider barriers and stigma experienced by people with probable Long Covid.

METHODS:

An active case finding approach was employed to find adults with probable, but not yet clinically diagnosed, Long Covid in two localities in London (Camden and Merton) and Derbyshire, England. Interviews explored the barriers to care and the stigma faced by participants and were analysed thematically. This study forms part of the STIMULATE-ICP Collaboration.

FINDINGS:

Twenty-three interviews were completed. Participants reported limited awareness of what Long Covid is and the available pathways to management. There was considerable self-doubt among participants, sometimes reinforced by interactions with healthcare professionals (HCPs). Participants questioned their deservedness in seeking healthcare support for their symptoms. Hesitancy to engage with healthcare services was motivated by fear of needing more investigation and concerns regarding judgement about the ability to carry out caregiving responsibilities. It was also motivated by the complexity of the clinical presentation and fear of all symptoms being attributed to poor mental health. Participants also reported trying to avoid overburdening the health system. These difficulties were compounded by experiences of stigma and discrimination. The emerging themes reaffirmed a framework of epistemic injustice in relation to Long Covid, where creating, interpreting and conveying knowledge has varied credibility based on the teller's identity characteristics and/or the level of their interpretive resources.

CONCLUSION:

We have codeveloped recommendations based on the findings. These include early signposting to services, dedicating protected time to listening to people with Long Covid, providing a holistic approach in care pathways, and working to mitigate stigma. Regardless of the diagnosis, people experiencing new symptoms must be encouraged to seek timely medical help. Clear public health messaging is needed among communities already disadvantaged by epistemic injustice to raise awareness of Long Covid, and to share stories that encourage seeking care and to illustrate the adverse effects of stigma. PATIENT OR PUBLIC CONTRIBUTION This study was coproduced with a CAB made up of 23 members including HCPs, people with lived experience of Long Covid and other stakeholders.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: COVID-19 / Síndrome de COVID-19 Pós-Aguda Limite: Adult / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: COVID-19 / Síndrome de COVID-19 Pós-Aguda Limite: Adult / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article