Barriers and facilitators to pressure ulcer prevention behaviours by older people living in their own homes and their lay carers: a qualitative study.
case_series · Level IV
Where this comes from
- Record sourced from PubMed, PMID 38503413.
- Also identified by DOI 10.1136/bmjopen-2023-080398 and PMC identifier 10953097.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
To identify barriers and facilitators to pressure ulcer prevention behaviours in community-dwelling older people and their lay carers. Theoretically informed qualitative interviews with two-phase, deductive then inductive, thematic analysis. The study was conducted in one geographical region in the UK, spanning several community National Health Service Trusts. Community-dwelling older patients at risk of pressure ulcer development (n=10) and their lay carers (n=10). Six themes and subthemes were identified: (1) knowledge and beliefs about consequences (nature, source, timing and taboo); (2) social and professional role and influences (who does what, conflicting advice and disagreements); (3) motivation and priorities (competing self-care needs and carer physical ability); (4) memory; (5) emotion (carer exhaustion and isolation, carergiver role conflict and patient feelings) and (6) environment (human resource shortage and equipment). There is minimal research in pressure ulcer prevention in community-dwelling older people. This study has robustly applied the theoretical domains framework to understanding barriers and facilitators to pressure ulcer prevention behaviours. Our findings will support co-design of strategies to promote preventative behaviours and are likely to be transferable to comparable healthcare systems nationally and internationally.
Medical subject headings
- Caregivers
- Pressure Ulcer