Development of a Resource for Health Professionals to Raise Advance Care Planning Topics During Kidney Care Consultations: A Multiple User-Centered Design.

Winterbottom, Anna; Hurst, Helen; Murtagh, Fliss E.M.; Bekker, Hilary L.; Ormandy, Paula; Hole, Barnaby; Russon, Lynne; Murphy, Emma; Bucknall, Keith; Mooney, Andrew

Abstract

Planning and delivering treatment pathways that integrate end-of-life care, frailty assessment, and enhanced supportive care is a service priority. Despite this, people with kidney failure are less likely to have an advance care plan and receive hospice and palliative care compared with other chronic illness populations. This is linked to health professionals feeling unskilled initiating conversations around future treatment and care options. This article describes research underpinning the development of a guide for kidney health professionals discussing end-of-life and advance care planning options with people with kidney failure and family members. The study comprised 2 parts: an initial cross-sectional qualitative approach using in-depth interviews with older adults with kidney failure and (bereaved) carers followed by resource development with input from multiple stakeholders. Older adults with kidney failure and (bereaved) carers recruited from 2 renal units in the North of England and by online advertisements with national United Kingdom-based kidney patient charities. Resource development included input from co-applicants, independent advisory committee, patient and public involvement team, multidisciplinary health professionals and academics in the United Kingdom and Denmark. Thematic analysis was used to analyze the data. Twenty-seven people were interviewed: older adults with kidney failure (n=18), carers (n=5), bereaved carers (n=4). Five themes are described: the context within which end-of-life conversations take place, preferences for end-of-life treatment and care, family members' role and needs in supporting people with kidney failure at the end-of-life, expectations and experience of dialysis treatment, and beliefs and experiences of death and dying. Participants were mainly White, British, and receiving hemodialysis. People with (lived) experience of kidney failure informed a guide which aims to build on health professionals existing skills and improve confidence having conversations about future treatment and care. Kidney teams have expressed interest implementing the guide in practice and within their broader communications training packages. [Abstract copyright: © 2024 The Authors.]

• Journal Article Type: Article
• Acceptance Date: May 1, 2024
• Online Publication Date: Jul 18, 2024
• Publication Date: 2024-07
• Deposit Date: Jul 25, 2024
• Publicly Available Date: Sep 11, 2024
• Journal: Kidney medicine
• Peer Reviewed: Peer Reviewed
• Volume: 6
• Issue: 9
• Pages: 100874
• DOI: https://doi.org/10.1016/j.xkme.2024.100874
• Keywords: health care professionals (renal physicians, clinicians, kidney doctors, nephrologists, dialysis nurses, renal nurses, kidney nurses, nephrology nurses), kidney failure (advanced kidney disease, end-stage kidney failure, end-stage kidney disease, chronic kidney disease), Advance care planning (personalized care planning, anticipatory care), palliative care (palliative treatment, hospice care), end-of-life care
• Additional Information: This article is maintained by: Elsevier; Article Title: Development of a Resource for Health Professionals to Raise Advance Care Planning Topics During Kidney Care Consultations: A Multiple User-Centered Design; Journal Title: Kidney Medicine; CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.xkme.2024.100874; Content Type: article; Copyright: © 2024 Published by Elsevier Inc. on behalf of the National Kidney Foundation, Inc.