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Thinking ahead - the need for early Advance Care Planning for people on haemodialysis: A qualitative interview study

Research output: Contribution to journalArticlepeer-review

Katherine Bristowe, Helen L Horsley, Kate Shepherd, Heather Brown, Irene Carey, Beverley Matthews, Donal O'Donoghue, Katie Vinen, Felicity Em Murtagh

Original languageEnglish
Pages (from-to)443-450
Number of pages8
JournalPalliative Medicine
Volume29
Issue number5
Early online date19 Dec 2014
DOIs
E-pub ahead of print19 Dec 2014
Published11 May 2015

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  • Palliat_Med_2015_Bristowe_443_50

    Palliat_Med_2015_Bristowe_443_50.pdf, 554 KB, application/pdf

    Uploaded date:17 Dec 2015

    Version:Final published version

    Licence:CC BY

King's Authors

Abstract

BACKGROUND: There is a need to improve end-of-life care for people with end-stage kidney disease, particularly due to the increasingly elderly, frail and co-morbid end-stage kidney disease population. Timely, sensitive and individualised Advance Care Planning discussions are acceptable and beneficial for people with end-stage kidney disease and can help foster realistic hopes and goals.

AIM: To explore the experiences of people with end-stage kidney disease regarding starting haemodialysis, its impact on quality of life and their preferences for future care and to explore the Advance Care Planning needs of this population and the timing of this support.

STUDY DESIGN: Semi-structured qualitative interview study of people receiving haemodialysis. Interviews were analysed using thematic analysis. Recruitment ceased once data saturation was achieved.

SETTING/PARTICIPANTS: A total of 20 patients at two UK National Health Service hospitals, purposively sampled by age, time on haemodialysis and symptom burden.

RESULTS: Themes emerged around: Looking Back, emotions of commencing haemodialysis; Current Experiences, illness and treatment burdens; and Looking Ahead, facing the realities. Challenges throughout the trajectory included getting information, communicating with staff and the 'conveyor belt' culture of haemodialysis units. Participants reported a lack of opportunity to discuss their future, particularly if their health deteriorated, and variable involvement in treatment decisions. However, discussion of these sensitive issues was more acceptable to some than others.

CONCLUSION: Renal patients have considerable unmet Advance Care Planning needs. There is a need to normalise discussions about preferences and priorities in renal and haemodialysis units earlier in the disease trajectory. However, an individualised approach is essential - one size does not fit all.

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