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Views of patients with progressive illness and carers about the role of digital advance care planning systems to record and share information: a qualitative study

Birtwistle, Jacqueline; Allsop, Matthew J.; Bradshaw, Andy; Millares Martin, Pablo; Sleeman, Katherine E.; Twiddy, Maureen; Evans, Catherine J.

Authors

Jacqueline Birtwistle

Matthew J. Allsop

Andy Bradshaw

Pablo Millares Martin

Katherine E. Sleeman

Catherine J. Evans



Abstract

Background: Digital approaches are being explored internationally to support the elicitation, documentation and sharing of advance care planning information. However, views and experiences of patients and carers are little understood, impeding development and impact of digital approaches to strengthen palliative and end-of-life care.
Aim: To explore perspectives of patients with progressive illness and their carers on digital approaches to advance care planning, anticipated impact from their use, and expectations for their future development.
Design: A qualitative study employing thematic framework analysis of data collected from focus groups and semi-structured interviews.
Setting/participants: Purposive sample of 29 patients and 15 current or bereaved carers in London and West Yorkshire from hospice settings, non-governmental support and advocacy groups, and care home residents.
Results: Four generated themes included: 1. ‘Why haven’t you read what’s wrong with me?’; uncertainty around professionals’ documenting, sharing and use of information; 2. The art of decision-making relies on the art of conversation; 3. The perceived value in having “a say in matters”: control and responsibility; 4. Enabling patient and carer control of their records: “custodianship is key”.
Conclusions: Lived experiences of information sharing influenced trust and confidence in digital advance care planning systems. Despite scepticism about the extent that care can be delivered in line with their preferences, patients and carers acknowledge digital systems could facilitate care through contemporaneous and accurately documented wishes and preferences. There remains a need to determine how independent patient and public-facing advance care planning resources might be integrated with existing digital health record systems

Citation

Birtwistle, J., Allsop, M. J., Bradshaw, A., Millares Martin, P., Sleeman, K. E., Twiddy, M., & Evans, C. J. (in press). Views of patients with progressive illness and carers about the role of digital advance care planning systems to record and share information: a qualitative study. Palliative medicine, https://doi.org/10.1177/02692163241255511

Journal Article Type Article
Acceptance Date May 1, 2024
Online Publication Date May 30, 2024
Deposit Date May 2, 2024
Publicly Available Date May 30, 2024
Journal Palliative medicine
Print ISSN 0269-2163
Publisher SAGE Publications
Peer Reviewed Peer Reviewed
DOI https://doi.org/10.1177/02692163241255511
Keywords Patients; Caregivers; Digital technology; Advance care planning; Qualitative research; Palliative care
Public URL https://hull-repository.worktribe.com/output/4659248

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Publisher Licence URL
http://creativecommons.org/licenses/by/4.0

Copyright Statement
© The Author(s) 2024.
This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).




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