Skip to main content

Research Repository

Advanced Search

Integration of primary care and palliative care services to improve equality and equity at the end-of-life: Findings from realist stakeholder workshops

Mitchell, Sarah; Turner, Nicola; Fryer, Kate; Aunger, Justin; Beng, Jude; Couchman, Emilie; Leach, Isabel; Bayly, Joanne; Gardiner, Clare; Sleeman, Katherine E.; Evans, Catherine J.

Integration of primary care and palliative care services to improve equality and equity at the end-of-life: Findings from realist stakeholder workshops Thumbnail


Authors

Sarah Mitchell

Kate Fryer

Justin Aunger

Jude Beng

Emilie Couchman

Isabel Leach

Joanne Bayly

Clare Gardiner

Katherine E. Sleeman

Catherine J. Evans



Abstract

Background:
Inequalities in access to palliative and end of life care are longstanding. Integration of primary and palliative care has the potential to improve equity in the community. Evidence to inform integration is scarce as research that considers integration of primary care and palliative care services is rare.

Aim:
To address the questions: ‘how can inequalities in access to community palliative and end of life care be improved through the integration of primary and palliative care, and what are the benefits?’

Design:
A theory-driven realist inquiry with two stakeholder workshops to explore how, when and why inequalities can be improved through integration. Realist analysis leading to explanatory context(c)-mechanism(m)-outcome(o) configurations(c) (CMOCs).

Findings:
A total of 27 participants attended online workshops (July and September 2022): patient and public members (n = 6), commissioners (n = 2), primary care (n = 5) and specialist palliative care professionals (n = 14). Most were White British (n = 22), other ethnicities were Asian (n = 3), Black African (n = 1) and British mixed race (n = 1). Power imbalances and racism hinder people from ethnic minority backgrounds accessing current services. Shared commitment to addressing these across palliative care and primary care is required in integrated partnerships. Partnership functioning depends on trusted relationships and effective communication, enabled by co-location and record sharing. Positive patient experiences provide affirmation for the multi-disciplinary team, grow confidence and drive improvements.

Conclusions:
Integration to address inequalities needs recognition of current barriers. Integration grounded in trust, faith and confidence can lead to a cycle of positive patient, carer and professional experience. Prioritising inequalities as whole system concern is required for future service delivery and research.

Citation

Mitchell, S., Turner, N., Fryer, K., Aunger, J., Beng, J., Couchman, E., Leach, I., Bayly, J., Gardiner, C., Sleeman, K. E., & Evans, C. J. (2024). Integration of primary care and palliative care services to improve equality and equity at the end-of-life: Findings from realist stakeholder workshops. Palliative Medicine, 38(8), 830-841. https://doi.org/10.1177/02692163241248962

Journal Article Type Article
Acceptance Date Apr 4, 2024
Online Publication Date May 11, 2024
Publication Date 2024-09
Deposit Date Jul 15, 2024
Publicly Available Date Jul 16, 2024
Journal Palliative Medicine
Electronic ISSN 1477-030X
Publisher SAGE Publications
Peer Reviewed Peer Reviewed
Volume 38
Issue 8
Pages 830-841
DOI https://doi.org/10.1177/02692163241248962
Keywords services, general practice, primary care, health care facilities, realist research, terminal care, manpower, Palliative care
Public URL https://nottingham-repository.worktribe.com/output/35425536
Publisher URL https://journals.sagepub.com/doi/10.1177/02692163241248962

Files





You might also like



Downloadable Citations