Managing medicines for patients dying at home: a review of family caregivers’ experiences

Wilson, Eleanor; Caswell, Glenys; Turner, Nicola; Pollock, Kristian

Abstract

Context: Increased life expectancy, technical advances in treatment and symptom control, and the extension of palliative care in community settings not only lengthen life, but make it possible for many patients to be cared for, and to die, at home. Moreover, death increasingly occurs in late old age and after a prolonged period of co-morbidity and/or frailty. This has far reaching consequences for the way that professional services are resourced and organised, and for the informal carers who are often responsible for providing the greater part of patient care, including management of complex medication regimes.

Objectives: To explore the literature focused on family caregivers’ experiences of medications management for patients being cared for and dying at home.

Methods: This literature review takes a Critical Interpretive Synthesis approach to the review of 15 identified papers.
Results: Findings show that family caregivers can struggle to manage medications for someone who is dying at home, yet there is an expectation that they will take on these roles and they are often judged by professional standards. Five key themes identified particular issues around administration, organisational skills, empowerment, relationships and support.

Conclusion: As increasing demands are placed on family caregivers, there remains limited acknowledgement or understanding of the challenges they face, how they cope, or could be best supported. Alongside training, family caregivers need access to 24hrs support and medication reviews to rationalise unnecessary medications. Furthermore, the ethical challenges arising from administering medicines at the end of life also need to be acknowledged and discussed.

Citation

Wilson, E., Caswell, G., Turner, N., & Pollock, K. (2018). Managing medicines for patients dying at home: a review of family caregivers’ experiences. Journal of Pain and Symptom Management, 56(6), 962-974. https://doi.org/10.1016/j.jpainsymman.2018.08.019

• Journal Article Type: Article
• Acceptance Date: Aug 29, 2018
• Online Publication Date: Sep 11, 2018
• Publication Date: Dec 1, 2018
• Deposit Date: Sep 17, 2018
• Publicly Available Date: Dec 19, 2018
• Journal: Journal of Pain and Symptom Management
• Print ISSN: 0885-3924
• Electronic ISSN: 1873-6513
• Publisher: Elsevier
• Peer Reviewed: Peer Reviewed
• Volume: 56
• Issue: 6
• Pages: 962-974
• DOI: https://doi.org/10.1016/j.jpainsymman.2018.08.019
• Keywords: Managing medication; End of life; Home care; Family caregivers’ experiences; Prescribing
• Public URL: https://nottingham-repository.worktribe.com/output/1077975
• Publisher URL: https://www.sciencedirect.com/science/article/pii/S0885392418304494?via%3Dihub
• Additional Information: This article is maintained by: Elsevier; Article Title: Managing Medicines for Patients Dying at Home: A Review of Family Caregivers' Experiences; Journal Title: Journal of Pain and Symptom Management; CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.jpainsymman.2018.08.019; Content Type: article; Copyright: Crown Copyright © 2018 Published by Elsevier Inc. on behalf of American Academy of Hospice and Palliative Medicine.
• Contract Date: Sep 17, 2018