Abstract
Background
Caregiver burden may influence individuals’ preferences for their own End-of-Life (EoL) care, but evidence remains limited.
Objective
Examine the association between caregiver burden and preferred EoL care settings across levels of anticipated care dependency.
Methods
A survey was conducted with 297 caregivers of functionally independent adults aged ≥75 in Sukagawa City, Japan. Participants selected preferred EoL care settings (“home/family home” vs. “hospital/nursing home/other”) across three hypothetical scenarios reflecting low, moderate, and high levels of care dependency at their own EoL. Caregiver burden was assessed using the Burden Index of Caregivers. Modified Poisson regression was applied.
Results
Higher caregiver burden was significantly associated with preference for non-home settings in high- and low-dependency scenarios.
Conclusion
Caregiver burden may shape future EoL care setting preferences. Recognizing its influence could help clinicians tailor care planning discussions that reflect individuals’ values and preferences. It may also inform policies aimed at reducing caregiver burden.
Keywords
Get full access to this article
View all access options for this article.
References
Supplementary Material
Please find the following supplemental material available below.
For Open Access articles published under a Creative Commons License, all supplemental material carries the same license as the article it is associated with.
For non-Open Access articles published, all supplemental material carries a non-exclusive license, and permission requests for re-use of supplemental material or any part of supplemental material shall be sent directly to the copyright owner as specified in the copyright notice associated with the article.
