Caregiving for older adults with hip fractures: Exploring the perspectives of caregivers, providers and decision-makers in Ontario, Canada

• Published in: Archives of gerontology and geriatrics 2021-03, Vol.93, p.104321-104321, Article 104321
• Main Authors: Guilcher, Sara J.T., Maunula, Laena, Cadel, Lauren, Everall, Amanda C., Li, Joyce, Kuluski, Kerry
• Format: Article
• Language: English
• Subjects: Aged; Caregivers; Frail elderly; Hip Fractures; Humans; Ontario; Qualitative Research; Social Support; Transitional care
• ISSN: 0167-4943; 1872-6976
• DOI: 10.1016/j.archger.2020.104321

•Differing perspectives of the caregiving role were identified•Caregivers often felt excluded from the decision-making process around patients’ care and discharge plan•Improving communication with caregivers could facilitate more positive experiences Caregivers play an important role in providing physical, emotional and social support to individuals with hip fracture. This study sought to explore perceptions of caregiving for older adults with hip fractures by comparing experiences of caregivers, providers and decision-makers. Semi-structured interviews were conducted both in-person and by telephone with caregivers, providers and decision-makers (n=32) from one rural and one urban hospital selected from two health regions in Ontario, Canada. Interviews were audio-recorded and transcribed verbatim. The data were coded descriptively and interpretively, and compared within and across participants types. Three main themes reflected tensions between caregivers and providers/decision-makers. Firstly, differing expectations of caregiver roles were identified. Several caregivers wanted more participation in the decision-making process but often felt excluded, while others expressed feeling stressed due to the expectations placed on them. Conversely, providers and decision-makers often described caregivers needing to strike a balance between providing supportive care while avoiding becoming too involved. Secondly, different expectations of what the healthcare system and providers could provide, with tensions particularly around timing of discharge were noted. Finally, there were differing perceptions of information needs. Providers spoke about the importance of providing education to caregivers and perceived themselves to be providing appropriate education. However, caregivers often described poor communication and not having a clear understanding of next steps and the care plan. Managing and tailoring expectations, improving communication (e.g., content, timing) and the consistency of information shared with caregivers from different providers could facilitate more positive caregiving experiences and interactions.