Dissonance on perceptions of end-of-life needs between health-care providers and members of the public: Quantitative cross-sectional surveys

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Abstract

Objective: To investigate views, determinants and barriers to end-of-life discussions for doctors, nurses and members of the public (MoP) and their acceptability of risk prediction tools. Methods: Concurrent surveys of 360 doctors and nurses and 497 MoP. Results: Sixty per cent of clinicians reported high confidence in initiating end-of-life discussions, and 55.8% regularly engaged in them. Barriers to end-of-life communication reported by clinicians were uncertainty on the likely time to death (44.7%) and family requests to withhold information from patients (44.2%). By contrast, most (92.8%) MoP wanted information about life expectancy; 89.9% wanted involvement in treatment decisions if the likelihood of death was high; and 23.8% already had an advance care directive. Conclusions: A dissonance exists between doctor/nurses perception of older peoples’ preference for receiving prognostic information and the public desire for involvement in decision-making at the end of life. As public attitudes change, strategies for greater involvement of patients in shared end-of-life planning are warranted.

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APA

Cardona, M., Lewis, E., Shanmugam, S., Nicholson, M., Williamson, M., Hanly, L., & Hillman, K. (2019). Dissonance on perceptions of end-of-life needs between health-care providers and members of the public: Quantitative cross-sectional surveys. Australasian Journal on Ageing, 38(3), e75–e84. https://doi.org/10.1111/ajag.12630

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