Improving Care Experiences for Patients and Caregivers at End of Life: A Systematic Review | Zendy

Denise D. Quigley | Zendy; Sara G. McCleskey | Zendy

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Improving Care Experiences for Patients and Caregivers at End of Life: A Systematic Review

Author(s) -

Denise D. Quigley,

Sara G. McCleskey

Publication year - 2020

Publication title -

american journal of hospice and palliative medicine®

Language(s) - English

Resource type - Journals

eISSN - 1938-2715

pISSN - 1049-9091

DOI - 10.1177/1049909120931468

Subject(s) - palliative care , end of life care , nursing , systematic review , medicine , grey literature , qualitative research , population , medline , quality of life (healthcare) , psychology , family medicine , social science , sociology , political science , law , environmental health

End-of-life care is increasing as the US population ages. Approaches to providing high-quality end-of-life care vary across setting, diseases, and populations. Several data collection tools measure patient and/or caregiver care experiences at end of life and can be used for quality improvement. Previous reviews examined palliative care improvements or available measures but none explicitly on improving care experiences. We reviewed literature on improving patient and/or caregiver end-of-life care experiences.

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