Donna Goodridge, John B Bond Jr, Cynthia Cameron, Elizabeth McKean
International Journal of Palliative Nursing, Vol. 11, Iss. 5, 26 May 2005, pp 226 - 232
Aim: To examine the perspectives of family members, registered nurses and healthcare aides regarding the last 72 hours of Canadian nursing home residentsí lives.
Study design: Exploratory, descriptive design using semistructured interviews.
Sample: Consisted of 14 registered nurses and eight healthcare aides who had provided care within the last 72 hours before a residentís death and four family members who had visited within the same time frame.
Setting: A 220-bed nursing home located within a larger long-term care facility in Canada.
Methods: Thematic analysis was conducted independently and through consensus identified themes and subthemes emerging from the interviews.
Findings: Dyspnea was a more common end-of-life (EoL) symptom for nursing home residents in this sample than was pain. Caring behaviours of staff were central to the residentís dying process and involved assessment, coordination of care, physical care, family education and nurturance. Family membersí ambivalence about the residentís death and fear of the resident dying alone were frequently noted.
Conclusions: Appropriate and timely symptom management and a range of caring behaviours of staff are critical elements in the dying experience of nursing home residents. Additional education and support for personnel involved with caring for this group will enhance end-of-life care.