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The effects of hospice interventions on behaviors, discomfort, and physical complications of end stage dementia nursing home residents

Marquette University; Research Development, Helen Bader Center, Milwaukee, Wisconsin

Sarah A. Wilson, PhD, RN

Faculty of Marquette University, Milwaukee, Wisconsin.

Patricia E. Noonan, MS, RN

St. Camillus Health Center Milwaukee, Wisconsin.

This project was guided by the question—what is the effect of hospice-oriented care on discomfort, physiological complications, and behaviors associated with dementia for residents of long term care facilities with an end stage dementing illness? Convenience sampling from three long term care facilities was used and 62 residents completed the project. The intervention was implemented through a four pronged approach:

• Interdisciplinary development of the intervention strategies for the new hospice households;

• Development of the households;

• Use of a hospice nurse as a case manager; and

• Education of staff

A pretest-posttest experimental design with random assignment to groups was used. Two months after the interventions were implemented, there was a statistically significant difference in discomfort levels between the treatment and control groups (t = 3.88, p < .001). Even though the treatment group showed lower scores on the tool that assessed behavior problems, the differences were not large enough to be statistically significant (t = 1.44, p = .155). There was no difference in the number of physical iatrogenic problems between the treatment and control groups (t = .054, p = .957). Staff reaction to the project was positive with staff reporting greater job satisfaction and empathy, and describing a variety of improvements in residents.

American Journal of Alzheimer's Disease and Other Dementias®, Vol. 11, No. 4, 7-15 (1996)
DOI: 10.1177/153331759601100402


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