Paper
Friday, July 23, 2004
10:00 AM - 10:30 AM
Friday, July 23, 2004
3:00 PM - 3:30 PM
This presentation is part of : Posters II
Family Perceptions of End-of-Life Care in the ICU Setting
Maria Kjerulf, RN, MScN, School of Nursing, School of Nursing, Ryerson University, Toronto, ON, Canada
Learning Objective #1: n/a
Learning Objective #2: n/a

Objective: This study reviews the satisfaction experienced by families of patients who died in the ICU of a large urban teaching hospital. This study attempts to determine whether these goals were adequately met. Design: Descriptive, quantitative Population: Families of critically ill patients in an urban teaching ICU Sample: N=53, 35% Return rate Years: Families surveyed had a loved that had died from 1994-1997, for a study period 2001. Variables: Perceptions of care, access to information, family support and attitudes toward organ donation Methods: Quantitative, survey method, likert-type scale. Results were analyzed using descriptive statistics and correlational analysis. Results: Information factors associated with perceptions of care included feeling the nurses were open and honest; believing that they were informed of changes; and having the physician do the death notification. Factors associated with the perception that information was not forthcoming included: feeling visiting hours were too limited; wanting to spend more time with loved ones; not being with the loved one when they died; believing that the loved one’s pain was not properly controlled; feeling that no trained health care professionals were able to help them with their grieving; feeling the nurses were too busy; and feeling that the doctors did not spend enough time answering questions. Implications & Conclusions: These findings have important implications for ICU care. Consistency in care may be difficult in the fast pace of an ICU but are reasonable program objectives considering the positive influence this has on perceptions of care. Further, while the important contribution of being absent at the time of the patient’s death may represent anger or guilt on the part of family members that is independent of the ICU experience, this may point to the need for more flexible visitation policies.

Back to Posters II
Back to 15th International Nursing Research Congress
Sigma Theta Tau International
July 22-24, 2004