Family members' perceptions of end-of-life care across diverse locations of care

被引:49
作者
Gallagher, Romayne [1 ]
Krawczyk, Marian [2 ]
机构
[1] Univ British Columbia, Dept Family & Community Med, Providence Hlth Care, Div Palliat Care, Vancouver, BC V5Z 1M9, Canada
[2] Simon Fraser Univ, Dept Sociol & Anthropol, Burnaby, BC V5A 1S6, Canada
关键词
Family satisfaction; End-of-life care; Palliative care; Acute care; Hospice; Residential care; Bereaved relative; PALLIATIVE CARE; QUALITY; IMPROVE; PERSPECTIVES; DEPRESSION; GUIDELINES; CAREGIVERS; OUTCOMES; HOSPICE; ANXIETY;
D O I
10.1186/1472-684X-12-25
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background: The goal of the study was to assess perceived level of satisfaction with end-of-life care, focusing on the last 48 hours of life. Methods: A previously validated instrument was used in a telephone survey with bereaved family members (n=90) of patients who died within an organization in British Columbia. Results: Bereaved family members had many unmet needs for information about the patient's changing condition, the process of dying, how symptoms would be managed and what to do at the time of death. In addition, many bereaved relatives felt that the patient or resident had an unmet need for emotional support and that their own emotional needs were not addressed adequately. The last place of care had the most significant effect on all of these variables, with acute care and residential care having the most unmet needs. Hospice had the fewest unmet needs, followed by the palliative and the intensive care units. Conclusions: We discuss these findings in relation to overall satisfaction with care, focus on individual, ethno-cultural and diversity issues, information and decision-making, symptom management and attending to the family. We conclude by offering possible practices address the end-of-life needs of patients and family members.
引用
收藏
页数:9
相关论文
共 26 条
[1]   Educating Nursing Home Staff About the Progression of Dementia and the Comfort Care Option: Impact on Family Satisfaction with End-of-Life Care [J].
Arcand, Marcel ;
Monette, Johanne ;
Monette, Michele ;
Sourial, Nadia ;
Fournier, Lynn ;
Gore, Brian ;
Bergman, Howard .
JOURNAL OF THE AMERICAN MEDICAL DIRECTORS ASSOCIATION, 2009, 10 (01) :50-55
[2]  
Barry LC, 2002, AM J GERIAT PSYCHIAT, V10, P447
[3]  
Canadian Institute of Health Research, 2013, PALL END LIF CAR
[4]   The health impact of health care on families: a matched cohort study of hospice use by decedents and mortality outcomes in surviving, widowed spouses [J].
Christakis, NA ;
Iwashyna, TJ .
SOCIAL SCIENCE & MEDICINE, 2003, 57 (03) :465-475
[5]   Measuring success of interventions to improve the quality of end-of-life care in the intensive care unit [J].
Curtis, J. Randall ;
Engelberg, Ruth A. .
CRITICAL CARE MEDICINE, 2006, 34 (11) :S341-S347
[6]  
El-Jawahri Areej, 2011, J Support Oncol, V9, P87
[7]   Does palliative care improve quality? A survey of bereaved family members [J].
Gelfman, Laura P. ;
Meier, Diane E. ;
Morrison, R. Sean .
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2008, 36 (01) :22-28
[8]  
Government of Canada, 2013, CAN EC ACT PLAN PALL
[9]   Anxiety, depression, and quality of life in caregivers of patients with cancer in late palliative phase [J].
Grov, EK ;
Dahl, AA ;
Moum, T ;
Fosså, SD .
ANNALS OF ONCOLOGY, 2005, 16 (07) :1185-1191
[10]   What Is the Evidence That Palliative Care Teams Improve Outcomes for Cancer Patients and Their Families? [J].
Higginson, Irene J. ;
Evans, Catherine J. .
CANCER JOURNAL, 2010, 16 (05) :423-435