CONCORDANCE OF PREFERENCES FOR END- OF-LIFE CARE BETWEEN TERMINALLY ILL CANCER PATIENTS AND THEIR FAMILY CAREGIVERS IN TAIWAN
Resource
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT v.30 n.6 pp.510-518
Journal
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
Journal Volume
v.30
Journal Issue
n.6
Pages
510-518
Date Issued
2005
Date
2005
Author(s)
TANG, SIEW-TZUH
LIU, TSANG-WU
LAI, MEI-SHU
LIU, LI-NIUH
Abstract
There is a dearth of information in the literature about the concordance of-life care between terminally ill patients and their family surrogates outside the Western countries. The purpose of this study was to examine the extent of concordance, in preferences for end-of-life care goals and life-sustaining treatments between 1 Taiwanese terminally ill cancer patients and their primary family caregivers. A total of 617 dyads of patients-family caregivers across 21 hospitals throughout Taiwan were surveyed. Overall agreements on the or end-of-life care and preferences for initiating life-sustaining treatment ranged front goals for end-of-life care and preferences for initiating life- sustaining treatments ranged from 62.4% to 96.9% (average: 71.0%). Kappa values for the extent of concordance ranged from 0.1.3 to 0.46 (average: 0.29), indicating poor to moderate consistency in personal preferences. Family caregivers had a significantly more aggressive attitude toward each examined life-sustaining treatment for their ill family members than the patients' own stated preferences. In societies, such as in Asian countries, where physicians' respect for patient autonomy is frequently subordinate to the power of family, disagreements between a patient and family about end-of-life care may result in the patients' preferences being overridden at the end-of-life care, an open dialogue between patients and their primary family caregivers should become standard.
Subjects
preferences for life-sustaining treatments
concordance of preferences
end-of-life care
SDGs
Type
journal article