Detailed Information

Cited 0 time in webofscience Cited 0 time in scopus
Metadata Downloads

Attitudes of the General Public, Cancer Patients, Family Caregivers, and Physicians Toward Advance Care Planning: A Nationwide Survey Before the Enforcement of the Life-Sustaining Treatment Decision-Making Act

Authors
Park, Hye YoonKim, Young AeSim, Jin-AhLee, JihyeRyu, HyewonLee, Jung LimMaeng, Chi HoonKwon, Jung HyeKim, Yu JungNam, Eun MiShim, Hyun-JeongSong, Eun-KeeJung, Kyung HaeKang, Eun JooKang, Jung HunYun, Young Ho
Issue Date
Apr-2019
Publisher
ELSEVIER SCIENCE INC
Keywords
Advance care planning; advance directives; decision-making; life support care; terminal care
Citation
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, v.57, no.4, pp.774 - 782
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
Volume
57
Number
4
Start Page
774
End Page
782
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/66439
DOI
10.1016/j.jpainsymman.2018.12.332
ISSN
0885-3924
Abstract
Context. To respect a patient's wish for end-of-life care, "the Act on Decisions on Life-Sustaining Treatment for Patients at the End-of-Life" was enacted in South Korea in 2016. Current understanding of people who would be involved in advance care planning (ACP) is crucial to disseminate it systematically. Objectives. The objective of this study was to investigate awareness and attitudes toward ACP in South Korea. Methods. A multicenter, nationwide cross-sectional study was conducted, a survey regarding ACP among four groups that would have different positions and experiences: 1001 cancer patients, 1006 family caregivers, 928 physicians, and 1241 members of the general public. Results. A total of 15% of the general population, 33% of the patients and caregivers, and 61% of the physicians had knowledge of advance directives. More than 64% of the general population, above 72% of the patients and caregivers, and 97% of the physicians were willing to do so when the disease status was aggravated or terminal. The possibility for changing the plan, uncertainty as to whether directives would actually be followed, and psychological discomfort were common reasons for not wanting to engage in ACP. Routine recommendations for a specific medical condition, heightened accessibility, and health insurance support were common factors that could help facilitate ACP. Conclusion. Our findings suggest that strategies for promoting ACP should reflect different perspectives among the general public, patients, family caregivers, and physicians. Public advocacy, resources for approaching and integrating ACP into routine health care, as well as systematic support provisions are needed. (C) 2018 American Academy of Hospice and Palliative Medicine. Published by Elsevier Inc. All rights reserved.
Files in This Item
There are no files associated with this item.
Appears in
Collections
College of Medicine > Department of Medical Science > 1. Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Altmetrics

Total Views & Downloads

BROWSE