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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

Title
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
Ewha Authors
남은미
SCOPUS Author ID
남은미scopusscopus
Issue Date
2019
Journal Title
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
ISSN
0885-3924JCR Link

1873-6513JCR Link
Citation
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT vol. 57, no. 4, pp. 774 - 782
Keywords
Advance care planningadvance directivesdecision-makinglife support careterminal care
Publisher
ELSEVIER SCIENCE INC
Indexed
SCIE; SCOPUS WOS scopus
Document Type
Article
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.
DOI
10.1016/j.jpainsymman.2018.12.332
Appears in Collections:
의과대학 > 의학과 > Journal papers
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