Palliative Care in the Greater China Region: A Systematic Review of Needs, Models, and Outcomes

被引:25
|
作者
Chung, Huei [1 ]
Harding, Richard [2 ]
Guo, Ping [2 ,3 ]
机构
[1] Taipei City Hosp, Dept Pharm, Zhongxiao Branch, Taipei, Taiwan
[2] Kings Coll London, Florence Nightingale Fac Nursing Midwifery & Pall, Cicely Saunders Inst Palliat Care Policy & Rehabi, London, England
[3] Univ Birmingham, Coll Med & Dent Sci, Sch Nursing, Inst Clin Sci, Birmingham B15 2TT, W Midlands, England
关键词
Palliative care needs; interventions; outcomes; Greater China; systematic review; ILL CANCER-PATIENTS; QUALITY-OF-LIFE; PATIENTS LAST YEAR; TERMINALLY-ILL; HONG-KONG; FAMILY CAREGIVERS; PAIN MANAGEMENT; DEATH; PREFERENCES; IMPACT;
D O I
10.1016/j.jpainsymman.2020.08.040
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
Context. There is rapidly increasing need for palliative care in Greater China because of rapidly aging populations. Objectives. This study aimed to systematically review and appraise evidence for palliative care needs, models of care, interventions, and outcomes in Greater China. Methods. Four databases (MEDLINE, EMBASE, CINAHL, and PsycINFO) were searched, with hand searching of local journals and databases. Narrative synthesis was applied to the qualitative and quantitative evidence. Results. Nineteen qualitative studies and 47 quantitative studies were retained. With respect to care needs, nine themes were synthesized: pain control, reduced aggressive end-of-life care, truth telling, physical, emotional, and spiritual supports, and achieving preferred place of care/death. Informal caregivers expressed their needs for education and burden reduction. Health care professionals called for training and national policy support. Twenty-four studies evaluated interventions, mostly among patients with advanced cancer. Positive effects were suggested for improvements in quality of life, pain, anxiety and depression, readmission rate, and costs. Models of care evaluated were mostly specialist palliative care delivered in various settings (hospitals, residential care, and home). Outcome measures used were grouped into six categories of construct: quality of life, pain, physical assessment, psychospiritual assessment, quality of care, and implementation assessment. Limited rigorous randomized controlled trials are available to document intervention outcomes, and some problems (such as high attrition rates) reduced the strength of the evidence. Conclusion. Palliative care services within Greater China should pay more attention to management of nonmalignant disease and to integration into primary services. Policy support is key to establishing culturally appropriate person-centered services. (C) 2020 American Academy of Hospice and Palliative Medicine. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:585 / 612
页数:28
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