4.5 Article

Different Experiences and Goals in Different Advanced Diseases: Comparing Serial Interviews With Patients With Cancer, Organ Failure, or Frailty and Their Family and Professional Carers

期刊

JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
卷 50, 期 2, 页码 216-224

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jpainsymman.2015.02.017

关键词

Cancer; organ failure; frailty; serial interviews; qualitative longitudinal research; palliative care; end-of-life care; illness trajectories

资金

  1. Chief Scientist Office, Scotland
  2. Department of Health, England
  3. Economic and Social Research Council
  4. Commonwealth Fund, a private independent foundation based in New York City
  5. Chief Scientist Office [CZH/4/320, PCRCA/08/01] Funding Source: researchfish

向作者/读者索取更多资源

Context. Quality care for people living with life-limiting illnesses is a global priority. A detailed understanding of the varied experiences of people living and dying with different conditions and their family and professional caregivers should help policymakers and clinicians design and deliver more appropriate and person-centered care. Objectives. To understand how patients with different advanced conditions and their family and professional caregivers perceive their deteriorating health and the services they need. Methods. We used a narrative framework to synthesize eight methodologically comparable, longitudinal, and multiperspective interview studies. We compared the end-of-life experiences of people dying from cancer (lung, glioma, and colorectal cancer), organ failure (heart failure, chronic obstructive pulmonary disease, and liver failure), and physical frailty and those of their family and professional caregivers in socioeconomically and ethnically diverse populations in Scotland. Results. The data set comprised 828 in-depth interviews with 156 patients, 114 family caregivers, and 170 health professionals. Narratives about cancer typically had a clear beginning, middle, and an anticipated end. Cancer patients gave a well-rehearsed account of their illness, hoping for recovery alongside fear of dying. In contrast, people with organ failure and their family caregivers struggled to pinpoint when their illness began, or to speak openly about death, hoping instead to avoid further deterioration. Frail older people tended to be frustrated by their progressive loss of independence, fearing dementia or nursing home admission more than dying. Conclusion. These contrasting illness narratives affect and shape the experiences, thoughts, and fears of patients and their carers in the last months of life. Palliative care offered by generalists or specialists should be provided more flexibly and equitably, responding to the varied concerns and needs of people with different advanced conditions. (C) 2015 American Academy of Hospice and Palliative Medicine. Published by Elsevier Inc. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据