Unsolved problems and unwanted decision-making in the last year of life: A qualitative analysis of comments from bereaved caregivers

被引:4
|
作者
Knop, Jannis [1 ,2 ]
Dust, Gloria [1 ,2 ]
Kasdorf, Alina [1 ,2 ]
Schippel, Nicolas [1 ,2 ]
Rietz, Christian [3 ]
Strupp, Julia [1 ,2 ]
Voltz, Raymond [1 ,2 ,4 ,5 ,6 ]
机构
[1] Univ Cologne, Fac Med, Dept Palliat Med, Cologne, Germany
[2] Univ Cologne, Univ Hosp, Cologne, Germany
[3] Univ Educ Heidelberg, Fac Educ & Social Sci, Dept Educ Sci, Heidelberg, Germany
[4] Univ Cologne, Fac Med, Clin Trials Ctr ZKS, Cologne, Germany
[5] Univ Cologne, Fac Med, Ctr Hlth Serv Res, Cologne, Germany
[6] Univ Cologne, Fac Med, Ctr Integrated Oncol Aachen Bonn Cologne Dusseldo, Cologne, Germany
关键词
Bereaved caregivers; End of life; End-of-life care; Last year of life; Qualitative analysis; ASSESSMENT TOOL CSNAT; PALLIATIVE CARE; CANCER-PATIENTS; HEALTH-CARE; END; NEEDS; PAIN; HOME; COMMUNICATION; EXPERIENCE;
D O I
10.1017/S1478951522000165
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
Objectives Patients in their last year of life, as well as their relatives, often feel that existent care structures of the healthcare system do not adequately address their individual needs and challenges. This study analyzes unmet needs in terms of unsolved problems and unwanted decision-making in the health and social care of patients in their last year of life from the perspective of bereaved caregivers. Methods This qualitative study is based on free-text comments from informal caregivers of deceased patients collected as part of the Last-Year-of-Life-Study-Cologne (LYOL-C) using a postal survey. With qualitative content analysis, a category system with main and subcategories was developed in a multi-step process. Results Free-text commentaries and demographic data were collected from 240 bereaved caregivers. Particularly outside of hospice and palliative care services, study participants addressed the following unsolved problems: poor communication with medical and nursing staff, insufficient professional support for informal caregivers, inadequate psycho-social support for patients, and poor management of pain and other symptoms. Respondents often stated that their relative had to be cared for and die outside their own home, which the relative did not want. Significance of results Our findings suggest the necessity for greater awareness of patients' and their relatives' needs in the last year of life. Addressing individual needs, integrating palliative and hospice care in acute hospitals and other healthcare structures, and identifying patients in their last year of life and their caregivers could help to achieve more targeted interventions and optimization of care.
引用
收藏
页码:261 / 269
页数:9
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