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Living at the end-of-life: experience of time of patients with cancer.
- Source :
-
BMC Palliative Care . 5/14/2019, Vol. 18 Issue 1, pN.PAG-N.PAG. 1p. - Publication Year :
- 2019
-
Abstract
- Background: The aim of this study was to gain insight into the experience of time of terminal patients with cancer. Experience of time is relevant in palliative care in both policy and practice. On a policy level, the Quality Adjusted Life Year (QALY), the most used outcome measure for cost-effectiveness analysis in healthcare, assumes time to be a linear and additive variable, which is one of the reasons that its applicability in palliative care is questioned. On a practice level, a better understanding of the experience of time of patients with limited time left, could help to recognize if and how these patients can have a more meaningful use of time. The main focus of this study was to discover whether time perception of these patients in their last months of life had changed as compared to earlier periods of time in their lives in good physical health. The pace of time and time dominance (comparison of past, present and future) were investigated. Methods: In several hospices and palliative care units in the Netherlands, twelve semi-structured interviews were conducted with terminal patients with cancer. Results: Time perception at the end of life had changed for most participants. They all lived on a day-to-day basis in the terminal phase, independent of their way of life in the healthy phase. Furthermore, the experienced duration of a day turned out to be very different between patients, but also between days, depending on daily activities. Besides, for most patients for whom the future was the dominant period of time in the healthy phase, the dominant period of time in the terminal phase had become the past. Conclusions: Time perception of terminal patients with cancer differed from the time perception in their relatively healthy phase of life. This suggests that the LY part of the QALY is not comparable for all phases of life. [ABSTRACT FROM AUTHOR]
- Subjects :
- *CANCER patient medical care
*CANCER patient psychology
*COST effectiveness
*HEALTH status indicators
*HOSPICE care
*INTERVIEWING
*RESEARCH methodology
*MEDICAL care costs
*HEALTH policy
*MEDICAL practice
*PALLIATIVE treatment
*PSYCHOLOGY of the terminally ill
*TIME
*ACTIVITIES of daily living
*QUALITY-adjusted life years
Subjects
Details
- Language :
- English
- ISSN :
- 1472684X
- Volume :
- 18
- Issue :
- 1
- Database :
- Academic Search Index
- Journal :
- BMC Palliative Care
- Publication Type :
- Academic Journal
- Accession number :
- 136441114
- Full Text :
- https://doi.org/10.1186/s12904-019-0424-7