The attitudes of brain cancer patients and their caregivers towards death and dying: A qualitative study

被引：37
作者：
Lipsman N. [1 ]
Skanda A. [1 ]
Kimmelman J. [2 ]
Bernstein M. [1 ]
机构：
[1] Division of Neurosurgery, Toronto Western Hospital, Toronto, ON M5T 2S8, 399 Bathurst Street
[2] Medical Bioethics Unit, McGill University, Montreal, QC H3A 1X1
来源：
BMC Palliative Care | / 6卷 / 1期
关键词：
Palliative Care; Brain Cancer; Terminal Illness; Illness Experience; Physician Assisted Suicide;
D O I：
10.1186/1472-684X-6-7
中图分类号：
学科分类号：
摘要：
Background. Much money and energy has been spent on the study of the molecular biology of malignant brain tumours. However, little attention has been paid to the wishes of patients afflicted with these incurable tumours, and how this might influence treatment considerations. Methods. We interviewed 29 individuals - 7 patients dying of a malignant brain tumor and 22 loved ones. One-on-one interviews were conducted according to a pre-designed interview guide. A combination of open-ended questions, as well as clinical scenarios was presented to participants in order to understand what is meaningful and valuable to them when determining treatment options and management approaches. The results were analyzed, coded, and interpreted using qualitative analytic techniques in order to arrive at several common overarching themes. Results. Seven major themes were identified. In general, respondents were united in viewing brain cancer as unique amongst malignancies, due in large part to the premium placed on mental competence and cognitive functioning. Importantly, participants found their experiences, however difficult, led to the discovery of inner strength and resilience. Responses were usually framed within an interpersonal context, and participants were generally grateful for the opportunity to speak about their experiences. Attitudes towards religion, spirituality, and euthanasia were also probed. Conclusion. Several important themes underlie the experiences of brain cancer patients and their caregivers. It is important to consider these when managing these patients and to respect not only their autonomy but also the complex interpersonal toll that a malignant diagnosis can have. © 2007 Lipsman et al; licensee BioMed Central Ltd.
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