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JCO Early Release, published online ahead of print Nov 9 2009
Journal of Clinical Oncology, 10.1200/JCO.2009.23.2793

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Received March 27, 2009
Accepted September 15, 2009

Care for Imminently Dying Cancer Patients: Family Members' Experiences and Recommendations

Takuya Shinjo,* Tatsuya Morita, Kei Hirai, Mitsunori Miyashita, Kazuki Sato, Satoru Tsuneto, and Yasuo Shima

From the Palliative Care Unit, Shakaihoken Kobe Central Hospital, Kobe; Department of Palliative and Supportive Care, Palliative Care Team and Seirei Hospice, Seirei Mikatahara Hospital, Hamamatsu; Center of the Study for Communication Design, Psychology and Behavioral Sciences, Graduate School of Human Science, Departments of Complementary and Alternative Medicine and Palliative Medicine, Graduate School of Medicine, Osaka University, Osaka; Department of Adult Nursing/Palliative Care Nursing, School of Health Sciences and Nursing, Graduate School of Medicine, The University of Tokyo, Tokyo; and Department of Palliative Medicine, Tsukuba Medical Center Hospital, Tsukuba, Japan.

* To whom correspondence should be addressed. E-mail: shinjo{at}doctor.email.ne.jp

Purpose: The aim of this study was to clarify the level of emotional distress experienced by bereaved family members and the perceived necessity for improvement in the care for imminently dying patients and to explore possible causes of distress and alleviating measures.

Methods: A cross-sectional nationwide survey was performed in 2007 of bereaved families of cancer patients at 95 palliative care units across Japan.

Results: Questionnaires were sent to 670 families, and 76% responded. Families reported their experiences as very distressing in 45% of cases. Regarding care, 1.2% of respondents believed that a lot of improvement was needed, compared with 58% who believed no improvement was needed. Determinants of high-level distress were a younger patient age, being a spouse, and overhearing conversations between the medical staff outside the room at the time of the patient's death; those reporting high-level necessity of improvement were less likely to have encountered attempts to ensure the patient's comfort, received less family coaching on how to care for the patient, and felt that insufficient time was allowed for the family to grieve after the patient's death.

Conclusion: A considerable number of families experienced severe emotional distress when their family member died. Thus, we propose that a desirable care concept for imminently dying cancer patients should include relief of patient suffering, family advisement on how to care for the patient, allowance of enough time for the family to grieve, and ensuring that family members cannot overhear medical staff conversations at the time of the patient's death.


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Copyright © 2009 by the American Society of Clinical Oncology, Online ISSN: 1527-7755. Print ISSN: 0732-183X
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