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American Journal of Hospice and Palliative Medicine®
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*Cancer
*Cancer--Living with Cancer
*Family Issues
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Perceptions and decision-making on rehydration of terminally ill cancer patients and family members

Tatsuya Morita, MD

Seirei Mikatabara Hospital, Hamamatsu, Shizuoka, Japan

Junichi Tsunoda, MD

Seirei Mikatabara Hospital, Hamamatsu, Shizuoka, Japan

Satoshi Inoue, MD

Seirei Mikatabara Hospital, Hamamatsu, Shizuoka, Japan

Satoshi Chihara, MD

Seirei Mikatabara Hospital, Hamamatsu, Shizuoka, Japan

Although the appropriateness of forced rehydration for terminally ill cancer patients has been actively discussed, few studies have investigated its psychological aspects. To clarify patients’ and family members’ perceptions about rehydration and identify contributing factors for decision-making, a prospective structured survey was performed on 121 hospice inpatients with insufficient oral intake.

Physicians did not recommend rehydration in 78 percent of patients, and 75 percent decided not to receive artificial fluid therapy. Various concerns affected decision-making: 76 percent of patients and 85 percent of family members believed patients could not get appropriate nutrition without artificial rehydration. Some 56 percent of patients and 84 percent of family members said that withholding rehydration would cause premature death, while more than half agreed that forced rehydration might worsen the patients’ suffering.

Patients’ performance status, fluid retention signs, denial, physicians’ recommendations, patients’ and family members’ beliefs about the effect of hydration on patients’ distress, and family members’ anxiety about withholding rehydration were significantly associated with decision-making. Multiple regression analyses revealed patients’ denial, physicians’ recommendations determined by patients’ performance status and fluid retention symptoms, and family members’ belief that rehydration could worsen patients’ distress as independent determinants for rehydration.

In conclusion, hospice care receivers had various concerns about rehydration, related to patients’ nutrition, survival, and distress. The main determinants for rehydration therapy were patients’ performance status, fluid retention symptoms, denial, and care receivers’ beliefs about the effect of hydration on the patients’ distress.

American Journal of Hospice and Palliative Medicine®, Vol. 16, No. 3, 509-516 (1999)
DOI: 10.1177/104990919901600306


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This article has been cited by other articles:


Home page
AM J HOSP PALLIAT CAREHome page
M. Miyashita, T. Morita, Y. Shima, R. Kimura, M. Takahashi, and I. Adachi
Nurse Views of the Adequacy of Decision Making and Nurse Distress Regarding Artificial Hydration for Terminally Ill Cancer Patients: A Nationwide Survey
American Journal of Hospice and Palliative Medicine, January 1, 2008; 24(6): 463 - 469.
[Abstract] [PDF]


Home page
AM J HOSP PALLIAT CAREHome page
M. Miyashita, T. Morita, Y. Shima, R. Kimura, M. Takahashi, and I. Adachi
Physician and Nurse Attitudes Toward Artificial Hydration for Terminally Ill Cancer Patients in Japan: Results of 2 Nationwide Surveys
American Journal of Hospice and Palliative Medicine, November 1, 2007; 24(5): 383 - 389.
[Abstract] [PDF]



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