Care Strategy for Death Rattle in Terminally Ill Cancer Patients and Their Family Members: Recommendations From a Cross-Sectional Nationwide Survey of Bereaved Family Members' Perceptions
Journal of Pain and Symptom Management
Volume 48, Issue 1 , Pages 2-12, July 2014
Abstract
Context
Bereaved
family members witnessing a patient's death rattle often experience
distress. However, the benefits of specific care measures aimed at
decreasing death rattle-associated family distress have not yet been
evaluated.
Objectives
To clarify death rattle-related
emotional distress levels among family members and their perceptions of
the need for death rattle care improvement and explore the factors
influencing both these issues.
Methods
A cross-sectional
questionnaire survey of bereaved family members of cancer patients was
conducted in 95 palliative care units in June 2007.
Results
Six
hundred sixty-three questionnaires were mailed out, and 390 (61%)
responses were analyzed. Among these, 181 (46%) respondents experienced
death rattle. Of these, 66% reported high distress levels and 53%
perceived a strong need for improved death rattle care. Factors
influencing high distress levels were the gender (female) of family
members, unawareness about death rattle being a natural phenomenon, and
their fear and distressing interpretations of death rattle. Factors
influencing perceptions of a strong need for improved care were the
gender (male) of family members, severity of death rattle, death
rattle-associated discomfort to patients, family members' experiences of
inadequate nursing care (e.g., repositioning) and insufficient
consultation about suctioning, and their perception of uncomfortable
smells.
Conclusion
To decrease family-perceived distress,
medical staff should alleviate patient symptoms and suffering with a
comprehensive care strategy, try to decrease uncomfortable smells, and
communicate with family members to address distressing interpretations
and fears.
Key Words: Death rattle, respiratory sounds, neoplasm, terminal care
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