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Teno JM, Weitzen S, Fennell ML, Mor V. J of Palliative Medicine
2001; 4(4):457-464.
Prepared by: : Dr. Robin
Fainsinger
Received during: Journal
Rounds on the Tertiary Palliative Care Unit, Grey Nuns Hospital
Abstract:
Purpose: To examine differences in the pattern of
functional decline among persons dying of cancer and other
leading non-cancer causes of death.
Design: Mortality followback survey of next of kin
listed on death certificate.
Setting: Probability sample of all deaths in the United
States.
Participants: Next of kin for 3,614 decedents that
represented 914,335 deaths.
Measurements: Days of difficulty with activities of
daily living and mobility in the last year of life.
Results: Relative to other decedents, patients with
cancer experienced an increased rate of functional impairment
beginning as late as 5 months prior to death. For example,
only 13.9% of patients with cancer had difficulty getting
out of bed or a chair 1-year prior to death. This increased
from 22.2% to 63.0% in the last five months of life. In contrast,
decedents from other disease had higher rates of functional
impairment 1 year prior to death (approximately 35% had difficulty
getting out of bed or chair) and they manifested a more gradual
increase in the level of functional decline (approximately
50% had difficulty getting out of bed). Precipitous functional
decline was associated with hospice involvement and dying
at home.
Conclusion: Persons dying of cancer experienced sharp
functional decline in the last months of life whereas other
decedents' have a more gradual decline. The more precipitous
functional decline was associated with hospice involvement
and dying at home.
Comments:
Strengths/uniqueness: This is a well described study
that is easy to follow, and uses data from a large national
representative data base.
Weaknesses: The use of potentially inaccurate proxy
reporting and secondary analyses of existing national data
that is already 9 years old.
Relevance to Palliative Care: This report confirms
the difficulty of anticipating prognosis in non-cancer palliative
populations, and the need for criteria that are different
to palliative cancer populations. It is also a reminder of
the challenge of incorporating non-cancer populations into
palliative care programs.
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