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The conditon of the caregiver as well as the patient plays a big
role in determining whether medications are used to treat Alzheimer's
disease, according to a study reported in the October 3 issue
of the Journal of the American Geriatric Society.
The two-year
study evaluated 102 caregivers for patients with mild to severe
stages of Alzheimer's disease.
Caregiver
chararcteristics drove medication decisions. Seventeen
percent did not want their relatives to take a risk-free medication
that could slow the disease, and half did not want their relatives
to take medication with a risk of side effects.
Study participants
who ranked themselves as having "just enough" or "not
enough" funds at the end of the month were more likely to
decline treatment. Non-whites were also more likely to decline
treatment, although no data confirmed why this was the case.
"Now
that we understand why caregivers refuse a dementia-slowing treatment,
we can better plan for patient care and develop future treatment
guidelines that incorporate the caregiver's experience,"
said study author Dr. Jason Karlawish, of University of Pennsylvania
School of Medicine. "This planning could ultimately help
caregivers and physicians in determining an appropriate time to
end treatment for Alzheimer's disease, based on factors influencing
quality of life."
Karlawish
said the study also shows that managing the health of the caregiver is an integral
part to treating a patient with Alzheimer's disease. "When you have one person
with Alzheimer's disease, you have at least two people to take care of,"
he added. Other
sources: University of Pennsylvania Medical Center
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