Caring for a loved one with Alzheimer's disease isn't easy under the
best of circumstances, but it may be much more stressful for spouses and
people who suffer from depression, a Finnish study suggests.
Researchers
followed 236 family caregivers of Alzheimer's patients for three years
after the diagnosis. Caregiving appeared to be much more stressful for
people who were married to the patients or who suffered from depression
when the study began.
"Even minor depressive symptoms at the
beginning of caregiving are a significant predictor of psychological
distress during the years of caregiving," lead study author Tarja
Valimaki of the University of Eastern Finland said by email.
The
findings suggest that spousal caregivers should receive mental health
evaluations at the time that their loved one is diagnosed with
Alzheimer's, Valimaki added.
"Alzheimer's disease patients' home
care is reliant on caregivers, and it is not reasonable for spousal
caregivers to put their own health at risk due to the caregiving,"
Valimaki said.
Alzheimer's disease is an irreversible, progressive
brain disorder that slowly destroys memory and thinking skills and
eventually, the ability to carry out the simplest tasks.
It is the most
common cause of dementia among older adults and a leading cause of death
among the elderly.
The study included 166 Alzheimer's patients
being cared for by their spouses, as well as 70 patients being cared for
by other loved ones. Researchers assessed psychological stress by
asking caregivers about their ability carry out daily activities, social
functioning, and the appearance of new sources of distress or concern
in their lives.
At the start of the study, caregivers and patients
who lived together had typically been sharing a home for more than
three decades. Spousal caregivers were older and reported more
depression than caregivers who weren't married to the patients.
Over
three years, psychological distress appeared to increase significantly
among spousal caregivers but not among non-spousal caregivers, the study
found.
One limitation of the study is that almost half of the participants dropped out before the end, the authors acknowledge in the Journal of Geriatric Psychiatry and Neurology.
Even
so, the study highlights the need for doctors and nurses to consider
two people patients in an Alzheimer's diagnosis – both the person
diagnosed and their partner or spouse, said Barbara Given, a researcher
at the college of nursing at Michigan State University in East Lansing.
"Not
everyone can be a good caregiver and as professionals we need to do an
assessment and determine who can do it, who wants to do it, and who
needs other support to do it," Given, who wasn't involved in the study,
said by email.
Another challenge may be financial, noted Carol
Levine, director of the families and health care project at the United
Hospital Fund in New York City.
"Perhaps there are alternatives in
the Finnish system; in the U.S. there are few alternatives and those
that do exist are expensive and beyond the reach of most families
(assisted-living or full-time home care) or considered unacceptable (a
long-term care facility)," Levine, who wasn't involved in the study,
said by email.
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