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Living With Dementia and Caregivers: So Many Unmet Needs
Posted By Sally Abrahms On February 20, 2014 @ 9:15 am In Take Care | Comments Disabled
A four-year Johns Hopkins School of Medicine study published in the Journal of the American Geriatrics Society examined the unmet needs of people with dementia (PWD) living in the community (as opposed to long-term care) and their family caregivers.
Researchers wanted to determine if there were a lot of unmet needs (an unequivocal “yes”). Insufficient care, supports or services can often lead to poor health outcomes, hospitalization and early placement in a nursing home. And something else we knew before the study: Those taking care of loved ones with dementia often have more stress, as well as more tasks to do, than caregivers dealing with other illnesses.
The research looked at 254 older adults with dementia from Baltimore and 246 of their caregivers; eight caregivers took care of two people with the disease. Most of those in the PWD sample lived with someone else; a few lived alone.
“Health problems that require hospitalization and nursing homes are all high-cost forms of care and things people want to avoid,” says Betty Black, an associate professor of psychiatry and behavioral sciences at Johns Hopkins and a coauthor of the study. The goal, she said, is to meet both groups’ needs so that PWD can stay in the community longer.
The research found that for adults with dementia:
What did caregivers need but not receive?
The report revealed that caregivers and PWD who were nonwhite or had clinical symptoms of depression seemed to have more unmet needs, as did caregivers with lower educational levels.
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