Because people are now living longer and often healthier lives, the rate of some illnesses that are more likely to develop with age has risen. These illnesses include dementia. In fact, the number of us living with dementia was already 47 million worldwide in 2015. It could reach 131 million by 2050.
Dementia is a general term that includes different types of mental decline. The most common type of dementia is Alzheimer's disease, which accounts for 60 to 80 percent of all dementia cases.
As Alzheimer's disease worsens, older adults may become more likely to have trouble performing daily activities, can develop trouble swallowing, and may become less active. This increases the risk for other concerns like infections. These infections, such as pneumonia, can increase the risk for death. As a result, the cause of death for people living with Alzheimer's disease is often infections or some other cause, rather than the Alzheimer's disease itself.
A team of researchers from Belgium recently studied how people with Alzheimer's disease use medical services during their final months. The goal was to learn more about the best ways to help older adults with dementia at the end of their lives. Their study was published in the Journal of the American Geriatrics Society.
The researchers studied information from people with Alzheimer's disease living in Belgium who died during 2012. They compared two groups of people who were diagnosed with Alzheimer's disease.
One group had death certificates that listed Alzheimer's disease as the cause of death. This was the group who died because of Alzheimer's disease.
The second group included individuals diagnosed with Alzheimer's disease but with death certificates that listed another cause of death (like infections). This was the group who died with Alzheimer's disease (but not of Alzheimer's disease).
The researchers looked at the healthcare resources the two groups used in the last six months of life.
Of the more than 11,000 people in the study, 77 percent had something other than Alzheimer's disease listed as the cause of death on their death certificate while 22 percent died of Alzheimer's disease. The average age of these individuals was 85, and most were women.
People who died with Alzheimer's disease were more likely to have at least one hospital admission and more intensive care unit (ICU) stays. People in both groups had about 12 visits with a doctor during the last six months of their lives.
However, the people who died with Alzheimer's disease received fewer palliative care services. Palliative care helps keep us comfortable when we are near death or dealing with a serious illness. This included fewer palliative home care services during the last six months of their lives. They also spent fewer days in a nursing home.
People in the study whose cause of death was listed as something other than Alzheimer's disease were also more likely to have invasive procedures compared to people who died of Alzheimer's disease. These invasive procedures included being put on breathing machines and being resuscitated (the medical term for reviving someone from unconsciousness or apparent death).
The researchers concluded that older adults whose cause of death was Alzheimer's disease used fewer healthcare resources than people whose cause of death was listed as something else even though they had been diagnosed with Alzheimer's disease. The researchers suggested that recognizing late-stage Alzheimer's disease as an end-of-life condition could influence healthcare providers to use more palliative care resources and fewer invasive procedures.
This summary is from "Resource Use During the Last Six Months of Life Among Those Dying with and of Alzheimer's Disease". It appears online ahead of print in the Journal of the American Geriatrics Society. The study authors are Kristof Faes, MSc; Joachim Cohen, PhD; and Lieven Annemans, PhD.
About the Health in Aging Foundation
This research summary was developed as a public education tool by the Health in Aging Foundation. The Foundation is a national non-profit established in 1999 by the American Geriatrics Society to bring the knowledge and expertise of geriatrics healthcare professionals to the public. We are committed to ensuring that people are empowered to advocate for high-quality care by providing them with trustworthy information and reliable resources. Last year, we reached nearly 1 million people with our resources through HealthinAging.org. We also help nurture current and future geriatrics leaders by supporting opportunities to attend educational events and increase exposure to principles of excellence on caring for older adults. For more information or to support the Foundation's work, visit http://www.
About the Journal of the American Geriatrics Society
Included in more than 9,000 library collections around the world, the Journal of the American Geriatrics Society (JAGS) highlights emerging insights on principles of aging, approaches to older patients, geriatric syndromes, geriatric psychiatry, and geriatric diseases and disorders. First published in 1953, JAGS is now one of the oldest and most impactful publications on gerontology and geriatrics, according to ISI Journal Citation Reports®. Visit wileyonlinelibrary.com/journal/JGS for more details.
About the American Geriatrics Society
Founded in 1942, the American Geriatrics Society (AGS) is a nationwide, not-for-profit society of geriatrics healthcare professionals that has--for 75 years--worked to improve the health, independence, and quality of life of older people. Its nearly 6,000 members include geriatricians, geriatric nurses, social workers, family practitioners, physician assistants, pharmacists, and internists. The Society provides leadership to healthcare professionals, policymakers, and the public by implementing and advocating for programs in patient care, research, professional and public education, and public policy. For more information, visit AmericanGeriatrics.org.