A new national survey conducted by researchers from Indiana University and the Regenstrief Institute has found that while palliative care may be available for those with dementia, there are significant barriers to providing or receiving services to relieve the pain, eating difficulties, and other symptoms associated with dementia.
The survey’s findings are reported in the November 2010 issue of the Journal of the American Geriatrics Society.
“Although the general public and many physicians do not associate palliative or hospice care with dementia, dementia is a terminal disease and should be respected as such. Palliative care is needed throughout the illness and can provide those who are unable to communicate their needs with a better quality of life as well as lowering the stress the illness places on caregivers and the entire family,” said study first author Alexia M. Torke, M.D., M.S., who is an IU School of Medicine assistant professor of medicine and geriatrics and a Regenstrief Institute investigator. She is also on the faculty of the IU Center for Aging Research and the Fairbanks Center for Clinical Medical Ethics.
According to National Hospice and Palliative Care Organization data, only 11% of hospice patients in the facilities had a primary diagnosis of dementia. That may be because it is often difficult to determine how close to the end of life dementia patients may be and they therefore are not provided with hospice care, researchers said.
In the new study, researchers conducted telephone interviews about the provision of palliative care to patients with dementia with directors of 426 hospice and palliative care programs. A detailed online survey was completed by 80 program directors.
The study found that 94% of hospice and 72% of palliative care program directors reported that their programs have recently cared for patients with dementia. This is a substantial increase from a 1995 study that found only 21% of hospice programs had provided this care.
Non-hospice palliative care programs are relatively new and typically care for patients earlier in the disease before the patient is hospice eligible. To learn more about these programs, researchers asked in-depth questions of palliative care program directors. The directors indicated the existence of significant barriers to providing non-hospice palliative care. These obstacles included inadequate insurance coverage for home services by Medicare and other insurers, home health benefits that expired before the individual was eligible for hospice care, as well as insufficient family and healthcare provider knowledge of palliative care for dementia.
Strategies highlighted as critical for successful palliative care for dementia and reduction of caregiver burden were: an interdisciplinary team usually composed of a nurse, social worker, physician and chaplain; collaboration with community organizations; and campaigns to provide information to families and physicians.
“Palliative Care for Patients with Dementia: A National Survey” was funded by the Alzheimer's Association.