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Dementia and Palliative Care

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Dementia and Palliative Care
Thomas Edison State College

Introduction According to the Palliative Medicine article “global prevalence of dementia is almost 36 million people and the numbers are expected to double every 20 years (Ryan, Gardiner, Bellamy, Gott & Ingleton, 2011). With this in mind, in seems dementia is just as prevalent as cancer but these patients do not seem to receive the same end of life care or palliative care. The World Health Organization defines palliative care as An approach that improves quality of life in patients and families facing problems associated with life threatening illness, through prevention and relief of suffering by means of early identification, impeccable assessment and treatment of pain and the problems with physical, psychosocial and spiritual. ("Who definition of," 2013)
The two article summaries that follow will help healthcare staff understand the great need for palliative care in dementia, from the diagnosis to death.

Annotated Bibliography
Ryan, T., Gardiner, C., Bellamy, G., Gott, M., & Ingleton, C. (2011). Barriers and facilitators to the receipt of palliative care for people with dementia: The views of medical and nursing staff. Palliative Medicine, 26(7), 879-886. doi: 10.1177/0269216311423443

Tony Ryan and colleagues discuss how “people with dementia often receive too little care whereas end of life care is often characterized by too much” (Ryan, Gardiner, Bellamy, Gott & Ingleton, 2011). A study was performed to discuss three questions; 1) does diagnosis influence end of life care? 2) are there specific issues relating to people with dementia and end of life care they receive? 3) is it more difficult to achieve palliative care for people with dementia? One finding was the knowledge that not all disciplines recognize dementia as a cause of death. Quotes from

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