A&E attendance for people with dementia is common and increasing
Posted on 21/02/2019
A new paper published today in the journal Alzheimer’s & Dementia: The Journal of the Alzheimer’s Association found that Accident and Emergency (A&E) attendance among people with dementia in their last year of life is common and is increasing.
In recent years, there has been a drop in the number of people with dementia dying in hospital, which has widely been seen as demonstrating better end of life care. However, the team of researchers from King’s College London found that over three quarters of people with dementia were seen in A&E in their last year of life. This has also been increasing over time.
For people who are approaching the end of life, attending A&E can be distressing. It is also often unnecessary and can be prevented. Sometimes people with dementia do need to be admitted to hospital, but admissions can also lead to deterioration, with an increased risk of infections, bedsores and distress.
In the study, the researchers identified people who had dementia and who had died over a five year period (2008 - 2013).
The paper’s main findings include:
- Out of 4,867 people with dementia who had died, 78.6% had at least one A&E attendance during their last year of life.
- These findings are similar to those from the USA and Australia, where 81% and 73% of people with dementia had an A&E attendance in their last year of life.
- A&E attendance became more common the closer people were to death, with just under half (44.5%) having an A&E attendance in their last month of life, and a fifth of people with dementia attending A&E in their last week of life.
- People living in a care home had fewer A&E attendances, which may be because plans were put in place to avoid this.
- The likelihood of attending A&E increased over time: people who died in the most recent year studied were 1.6 times more likely to attend A&E then in the previous years.
Lead author, Dr Katherine Sleeman from the Cicely Saunders Institute at King’s College London, said: “Recognition of the need to improve end of life for people with dementia has been increasing. This includes enabling them to be cared for in their home or a care home. However, our results show a worrying increase in the reliance on emergency care. In light of the current pressures on the health service, our ageing population and the associated increase in deaths from dementia, there is an urgent need to look at ways we can provide better support for care in the community.”
“A strong policy focus on dying out of hospital as a marker of good end of life care may have contributed to the fall in hospital deaths in dementia in recent years. However, our results show that A&E attendance in the last year of life follows the opposite trend. Policy makers need to consider a broader range of indicators of the quality of end of life care alongside the place of death.”
Co-author Professor Robert Stewart, CRIS Lead and Consultant Old Age Psychiatrist at King’s College London said: “Most people with dementia have a number of other health problems as well as difficulties arising from the dementia itself. Sometimes people do need to be taken to A&E and sometimes time in hospital is needed; however, this is often distressing and disruptive and most people want to keep it to a minimum. A lot of hospital use could be avoided if there was a higher level of support in the community. This includes clearer plans in place for dealing with illnesses when they occur and when they don’t necessarily need hospital services.”
The team used the NIHR Maudsley Biomedical Research Centre (BRC) Clinical Record Interactive Search (CRIS) database linked to Hospital Episodes Statistics from NHS Digital to provide information on Emergency Department use among people with dementia in their last year of life. Dr Katherine Sleeman is also a NIHR Clinician Scientist.
Notes to Editors:
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About the Cicely Saunders Institute
The Cicely Saunders Institute is the world’s first purpose built Institute for Palliative Care and Rehabilitation, named after Dame Cicely Saunders (1918–2005), recognised internationally as the founder of the modern hospice movement 50 years ago. The Institute is a partnership of Cicely Saunders International, King’s College London and associated local clinical services to bring together clinical and academic teams to innovate, discover, evaluate and translate solutions to improve care, symptom control and quality of life for patients and families affected by serious and progressive illnesses.
About Cicely Saunders International
Cicely Saunders International (Registered Charity No. 1087195) is the world’s leading charity promoting and supporting best practice and quality research in end of life and palliative care to improve the care and treatment of all those affected by progressive illness and to make high quality palliative care available to everyone who needs it.
About the National Institute for Health Research
The National Institute for Health Research (NIHR): improving the health and wealth of the nation through research. Established by the Department of Health, the NIHR:
- funds high quality research to improve health
- trains and supports health researchers
- provides world-class research facilities
- works with the life sciences industry and charities to benefit all
- involves patients and the public at every step
For further information, visit the NIHR website (www.nihr.ac.uk).