Published 2 October 2009, doi:10.1136/bmj.b3993
Cite this as: BMJ 2009;339:b3993

Editorials

Ethical care in dementia

Requires respect for patient autonomy, partnership with families, and education

The first 150 words of the full text of this article appear below.

More than 24 million people are living with dementia worldwide,1 and this figure is expected to double every 20 years.1 Dementia is an age related disease—about 25% of Europeans aged 85 or more are affected.1 The increasing number of people with dementia is challenging for their families and carers, and for health services. In addition to the physical, emotional, and social aspects of caring for someone with dementia, there are also ethical aspects, which are often poorly understood and overlooked. On 1 October 2009, the Nuffield Council on Bioethics published the report Dementia: ethical issues,2 which provides practical tools to help health professionals understand and support patients with dementia and their carers. The report emphasises that offering these patients and their carers certain services is not enough; rather, we should be aware of our attitudes and values and how we communicate with them.

The report considers general ethical questions . . . [Full text of this article]

Marja-Liisa Laakkonen, geriatrician 1, Kaisu Pitkälä, professor of general practice and primary health care2

1 Helsinki Health Centre, Geriatric Memory Clinic, Laakso Hospital, PO Box 6600, FIN-00099, Helsinki, Finland, 2 Helsinki University Hospital, Unit of General Practice, Tukholmankatu 8 B, 00290 Helsinki, Finland

marja-liisa.laakkonen@hel.fi


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