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BMJ 2005;330:471-472 (26 February), doi:10.1136/bmj.330.7489.471
Shirley Nurock, London region coordinator, Alzheimer's Society quality research in dementia consumer network1
1 London SW3 4BD s_nurock@hotmail.com
| The first 150 words of the full text of this article appear below. |
Ethical considerations should apply to all medical practice and interventions that affect patients. This should include social caregiving, which at present is not seen as being in need of moral or ethical consideration. And if audit is potentially more likely to lead to change than research, as Wade claims,1 clearly it should be given equal consideration and outcomes followed up.
Sometimes, however, it feels as though ethics committees are putting up barriers to much needed research. As a former carer for my husband, a general practitioner who developed Alzheimer's disease in his 50s, I know that some people with dementia and their carers perceive acceptable risk differently from ethics committees and are more willing to take risks, feeling there is little to lose. Indeed, research has shown that carers and people with dementia are particularly altruistic in their desire to be included in research.2
Affected patients should be given a
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