The Library
Best interests, dementia and the Mental Capacity Act (2005)
Tools
Hope, R. A., Slowther, Anne and Eccles, J.. (2009) Best interests, dementia and the Mental Capacity Act (2005). Journal of Medical Ethics, Vol.35 (No.12). pp. 733-738. ISSN 0306-6800
|
PDF
WRAP_Slowther_best-interests.pdf - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader Download (198Kb) |
Official URL: http://dx.doi.org/10.1136/jme.2009.030783
Abstract
The Mental Capacity Act (2005) is an impressive piece of legislation that deserves serious ethical attention, but much of the commentary on the Act has focussed on its legal and practical implications rather than the underlying ethical concepts. This paper examines the approach that the Act takes to best interests. The Act does not provide an account of the underlying concept of best interests. Instead it lists factors that must be considered in determining best interests, and the Code of Practice to the Act states that this list is incomplete. This paper argues that this general approach is correct, contrary to some accounts of best interests. The checklist includes items that are unhelpful. Furthermore, neither the Act nor its Code of Practice provides sufficient guidance to carers faced with difficult decisions concerning best interests. This paper suggests ways in which the checklist can be developed and discusses cases that could be used in an updated Code of Practice.
| Item Type: | Journal Article |
|---|---|
| Subjects: | R Medicine > RC Internal medicine |
| Divisions: | Faculty of Medicine > Warwick Medical School > Health Sciences Faculty of Medicine > Warwick Medical School |
| Library of Congress Subject Headings (LCSH): | Psychiatric ethics, Dementia -- Moral and ethical aspects, Mental Capacity Act 2005 |
| Journal or Publication Title: | Journal of Medical Ethics |
| Publisher: | BMJ Group |
| ISSN: | 0306-6800 |
| Date: | December 2009 |
| Volume: | Vol.35 |
| Number: | No.12 |
| Number of Pages: | 6 |
| Page Range: | pp. 733-738 |
| Identification Number: | 10.1136/jme.2009.030783 |
| Status: | Peer Reviewed |
| Publication Status: | Published |
| Access rights to Published version: | Open Access |
| References: | 1. Dostoevsky F. Notes from underground. Translated by J Coulson. London: Penguin Books 1972 (first published in 1864). 2. Office of Public Sector Information (OPSI). Mental Capacity Act 2005. http:// www.opsi.gov.uk/acts/acts2005/ukpga_20050009_en_1 (accessed 9 April 2009). 3. Department for Constitutional Affairs. Mental Capacity Act 2005: Code of practice. London: The Stationery Office, 2007. 4. Degrazia D. Value theory and the best interests standard. Bioethics 1995;9:50–61. 5. McCubbin M, Weisstub D. Toward a pure best interests model of proxy decision making for incompetent psychiatric patients. Intl J Law Psychiatry 1998;21:1–30. 6. Berghmans R. Ethical hazards of substituted judgment test in decision making concerning the end of life of dementia patients. Intl J Geriatr Psychiatry 1997;12:283–7. 7. Dworkin R. Autonomy and the demented self. The Millbank Quarterly 1986;64:4–16. 8. Treloar A. Advance directives: limitations upon their applicability in elderly care. Intl J Geriatr Psychiatry 1999;14:1039–43. 9. Berghmans R. Advance directives and dementia. Ann NY Acad Sci 2000;913:105–10. 10. Biegler P, Stewart C, Savulescu J, et al. Determining the validity of advance directives. Med J Aust 2000;172:545–8. 11. Widdershoven G, Berghmans R. Advance directives in psychiatric care: a narrative approach. J Med Ethics 2001;27:92–7. 12. Widdershoven G, Berghmans R. Advance directives in dementia care: from instructions to instruments. Patient Educ Counsel 2001;44:179–86. 13. Fagerlin A, Schnieder C. Enough: the failure of the living will. Hastings Center Rep 2004;34:30–42. 14. Buchanan A, Brock D. Deciding for others: the ethics of surrogate decision making. Cambridge: Cambridge University Press, 1989. 15. Savulescu J, Dickenson D. The time frame of preferences, dispositions, and the validity of advance directives for the mentally ill. Philos, Psychiatry, Philos 1998;5:225–46. 16. Firlik A. Margo’s logo. JAMA 1991;265:201. 17. Dworkin R. Life’s dominion: an argument about abortion and euthanasia. London: HarperCollins, 1993. 18. Dresser R. Dworkin on dementia: elegant theory, questionable policy. Hastings Center Rep 1995;25:32–8. 19. Holm S. Autonomy, authenticity, or best interests: everyday decision-making and persons with dementia. Med, Health Care Philos 2001;4:153–9. 20. Jaworska A. Respecting the margins of agency: Alzheimer’s patients and the capacity to value. Philos Public Aff 1999;28:105–38. 21. Hughes J. Views of the person with dementia. J Med Ethics 2001;27:86–91. 22. Dresser R, Whitehouse P. The incompetent patient on the slippery slope. Hastings Center Rep 1994;24:6–12. 23. Kopelman L. The best interests standard for incompetent or incapacitated persons of all ages. J Law, Med Ethics 2007;35:187–96. 24. Kuhse H. Some reflections on the problem of advance directives, personhood, and personal identity. Kennedy Inst Ethics J 1999;9:347–64. 25. Hope T. Advance directives. J Med Ethics 1996;22:67–8. |
| URI: | http://wrap.warwick.ac.uk/id/eprint/3136 |
Data sourced from Thomson Reuters' Web of Knowledge
Actions (login required)
![]() |
View Item |
Tools
Tools

