"If you think you've got a lump, they'll screen you." Informed consent, health promotion, and breast cancer
David Bourget (Western Ontario)
David Chalmers (ANU, NYU)
Rafael De Clercq
Jack Alan Reynolds
Learn more about PhilPapers
Journal of Medical Ethics 30 (2):227-230 (2004)
A great deal has been written about information that is or should be provided when seeking consent to medical research and treatment. Relatively little attention has been paid to information describing health promotion interventions. This paper critically examines some information material describing three different methods of encouraging early presentation of breast cancer in the UK: the NHS breast screening programme, breast self examination, and breast awareness. Findings from a content analysis of printed material and a series of focus group discussions that included women who speak little or no English were organised around the Department of Health’s recommendations about the information which should be provided when seeking consent to treatment and research. They exposed inconsistencies, ambiguities, and gaps, which when taken together suggest both compliance and non-compliance are being achieved in the absence of informed consent. The findings also provide a starting point for a discussion about how informed consent to health promotion might be sought
|Keywords||No keywords specified (fix it)|
|Categories||categorize this paper)|
Setup an account with your affiliations in order to access resources via your University's proxy server
Configure custom proxy (use this if your affiliation does not provide a proxy)
|Through your library|
References found in this work BETA
No references found.
Citations of this work BETA
J. Neuberger (2015). The Patient/Client/Consumer/Service User and Medical Ethics 40 Years On. Journal of Medical Ethics 41 (1):22-24.
Similar books and articles
Megan Eide & Ann Milliken Pederson (2009). God, Disease, and Spiritual Dilemmas: Reading the Lives of Women with Breast Cancer. Zygon 44 (1):85-96.
Lisa S. Parker (1995). Beauty and Breast Implantation: How Candidate Selection Affects Autonomy and Informed Consent. Hypatia 10 (1):183 - 201.
Maya J. Goldenberg (2010). Working for the Cure: Challenging Pink Ribbon Activism [Book Chapter]. In Roma Harris, Nadine Wathen & Sally Wyatt (eds.), [Book] Configuring Health Consumers: Health Work and the Imperative of Personal Responsibility. Eds. R. Harris, N. Wathen, S. Wyatt. Amsterdam: Palgrave Macmillan, 2010. Palgrave Macmillan
Sandra Woien, Mohamad Rady, Joseph Verheijde & Joan McGregor (2006). Organ Procurement Organizations Internet Enrollment for Organ Donation: Abandoning Informed Consent. [REVIEW] BMC Medical Ethics 7 (14):1-9.
Deborah Bowman (2011). Informed Consent: A Primer for Clinical Practice. Cambridge University Press.
Leonard J. Haas (1991). Hide-and-Seek or Show-and-Tell? Emerging Issues of Informed Consent. Ethics and Behavior 1 (3):175 – 189.
Peter R. Mansfield (2005). Banning All Drug Promotion is the Best Option Pending Major Reforms. Journal of Bioethical Inquiry 2 (2):75-81.
M. P. M. Richards (2003). Issues of Consent and Feedback in a Genetic Epidemiological Study of Women with Breast Cancer. Journal of Medical Ethics 29 (2):93-96.
M. Sheehan (2011). Can Broad Consent Be Informed Consent? Public Health Ethics 4 (3):226-235.
Stewart Justman (2012). Uninformed Consent: Mass Screening for Prostate Cancer. Bioethics 26 (3):143-148.
Peter J. Schulz & Bert Meuffels (2012). It is About Our Body, Our Own Body!”: On the Difficulty of Telling Dutch Women Under 50 That Mammography is Not for Them. Journal of Argumentation in Context 1 (1):130-142.
Akira Akabayashi & Brian Taylor Slingsby (2006). Informed Consent Revisited: Japan and the U.S. American Journal of Bioethics 6 (1):9 – 14.
Benedetto Vitiello (2008). Effectively Obtaining Informed Consent for Child and Adolescent Participation in Mental Health Research. Ethics and Behavior 18 (2 & 3):182 – 198.
Roy Gilbar & Ora Gilbar (2009). The Medical Decision-Making Process and the Family: The Case of Breast Cancer Patients and Their Husbands. Bioethics 23 (3):183-192.
Michael C. Rea (2000). Constitution and Kind Membership. Philosophical Studies 97 (2):169-193.
Added to index2010-08-24
Total downloads4 ( #405,599 of 1,725,607 )
Recent downloads (6 months)2 ( #268,736 of 1,725,607 )
How can I increase my downloads?