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ARTICLES

Metaphors in a Patient's Narrative: Picturing Good Care

References

  • Barnes, M. 2011. “Abandoning Care? A Critical Perspective on Personalisation from an Ethic of Care.” Ethics and Social Welfare 5 (2): 153–167.
  • Beauchamp, T., and J. Childress. 2009. Principles of Biomedical Ethics. 6th ed. New York: Oxford University Press.
  • Ceci, C., and M. E. Purkis. 2009. “Bridging Gaps in Risk Discourse: Home Care Case Management and Client Choices.” Sociology of health & illness 31 (2): 201–214.
  • Clarke, J., J. E. Newman, N. Smith, E. Vidler, and E. Westmarland. 2007. Creating Citizen-Consumers: Changing Publics and Changing Public Services. London: Sage.
  • Coffey, A., and P. Atkinson. 1996. “Meanings and Metaphors.” In Making Sense of Qualitative Data, 83–107. Thousand Oaks: Sage.
  • Donetto, S., and A. Cribb. 2011. “Researching Involvement in Health Care Practices: Interrupting or Reproducing Medicalization?” Journal of Evaluation in Clinical Practice 17 (5): 907–912.
  • Ells, C., M. R. Hunt, and J. Chambers-Evans. 2011. “Relational Autonomy as an Essential Component of Patient-centered Care.” International Journal of Feminist Approaches to Bioethics 4 (2): 79–101.
  • Entwistle, V., D. Firnigl, M. Ryan, J. Francis, and P. Kinghorn. 2012. “Which Experiences of Health Care Delivery Matter to Service Users and Why? A Critical Interpretive Synthesis and Conceptual Map.” Journal of Health Services Research & Policy 17 (2): 70–78.
  • Entwistle, V., D. McCaughan, I. Watt, Y. Birks, J. Hall, M. Peat, B. Williams, and J. Wright. 2010. “Speaking Up about Safety Concerns: Multi-setting Qualitative Study of Patients' Views and Experiences.” Quality and Safety in Health Care 19 (6): 1–7.
  • Entwistle, V., M. Mello, and T. Brennan. 2005. “Advising Patients about Patient Safety: Current Initiatives Risk Shifting Responsibility.” Joint Commission Journal on Quality and Patient Safety 31 (9): 483–494.
  • Fox, N. J., K. J. Ward, and A. J. O'Rourke. 2005. “The ‘Expert Patient’: Empowerment or Medical Dominance? The Case of Weight Loss, Pharmaceutical Drugs and the Internet.” Social Science & Medicine 60 (6): 1299–1309.
  • Globerman, J., J. White, and G. McDonald. 2002. “Social Work in Restructuring Hospitals: Program Management Five Years Later.” Health & Social Work 27 (4): 274–284.
  • Harris, R., N. Wathen, and S. Wyatt. 2010a. Configuring Health Consumers: Health Work and the Imperative of Personal Responsibility. Basingstoke: Palgrave Macmillan.
  • Harris, R., N. Wathen, and S. Wyatt. 2010b. “Working to be Healthy: Empowering Consumers or Citizens?” In Configuring Health Consumers: Health Work and the Imperative of Personal Responsibility, edited by R. Harris, N. Wathen, and S. Wyatt, 211–224. Basingstoke: Palgrave Macmillan.
  • Henwood, F., R. Harris, and P. Spoel. 2011. “Informing Health? Negotiating the Logics of Choice and Care in Everyday Practices of ‘Healthy Living’.” Social Science & Medicine 72 (12): 2026–2032.
  • Henwood, F., S. Wyatt, A. Hart, and J. Smith. 2003. “‘Ignorance is Bliss Sometimes’: Constraints on the Emergence of the ‘Informed Patient’ in the Changing Landscapes of Health Information.” Sociology of Health & Illness 25 (6): 589–607.
  • Hunt, M. R., and C. Ells. 2011. “Partners Towards Autonomy: Risky Choices and Relational Autonomy in Rehabilitation Care.” Disability & Rehabilitation 33 (11): 961–967
  • Koggel, C., and J. Orme. 2010. “Care Ethics: New Theories and Applications.” Ethics and Social Welfare 4 (2): 109–114.
  • Lakoff, G., and M. Johnson. 1980. Metaphors We Live By. Chicago: University of Chicago Press.
  • Lupton, D. 1994. Medicine as Culture: Illness, Disease and the Body in Western Societies. Thousand Oaks, CA: Sage.
  • Lupton, D. 1997. “Consumerism, Reflexivity and the Medical Encounter.” Social Science & Medicine 45 (3): 373–381.
  • McCoy, L. 2009. “Time, Self and the Medication Day: A Closer Look at the Everyday Work of ‘Adherence’.” Sociology of Health & Illness 31 (1): 128–146.
  • McDonald, C. 2006. Challenging Social Work: The Context of Practice. New York: Palgrave Macmillan.
  • Meagher, G., and N. Parton. 2004. “Modernising Social Work and the Ethics of Care.” Social Work & Society 2 (1): 10–27.
  • Mol, A. 2008. The Logic of Care: Health and the Problem of Patient Choice. London: Routledge.
  • Mykhalovskiy, E. 2002. “Understanding the Social Character of Treatment Decision Making.” In Making Care Visible: Antiretroviral Therapy and the Health Work of People Living with HIV/AIDS, edited by M. Bresalier, L. Gillis, C. McClure, L. McCoy, E. Mykhalovskiy, D. Taylor, and M. Webber, 37–64. Toronto: Making Care Visible Working Group.
  • Noerreslet, M., G. B. E. Jemec, and J. M. Traulsen. 2009. “Involuntary Autonomy: Patients Perceptions of Physicians, Conventional Medicines and Risks in the Management of Atopic Dermatitis.” Social Science & Medicine 69 (9): 1409–1415.
  • Porter, S., P. O'Halloran, and E. Morrow. 2011. “Bringing Values Back Into Evidence-Based Nursing: The Role of Patients in Resisting Empiricism.” Advances in Nursing Science 34 (2): 106–118.
  • Salander, P., and C. Moynihan. 2010. “Facilitating Patients' Hope Work through Relationships: A Critique of the Discourse of Autonomy.” In Configuring Health Consumers: Health Work and the Imperative of Personal Responsibility, edited by R. Harris, N. Wathen, and S. Wyatt, 113–125. Basingstoke: Palgrave Macmillan.
  • Salmon, P. 2010. “The Work of Clinical Communication in Cancer Care.” In Configuring Health Consumers: Health Work and the Imperative of Personal Responsibility, edited by R. Harris, N. Wathen, and S. Wyatt, 126–139. Basingstoke: Palgrave Macmillan.
  • Salmon, P., and B. Young. 2005. “Core Assumptions and Research Opportunities in Clinical Communication.” Patient Education and Counseling 58 (3): 225–234.
  • Sherwin, S. 1998. “A Relational Approach to Autonomy in Health Care.” In The Politics of Women's Health: Exploring Agency and Autonomy, edited by S. Sherwin and the Feminist Health Care Ethics Research Network, 122–149. Philadelphia, PA: Temple University Press.
  • Sinding, C., P. Hudak, J. Wiernikowski, J. Aronson, P. Miller, J. Gould, and D. Fitzpatrick-Lewis. 2010. “‘I Like to Be an Informed Person But..’ Negotiating Responsibility for Treatment Decisions in Cancer Care.” Social Science & Medicine 71 (6): 1094–1101.
  • Sinding, C., P. Miller, P. Hudak, S. Keller-Olaman, and J. Sussman. 2012. “Of Time and Troubles: Patient Involvement and the Production of Health Care Disparities.” Health:An Interdisciplinary Journal for the Social Study of Health, Illness and Medicine 16 (4): 400–417.
  • Sinding, C., L. Watt, P. Miller, J. Silliker, L. Lawson, C. Kislinsky, C. Stanzlik-Elliot, J. O'Neill, J. Pereira, and P. McGillicuddy. 2013. “Stigmas and Silos: Social Workers' Accounts of Care for People Diagnosed with Serious Mental Illness and Cancer.” Social Work in Mental Health 11 (3): 288–309.
  • Smith, D. E. 2005. Institutional Ethnography: A Sociology for People. Toronto: AltaMira Press.
  • Smith, D. E., ed. 2006. Institutional Ethnography as Practice. Lanham: Rowman & Littlefield.
  • Smith, S. K., A. Dixon, L. Trevena, D. Nutbeam, and K. J. McCaffery. 2011. “Exploring Patient Involvement in Healthcare Decision Making across Different Education and Functional Health Literacy Groups.” Social Science & Medicine 69 (12): 1805–1812.
  • Spoel, P. 2006. “Midwifery, Consumerism, and the Ethics of Informed Choice.” In Bordering Biomedicine: Interdisciplinary Perspectives on Health, Illness, and Disease, edited by V. Kalitzkus, and P. Twohig, 197–214. Amsterdam: Rodopi.
  • Spoel, P. 2007. “A Feminist Rhetorical Perspective on Informed Choice in Midwifery.” Rhetor: Journal of the Canadian Society for the Study of Rhetoric 2: 1–25.
  • Waterworth, S., and K. A. Luker. 1990. “Reluctant Collaborators: Do Patients Want to Be Involved in Decisions Concerning Care?” Journal of Advanced Nursing 15 (8): 971–976.
  • Willems, S., S. De Maesschalck, M. Deveugele, A. Derese, and J. De Maeseneer. 2005. “Socio-economic Status of the Patient and Doctor-Patient Communication: Does It Make a Difference?” Patient Education and Counseling 56 (2): 139–146.
  • Willow Breast Cancer Support Canada. 2010. Managing Your Cancer Care: A Self Advocacy Guide for Breast Cancer Patients. Toronto, ON: Willow Breast Cancer Support Canada.
  • Ziebland, S., J. Evans, and A. McPherson. 2006. “The Choice Is Yours? How Women with Ovarian Cancer Make Sense Of Treatment Choices.” Patient Education and Counseling 62 (3): 361–367.

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