The Wiley Blackwell Companion to Medical Sociology. Группа авторов
Чтение книги онлайн.
Читать онлайн книгу The Wiley Blackwell Companion to Medical Sociology - Группа авторов страница 54
![The Wiley Blackwell Companion to Medical Sociology - Группа авторов The Wiley Blackwell Companion to Medical Sociology - Группа авторов](/cover_pre881010.jpg)
88 Rothman, David. 1991. Strangers at the Bedside. New York: Basic Books.
89 Schneider, Carl E. 1998. The Practice of Autonomy, Patients, Doctors and Medical Decision. New York: Oxford University Press.
90 Schneiderman, L., T. Glimer, H. D. Teetzel, D. O. Dugan, J. Blustein, R. Cranford, K. B. Briggs, G. I. Komatsu, P. Goodman-Crews, F. Cohn, and E. W. W Young. 2003. “Effects of Ethics Consultations on Non-Beneficial Life Sustaining Treatments in the Intensive Care Setting: A Randomized Controlled Trial.” Journal of American Medical Association 290(9):1166–1172.
91 Sheehan, Mark and Dunn Michael. 2013. “On the Nature and Sociology of Bioethics.” Health Care Analysis 21:54–69.
92 Silverman, Henry, Sara C Hull, and Jeremy Sugarman. 2001. “Variability among Institutional Review Boards’ Decisions within the Context of a Multi-Center Trial.” Critical Care Medicine 29:235–241.
93 Simmel, Georg. [1908] 1971. “Der Fremde” [“The Stranger”] Pp. 685–691 in Soziologie [Sociology]. Munich and Liepzig: Duncker and Humblot. Translated and reprinted in Georg Simmel, On Individuality and Social Forms: Selected Writings, pp. 143–149, Donald Levine (ed.). Chicago, IL: University of Chicago Press.
94 Stair, Thomas, Caitlin Reed, Michael Radeos, Greg Koski, and Carlos A. Camargo; MARC investigators. Multicenter Research Collaboration. 2001. “Variation in Institutional Review Board Responses to a Standard Protocol for a Multicenter Trial.” Academic Emergency Medicine 8:636–641.
95 Stark, Laura. 2012. Behind Closed Doors: IRBs and the Making of Ethical Research. Chicago, IL: University of Chicago Press.
96 Stevens, Tina M L. 2000. Bioethics in America: Origin and Cultural Politics. Baltimore, MD: John Hopkins University Press.
97 Stolper, Margreet, Reidar Pedersen, and Bert Molewijk. 2020. “Examining the Doing of Ethics Support Staff. A Dialogical Approach toward Assessing the Quality of Facilitators of Moral Case Deliberation.” The American Journal of Bioethics 20(3):42–44.
98 Strauss, Anselm, Shizuko Fagerhaugh, Barbara Suczek, and Carolyn Wiener. 1985. The Social Organization of Medical Work. Chicago, IL: University of Chicago Press.
99 Strauss, Anselm and Barney G. Glaser. 1975. Chronic Illness and the Quality of Life. St. Louis, MO: Mosby.
100 Strong Philip M. 1979. “Sociological imperialism and the profession of medicine. A critical examination of the thesis of medical imperialism.” Social Science & Medicine, Mar; 13A (2):199–215
101 The SUPPORT Principal Investigators. 1995. “A Controlled Trial to Improve Care for Seriously Ill Hospitalized Patients: The Study to Understand Prognoses and Preferences for Outcomes and Risks of Treatments (SUPPORT).” Journal of American Medical Association 274:1591–1598.
102 Tomlinson, Tom, Raymond De Vries, Kerry Ryan, Myra Kim Hyungjin, Nicole Lehpamer, and Scott Y H Kim. 2015. “Moral Concerns and the Willingness to Donate to a Research Biobank.” Journal of American Medical Association 313(4):417–419.
103 Touraine, Alain. 1995. Critique of Modernity. Oxford: Blackwell.
104 Turner, Leigh. 2009. “Anthropological and Sociological Critiques of Bioethics.” Journal of Bioethical Inquiry 6(1):83–98.
105 Van der Scheer, Lieke and Guy Widdershoven. 2004. “Integrated Empirical Ethics: Loss of Normativity?” Medicine, Health Care and Philosophy 7:71–79.
106 Wainwright, Steven P, Clare Williams, Mike Michael, Bobbie Frasides, and Alen Cribb. 2007. “Ethical Boundary-work in the Embryonic Stem Cell Laboratory.” Pp. 67–82 in The View from Here, Bioethics and the Social Sciences, edited by Raymond DeVries, Leigh Turner, Kristina Orfali, and Charles Bosk. Oxford: Blackwell.
107 Wolf, Suzan M. 2004. “Law & Bioethics: From Values to Violence.” Journal of Law, Medicine and Ethics 32:293–306.
108 Wolpe, Paul R. 1998. “The Triumph of Autonomy in American Bioethics: A Sociological View.” Pp. 38–59 in Bioethics and Society: Constructing the Ethical Enterprise, edited by Raymond DeVries and Janardan Subedi. Upper Saddle River, NJ: Prentice Hall.
109 Zussman, Robert. 1997. Intensive Care. Chicago, IL: The University of Chicago Press.
110 Zussman, Robert. 2000. “The Contributions of Sociology to Medical Ethics.” Hastings Center Report 10(1):7–11.
6 The Sociology of the Body
SARAH NETTLETON
In Tom Stoppard’s (1967) play Rosencrantz and Guildenstern are Dead, the two central characters lament the precariousness of their lives. Rosencrantz seeks solace in life’s only certainty when he comments that “the only beginning is birth and the only end is death – if we can’t count on that what can we count on?” To this he might have added that he could reliably count on the fact that he had a body. The “fact” that we are born, have a body, and then die is of course something that does seem to be beyond question. It is something that we can hold on to, as we live in a world that appears to be ever more uncertain and ever more risky (Shilling and Mellor 2017).
But is this fact so obvious? Ironically, the more sophisticated our medical, technological, and scientific knowledge of bodies becomes, the more uncertain we are as to what the body actually is. For example, technological innovations can disrupt boundaries between the physical (or seemingly natural) and social body. With the development of assisted conception, when does birth begin? With the development of life-extending technologies, when does the life of a physical body end? With the development of prosthetic technologies, what constitutes a “pure” human? It seems the old certainties around birth, life, and death are becoming increasingly unstable. It is perhaps not surprising, therefore, that attempts to understand the social and ethical significance of the body have become central to sociological debates. Attempts to develop a sociological appreciation of the body important in the subdiscipline of the sociology of health and illness. Health, disease and illness are fundamentally embodied experiences that are embedded in social contexts (Nettleton 2020). How bodies are conceptualized, maintained, monitored and managed is therefore profoundly political and so contentious. The aim of this chapter is to delineate some of the key developments in the sociological theorizing of the body and to assess their significance for a number of substantive issues in medical sociology. To meet this aim, the chapter will first review the main perspectives on the sociology of the body and social theorists who have informed each of these approaches. Second, the chapter will outline the parameters of the sociology of embodiment or perhaps more appropriately an embodied sociology. Concepts which have emerged from these debates such as flexible immunity bodies, body projects, biovalue and virtual bodies will also be discussed. Finally, a number of substantive issues which are central to medical sociology will be considered to highlight the merits of incorporating the body into the analysis of matters associated with health and illness. These issues are: illness and injury, body work, and embodied health inequalities.
SOCIOLOGICAL PERSPECTIVES ON THE SOCIOLOGY OF THE BODY
There is a substantial literature on the sociology of the body which spans a range