• Title of article

    Contending visions in the evolution of genetic medicine: The case of cancer genetic services in Ontario, Canada

  • Author/Authors

    Fiona Alice Miller، نويسنده , , Mita Giacomini، نويسنده , , Catherine Ahern، نويسنده ,

  • Issue Information
    دوهفته نامه با شماره پیاپی سال 2008
  • Pages
    9
  • From page
    152
  • To page
    160
  • Abstract
    Growth in genetic medicine has provoked debate about how new and emerging genetic services should be provided, and specifically, what roles non-genetic clinicians should assume. We address this question through a qualitative interview based case study of the program in genetic testing for the hereditary cancer syndromes (breast/ovarian and colorectal) in Ontario, Canada. We argue that two communities offer parallel visions of cancer genetic care: one “genetic,” the other “oncologic.” Both communities argue from precedent that cancer genetics is a natural extension of their work: it is “what we do.” Both communities also highlight the importance of their own expertise in providing core elements of cancer genetic care: it requires “what we know.” Further, both communities perceive the need for leadership by their own (or a related) community as genetic medicine expands to include a broader array of more common and complex diseases: it is expanding “where weʹre leading.” Yet, the “weʹs” articulating these visions are not reducible to professional identity; rather, both represent distinctive “communities of practice and discourse” that are constructed in relation to institutionalized professional roles, and interactions with the genetic technologies (both tests and counselling) themselves. Available literature on the role of diverse health care professionals in the provision of genetic health care presumes a fixed identity and set of approaches for each professional group that might play a role. Further, existing models tend to assume that genetic technologies are given as tools, and that service organization concerns primarily questions of who will have access to these tools and their powers, as well as the consequent professional and ethical responsibilities. Yet questions about who will control genetic technologies are not simply turf battles between the professions: they are also inescapably questions about what the genetic technologies should and will accomplish clinically.
  • Keywords
    CanadaCancer geneticsGenetic risk assessmentModels of careProfessions
  • Journal title
    Social Science and Medicine
  • Serial Year
    2008
  • Journal title
    Social Science and Medicine
  • Record number

    603869