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Truth and lies: Disclosure and the power of diagnosis

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  • Jutel, Annemarie

Abstract

The moment at which a diagnosis is delivered to a patient, particularly when it is serious, is an important social moment. It not only dictates the clinical pathway, it also rewrites the patient narrative, shifts their identity, predicts potential outcomes, and foregrounds mortality. It may provide a sense of relief, or one of despair. Over time, and across cultures, there have been many different approaches used to palliate the potential impact of the diagnostic utterance on the patient. France, as one example, provides an interesting case study. Until the turn of the century, cancer diagnoses were often concealed from patients. However, recent legislation now requires full diagnostic disclosure according to prescribed protocols. Using Zerubavel's social patterning methodology, and transcultural historical methods, I seek to understand beliefs about the potential impact of the diagnostic moment by identifying common features across cultural and historical social contexts. I examine writings of French oncologists, and physicians in related fields, from the pre- and post-legislation era who discuss if and how a cancer diagnosis should be disclosed to the patient. While the approach to diagnostic disclosure has changed significantly, medical representations of diagnostic power have not. The diagnostic utterance is still cast by medical professionals as a terrifying and life-disrupting moment.

Suggested Citation

  • Jutel, Annemarie, 2016. "Truth and lies: Disclosure and the power of diagnosis," Social Science & Medicine, Elsevier, vol. 165(C), pages 92-98.
  • Handle: RePEc:eee:socmed:v:165:y:2016:i:c:p:92-98
    DOI: 10.1016/j.socscimed.2016.07.037
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    References listed on IDEAS

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    1. Dumit, Joseph, 2006. "Illnesses you have to fight to get: Facts as forces in uncertain, emergent illnesses," Social Science & Medicine, Elsevier, vol. 62(3), pages 577-590, February.
    2. Jutel, Annemarie, 2010. "Framing disease: The example of female hypoactive sexual desire disorder," Social Science & Medicine, Elsevier, vol. 70(7), pages 1084-1090, April.
    3. Nettleton, Sarah, 2006. "'I just want permission to be ill': Towards a sociology of medically unexplained symptoms," Social Science & Medicine, Elsevier, vol. 62(5), pages 1167-1178, March.
    4. Jutel, Annemarie & Nettleton, Sarah, 2011. "Towards a sociology of diagnosis: Reflections and opportunities," Social Science & Medicine, Elsevier, vol. 73(6), pages 793-800, September.
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    Cited by:

    1. Mei, Xiao & Tu, Jiong, 2021. "Values, skills, and decision-making: A cultural sociological approach to explaining diagnostic disclosure," Social Science & Medicine, Elsevier, vol. 279(C).
    2. Joyce, Kelly & Jeske, Melanie, 2020. "Using autoimmune strategically: Diagnostic lumping, splitting, and the experience of illness," Social Science & Medicine, Elsevier, vol. 246(C).
    3. Engman, Athena, 2019. "Embodiment and the foundation of biographical disruption," Social Science & Medicine, Elsevier, vol. 225(C), pages 120-127.

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