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Patients with medically unexplained symptoms: Sources of patients' authority and implications for demands on medical care

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  • Peters, Sarah
  • Stanley, Ian
  • Rose, Michael
  • Salmon, Peter

Abstract

Lay and medical beliefs are not separate systems. The beliefs of somatizing patients, in particular, incorporate medical understanding and it has been argued that this increases the power that such patients exert in seeking treatment from doctors. To understand the nature and use of this power requires investigation of (i) how patients use medical ideas and language to explain their symptoms and (ii) how this process influences patients' expectations and evaluations of their doctors. We interviewed 68 patients, in whom no physical cause had been found for persistent physical symptoms. Their accounts of symptoms and of their experience of doctors were subjected to qualitative thematic analysis. As expected, patients used medical terms to explain their symptoms. However, these depicted explanatory themes which have long been familiar in traditional lay models: disease as a malign entity and imbalance between bodily forces. Patients' sense of authority over doctors derived, not from facility with medical language and ideas but from contrasting their own sensory, and therefore infallible, experience of symptoms with doctors' indirect and fallible knowledge. By providing explanations that questioned the reality of symptoms, doctors were perceived as incompetent and inexpert. Patients used their authority, not to seek treatment, but to secure naming of, and collaboration against, the disorder. Although these patients saw the doctors' role as limited and inexpert by comparison with their own, our analysis suggests ways in which doctors might more effectively engage with persistent somatizing patients.

Suggested Citation

  • Peters, Sarah & Stanley, Ian & Rose, Michael & Salmon, Peter, 0. "Patients with medically unexplained symptoms: Sources of patients' authority and implications for demands on medical care," Social Science & Medicine, Elsevier, vol. 46(4-5), pages 559-565, February.
  • Handle: RePEc:eee:socmed:v:46:y::i:4-5:p:559-565
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    Cited by:

    1. Clemente, Ignasi & Lee, Seung-Hee & Heritage, John, 2008. "Children in chronic pain: Promoting pediatric patients' symptom accounts in tertiary care," Social Science & Medicine, Elsevier, vol. 66(6), pages 1418-1428, March.
    2. Stockl, Andrea, 2007. "Complex syndromes, ambivalent diagnosis, and existential uncertainty: The case of Systemic Lupus Erythematosus (SLE)," Social Science & Medicine, Elsevier, vol. 65(7), pages 1549-1559, October.
    3. Budych, Karolina & Helms, Thomas M. & Schultz, Carsten, 2012. "How do patients with rare diseases experience the medical encounter? Exploring role behavior and its impact on patient–physician interaction," Health Policy, Elsevier, vol. 105(2), pages 154-164.
    4. Vikas Menon & Balasubramanian Shanmuganathan & Anand Babu Arun & Jaiganesh Selvapandian Thamizh & Nivedhitha Selvakumar & Siddharth Sarkar, 2016. "A qualitative analysis of explanatory models in medically unexplained physical symptoms presenting to a tertiary health care psychiatric facility in South India," International Journal of Social Psychiatry, , vol. 62(7), pages 608-615, November.
    5. Madden, Sue & Sim, Julius, 2006. "Creating meaning in fibromyalgia syndrome," Social Science & Medicine, Elsevier, vol. 63(11), pages 2962-2973, December.
    6. Ring, Adele & Dowrick, Christopher F. & Humphris, Gerry M. & Davies, John & Salmon, Peter, 2005. "The somatising effect of clinical consultation: What patients and doctors say and do not say when patients present medically unexplained physical symptoms," Social Science & Medicine, Elsevier, vol. 61(7), pages 1505-1515, October.
    7. Lawrence, Vanessa & McCombie, Catherine & Nikolakopoulos, Georgios & Morgan, Craig, 2021. "Navigating the mental health system: Narratives of identity and recovery among people with psychosis across ethnic groups," Social Science & Medicine, Elsevier, vol. 279(C).

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