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The power of compassion: Truth-telling among American doctors in the care of dying patients

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  • Miyaji, Naoko T.

Abstract

The perceptions of American doctors about their practice regarding truth-telling in the care of dying patients were examined based on semi-structured interviews with 32 physicians in a teaching hospital. The doctors inform patients of their disease using three basic styles; 'telling what patients want to know', 'telling what patients need to know' and 'translating information into terms that patients can take'. These styles are supported by five basic normative principles; 'respect the truth', 'patients rights', 'doctors' duty to inform', 'preserve hope' and 'individual contract between patients and doctors'. These styles and principles suggest that physicians adhere to the recent trends of American medical ethics based on informed consent doctrine, and give the impression that patients have control over obtaining information. But close analysis of their accounts shows that physicians still hold power to control information through their management of the information-giving process. The styles and principles are flexibly interpreted and selectively used in the process so that they facilitate a discourse which justifies, rather than eliminates, the information control. Clinical contexts of information control are analyzed by examining dissimilar manners of providing information about treatment as opposed to prognosis. Physicians give less, and vaguer information about prognosis, citing its uncertainty and lesser relevance to future actions as reasons. Information about treatment is more readily shared in order to counterbalance the negative impact of the news on patients. The analysis reveals that the way doctors control information is closely related to the way they handle aspects of the reality of clinical practice, such as physicians' own emotional coping, institutional and legal constraints, and power relationships among patients, doctors and other care-givers. Situating the findings in the historical context of normative discourse in American medicine, discussion focuses on the issues of trust and power of doctors. The humanistic role of the doctor, although suppressed in the currently dominant, contractual ethical framework, is still powerful in doctors' narratives. It expresses doctors' commitment to patients while preserving their authority. Implications of the individualistic approach to the doctor-patient relationship are also discussed.

Suggested Citation

  • Miyaji, Naoko T., 1993. "The power of compassion: Truth-telling among American doctors in the care of dying patients," Social Science & Medicine, Elsevier, vol. 36(3), pages 249-264, February.
  • Handle: RePEc:eee:socmed:v:36:y:1993:i:3:p:249-264
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    Cited by:

    1. N. C. A. van der Velden & M. B. A. van der Kleij & V. Lehmann & E. M. A. Smets & J. M. L. Stouthard & I. Henselmans & M. A. Hillen, 2021. "Communication about Prognosis during Patient-Initiated Second Opinion Consultations in Advanced Cancer Care: An Observational Qualitative Analysis," IJERPH, MDPI, vol. 18(11), pages 1-15, May.
    2. Kirby, Emma & Broom, Alex & MacArtney, John & Lewis, Sophie & Good, Phillip, 2021. "Hopeful dying? The meanings and practice of hope in palliative care family meetings," Social Science & Medicine, Elsevier, vol. 291(C).
    3. 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).
    4. Stacey, Clare L. & Pai, Manacy & Novisky, Meghan A. & Radwany, Steven M., 2019. "Revisiting ‘awareness contexts’ in the 21st century hospital: How fragmented and specialized care shape patients' Awareness of Dying," Social Science & Medicine, Elsevier, vol. 220(C), pages 212-218.

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