Information control and the micropolitics of health care: Summary of an ongoing research project

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Abstract

Policy changes suggested by “macro” research on the medical care system will not in themselves correct critical gaps and misunderstandings that persist at the “micro” level of the doctor-patient relationship. This paper presents a summary of an ongoing research project concerning one element of this relationship—the doctor's communication of information about illness to the patient.

Information transmittal is closely related to the clinical problems of history taking, medical records, compliance, satisfaction, physiologic response to therapy and patient delay in reporting symptoms.

The sociological considerations guiding the research are summarized under four headings: (1) the problems of uncertainty and power; (2) the definition of information; (3) sociolinguistics and the diffidence of the sick poor; and (4) ethnomethodology and common-sense constructs. The doctor-patient relationship is viewed as a micropolitical situation, in which information control is used, at least in part, to maintain patterns of dominance and subordination.

The over-all methodological objective of the research project is to develop a research design, linked to these sociological perspectives, which allows reproducible and generalizable conclusions about the informative process in a variety of clinical settings. Based on a pre-test,a multivariate model has been operationalized; an association is hypothesized between transmitted information—the dependent variable—and several independent variable, which are classified as physician characteristics, patient characteristics, and situational characteristics. The measures of the dependent and independent variables, sampling procedures, and approach to data analysis are described. Questionnaire materials are presented in appendices.

References (119)

  • H.L. Blumgart

    Caring for the patient

    New Engl. J. Med.

    (1964)
  • P.H. Brauer

    Should the patient be told the truth?

  • A. Verwoerdt

    Communication with the Fatally Ill

    (1966)
  • I. Kant

    Critique of Practical Reason

    (1956)
  • R.C. Cabot

    The use of truth and falsehood in medicine: An experimental study

    Am. Med.

    (1903)
  • R.C. Cabot

    Ethical forces in the practice of medicine

    (1905)
  • R.C. Cabot

    Social Service and the Art of Healing

    (1909)
  • R.C. Cabot

    The Meaning of Right and Wrong

    (1936)
  • A.C. Eustene

    Explaining to the patient: A therapeutic tool and a professional obligation

    J.A.M.A.

    (1957)
  • J. Fletcher

    Morals and Medicine

    (1954)
  • J. Katz

    The education of the physician-investigator

    Daedalus

    (1969)
  • L.P. White

    The self-image of the physician and the care of dying patients

    Ann. N.Y. Acad. Sci.

    (1969)
  • J. Collins

    Should doctors tell the truth?

    Harper's Mag.

    (1927)
  • L.J. Henderson

    Physician and patient as a social system

    New Engl. J. Med.

    (1935)
  • B. Sachs

    Be an optimist

    J. Mt. Sinai Hosp.

    (1942)
  • F. Treves

    A modern religio medici: Sir Thomas Browne

    Br. Med. J.

    (1902)
  • H. Waitzkin et al.

    The communication of information about illness: Clinical, sociological and methodological considerations

    Adv. Psychosom. Med.

    (1972)
  • H. Waitzkin et al.

    The Exploitation of Illness in Capitalist Society

    (1974)
  • L.L. Weed

    Medical Records, Medical Education and Patient Care

    (1969)
  • M.S. Davis

    Variations in patients' compliance with doctors' advice: An empirical analysis of patterns of communication

    Am. J. publ. Hlth

    (1968)
  • V. Francis et al.

    Gaps in doctor-patient communication: Patients' response to medical advice

    New Engl. J. Med.

    (1969)
  • M.S. Davis

    Variation in patients' compliance with doctors' orders: Medical practice and doctor-patient interaction

    Psychiat. Med.

    (1971)
  • T.F. Williams et al.

    The clinical picture of diabetes control, studied in four settings

    Am. J. publ. Hlth

    (1967)
  • B. Blackwell

    Patient compliance

    New Engl. J. Med.

    (1973)
  • T.S. Inui

    Effects of Post-Graduate Physician Education on the Management and Outcomes of Patients with Hypertension

    (1973)
  • B.M. Korsch et al.

    Gaps in doctor-patient communication: Doctor-patient interaction and patient satisfaction

    Pediat.

    (1968)
  • B.M. Korsch et al.

    Doctor-patient communication

    Sci. Am.

    (1972)
  • I.L. Janis

    Psychological Stress: Psychoanalytic and Behavioral Studies of Surgical Patients

    (1958)
  • L.D. Egbert et al.

    Reduction of post-operative pain by encouragement and instruction of patients

    New Engl. J. Med.

    (1964)
  • J.K. Skipper et al.

    Children, stress, and hospitalization: A field experiment

    J. Hlth Soc. Behav.

    (1968)
  • T.P. Hackett et al.

    Patient delay in cancer

    New Engl. J. Med.

    (1973)
  • M.H. Bartlett et al.

    Dial access library—Patient information service: An experiment in health education

    New Engl. J. Med.

    (1973)
  • C.O. Leonard et al.

    Genetic counseling: A consumers' view

    New Engl. J. Med.

    (1972)
  • E. Glogow

    The “bad” patient gets better quicker

    Soc. Policy

    (1973)
  • C.G. Schwartz

    Strategies and tactics of mothers of mentally retarded children for dealing with the medical care system

  • B.N. Shenkin

    Giving the patient his medical record: A proposal to improve the system

    New Engl. J. Med.

    (1973)
  • J.F. Horty

    Informed consent: New rule puts burden of proof on patients

    Mod. Hosp.

    (1971)
  • F.J. Ingelfinger

    Informed (but uneducated) consent

    New Engl. J. Med.

    (1972)
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    This report is based on Working Paper No. 9, which was prepared as part of the research project. “The Informative Process in Medical Care,” sponsored by grants HS 01565 and 5F01HS54.957 from the National Center for Health Services Research, and by the Robert Wood Johnson Foundation Clinical Scholars Program at Stanford University. Portions of the report were presented at the Annual Meeting of the Clinical Scholars Program, Rye, New York, April, 1975.

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