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Patient desire for information and decision making in health care decisions

The autonomy preference index and the health opinion survey

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Abstract

OBJECTIVES: To compare results on the Autonomy Preference Index (API) and the Health Opinion Survey (HOS), two instruments that measure patient desire for information and involvement in decision making.

DESIGN: Cross-sectional survey.

SETTING: University-based primary care outpatient longitudinal and acute care clinic.

PATIENTS: 167 patients with benign prostatic hyperplasia, back pain, or mild hypertension seen from October 1991 to December 1992.

MEASUREMENTS AND MAIN RESULTS: On the API and the HOS (both scaled from 0 to 1), the patients had intermediate desire for involvement in decision making (median API: 0.42; HOS: 0.36) and higher desire for information (median API: 0.97; HOS: 0.57). With either instrument, the desire for information exceeded that for involvement in decision making (p<0.0001). The API information scores were higher than the HOS information scores (p < 0.0001), probably because the HOS focuses on patient behavior rather than desire. Variation in desire for information and involvement in decision making was substantial and largely unexplained.

CONCLUSIONS: Most patients have a high desire for information, the desire for information and involvement in decision making varies substantially among patients, and the API is preferable to the HOS for researchers interested in focusing solely on patient desire for information.

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Received from the Department of Medicine, Dartmouth — Hitchcock Medical Center, Lebanon, New Hampshire.

Preliminary analyses were presented at the annual meeting of the Society for Medical Decision Making, Portland, Oregon, October 17–20, 1992.

Supported by a grant from the Pew Charitable Trusts. Dr. Nease is a Picker/Commonwealth Scholar.

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Nease, R.F., Brooks, W.B. Patient desire for information and decision making in health care decisions. J Gen Intern Med 10, 593–600 (1995). https://doi.org/10.1007/BF02602742

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