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Disparities in patient reports of communications to inform decision making in the DECISIONS survey
Brian J Zikmund-Fisher1, Mick P Couper, Angela Fagerlin
1Department of Health Behavior and Health Education, University of Michigan, Ann Arbor, MI 48109-2029, USA. bzikmund@umich.edu
Objective:
To identify patient- and decision-type predictors of two key aspects of informed decision making: discussing the cons (not just the pros) of medical interventions and asking patients what they want to do.
Methods:
Using data from 2473 members of the DECISIONS survey, a nationally representative sample of U.S. adults age 40+, we used logistic regression analysis to identify which patient characteristics predicted patient reports of healthcare providers discussing cons or eliciting preferences about one of 9 common medical decisions.
Results:
Multiple demographic characteristics predicted both discussions of cons and elicitations of preferences, although the specific characteristics varied between decision contexts. In particular, African-American respondents reported being more likely to receive a discussion of the cons of cancer screening (OR=1.69, p<0.05) yet less likely to have been asked their opinion about either getting a cancer screening test (OR=0.56, p<0.05) or initiating medications (OR=0.53, p<0.05). Significant cross-decision variations remained even after controlling for patient characteristics.
Conclusions:
Important disparities in patient communication and involvement appear to exist both between different types of medical decisions and between different types of patients.
Practice Implications:
Providers must make sure to consistently discuss the cons of treatment and to solicit input from all patients, especially African-Americans.
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