Background
Determining whether observed differences in healthcare can be called disparities requires persistence of differences after adjustment for relevant patient, provider and health system factors. We examined whether providing dual energy x-ray absorptiometry (DXA) test results directly to patients might reduce or eliminate racial differences in osteoporosis-related healthcare.
Design, Subjects, and Measures
We analyzed data from 3,484 White and 1,041 Black women who underwent DXA testing at two health systems participating in the Patient Activation after DXA Result Notification (PAADRN) pragmatic clinical trial (ClinicalTrials.gov NCT-01507662) between February 2012 and August 2014. We examined seven outcomes related to bone health at 12- and 52-weeks post-DXA: (1) whether the patient correctly identified their DXA baseline results; (2) whether the patient was on guideline-concordant osteoporosis pharmacotherapy; (3) osteoporosis-related satisfaction; (4) osteoporosis knowledge; (5 and 6) osteoporosis self-efficacy for exercise and for diet; and, (7) patient activation. We examined whether unadjusted differences in outcomes between Whites and Blacks persisted after adjusting for patient, provider and health system factors.
Results
Mean age was 66.5 years and 29% were Black. At baseline Black women had less education, poorer health status, and were less likely to report a history of osteoporosis (p < 0.001 for all). In unadjusted analyses Black women were less likely to correctly identify their actual DXA results, more likely to be on guideline concordant therapy, and had similar patient activation. After adjustment for patient demographics, baseline health status and other factors, Black women were still less likely to know their actual DXA result and less likely to be on guideline-concordant therapy, but Black women had greater patient activation.
Conclusions
Adjustment for patient and provider level factors can change how racial differences are viewed, unmasking new disparities and providing explanations for others.
Trial Registration
ClinicalTrials.gov Identifier: NCT01507662