Table 4.
At 52 weeks
|
Crude Adjusted
|
||||
---|---|---|---|---|---|
Crude | Adjusted | Crude | Adjusted | ||
Patient was on guideline-concordant pharmacotherapy | AOR 95 % CI |
1.04 (0.93, 1.16) |
1.03 (0.91, 1.17) |
1.07 (0.96, 1.19) |
1.06 (0.93, 1.21) |
Patient recalled receiving a letter with their DXA results | AOR 95 % CI |
3.10*** (2.66, 3.63) |
3.14*** (2.71, 3.63) |
N/A | |
Patient correctly identified the results of their baseline DXA | AOR 95 % CI |
1.44*** (1.29, 1.62) |
1.47*** (1.31, 1.64) |
1.26** (1.10, 1.44) |
1.27** (1.11, 1.45) |
Patient reported having contact with their provider after their DXA | AOR 95 % CI |
1.02 (0.92, 1.12) |
1.01 (0.91, 1.12) |
1.21* (1.05, 1.40) |
1.21* (1.05, 1.39) |
Patient discussed their DXA results with their provider | AOR 95 % CI |
1.15* (1.02, 1.30) |
1.13 (1.01, 1.27) |
1.22** (1.09, 1.37) |
1.24*** (1.11, 1.39) |
The covariates that were adjusted for included clinical site, patient age, sex, race, education, self-rated health, COPD, depression, smoking status, alcohol use, weight-bearing exercise, fractures after age 40, parental hip fractures after age 50, prior DXA testing, index FRAX risk, prior diagnoses for osteopenia or osteoporosis, and current or former osteoporosis medication use
p < 0.025,
p < 0.005,
p < 0.0005