Table 5.
Women Within Each BMI Group Who Were on Treatment Before and After Fracture
Underweight (1) | Non-obese (2) | Obese (3) | Significant P values | |
---|---|---|---|---|
AOM use | ||||
Before fracture | 51.5 (39.6-63.3) | 40.6 (38.7-42.5) | 27.9 (24.7-31.2) | (1) vs. (3)b, (2) vs. (3)b |
After fracture | 63.2 (51.8-74.7) | 46.3 (44.4-48.2) | 33.2 (29.8-36.6) | (1) vs. (3)b, (2) vs. (3)b, (1) vs. (2)a |
Calcium & vitamin D | ||||
Before fracture | 34.9 (24.7-45.2) | 39.9 (38.1-41.6) | 38.6 (35.4-41.8) | |
After fracture | 45.8 (35.1-56.5) | 45.2 (43.4-46.9) | 45.5 (42.2-48.7) | |
AOM, calcium & vitamin D | ||||
Before fracture | 26.6 (15.7-37.4) | 22.2 (20.6-23.8) | 15.8 (13.1-18.4) | (2) vs. (3)b |
After fracture | 34.4 (22.7-46.0) | 26.0 (24.3-27.7) | 20.9 (17.9-23.9) | (1) vs. (3)a, (2) vs. (3)a |
Data are unadjusted percentages (95% confidence intervals)
AOM anti-osteoporosis medication, BMI body mass index
Alpha level ≤ 0.017 for pair-wise unadjusted comparisons
Alpha level ≤ 0.017 for pair-wise unadjusted and adjustedc comparisons
Adjusted for age, comorbidities (hypertension, heart disease, high cholesterol, asthma, emphysema, osteoarthritis and diabetes), and fracture type (clavicle, upper arm, wrist, spine, rib, hip, pelvis, ankle, upper and lower leg)