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. 2020 May 30;31(10):1935–1942. doi: 10.1007/s00198-020-05463-4

Table 3.

Cumulative incidence of patients with ≥ 1 pooled clinical fractures (clinical vertebral and non-vertebral) and adjusted hazard ratios estimated with an extended Cox regression model at different time points of follow-up

Teriparatide (n = 680) Risedronate (n = 680) HR (95% CI) p value
At 3 months 6 (0.9%) 7 (1.0%) 0.70 (0.36, 1.37) 0.299
At 6 months 12 (1.8%) 17 (2.6%) 0.62 (0.37, 1.07) 0.085
At 7 months 12 (1.8%) 23 (3.6%) 0.60 (0.36, 0.99) 0.046
At 8 months 13 (2.0%) 25 (3.9%) 0.58 (0.36, 0.93) 0.024
At 9 months 14 (2.1%) 26 (4.0%) 0.56 (0.35, 0.88) 0.012
At 12 months 18 (2.8%) 34 (5.3%) 0.49 (0.31, 0.78) 0.003
At 15 months 22 (3.5%) 39 (6.1%) 0.44 (0.26, 0.76) 0.003
At 18 months 26 (4.1%) 49 (7.8%) 0.39 (0.20, 0.77) 0.007
At 21 months 27 (4.3%) 55 (8.8%) 0.35 (0.15, 0.81) 0.014
At 24 months 30 (4.8%) 61 (9.8%) 0.31 (0.11, 0.86) 0.024

BMD, bone mineral density; CI, confidence interval; HR, hazard ratio (teriparatide versus risedronate). Adjusted by treatment, antecedent of recent clinical vertebral fracture, recent use of bisphosphonate, age, baseline femoral neck BMD, baseline 25-hydroxy-vitamin D concentration, geographical region, and time-varying covariate treatment-by-time interaction