Real-world effectiveness of osteoporosis therapies for fracture reduction in post-menopausal women

被引:56
|
作者
Yusuf, Akeem A. [1 ]
Cummings, Steven R. [2 ]
Watts, Nelson B. [3 ]
Feudjo, Maurille Tepie [4 ]
Sprafka, J. Michael [1 ]
Zhou, Jincheng [5 ]
Guo, Haifeng [6 ]
Balasubramanian, Akhila [1 ]
Cooper, Cyrus [7 ]
机构
[1] Ctr Observat Res, 1 Amgen Ctr Dr,MS 24-2-A, Thousand Oaks, CA 91320 USA
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
[3] Mercy Hlth Osteoporosis & Bone Hlth Serv, Cincinnati, OH USA
[4] Amgen Inc, Uxbridge, Middx, England
[5] Univ Minnesota, Sch Publ Hlth, Div Biostat, Minneapolis, MN 55455 USA
[6] Chron Dis Res Grp, Minneapolis, MN USA
[7] Univ Southampton, MRC Lifecourse Epidemiol Unit, Southampton, Hants, England
关键词
Osteoporosis; Fracture risk reduction; Effectiveness; Anabolics; Antiresorptives; FRAGILITY FRACTURES; LONGITUDINAL CHANGE; IDENTIFICATION; PREVENTION; DRUGS;
D O I
10.1007/s11657-018-0439-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Studies examining real-world effectiveness of osteoporosis therapies are beset by limitations due to confounding by indication. By evaluating longitudinal changes in fracture incidence, we demonstrated that osteoporosis therapies are effective in reducing fracture risk in real-world practice settings. Introduction Osteoporosis therapies have been shown to reduce incidence of vertebral and non-vertebral fractures in placebo-controlled randomized clinical trials. However, information on the real-world effectiveness of these therapies is limited. Methods We examined fracture risk reduction in older, post-menopausal women treated with osteoporosis therapies. Using Medicare claims, we identified 1,278,296 women age >= 65 years treated with zoledronic acid, oral bisphosphonates, denosumab, teriparatide, or raloxifene. Fracture incidence rates before and after treatment initiation were described to understand patients' fracture risk profile, and fracture reduction effectiveness of each therapy was evaluated as a longitudinal change in incidence rates. Results Fracture incidence rates increased during the period leading up to treatment initiation and were highest in the 3-month period most proximal to treatment initiation. Fracture incidence rates following treatment initiation were significantly lower than before treatment initiation. Compared with the 12-month pre-index period, there were reductions in clinical vertebral fractures for denosumab (45%; 95% confidence interval [CI] 39-51%), zoledronic acid (50%; 95% CI 47-52%), oral bisphosphonates (24%; 95% CI 22-26%), and teriparatide (72%; 95% CI 69-75%) during the subsequent 12 months. Relative to the first 3 months after initiation, clinical vertebral fractures were reduced for denosumab (51%; 95% CI 42-59%), zoledronic acid (25%; 95% CI 17-32%), oral bisphosphonates (23%; 95% CI 20-26%), and teriparatide (64%; 95% CI 58-69%) during the subsequent 12 months. Conclusion In summary, reductions in fracture incidence over time were observed in cohorts of patients treated with osteoporosis therapies.
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页数:10
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