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Different fracture risk profile in patients treated with anti-osteoporotic drugs in real-life

机译:在现实生活中抗骨质疏松药物治疗患者的不同骨折风险概况

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In this retrospective study, we intended to investigate the baseline fracture risk profile in patients who started treatment with different anti-osteoporotic medications. We analyzed retrospectively the fracture risk calculated with DeFRA, a validated FRAX derived tool, in women who started an anti-osteoporotic treatment from 2010 to 2017. We analyzed baseline data of 12,024 post-menopausal women aged over 50 years. Teriparatide initiators had a baseline 10-year risk of major osteoporotic fracture of 82.1% with a Standard Deviation (SD) of 66.5%. Denosumab initiators and zoledronic acid initiators had a greater 10-year baseline risk of fracture (54.3%, SD 46.5% and 47.0%, SD 42.0 respectively) than patients initiated on alendronate (24.9%, SD 34.6%) and patients initiated on risedronate (23.9%, SD 24.1%). Using DeFRA, a FRAX? derived tool, we showed significantly different fracture risk profiles in women who were started on various therapeutic agents for the treatment of osteoporosis in routine clinical practice.
机译:在这项回顾性研究中,我们旨在研究开始用不同抗骨质疏松药物治疗的患者的基线骨折风险概况。我们回顾性地分析了由2010年到2010年开始抗骨质疏松治疗的抗骨质疏松治疗的妇女用DEFRA计算的骨折风险。我们分析了50岁以上的12,024名后绝经妇女的基线数据。 Teriparatide Inentiators的基线10年的主要骨质疏松骨折风险为82.1%,标准差(SD)为66.5%。 Denosumab引发剂和唑醇酸引发剂的骨折的10年基线风险较大(分别为54.3%,SD 46.5%和47.0%,SD 42.0,SD 42.0),患者比在阿仑膦酸盐(24.9%,SD 34.6%)和在Ristronate上发起的患者( 23.9%,SD 24.1%)。使用defra,frax?衍生工具,我们在常规临床实践中展示了各种治疗剂的女性中展示了骨折的骨折风险型材显着不同。

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