Osteoporosis

特立帕肽 德诺苏马布 医学 骨质疏松症 重症监护医学 健骨 骨矿物 内科学 儿科
作者
Juliet Compston,Michael R. McClung,William D. Leslie
出处
期刊:The Lancet [Elsevier BV]
卷期号:393 (10169): 364-376 被引量:1838
标识
DOI:10.1016/s0140-6736(18)32112-3
摘要

Summary

Fractures resulting from osteoporosis become increasingly common in women after age 55 years and men after age 65 years, resulting in substantial bone-associated morbidities, and increased mortality and health-care costs. Research advances have led to a more accurate assessment of fracture risk and have increased the range of therapeutic options available to prevent fractures. Fracture risk algorithms that combine clinical risk factors and bone mineral density are now widely used in clinical practice to target high-risk individuals for treatment. The discovery of key pathways regulating bone resorption and formation has identified new approaches to treatment with distinctive mechanisms of action. Osteoporosis is a chronic condition and long-term, sometimes lifelong, management is required. In individuals at high risk of fracture, the benefit versus risk profile is likely to be favourable for up to 10 years of treatment with bisphosphonates or denosumab. In people at a very high or imminent risk of fracture, therapy with teriparatide or abaloparatide should be considered; however, since treatment duration with these drugs is restricted to 18–24 months, treatment should be continued with an antiresorptive drug. Individuals at high risk of fractures do not receive adequate treatment and strategies to address this treatment gap—eg, widespread implementation of Fracture Liaison Services and improvement of adherence to therapy—are important challenges for the future.
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