McCloskey Eugene
Academic Unit of Bone Metabolism, University of Sheffield.
Practitioner. 2011 Jan;255(1736):19-22, 2-3.
While fractures at the spine, wrist and hip are regarded as classical osteoporotic fractures, all fragility fractures in the elderly should be considered as osteoporotic once pathological fracture (e.g. metastatic disease) has been excluded. The assessment of fracture risk should take account of specific risk factors in addition to bone mineral density (BMD). The WHO has produced FRAX, a well validated tool that estimates the probability of a major osteoporotic fracture in the next 10 years. The algorithm is specifically designed for primary care. After age and prior fragility fracture, BMD is the next major determinant of fracture risk. Rather than scanning all individuals with a risk factor, measurements should be targeted to those whose probability of fracture lies close to the intervention threshold where knowledge of BMD will influence management. Individuals with a low trauma vertebral fracture or low BMD for age should be investigated for underlying causes of osteoporosis. Secondary causes account for up to 40% of cases of osteoporosis in women and 60% in men. The goal of osteoporosis management is to reduce the future risk of fracture. Lifestyle modification includes measures to reduce falls risk and bone loss such as exercise, adequate dietary calcium and avoidance of smoking and excessive alcohol consumption. All patients with an osteoporotic fracture and those at high risk should be assessed for falls risk. Combined therapy, with calcium and vitamin D, has been shown to reduce hip fracture risk in the frail elderly and should be considered in all older patients who are housebound or in residential care. Alendronate and risedronate are available as once-weekly preparations with evidence for significant reductions in vertebral and non-vertebral fractures. Denosumab is approved for osteoporosis in postmenopausal women at increased risk of fractures. Strontium ranelate has been shown to reduce fracture risk significantly in postmenopausal women.
虽然脊柱、腕部和髋部骨折被视为典型的骨质疏松性骨折,但一旦排除病理性骨折(如转移性疾病),老年人的所有脆性骨折都应被视为骨质疏松性骨折。骨折风险评估除骨密度(BMD)外,还应考虑特定风险因素。世界卫生组织(WHO)制定了FRAX,这是一种经过充分验证的工具,可估计未来10年内发生主要骨质疏松性骨折的概率。该算法专为初级保健设计。除年龄和既往脆性骨折外,骨密度是骨折风险的下一个主要决定因素。不应扫描所有有风险因素的个体,而应针对骨折概率接近干预阈值的人群进行测量,因为了解骨密度会影响治疗管理。对于年龄相关的低创伤性椎体骨折或低骨密度个体,应调查骨质疏松的潜在原因。继发性原因在女性骨质疏松病例中占比高达40%,在男性中占比60%。骨质疏松管理的目标是降低未来骨折风险。生活方式的改变包括采取措施降低跌倒风险和骨质流失,如运动、摄入足够的膳食钙以及避免吸烟和过量饮酒。所有骨质疏松性骨折患者和高危患者都应评估跌倒风险。钙和维生素D联合治疗已被证明可降低体弱老年人的髋部骨折风险,所有居家或接受机构护理的老年患者都应考虑使用。阿仑膦酸钠和利塞膦酸钠有每周一次的制剂,有证据表明可显著降低椎体和非椎体骨折的发生率。地诺单抗被批准用于骨折风险增加的绝经后女性的骨质疏松治疗。雷奈酸锶已被证明可显著降低绝经后女性的骨折风险。