首页> 外文期刊>Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research >Managing Osteoporosis in Patients on Long-Term Bisphosphonate Treatment: Report of a Task Force of the American Society for Bone and Mineral Research
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Managing Osteoporosis in Patients on Long-Term Bisphosphonate Treatment: Report of a Task Force of the American Society for Bone and Mineral Research

机译:长期接受双膦酸盐治疗的患者的骨质疏松症的处理:美国骨与矿物质研究学会工作队的报告

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Bisphosphonates (BPs) are the most commonly used medications for osteoporosis. This ASBMR report provides guidance on BP therapy duration with a risk-benefit perspective. Two trials provided evidence for long-term BP use. In the Fracture Intervention Trial Long-term Extension (FLEX), postmenopausal women receiving alendronate for 10 years had fewer clinical vertebral fractures than those switched to placebo after 5 years. In the HORIZON extension, women who received 6 annual infusions of zoledronic acid had fewer morphometric vertebral fractures compared with those switched to placebo after 3 years. Low hip T-score, between -2 and -2.5 in FLEX and below -2.5 in HORIZON extension, predicted a beneficial response to continued therapy. Hence, the Task Force suggests that after 5 years of oral BP or 3 years of intravenous BP, reassessment of risk should be considered. In women at high risk, for example, older women, those with a low hip T-score or high fracture risk score, those with previous major osteoporotic fracture, or who fracture on therapy, continuation of treatment for up to 10 years (oral) or 6 years (intravenous), with periodic evaluation, should be considered. The risk of atypical femoral fracture, but not osteonecrosis of the jaw, clearly increases with BP therapy duration, but such rare events are outweighed by vertebral fracture risk reduction in high-risk patients. For women not at high fracture risk after 3 to 5 years of BP treatment, a drug holiday of 2 to 3 years can be considered. The suggested approach for long-term BP use is based on limited evidence, only for vertebral fracture reduction, in mostly white postmenopausal women, and does not replace the need for clinical judgment. It may be applicable to men and patients with glucocorticoid-induced osteoporosis, with some adaptations. It is unlikely that future trials will provide data for formulating definitive recommendations. (C) 2015 American Society for Bone and Mineral Research.
机译:双膦酸盐(BPs)是骨质疏松症最常用的药物。该ASBMR报告从风险获益的角度为BP治疗的持续时间提供了指导。两项试验为长期使用BP提供了证据。在骨折干预试验长期延长(FLEX)中,接受阿仑膦酸盐治疗10年的绝经后妇女的临床椎骨骨折少于5年后转用安慰剂的妇女。在HORIZON扩展方案中,与3年后改用安慰剂的女性相比,每年接受6次唑来膦酸输注的女性的椎体形态骨折较少。低髋关节T分评分(FLEX介于-2至-2.5之间,HORIZON伸展范围低于-2.5之间)预示着对持续治疗的有益反应。因此,工作队建议口服BP 5年或静脉BP 3年后,应考虑重新评估风险。在高风险女性中,例如老年女性,髋部T分数低或骨折风险评分高的女性,先前患有严重骨质疏松性骨折的女性,或因治疗而骨折,持续治疗长达10年的患者(口服)或6年(静脉),应考虑定期评估。随着BP治疗持续时间的增加,非典型股骨骨折的风险明显增加,但颌骨坏死的风险却没有明显增加,但是这种高风险患者降低椎骨骨折的风险却远远超过了这种罕见的事件。对于在BP治疗3至5年后没有高骨折风险的女性,可以考虑2至3年的停药期。长期使用BP的建议方法是基于有限的证据,仅适用于绝大部分白人绝经后妇女的椎体骨折复位术,并不能代替临床判断的需要。经过一些修改,它可能适用于糖皮质激素诱发的骨质疏松症的男性和患者。未来的试验不太可能为制定明确的建议提供数据。 (C)2015年美国骨矿物质研究学会。

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