Osteoporosis and Bone Metabolism Unit, Department of Endocrinology, Singapore General Hospital, DUKE NUS Medical School, Singapore, Singapore.
Clinical and Molecular Osteoporosis Research Unit, Department of Clinical Sciences, Lund University, Department of Orthopedics, Skåne University Hospital, Malmö, Sweden.
Osteoporos Int. 2024 Aug;35(8):1337-1358. doi: 10.1007/s00198-024-07059-8. Epub 2024 Apr 8.
Antiresorptive medications do not negatively affect fracture healing in humans. Teriparatide may decrease time to fracture healing. Romosozumab has not shown a beneficial effect on human fracture healing.
Fracture healing is a complex process. Uncertainty exists over the influence of osteoporosis and the medications used to treat it on fracture healing.
Narrative review authored by the members of the Fracture Working Group of the Committee of Scientific Advisors of the International Osteoporosis Foundation (IOF), on behalf of the IOF and the Société Internationale de Chirurgie Orthopédique et de Traumatologie (SICOT).
Fracture healing is a multistep process. Most fractures heal through a combination of intramembranous and endochondral ossification. Radiographic imaging is important for evaluating fracture healing and for detecting delayed or non-union. The presence of callus formation, bridging trabeculae, and a decrease in the size of the fracture line over time are indicative of healing. Imaging must be combined with clinical parameters and patient-reported outcomes. Animal data support a negative effect of osteoporosis on fracture healing; however, clinical data do not appear to corroborate with this. Evidence does not support a delay in the initiation of antiresorptive therapy following acute fragility fractures. There is no reason for suspension of osteoporosis medication at the time of fracture if the person is already on treatment. Teriparatide treatment may shorten fracture healing time at certain sites such as distal radius; however, it does not prevent non-union or influence union rate. The positive effect on fracture healing that romosozumab has demonstrated in animals has not been observed in humans.
Overall, there appears to be no deleterious effect of osteoporosis medications on fracture healing. The benefit of treating osteoporosis and the urgent necessity to mitigate imminent refracture risk after a fracture should be given prime consideration. It is imperative that new radiological and biological markers of fracture healing be identified. It is also important to synthesize clinical and basic science methodologies to assess fracture healing, so that a convergence of the two frameworks can be achieved.
抗吸收药物不会对人体骨折愈合产生负面影响。特立帕肽可能会缩短骨折愈合时间。罗莫佐单抗尚未显示对人类骨折愈合有益的影响。
骨折愈合是一个复杂的过程。骨质疏松症及其治疗药物对骨折愈合的影响存在不确定性。
国际骨质疏松基金会(IOF)科学顾问委员会骨折工作组的成员撰写的叙述性评论,代表 IOF 和国际矫形与创伤外科学会(SICOT)。
骨折愈合是一个多步骤的过程。大多数骨折通过膜内和软骨内骨化的结合愈合。影像学检查对于评估骨折愈合和检测延迟愈合或不愈合非常重要。随着时间的推移,骨痂形成、桥接小梁和骨折线大小的减小表明正在愈合。影像学必须与临床参数和患者报告的结果相结合。动物数据支持骨质疏松症对骨折愈合有负面影响;然而,临床数据似乎并不支持这一点。证据不支持在发生脆性骨折后延迟开始抗吸收治疗。如果患者已经在接受治疗,则骨折时没有理由暂停骨质疏松症药物治疗。特立帕肽治疗可能会缩短某些部位(如桡骨远端)的骨折愈合时间;然而,它不会预防不愈合或影响愈合率。罗莫佐单抗在动物身上表现出的对骨折愈合的积极影响在人类身上并未观察到。
总体而言,骨质疏松症药物似乎对骨折愈合没有不良影响。治疗骨质疏松症和在骨折后立即降低再次骨折风险的迫切必要性应被优先考虑。确定新的骨折愈合的放射学和生物学标志物至关重要。综合临床和基础科学方法来评估骨折愈合也很重要,以便实现两个框架的融合。