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首页> 外文期刊>Asian spine journal. >Effects of Weekly Teriparatide Administration for Vertebral Stability and Bony Union in Patients with Acute Osteoporotic Vertebral Fractures
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Effects of Weekly Teriparatide Administration for Vertebral Stability and Bony Union in Patients with Acute Osteoporotic Vertebral Fractures

机译:每周服用特立帕肽对急性骨质疏松性椎体骨折患者的椎骨稳定性和骨结合的影响

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Study Design An open-label, non-randomized prospective study. Purpose Teriparatide (TPTD) is known to be an antiosteoporotic agent that may accelerate the healing of fractures. This study was designed to investigate the effect of once-weekly TPTD administration on vertebral stability and bony union after acute osteoporotic vertebral fracture (OVF). Overview of Literature Once-weekly TPTD administration can lead to early vertebral stability and promote bony union of fractured vertebrae in patients with severe osteoporosis. Methods Forty-eight subjects with acute OVF were assigned to receive activated vitamin D3 and calcium supplementation or onceweekly subcutaneous injection of TPTD (56.5 μg) in combination with activated vitamin D3 and calcium supplementation for 12 weeks. Vertebral stability was assessed using lateral plain radiography. Vertebral height at the anterior location (VHa) and the difference in VHa {ΔVHa=VHa (supine position)?VHa (weight-bearing position)} were measured at baseline and 12 weeks after starting treatment. Bony union was defined as the absence of a vertebral cleft or abnormal motion (ΔVHa 2 mm). Results Although not significant, ΔVHa, indicating vertebral stability, tended to be lower in the TPTD group at 12 weeks ( p =0.17). As for subjects with severe osteoporosis, ΔVHa at 12 weeks was significantly lower in the TPTD group than in the control group (mean ΔVHa: control group, 3.1 mm (n=15); TPTD group, 1.4 mm (n=16); p =0.02). The rate of bony union was significantly higher in the TPTD group than in the control group (control group, 40%; TPTD group, 81%; p =0.03). Conclusions Once-weekly TPTD administration may facilitate early bony union after acute OVF accompanied by severe osteoporosis.
机译:研究设计开放标签,非随机的前瞻性研究。目的特立帕肽(TPTD)是一种抗骨质疏松剂,可以加速骨折的愈合。本研究旨在研究每周一次TPTD给药对急性骨质疏松性椎体骨折(OVF)后椎体稳定性和骨结合的影响。文献综述每周一次TPTD给药可导致严重骨质疏松症患者早期椎体稳定并促进骨折椎骨的骨性结合。方法选择48例急性OVF受试者接受活化维生素D3和钙补充,或每周一次皮下注射TPTD(56.5μg)并联合活化维生素D3和钙补充12周。使用侧面平片检查评估椎骨稳定性。在基线和开始治疗后12周测量前位椎骨高度(VHa)和VHa之差{ΔVHa= VHa(仰卧位)→VHa(负重位置)}。骨结合定义为不存在椎骨裂或异常运动(ΔVHa> 2 mm)。结果TPTD组在第12周时,虽然不显着,但表明椎骨稳定性的ΔVHa趋于降低(p = 0.17)。对于患有严重骨质疏松症的受试者,TPTD组在12周时的ΔVHa显着低于对照组(平均值ΔVHa:对照组3.1 mm(n = 15); TPTD组1.4 mm(n = 16); p = 0.02)。 TPTD组的骨结合率明显高于对照组(对照组为40%; TPTD组为81%; p = 0.03)。结论每周一次TPTD给药可促进急性OVF伴有严重骨质疏松症后的早期骨结合。

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