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The use of an injectable, biodegradable calcium phosphate bone substitute for the prophylactic augmentation of osteoporotic vertebrae and the management of vertebral compression fractures.

机译:可注射,可生物降解的磷酸钙骨替代物在预防性增加骨质疏松性椎骨和处理椎体压缩性骨折中的用途。

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STUDY DESIGN: A biomechanical study comparing two materials for augmentation of osteoporotic vertebral bodies and vertebral bodies after compression fracture. OBJECTIVES: To compare an injected, biodegradable calcium phosphate bone substitute with injected polymethylmethacrylate bone cement for strengthening osteoporotic vertebral bodies and improving the integrity of vertebral compression fractures. SUMMARY OF BACKGROUND DATA: Injection of polymethylmethacrylate bone cement into fractured vertebral bodies has been used clinically. However, there is concern about thermal damage to the neural elements during polymerization of the polymethylmethacrylate bone cement as well as its negative effects on bone remodeling. Biodegradable calcium phosphate bone substitutes have been studied for enhancement of fixation in fractured vertebrae. METHODS: Forty fresh osteoporotic thoracolumbar vertebrae were used for two separate parts of this study: 1) injection into osteoporotic vertebrae: intact control (n = 8), calcium phosphate (n = 8), and polymethylmethacrylate bone cement (n = 8) groups. Each specimen then was loaded in anterior compression until failure; 2) injection into postfractured vertebrae: calcium phosphate (n = 8) and polymethylmethacrylate bone cement (n = 8) groups. Before and after injection, the specimens were radiographed in the lateral projection to determine changes in vertebral body height and then loaded to failure in anterior bending. RESULTS: For intact osteoporotic vertebrae, the average fracture strength was 527 +/- 43 N (stiffness, 84 +/- 11 N/mm), 1063 +/- 127 N (stiffness, 157 +/- 21 N/mm) for the group injected with calcium phosphate, and 1036 +/- 100 N (stiffness, 156 +/- 8 N/mm) for the group injected with polymethylmethacrylate bone cement. The fracture strength and stiffness in the calcium phosphate bone substitute group and those in the polymethylmethacrylate bone cement group were similar and significantly stronger than those in intact control group (P < 0.05). For the compression fracture study, anterior vertebral height was increased 58.5 +/- 4.6% in the group injected with calcium phosphate and 58.0 +/- 6.5% in the group injected with polymethylmethacrylate bone cement as compared with preinjection fracture heights. No significant difference between the two groups was found in anterior vertebral height, fracture strength, or stiffness. CONCLUSION: This study demonstrated that the injection of a biodegradable calcium phosphate bone substitute to strengthen osteoporotic vertebral bodies or improve vertebral compression fractures might provide an alternative to the use of polymethylmethacrylate bone cement.
机译:研究设计:一项生物力学研究,比较了两种材料以增强骨质疏松性椎体和压缩性骨折后的椎体。目的:比较注射用可生物降解的磷酸钙骨替代物和注射用聚甲基丙烯酸甲酯骨水泥,以增强骨质疏松性椎体并改善椎体压缩性骨折的完整性。背景技术概述:在临床上已经将聚甲基丙烯酸甲酯骨水泥注射到骨折的椎体中。然而,人们担心在聚甲基丙烯酸甲酯骨水泥聚合过程中对神经元的热损伤及其对骨骼重塑的负面影响。已经研究了可生物降解的磷酸钙骨替代物以增强骨折椎骨的固定。方法:将四十个新鲜的骨质疏松性胸腰椎椎骨用于该研究的两个独立部分:1)注射到骨质疏松性椎骨中:完整对照组(n = 8),磷酸钙(n = 8)和聚甲基丙烯酸甲酯骨水泥(n = 8)组。然后将每个标本以前压缩方式加载,直到失效; 2)注射到骨折后的椎骨中:磷酸钙(n = 8)和聚甲基丙烯酸甲酯骨水泥(n = 8)组。在注射之前和之后,将标本在侧面投影中进行射线照相,以确定椎体高度的变化,然后将其加载至前弯失败。结果:对于完整的骨质疏松椎骨,平均断裂强度为527 +/- 43 N(刚度,84 +/- 11 N / mm),1063 +/- 127 N(刚度,157 +/- 21 N / mm)。注射磷酸钙的组,注射聚甲基丙烯酸甲酯骨水泥的组为1036 +/- 100 N(刚度,156 +/- 8 N / mm)。磷酸钙骨替代物组和聚甲基丙烯酸甲酯骨水泥组的断裂强度和刚度相近,并且明显强于完整对照组(P <0.05)。对于压迫性骨折研究,与注射前骨折高度相比,注射磷酸钙组的前椎骨高度增加58.5 +/- 4.6%,而注射聚甲基丙烯酸甲酯骨水泥的组中椎骨高度增加58.0 +/- 6.5%。两组之间在椎体高度,骨折强度或刚度方面无明显差异。结论:这项研究表明,注射可生物降解的磷酸钙骨替代品以增强骨质疏松性椎体或改善椎体压缩性骨折可能是使用聚甲基丙烯酸甲酯骨水泥的另一种选择。

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