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Comparative biomechanical investigation of a modular dynamic lumbar stabilization system and the Dynesys system

机译:模块化动态腰椎稳定系统和Dynesys系统的比较生物力学研究

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The goal of non-fusion stabilization is to reduce the mobility of the spine segment to less than that of the intact spine specimen, while retaining some residual motion. Several in vitro studies have been conducted on a dynamic system currently available for clinical use (Dynesys®). Under pure moment loading, a dependency of the biomechanical performance on spacer length has been demonstrated; this variability in implant properties is removed with a modular concept incorporating a discrete flexible element. An in vitro study was performed to compare the kinematic and stabilizing properties of a modular dynamic lumbar stabilization system with those of Dynesys, under the influence of an axial preload. Six human cadaver spine specimens (L1–S1) were tested in a spine loading apparatus. Flexibility measurements were performed by applying pure bending moments of 8 Nm, about each of the three principal anatomical axes, with a simultaneously applied axial preload of 400 N. Specimens were tested intact, and following creation of a defect at L3–L4, with the Dynesys implant, with the modular implant and, after removal of the hardware, the injury state. Segmental range of motion (ROM) was reduced for flexion–extension and lateral bending with both implants. Motion in flexion was reduced to less than 20% of the intact level, in extension to approximately 40% and in lateral bending a motion reduction to less than 40% was measured. In torsion, the total ROM was not significantly different from that of the intact level. The expectations for a flexible posterior stabilizing implant are not fulfilled. The assumption that a device which is particularly compliant in bending allows substantial intersegmental motion cannot be fully supported when one considers that such devices are placed at a location far removed from the natural rotation center of the intervertebral joint.
机译:非融合稳定的目的是将脊柱节段的活动性降低到小于完整脊柱标本的活动性,同时保留一些残余运动。在目前可用于临床的动态系统(Dynesys ®)上进行了几项体外研究。在纯力矩载荷下,已经证明了生物力学性能对间隔物长度的依赖性。植入特性的可变性通过结合了离散柔性元件的模块化概念得以消除。在轴向预紧力的影响下,进行了一项体外研究,以比较模块化动态腰椎稳定系统与Dynesys的运动学和稳定特性。在脊柱加载设备中测试了六个人体尸体脊柱标本(L1-S1)。通过在三个主要解剖轴上分别施加8 Nm的纯弯矩并同时施加400 N的轴向预紧力来进行挠性测量。对样品进行完整测试,然后在L3–L4处产生缺陷, Dynesys植入物,模块化植入物以及在移除硬件后的受伤状态。两种植入物的屈伸和横向弯曲都减小了节段运动(ROM)。屈曲运动降低到完整水平的20%以下,伸展运动降低到大约40%,横向弯曲运动降低到40%以下。扭转时,总ROM与完整水平没有显着差异。柔性后路稳定植入物的期望没有得到满足。当人们认为这样的装置被放置在远离椎间关节自然旋转中心的位置时,就不能完全支持这样一种假设,即特别适合于弯曲的装置允许明显的节段运动。

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