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Clinical and biomechanical researches of polyetheretherketone (PEEK) rods for semi-rigid lumbar fusion: a systematic review

机译:半刚性腰椎融合酮(PEEK)棒的临床和生物力学研究:系统评价

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摘要

Lumbar spinal fusion using rigid rods is a common surgical technique. However, adjacent segment disease and other adverse effects can occur. Dynamic stabilization devices preserve physiologic motion and reduce painful stress but have a high rate of construct failure and reoperation. Polyetheretherketone (PEEK) rods for semi-rigid fusions have a similar stiffness and adequate stabilization power compared with titanium rods, but with improved load sharing and reduced mechanical failure. The purpose of this paper is to review and evaluate the clinical and biomechanical performance of PEEK rods. A systematic review of clinical and biomechanical studies was conducted. A literature search using the PubMed, EMBASE, and Cochrane Library databases identified studies that met the eligibility criteria. Eight clinical studies and 15 biomechanical studies were included in this systematic review. The visual analog scale and the Oswestry disability index improved significantly in most studies, with satisfactory fusion rates. The occurrence of adjacent segment disease was low. In biomechanical studies, PEEK rods demonstrated a superior load-sharing distribution, a larger adjacent segment range of motion, and reduced stress at the rod-screw/screw-bone interfaces compared with titanium rods. The PEEK rod construct was simple to assemble and had a reliable in vivo performance compared with dynamic devices. The quality of clinical studies was low with confounding results, although results from mechanical studies were encouraging. There is no evidence strong enough to confirm better outcomes with PEEK rods than titanium rods. More studies with better protocols, a larger sample size, and a longer follow-up time are needed.
机译:使用刚性杆的腰椎融合是一种常见的手术技术。然而,相邻的细分疾病和其他不利影响可能会发生。动态稳定装置保留生理运动并降低疼痛压力,但具有高的构建性能和重新进食。与钛棒相比,聚醚醚酮(PEEK)杆具有类似的刚度和足够的稳定功率,但具有改善的负载分配和机械故障减少。本文的目的是审查和评估Peek Rods的临床和生物力学性能。对临床和生物力学研究进行了系统综述。使用PubMed,Embase和Cochrane库数据库进行文献搜索确定的研究符合资格标准。八项临床研究和15项生物力学研究包括在该系统审查中。在大多数研究中,视觉模拟规模和OsWestry残疾指数在大多数研究中得到了显着改善,具有令人满意的融合率。相邻分段疾病的发生低。在生物力学研究中,PEEK棒证明了较高的载荷分布,更大的相邻段运动范围,以及与钛杆相比的杆螺杆/螺杆骨界面处的应力减小。 PEEK杆构造简单易于组装,与动态设备相比,体内性能可靠。临床研究质量较低,结果较低,虽然机械研究的结果令人鼓舞。没有证据表明足以确认与钛棒的垂直杆更好的结果。需要更好的协议,更大的样本大小和更长的随访时间进行更多研究。

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