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Dynesys(®)脊柱植入物的体内相容性:五例取出的假体周围组织样本及相应植入物的病例系列

In vivo compatibility of Dynesys(®) spinal implants: a case series of five retrieved periprosthetic tissue samples and corresponding implants.

作者信息

Neukamp M, Roeder C, Veruva S Y, MacDonald D W, Kurtz S M, Steinbeck M J

机构信息

Institute for Evaluative Research in Medicine, University of Bern, Bern, Switzerland.

出版信息

Eur Spine J. 2015 May;24(5):1074-84. doi: 10.1007/s00586-014-3705-0. Epub 2014 Dec 6.

Abstract

PURPOSE

To determine whether particulate debris is present in periprosthetic tissue from revised Dynesys(®) devices, and if present, elicits a biological tissue reaction.

METHODS

Five Dynesys(®) dynamic stabilization systems consisting of pedicle screws (Ti alloy), polycarbonate-urethane (PCU) spacers and a polyethylene-terephthalate (PET) cord were explanted for pain and screw loosening after a mean of 2.86 years (1.9-5.3 years). Optical microscopy and scanning electron microscopy were used to evaluate wear, deformation and surface damage, and attenuated total reflectance Fourier transform infrared spectroscopy to assess surface chemical composition of the spacers. Periprosthetic tissue morphology and wear debris were determined using light microscopy, and PCU and PET wear debris by polarized light microscopy.

RESULTS

All implants had surface damage on the PCU spacers consistent with scratches and plastic deformation; 3 of 5 exhibited abrasive wear zones. In addition to fraying of the outer fibers of the PET cords in five implants, one case also evidenced cord fracture. The pedicle screws were unremarkable. Patient periprosthetic tissues around the three implants with visible PCU damage contained wear debris and a corresponding macrophage infiltration. For the patient revised for cord fracture, the tissues also contained large wear particles (>10 μm) and giant cells. Tissues from the other two patients showed comparable morphologies consisting of dense fibrous tissue with no inflammation or wear debris.

CONCLUSIONS

This is the first study to evaluate wear accumulation and local tissue responses for explanted Dynesys(®) devices. Polymer wear debris and an associated foreign-body macrophage response were observed in three of five cases.

摘要

目的

确定翻修后的Dynesys®装置周围假体组织中是否存在颗粒性碎片,若存在,是否会引发生物组织反应。

方法

5个Dynesys®动态稳定系统被取出,这些系统由椎弓根螺钉(钛合金)、聚碳酸酯-聚氨酯(PCU)垫片和聚对苯二甲酸乙二酯(PET)绳组成,取出原因是疼痛和螺钉松动,平均使用时间为2.86年(1.9 - 5.3年)。采用光学显微镜和扫描电子显微镜评估磨损、变形和表面损伤情况,并用衰减全反射傅里叶变换红外光谱法评估垫片的表面化学成分。使用光学显微镜确定假体周围组织形态和磨损碎片,通过偏光显微镜确定PCU和PET磨损碎片。

结果

所有植入物的PCU垫片均有与划痕和塑性变形一致的表面损伤;5个中有3个出现磨料磨损区域。除5个植入物中PET绳外部纤维磨损外,1例还出现绳断裂。椎弓根螺钉未见异常。3个PCU有明显损伤的植入物周围的患者假体周围组织含有磨损碎片和相应的巨噬细胞浸润。对于因绳断裂而翻修的患者,组织中还含有大的磨损颗粒(>10μm)和巨细胞。其他两名患者的组织显示出类似的形态,由致密纤维组织组成,无炎症或磨损碎片。

结论

这是第一项评估取出的Dynesys®装置磨损积累和局部组织反应的研究。5例中有3例观察到聚合物磨损碎片和相关的异物巨噬细胞反应。

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