Choma Theodore J, Miranda Jose, Siskey Ryan, Baxter Ryan, Steinbeck Marla J, Kurtz Steven M
Orthopaedic Surgery Department, University of Missouri, Columbia, MO 65212, USA.
J Spinal Disord Tech. 2009 Jun;22(4):290-6. doi: 10.1097/BSD.0b013e31816dd2b6.
We retrieved a functioning ProDisc-L total disc replacement and associated tissues at 16 months of service life.
To analyze a previously unreported mode of implant malpositioning, wear mechanisms, and polyethylene locking mechanism, and to study retrieved periprosthetic tissues.
The clinical performance of polyethylene in the context of total disc replacements remains poorly understood. In the ProDisc-L, the polyethylene core is fixed to the inferior metal endplate through a mechanical interference locking mechanism similar to those used in tibial total knee components. This case represents the third report of an explanted ProDisc-L prosthesis, and the first reported case of posterior malpositioning with this device.
The implant was removed via a transperitoneal approach. Its polyethylene core was evaluated for burnishing, fracture, third-body abrasion, and permanent deformation. An identical, never-implanted set of polyethylene and endplate components served as controls for the microscopic evaluation of wear. Two tissue samples were collected from a region adjacent to the failed implant to evaluate tissue morphology and inflammation. Hematoxylin and eosin-stained tissue sections were also evaluated for the presence of polyethylene debris by polarized light microscopy.
The implant was removed without serious incident, although there were incidental venotomies. The patient went on to solid arthrodesis. We found minimal wear, oxidation, and periprosthetic tissue reaction, as might be expected given the short-term duration of implantation and its reason for revision. No evidence was found of malfunction or improper deployment of the locking mechanism. Burnishing seemed to be the result of short-term impingement. Some areas of the tissue matrix showed evidence of early cell degeneration, and some of these areas contained polyethylene particles identified by polarized light microscopy.
A larger series of implant retrievals will be needed to investigate possible wear and the biologic response to increased particle generation.
我们获取了一个使用寿命为16个月的正常工作的ProDisc-L全椎间盘置换假体及相关组织。
分析一种此前未报道的植入物错位模式、磨损机制及聚乙烯锁定机制,并研究取出的假体周围组织。
在全椎间盘置换中,聚乙烯的临床性能仍知之甚少。在ProDisc-L中,聚乙烯核心通过一种类似于胫骨全膝关节组件中使用的机械干涉锁定机制固定于下方的金属终板。本病例是第三例关于取出的ProDisc-L假体的报告,也是首例报道的该装置后位错位病例。
通过经腹途径取出植入物。对其聚乙烯核心进行抛光、骨折、三体磨损及永久变形评估。一组相同的、从未植入过的聚乙烯和终板组件用作磨损微观评估的对照。从失败植入物附近区域采集两份组织样本,以评估组织形态和炎症。苏木精-伊红染色的组织切片也通过偏振光显微镜评估聚乙烯碎片的存在情况。
尽管有意外的静脉切开,但植入物顺利取出。患者随后实现了牢固的关节融合。鉴于植入时间短及其翻修原因,我们发现磨损、氧化和假体周围组织反应极小。未发现锁定机制故障或部署不当的证据。抛光似乎是短期撞击的结果。组织基质的一些区域显示出早期细胞变性的迹象,其中一些区域含有通过偏振光显微镜鉴定的聚乙烯颗粒。
需要更多系列的植入物取出研究来调查可能的磨损情况以及对颗粒产生增加的生物学反应。