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聚乙烯磨损颗粒与Charité椎间盘假体的长期临床失败:4例患者的研究

Polyethylene wear debris and long-term clinical failure of the Charité disc prosthesis: a study of 4 patients.

作者信息

van Ooij André, Kurtz Steven M, Stessels Filip, Noten Huub, van Rhijn Lodewijk

机构信息

Department of Orthopaedic Surgery, University Hospital Maastricht, Maastricht, The Netherlands.

出版信息

Spine (Phila Pa 1976). 2007 Jan 15;32(2):223-9. doi: 10.1097/01.brs.0000251370.56327.c6.

Abstract

STUDY DESIGN

A clinical case series of 4 patients undergoing anterior lumbar revision due to failure of total disc replacement surgery.

OBJECTIVES

To assess the clinical significance of polyethylene wear debris in salvage surgery after initial total disc replacement, the pattern and the mechanisms of polyethylene wear in the retrieved cores, and the extent of polyethylene debris in the periprosthetic tissues obtained from 4 patients.

SUMMARY OF BACKGROUND DATA

Previous in vitro wear tests have demonstrated low wear rates for lumbar artificial discs, suggesting that implant wear may not be a clinically relevant issue with total disc replacement. However, only long-term clinical investigations with analysis of retrieved implants and periprosthetic tissue can ultimately establish the significance of polyethylene wear debris for total disc arthroplasty.

METHODS

Starting in 2004, we began routinely performing salvage procedures in patients with failed total disc replacements. We report on the short-term outcomes of 4 patients at our institution who were revised with a Charité prosthesis (DePuy Spine, Raynham, MA). Wear analysis of the retrieved prosthesis and histologic examination of the periprosthetic tissue were also performed.

RESULTS

All of the retrieved polyethylene cores showed evidence of wear, but the extent and severity varied among the 4 patients. Wear and fracture of the core were associated with osteolysis of the underlying sacrum in 1 patient. Histologic examination of the periprosthetic tissues confirmed the presence of wear debris lying in inflammatory fibrous tissue. In 3 of the 4 patients, implant wear was associated with an unfavorable biomechanical environment (e.g., subsidence, migration, undersizing, and adjacent fusion). The mechanisms of wear included adhesive/abrasive wear of the central domed region of the polyethylene core, as well as chronic rim impingement, resulting in rim fatigue and fracture.

CONCLUSIONS

This study demonstrates the clinical significance of polyethylene wear debris and the potential for osteolysis with total disc replacements. The authors recommend that patients undergoing lumbar disc arthroplasty receive long-term follow-up to monitor the wear and functional status of their implants.

摘要

研究设计

一项关于4例因全椎间盘置换手术失败而接受腰椎翻修手术患者的临床病例系列研究。

目的

评估初次全椎间盘置换术后翻修手术中聚乙烯磨损碎屑的临床意义、取出的假体芯中聚乙烯磨损的模式和机制,以及4例患者假体周围组织中聚乙烯碎屑的程度。

背景资料总结

以往的体外磨损试验表明腰椎人工椎间盘的磨损率较低,提示植入物磨损在全椎间盘置换中可能不是一个与临床相关的问题。然而,只有通过对取出的植入物和假体周围组织进行分析的长期临床研究,才能最终确定聚乙烯磨损碎屑对全椎间盘置换术的意义。

方法

从2004年开始,我们对全椎间盘置换失败的患者常规进行翻修手术。我们报告了我院4例接受Charité假体(DePuy Spine,Raynham,马萨诸塞州)翻修的患者的短期结果。还对取出的假体进行了磨损分析,并对假体周围组织进行了组织学检查。

结果

所有取出的聚乙烯芯均显示有磨损迹象,但4例患者的磨损程度和严重程度各不相同。1例患者的芯磨损和骨折与下方骶骨的骨溶解有关。假体周围组织的组织学检查证实了炎性纤维组织中存在磨损碎屑。4例患者中有3例,植入物磨损与不利的生物力学环境(如下沉、移位、尺寸过小和相邻融合)有关。磨损机制包括聚乙烯芯中央穹顶区域的粘着/磨料磨损,以及慢性边缘撞击,导致边缘疲劳和骨折。

结论

本研究证明了聚乙烯磨损碎屑的临床意义以及全椎间盘置换导致骨溶解的可能性。作者建议接受腰椎间盘置换术的患者应接受长期随访,以监测其植入物的磨损情况和功能状态。

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