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患者控制与力控制模拟器全膝关节置换运动学的直接比较。

A direct comparison of patient and force-controlled simulator total knee replacement kinematics.

作者信息

DesJardins John D, Banks Scott A, Benson Lisa C, Pace Thomas, LaBerge Martine

机构信息

Department of Bioengineering, Clemson University, 401 Rhodes Engineering Research Center, Clemson, SC 29634, USA.

出版信息

J Biomech. 2007;40(15):3458-66. doi: 10.1016/j.jbiomech.2007.05.022. Epub 2007 Jul 12.

Abstract

The need to critically evaluate the efficacy of current total knee replacement (TKR) wear testing methodologies is great. Proposed international standards for TKR wear simulation have been drafted, yet their methods continue to be debated. The "gold standard" to which all TKR wear testing methodologies should be compared is measured in vivo TKR performance in patients. The current study compared patient TKR kinematics from fluoroscopic analysis and simulator TKR kinematics from force-controlled wear testing to quantify similarities in clinical ranges of motion and contact bearing kinematics and to evaluate the proposed ISO force-controlled wear testing methodology. The treadmill walking kinematics from eight well-functioning, 13 month average post-op patients were compared to the 2 million cycle interval walking cycle kinematics from a force-controlled (Instron/Stanmore Knee Joint Simulator, Instron, Canton, MA) knee simulator using identical implant designs (Natural Knee II, Standard Congruent, Zimmer, Warsaw, IN). The in vivo and simulator data showed good agreement in kinematic patterns and ranges of clinical motion. Tribologically the data sets showed similar contact pathway ranges of motion and wear travel distances per cycle. Surgical and simulator alignments of the implant systems were determined to be a contributing factor in observed kinematic differences. This study's statistical findings offer supporting evidence that the simulation of in vivo walking cycle wear kinematics can be accurately reproduced with a force controlled testing methodology.

摘要

亟需对当前全膝关节置换术(TKR)磨损测试方法的有效性进行严格评估。TKR磨损模拟的国际标准草案已起草完成,但相关方法仍在讨论之中。所有TKR磨损测试方法都应与之比较的“金标准”,是患者体内TKR的实际表现。本研究比较了通过荧光透视分析得出的患者TKR运动学数据,以及通过力控磨损测试得出的模拟器TKR运动学数据,以量化临床活动范围和接触承载运动学方面的相似性,并评估国际标准化组织(ISO)提议的力控磨损测试方法。将8名术后平均13个月且功能良好的患者在跑步机上行走的运动学数据,与使用相同植入物设计(Natural Knee II,标准匹配型,捷迈公司,印第安纳州华沙)的力控膝关节模拟器(英斯特朗/斯坦莫尔膝关节模拟器,英斯特朗公司,马萨诸塞州坎顿)在200万次循环间隔的行走周期运动学数据进行比较。体内和模拟器数据在运动学模式和临床活动范围方面显示出良好的一致性。从摩擦学角度看,数据集显示出类似的接触路径活动范围和每个周期的磨损行程距离。植入系统的手术和模拟器校准被确定为观察到的运动学差异的一个促成因素。本研究的统计结果提供了支持性证据,表明使用力控测试方法能够准确再现体内行走周期磨损运动学。

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