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Three-dimensional implant position and orientation after total knee replacement performed with patient-specific instrumentation systems

机译:使用特定于患者的仪器系统进行全膝关节置换后的三维植入物位置和方向

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摘要

Patient-specific instrumentation systems are entering into clinical practice in total knee replacement, but validation tests have yet to determine the accuracy of replicating computer-based plans during surgery. We performed a fluoroscopic analysis to assess the final implant location with respect to the corresponding preoperative plan. Forty-four patients were analyzed after using a patient-specific system based on CT and MRI. Computer aided design implant models and models of the femur and tibia bone portions, as for the preoperative plans, were provided by the manufacturers. Two orthogonal fluoroscopic images of each knee were taken after surgery for pseudo-biplane imaging; 3D component locations with respect to the corresponding bones were estimated by a shape-matching technique. Assuming that the corresponding values at the preoperative plan were equal to zero, discrepancies were taken as an indication of accuracy for the systems. A repeatability test revealed that the technique was reliable within 1 mm and 1°. The maximum discrepancies for all the patients for the femoral component were 5.9 mm in a proximo-distal direction and 4.2° in flexion. Good matching was found between final implantations and preoperative plans with mean discrepancies smaller than 3.1 mm and 1.9°.
机译:特定于患者的仪器系统正在全膝关节置换中进入临床实践,但是验证测试尚未确定在手术期间复制基于计算机的计划的准确性。我们进行了透视检查,以评估相对于相应术前计划的最终植入物位置。使用基于CT和MRI的特定于患者的系统后,对44例患者进行了分析。制造商提供了计算机辅助设计的植入物模型以及股骨和胫骨骨部分的模型,以及术前计划。手术后拍摄每个膝盖的两个正交透视图像,以进行伪双平面成像。通过形状匹配技术估算相对于相应骨骼的3D组件位置。假设术前计划的相应值等于零,则差异被视为系统准确性的指标。重复性测试表明该技术在1 mm和1°范围内是可靠的。所有患者股骨组件的最大差异在近端方向上为5.9mm,在屈曲方向上为4.2°。在最终植入和术前计划之间发现良好的匹配,平均差异小于3.1mm和1.9°。

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