tl18051 -全踝关节置换术中患者特异性内固定的准确性

G. Saito, A. Sanders, M. O'Malley, J. Deland, S. Ellis, Constantine A. Demetracopoulos
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摘要

全踝关节置换术中植入物的正确定位是保证假体使用寿命的关键步骤。通过术前计算机断层扫描的TAA患者专用仪器(PSI)是由PROPHECY (Wright Medical, Memphis, TN)开发并提供的。本研究的目的是比较PSI与标准参考指南(SRG)在胫骨植入物定位的准确性、手术时间和透视时间方面的差异。方法:回顾性分析99例使用INFINITY假体进行原发性TAA的患者(Wright Medical, Memphis, TN)。根据TAA期间使用的器械类型将患者分为两组(PSI - PROPHECY组75例,SRG组24例)。结果:两组间胫骨植入物定位相似。在冠状面,SRG组胫骨种植体的绝对偏差为1.7±1.4度,PSI组为1.6±1.2度(P = 0.710)。在矢状面,SRG的绝对对中偏差为1.8±1.4度,PSI的绝对对中偏差为1.9±1.5度(P = 0.675)。PSI组手术时间(P = 0.040)和透视时间(P < 0.001)均显著缩短。PSI术前计划报告在73%的胫骨假体病例中正确预测了种植体的大小,而距骨假体只有51%的病例正确预测了种植体的大小。结论:PSI提供了与标准器械相似的胫骨假体对准,同时减少了手术和透视时间。然而,PSI术前计划报告不能很好地预测种植体的大小。因此,最终的决定应始终基于外科医生的经验,以防止错误的种植体的大小和定位。
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TL 18051 - Accuracy of patient-specific instrumentation in total ankle arthroplasty
Introduction: Correct positioning of implants in total ankle arthroplasty (TAA) is a key step to ensure the longevity of the prosthesis. Patient-specific instrumentation (PSI) via preoperative computed tomography for TAA was developed and made available through PROPHECY (Wright Medical, Memphis, TN). The purpose of this study was to compare the use of PSI with the standard referencing guide (SRG) in regard to the accuracy of tibial implant positioning, operative time, and fluoroscopy time. Methods: A retrospective analysis of 99 patients who underwent a primary TAA with the INFINITY prosthesis (Wright Medical, Memphis, TN) was performed. Patients were divided in two groups based on the type of instrumentation used during the TAA (75 in the PSI - PROPHECY group vs 24 in the SRG group). Results: Tibial implant positioning was similar between groups. In the coronal plane, the absolute deviation of the tibial implant was 1.7 ± 1.4 degrees for the SRG and 1.6 ± 1.2 degrees for PSI (P = 0.710). In the sagittal plane, the absolute alignment deviation of the tibial implant was 1.8 ± 1.4 degrees for the SRG and 1.9 ± 1.5 degrees for PSI (P = 0.675). Operative time (P = 0.040) and fluoroscopy time (P < 0.001) were significantly decreased in the PSI group. The PSI preoperative plan report correctly predicted the implant size in 73% of cases for the tibial component and in only 51% of cases for the talar component. Conclusions: PSI provided similar tibial component alignment to standard instrumentation while decreasing the operative and fluoroscopy time. However, PSI preoperative plan reports were poor predictors of implant sizing. Therefore, the final decision should always be based on the surgeon’s experience to prevent errors in implant sizing and positioning.
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