Saito Guilherme H, Sanders Austin E, O'Malley Martin J, Deland Jonathan T, Ellis Scott J, Demetracopoulos Constantine A
Foot and Ankle Service, Department of Orthopaedic Surgery, Hospital for Special Surgery, New York, NY 10021, United States.
Foot and Ankle Service, Department of Orthopaedic Surgery, Hospital for Special Surgery, New York, NY 10021, United States.
Foot Ankle Surg. 2019 Jun;25(3):383-389. doi: 10.1016/j.fas.2018.02.008. Epub 2018 Feb 16.
Patient-specific instrumentation (PSI) for TAA is a novel technology with several potential benefits. The primary goal of this study was to compare the use of PSI with the standard referencing guide (SRG) in regards to accuracy of tibial implant positioning. Operative time, fluoroscopy time and accuracy of PSI preoperative reports were also evaluated.
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 group vs 24 in the SRG group). There was no significant difference between groups in regards to age at the time of surgery (P=0.122), sex (P=0.138), number of concomitant procedures performed during surgery (P=0.567) and etiology (P=0.841). However, preoperative deformity was significantly smaller in the PSI group (P=0.002).
Tibial implant positioning was similar between groups. In the coronal plane, the absolute deviation of the tibial implant from the intended alignment was 1.7±1.4° for the SRG and 1.6±1.2° for PSI (P=0.710). In the sagittal plane, the absolute alignment deviation of the tibial implant was 1.8±1.4° for the SRG and 1.9±1.5° for PSI (P=0.675). Operative time (167 vs 190min, P=0.040) and fluoroscopy time (85 vs 158s, 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 51% of cases for the talar component.
PSI provided similar tibial component alignment as standard instrumentation. Additionally, PSI preoperative plan reports were poor predictors of implant sizing. Therefore, the final decision should always be based on surgeon's experience in order to prevent errors in implant sizing and positioning.
Level III, retrospective comparative study.
用于全踝关节置换术(TAA)的定制化器械(PSI)是一项具有多种潜在优势的新技术。本研究的主要目的是比较定制化器械与标准参考指南(SRG)在胫骨假体植入位置准确性方面的差异。同时还评估了手术时间、透视时间以及定制化器械术前报告的准确性。
对99例行初次全踝关节置换术并使用INFINITY假体(Wright Medical,孟菲斯,田纳西州)的患者进行回顾性分析。根据全踝关节置换术中使用的器械类型将患者分为两组(定制化器械组75例,标准参考指南组24例)。两组患者在手术时的年龄(P = 0.122)、性别(P = 0.138)、手术中同时进行的其他手术数量(P = 0.567)和病因(P = 0.841)方面无显著差异。然而,定制化器械组术前畸形明显更小(P = 0.002)。
两组之间胫骨假体的植入位置相似。在冠状面,标准参考指南组胫骨假体与预期对线的绝对偏差为1.7±1.4°,定制化器械组为1.6±1.2°(P = 0.710)。在矢状面,标准参考指南组胫骨假体的绝对对线偏差为1.8±1.4°,定制化器械组为1.9±1.5°(P = 0.675)。定制化器械组的手术时间(167分钟对190分钟,P = 0.040)和透视时间(85秒对158秒,P<0.001)显著缩短。定制化器械术前计划报告在73%的胫骨部件病例和51%的距骨部件病例中正确预测了假体尺寸。
定制化器械在胫骨部件对线方面与标准器械相似。此外,定制化器械术前计划报告对假体尺寸的预测能力较差。因此,最终决策应始终基于外科医生的经验,以防止假体尺寸和位置出现错误。
III级,回顾性比较研究。