Department of Orthopaedic Surgery, Zuyderland Medical Centre, Dr. H vd Hoffplein 1, 6162 BG, Sittard-Geleen, The Netherlands.
Department of Orthopaedic Surgery, Sint Maartenskliniek, Nijmegen, The Netherlands.
Knee Surg Sports Traumatol Arthrosc. 2017 Dec;25(12):3844-3848. doi: 10.1007/s00167-016-4345-1. Epub 2016 Oct 5.
Patients-specific instruments (PSI) for implantation of total knee arthroplasty (TKA) can be used to predict the implant size for both the femur and the tibia component. This study aims to determine the impact of approval of the PSI planning for TKA on the frequency of, and reason for intraoperative changes of implant sizes.
The clinical records of 293 patients operated with MRI- (90.4 %) and CT-based (9.6 %) PSI were reviewed for actual used implant size. Preoperative default planning from the technician and approved planning by the operating surgeon were compared with the intraoperative implanted component size for both the femur and tibia. Intraoperative reason for not following the default sizes was outdated. Furthermore, MRI- and CT-based PSI were compared for these outcomes.
In 93.9 and 91.1 % for, respectively, the femur and tibia (n.s.), the surgeon planned size was implanted during surgery. The predicted size of the femur (p < 0.00) and the tibia (p < 0.00) component planned by a technician differed from the implanted component sizes in 62 (21.2 %) and 51 (17.4 %) patients, respectively. In 17 cases, the femoral component size was adapted intraoperative based on the expert opinion of the operating surgeon. In 26 cases, the tibia component was changed during the surgery because of a mediolateral overhang, sclerotic bone, medial or lateral release, limited extension and/or fixed varus deformity. The results between the MRI- and CT-based PSI did not differ (n.s.).
PSI is a tool to help the surgeon to achieve the best possible results during TKA. The planning made by a technician should always be validated and approved by the operating surgeon who has the ultimate responsibility regarding the operation. With PSI, the operating surgeon is able to minimize intraoperative implant size errors in advance to improve operating room efficiency with possible lowering hospital costs per procedure.
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膝关节置换术(TKA)专用假体(PSI)可用于预测股骨和胫骨假体的尺寸。本研究旨在确定 TKA 使用 PSI 规划的批准对术中假体尺寸变化的频率和原因的影响。
回顾了 293 例接受 MRI(90.4%)和 CT (9.6%)PS 规划的患者的临床记录,以了解实际使用的假体尺寸。比较了技术员的术前默认规划和手术医生批准的规划与术中植入的股骨和胫骨假体的实际尺寸。术中不遵循默认尺寸的原因是过时的。此外,还比较了 MRI 和 CT 基础 PSI 的这些结果。
在股骨(n.s.)和胫骨(n.s.)中,分别有 93.9%和 91.1%的情况下,手术医生在术中植入了计划的假体尺寸。股骨(p<0.00)和胫骨(p<0.00)组件的预测尺寸分别与 62(21.2%)和 51(17.4%)名患者的植入组件尺寸不同。在 17 例中,根据手术医生的专家意见,术中对股骨组件的尺寸进行了调整。在 26 例中,由于股骨外侧过度覆盖、骨硬化、内侧或外侧松解、屈伸受限和/或固定的内翻畸形,术中改变了胫骨组件。MRI 和 CT 基础 PSI 的结果没有差异(n.s.)。
PSI 是帮助外科医生在 TKA 中获得最佳结果的工具。技术员的规划应由手术医生进行验证和批准,因为手术医生对手术结果负有最终责任。通过 PSI,手术医生能够提前最小化术中假体尺寸误差,提高手术室效率,并可能降低每次手术的医院成本。
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