Abstract
Purpose
Patient-specific instrumentation (PSI) is a technique to plan and position the prosthesis components in unicompartmental knee arthroplasty (UKA) surgery. This study assesses whether the definitive component position in the frontal, sagittal and axial plane is according to the preoperative plan, based on the hypothesis that PSI is accurate.
Methods
Twenty-six patients who had PSI Oxford UKA surgery were included prospectively. The component position in vivo was determined with a postoperative CT-scan and compared with the planned component position using MRI-based digital 3D imaging. Adjustments to the preoperative plan and implanted component sizes during surgery were recorded.
Results
Intraoperatively, no femoral adjustments were performed; 12 tibial re-resections were necessary. The median absolute deviation from the plan in degrees (range) in the frontal, sagittal and axial plane was 1.8° (− 1.5°–6.5°), 2.0° (− 6.5°–8.0°) and 1.0° (− 1.5°–5.0°) for the femoral component, and 2.5° (− 1.0°–6.0°), 3.0° (− 1.0°–5.0°) and 5.0° (− 6.5°–12.5°) for the tibial component. The femoral component is positioned 0.5 (− 1°–2.5°) mm more lateral and 0.8 (− 1.0°–2.5°) mm more anterior. The tibial component is positioned 2.0 (− 5.0–0.0) mm more lateral and 1.3 (− 3.0–6.0) mm more distal. The femoral and tibial default plans were changed four times (15.4%) and nine times (34.6%), respectively, before approval by the surgeon.
Conclusion
PSI in Oxford UKA surgery is reliable and accurately translates the preoperative plan into the in vivo situation, except for the tibial rotational position. The preoperative planning is a crucial step in avoiding re-resections that can cause angular deviations in prosthesis position, especially in tibial component rotational position. It is advised to avoid re-resections and to consider this while planning the PSI procedure.
Level of evidence
Prospective comparative study Level II.
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Acknowledgements
The authors would like to thank Drs. M. Keulen, M.D., from the Dell Medical School at the University of Texas in Austin, USA, who served as external reader, and for his comments that greatly improved the manuscript.
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BK participated in the design of the study, acquisition of data and writing of the manuscript. AL participated in the design of the study and helped to draft the manuscript. MS participated in the design of the study and acquisition of data and helped to draft the manuscript. BB participated in the design of the study and helped to draft the manuscript. WT participated in the statistical analysis and helped to draft the manuscript. BJ participated in the design of the study and helped to draft the manuscript. PE participated in the design of the study and helped to draft the manuscript. NK participated in the design of the study and helped to draft the manuscript. All authors read and approved the final manuscript.
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One author (NK) is a paid consultant for Zimmer-Biomet. The other authors have no conflict of interest to be reported.
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No funding has been received for this study.
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All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.
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Informed consent was obtained from all individual participants included in the study.
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Kerens, B., Leenders, A.M., Schotanus, M.G.M. et al. Patient-specific instrumentation in Oxford unicompartmental knee arthroplasty is reliable and accurate except for the tibial rotation. Knee Surg Sports Traumatol Arthrosc 26, 1823–1830 (2018). https://doi.org/10.1007/s00167-017-4826-x
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DOI: https://doi.org/10.1007/s00167-017-4826-x