Bone defects in knee revision arthroplasty-a therapy-oriented classification
- PMID: 40156618
- PMCID: PMC11954694
- DOI: 10.1007/s00402-025-05759-2
Bone defects in knee revision arthroplasty-a therapy-oriented classification
Abstract
Introduction: The complex field of revision knee arthroplasty displays a lack of standardized, intuitive pre- and intraoperative assessment of bone defects. In clinical practice revision surgeries are a common sight presenting with increasingly complex cases of bone loss and ligamentary dysfunction. To address these issues the Knee Defect Classification (KDC) is introduced to offer a reliable, reproducible and an intuitive classification system with a clear therapeutic guideline.
Materials and methods: Reliability was evaluated through comparison between intraoperative findings and preoperative gradings of 218 patients. To account for reproducibility inter- and intra-rater agreement was assessed.
Results: The mean agreement between intraoperative and radiographic grading of femoral and tibial defects was evaluated with a Cohens kappa of 0.79, representing a good agreement. For interrater reliability a mean Fleiss kappa of 0.71 could be evaluated for femoral and tibial defects falling into the good agreement range. In the subgroup analysis femoral defects presented with a Fleiss kappa of 0.652 ± 0.026 (good agreement), while tibial defects presented with a Fleiss kappa of 0.768 ± 0.024 (good agreement). For intrarater reliability a mean Cohens kappa was evaluated at 0.78 indicating good agreement.
Conclusion: The KDC is a reliable and reproducible classification system. Through its structured design it facilitates intuitive use and allows for consistent preoperative planning and intraoperative guidance. A therapeutic algorithm is provided based on a review of the literature in combination with expert opinion.
Keywords: AORI; Constrainment; Defect classification; Knee revision arthroplasty; Ligamentary instability; Reliability; Reproducability.
© 2025. The Author(s).
Conflict of interest statement
Declarations. Conflict of interest: All authors declare that they have no conflict of interest. The authors did not receive support from any organization for the submitted work. Ethical approval and informed consent: All procedures performed in this study were in accordance with the ethical standards of the institutional and national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. For this type of study formal consent is not required. All data obtained is part of in-house quality assessment in accordance with National Register procedures. Additional approval for this study was obtained from the institutional review board of our hospital.
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