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Published on: October 12, 2016
Medium-term osteolysis with the Wallaby I® deep-dished total knee prosthesis
1Service de chirurgie orthopédique, hôpital Bichat-Claude-Bernard, 46, rue Henri-Huchard, 75877 Paris cedex 18, France; EA REMES, université Paris-Diderot, Sorbonne Paris Cité, 75010 Paris, France.
The Wallaby I® total knee prosthesis showed inferior medium-term outcomes, with a high rate of aseptic loosening and osteolysis. This deep-dished design may increase wear and compromise insert fixation, leading to a recommendation against its use.
Area of Science:
- Orthopedic surgery
- Biomaterials science
- Medical device engineering
Background:
- Highly congruent total knee prostheses aim to reduce polyethylene wear and osteolysis.
- Conventional gamma-irradiated polyethylene inserts have shown high rates of aseptic loosening.
- The Wallaby I® prosthesis utilizes a deep-dished tibial insert made of conventional polyethylene.
Purpose of the Study:
- To assess the medium-term outcomes of the Wallaby I® total knee prosthesis.
- To compare the rates of aseptic loosening and osteolysis with posterior-stabilised prostheses.
- To evaluate the hypothesis that the Wallaby I® prosthesis has similar or lower rates of aseptic loosening and osteolysis.
Main Methods:
- Retrospective analysis of 121 consecutive total knee arthroplasty (TKA) patients between 2001-2005.
- Complete follow-up data over 4 years for 89 patients, with a mean follow-up of 96 months.
- Clinical and radiographic IKS scores were analyzed.
Main Results:
- 10 knees required revision TKA due to osteolysis and aseptic loosening after a mean of 81 months.
- Mean 9-year prosthesis survival was 88±17%.
- Insert delamination, fracture of the tibial baseplate, and insert mobility were observed in several cases.
Conclusions:
- Medium-term outcomes were inferior compared to posterior-stabilised components.
- Potential causes include polyethylene quality variations and increased shear stresses from the deep-dish design leading to backside wear.
- The Wallaby I® prosthesis is not recommended for use; CT follow-up is advised for patients with this implant.
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