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Orthopaedic Proceedings
Vol. 101-B, Issue SUPP_4 | Pages 139 - 139
1 Apr 2019
Nambu S Chang D
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Objective

Clinical wear depends on several factors such as implant specific factors (material, design, and sterilization), surgical factors/techniques, and patient-specific factors (weights and activities). The load magnitude for wear testing in the standard protocols (i.e., 2 kN as per ASTM F1714 or 3 kN as per ISO 14243-3) represent an average patient weight and does not address the other “what-if”’ scenarios (i.e., wear vs. patient weights, activities, duration, etc.,). The results from in-vitro testing report the data in wear (mg) or wear rate (mg/Mc) and are only applicable to the parameters (i.e., loads, bearing diameter, thickness, etc.,) used for the testing and not suitable to the variations seen in clinical scenarios. Therefore, it is essential to present the wear summary that can normalize the parameters and which is relevant in both in-vitro and in-vivo conditions. The goal of the current study is an attempt to present wear as a parameter (i.e., wear factor that combines the wear test data and established- theoretical relationship) and is thus applicable in both in-vivo and in-vitro scenarios.

Methods

Wear factor was first evaluated using actual wear testing conducted on metal on cross-linked polyethylene bearings along with well-established Dowson's wall bridge equation.

As per Dowson-Wallbridge, volumetric wear is V=2.376·KNWR+C or K=V/(2.376·NWR) where V is the volumetric wear in mm3, K is the wear factor in mm3/Nmm, N is the number of cycles, W is the load in Newtons, R is the bearing radius in mm, and C is the creep (assumed to be negligible, i.e., C=0 in this model.

28 mm simulator wear was first used to evaluate wear factor, but since simulator wear presented as a mass loss, these results were converted to volumetric wear using the equation

V = m / ρ ,

(m is the wear in mg and r is the density of XLPE in mg/mm3 (=0.923).

The Dowson-Wallbridge equation was then validated for predictive accuracy against actual wear testing on the predecessor THR system. The wear factor thus obtained was used to compute the theoretical-wear for other sizes (i.e., 42 and 46 mm bearings). The theoretical-wear was then compared to simulator wear for predictive accuracy.


The Journal of Bone & Joint Surgery British Volume
Vol. 92-B, Issue 12 | Pages 1710 - 1716
1 Dec 2010
Chia W Pan R Tseng F Chen Y Feng C Lee H Chang D Sytwu H

The patellofemoral joint is an important source of symptoms in osteoarthritis of the knee. We have used a newly designed surgical model of patellar strengthening to induce osteoarthritis in BALB/c mice and to establish markers by investigating the relationship between osteoarthritis and synovial levels of matrix metalloproteinases (MMPs). Osteoarthritis was induced by using this microsurgical technique under direct vision without involving the cavity of the knee. Degeneration of cartilage was assessed by the Mankin score and synovial tissue was used to determine the mRNA expression levels of MMPs. Irrigation fluid from the knee was used to measure the concentrations of MMP-3 and MMP-9. Analysis of cartilage degeneration was correlated with the levels of expression of MMP.

After operation the patellofemoral joint showed evidence of mild osteoarthritis at eight weeks and further degenerative changes by 12 weeks. The level of synovial MMP-9 mRNA correlated with the Mankin score at eight weeks, but not at 12 weeks. The levels of MMP-2, MMP-3 and MMP-14 mRNA correlated with the Mankin score at 12 weeks. An increase in MMP-3 was observed from four weeks up to 16 weeks. MMP-9 was notably increased at eight weeks, but the concentration at 16 weeks had decreased to the level observed at four weeks.

Our observations suggest that MMP-2, MMP-3 and MMP-14 could be used as markers of the progression of osteoarthritic change.