Demand for TKR surgery is rising, including a more diverse patient demographic with increasing expectations [1]. Therefore, greater efforts are being devoted to laboratory testing. As a result, laboratory testing may set a clinical performance presumption for surgeons and patients. For example, oxidized ZrNB (Oxinium) femoral components have been projected to show 85% less wear than CoCr femoral components in bench-top testing [2]. However, recent clinical data show no difference in outcomes between Oxinium® and CoCr for the same design [3]. While it does not show lagging peformance for the Oxinium components, it does call into question the predictive ability of simulation. To better understand the performance of these two materials, a non standardized simulator evaluation was conducted.

One commercially available design (Legion PS) was evaluated with two variations of femoral component material (n = 3/material) Oxinium® and Cobalt Chromium. All testing was conducted using a 7.5 kGy moderately crosslinked UHMWPE (XLPE). A 6-station knee simulator was utilized to simulate stair-climbing kinematics. The lubricant used was Alpha Calf Fraction serum which was replaced every 0.5 million cycles for a total of 5 million cycles. Soak controls were used to correct for fluid absorption and statistical analysis was performed using the Student's t-test.

Total wear rate results for the tibial inserts are shown in Figure 1. There was no statistical difference in volume loss (p = 0.8) or wear rate (p = 0.9) for the Oxinium® system when compared to the CoCrsystem under stair-climbing kinematics. Visual examination revealed typical wear scars and features on the condylar surfaces, including burnishing.

These results corroborate the recent clinical data showing no difference between Oxinium® components and their CoCr analogs [3]. The kinematics used here are not a combination of normal level walking with stair-climbing conditions as was published originally for the Oxinium® material [2], but stair-climbing kinematics only. Even though the stair-climbing profile utilized here does not represent standardized kinematics, it provided results that are in line with clinical observations for these femoral materials. Logic suggests that a combined duty cycle is more representative of patient behavior so there must be additional test factors contributing to the prediction previously reported. The goal of bench top testing is to simulate actual clinical performance so test models must be validated as clinicaly relevant in order to be predictive. Furthermore, the results of this test indicate that the different femoral materials evaluated in this study do not alter the wear characteristics of this TKR. This is further supported by a similar previous study showing the relative contribution of design versus materials in terms of wear behavior [4]. The main determination comes from clinical evidence, and as it has been demonstrated by Kim, et al [3], there is no significant difference in the clinical results of the two TKR devices analyzed.

It is difficult for surgeons to make the decision on which design or material to use given multiple available options for total knee arthroplasty. Due to the complex interaction of soft tissue, implant position, patient anatomy, and kinematic demands of the patient, the prosthetic design of a knee device has traditionally been more important than materials. The purpose of this study was to examine the overall influence of both implant design and materials on volumetric wear rates in an in vitro knee simulator study for two knee designs.

Two different designs (single radius and J-curve) with two highly crosslinked materials (Sequentially crosslinked and annealed PE (X3®, Stryker Orthopaedics, Mahwah, NJ) (7.5 kGy moderately crosslinked UHMWPE (XLPE, Smith and Nephew, Memphis, TN)) were evaluated. The two designs tested were the Triathlon® CR knee system (single radius design)(Stryker Orthopaedics, Mahwah, NJ) and the Legion™ Oxinium® CR knee system (J-curve design) (Verilast™, Smith and Nephew, Memphis, TN). Three inserts per condition were tested in this study. This comparison incorporates the effects of both materials and designs: different femoral component materials, different tibial bearing materials, and implant geometry (J-curve vs. single radius saggital profile). All devices were tested under ISO 14243-3 normal walking using an MTS knee simulator for a total of 5 million cycles. Standard test protocols were used for cleaning, weighing and assessing the wear loss of the tibial inserts (ASTM F2025). Soak control specimens were used to correct for fluid absorption with weight loss data converted to volumetric data (by material density). Statistical analysis was performed using the Student's t-test.

Total volume loss results are shown in Figure 1. Test results show a 36% reduction (p<0.05) in volume loss and a 30% reduction (p<0.05) in wear rate for the single radius design compared to the J-curve design, respectively. All comparisons are statistically significant by the t-test method (p<0.05). Visual examination of all worn inserts revealed typical wear scars and features on the condylar surfaces, including burnishing.

Results indicate superior wear resistance for the single radius system. This finding indicates that a combination of implant design and prosthesis material plays a significant role in knee wear rates. The in vitro low volumetric wear observed in the single-radius prosthesis could theoretically influence long term survivorship in vivo, and supports the potential for improved durability and long term wear performance for this design when compared to a J-curved femoral component. Longer term clinical evidence such as published studies or outcomes reported in the available joint registries will be needed to establish whether any material or design can achieve a 30-year or longer outcome.

Introduction: The results of total hip arthroplasty in patients with avascular necrosis of the hip have been variable. This study analyzed the clinical and radiographic outcome of young patients treated with Four different cementless systems, three with alumina-on-alumina bearings in comparison to a control metal-on-poly couple in young patients with avascular necrosis of the femoral head.

Materials and Methods: This was a US IDE multicenter prospective randomized clinical trial begun in 1996 to evaluate safety and effectiveness of alumina-alumina bearings in young patients. Four cementless systems were compared in 95 patients (105 hips), three alumina-on-alumina bearing systems: ABC System I, porous coated cup; ABC System II, hydroxyapatite coated cup; Trident system, hydroxyapatite coated cup with metal sleeve backing on ceramic cup liner. The control group was the ABC System III, porous coated cup with polyethylene and cobalt chromium bearing system. All patients received a cementless Omnifit HA femoral stem. Patients were randomized to receive ABC System I, II, or III. Trident patients (Study arm begun in 1999) were not randomized. Examinations were performed at 7 weeks, 6 months, 1 year, and yearly thereafter including x-rays, clinical exam and modified Harris Hip Scores (HHS).

Results: For the alumina-alumina hips patients had a mean age of 45 years (21–67) with 18 women (23%) and 61 men (77%) at a mean follow up of 4.2 years (range, 2–7). The mean HHS at latest evaluation was 96 points. There were three revisions: one revision of all components for hip pain (sepsis suspected but not confirmed); one stem and head for traumatic postoperative periprosthetic femoral fracture; and one insert and head for subluxation in a patient implanted with the Trident insert and head. For the metal-poly hips, there were similar demographics, follow-up, and clinical scores. There were two revisions; one stem and head for traumatic postoperative periprosthetic femoral fracture, and one insert only 2 days after index surgery for dislocation.

Discussion: Both bearing couples (alumina-alumina and metal-poly) did well in theses cementless hip arthroplasties performed in young patients with avascular necrosis of the femoral head. The low revision rate is encouraging for these previously difficult to treat patients.

Aims: To compare acetabular surface treatments in alumina on alumina clinical trial. Methods: Utilizing new improved alumina ceramic materials and implant design, 514 hips were implanted in a US IDE prospective randomized study. All patients received the same press-þt hydroxylapatite-coated (HA) femoral stem. Two-thirds (349 hips) received an alumina ceramic bearing surface, while one-third (165 hips) received a cobalt chrome on polyethylene bearing. The alumina group was further divided with approximately one-half receiving a porous-coated titanium shell and alumina insert (172 hips Ð System I), and one-half receiving an arc deposited titanium shell with HA coating and alumina insert (177 hips Ð System II). System III, the control group, had a porous-coated titanium shell and polyethylene insert. All acetabular shells were of identical external geometry. Results: At latest follow-up, minimum 2 years (2–4 year range), differences were noted in the pattern of development of radiolucent lines around the acetabular components. Radiolucent lines were noted most commonly in De Lee Charnley Zone 3 in porous-coated shells (25/164 hips Ð System I, 33/151 hips Ð System III respectively). Radiolucent lines in Zone 3 were absent in the arc deposited with HA shells (System II) (p=0.001). Conclusions: These results appear to demonstrate that PSL style cups with arc dep and HA coating may improve levels of primary þxation versus that of porous-coated acetabular components.

Utilising a new implant design and improved alumina ceramic materials, 514 hips were implanted in a US IDE prospective, randomised study. All patients received the same press-fit hydroxylapatite (HA) coated femoral stem. Two-thirds (349 hips) received alumina ceramic bearings, and one-third (165 hips) received CoCr heads on polyethylene liners. The alumina group was further divided. Approximately one-half (172 hips – System I) received a porous-coated titanium shell and an alumina insert, and one-half (177 hips – System II ) received a HA-coated, arc-deposited titanium shell and an alumina insert. System III (the control) consisted of a porous-coated titanium shell and a polyethylene insert. External geometry of all shells was identical.

An independent orthopaedic surgeon who did not participate in the study reviewed all radiographs. At latest follow-up, (minimum 2 years; range 2-4 years), differences were noted in the developmental pattern of the radiolucent line around the acetabular component. Radiolucent lines were most often noted with System I and System III (porous acetabular shells) in De Lee and Charnley Zone 3 and were absent in System II (arc-deposited titanium with HA) (p=0.001). Other standard radiographic parameters evaluated were found to be comparable, with one exception: In 10 cases in the control group, the development of a small erosive lesion (scalloping) in femoral Gruen Zone 8 was observed on the lateral film. This compares to two cases in System I, and no cases in System II (p=0.001).

Dislocation rates were comparable for all three Systems. Seven acetabular components were revised: one in System I, three in System II and System III. The two revisions for aseptic loosening were both in the control group.