Patients planning to undergo total knee arthroplasty (TKA), especially in Asian and Middle Eastern countries, usually expect to be able to perform activities requiring knee flexion such as sitting cross-legged or kneeling with ease after the surgery. Postoperative range of motion (ROM) can be affected by multiple factors such as the patient's gender, age, preoperative ROM, diagnosis, the surgeon's technique, the pre- and post-operative rehabilitation program, and the design of the prosthesis. Among these, the choice of the prosthesis depends on the surgeon's preference. As a result, several trials and studies have been conducted to improve postoperative ROM by modifying prosthesis design. The present study aimed to examine the results of TKA with the NexGen LPS-Flex system (Zimmer, Warsaw, Indiana), which is one of several high-flexion total knee prostheses that were designed to achieve a wide ROM for osteoarthritis in the valgus knee. A total of 27 primary TKAs in 26 osteoarthritis patients with valgus knee deformities (femorotibial angle (FTA) ≤ 170°) were performed using the NexGen LPS-Flex fixed prosthesis between July 2003 and December 2011. The patients included 2 men (7.7%, 2 knees) and 24 women (92.3%, 25 knees) with a mean age of 72.6 years (range, 59 to 83 years) at the time of the surgery. The mean duration of follow-up after surgery was 50.1 months (range, 24 to 126 months). Knee Society Knee Score (KSKS), Knee Society Function Score (KSFS), maximum flexion angle, maximum extension angle, and radiological femorotibial angle (FTA) were evaluated pre- and post-operatively. The mean preoperative KSKS and KSFS were 42.6 points (SD 7.5) and 41.1 points (SD 8.6), respectively, which improved after surgery to 82.2 points (SD 8.2) and 80.9 points (SD 7.6), respectively (P < 0.01). The maximum flexion angle improved from 109.1° (SD 23.1) to 117.3° (SD 12.4) postoperatively, but it did not reach statistical significance (P = 0.097). The preoperative maximum extension angle improved from −9.7° (SD 10.8) to −3.6° (SD 4.9) postoperatively (p < 0.05). The mean radiological FTA was 166.4° (SD 4.2; range: 155° − 170°) preoperatively and 172.4° (SD 2.7; range: 168° − 178°) at the final follow-up, and the difference was statistically significant (P < 0.01). None of the patients had undergone revision surgery by the final follow-up. As a conclusion, the results of the present study showed that the use of NexGen LPS-Flex implant in TKA for knee osteoarthritis with valgus deformity produced a satisfactory improvement in the clinical and radiological outcomes. Further studies on the outcomes of other prosthesis are needed to determine whether the NexGen LPS-Flex implant is advantageous for osteoarthritis patients with valgus knees who undergo TKA, and further large-scale studies with longer term follow-up are necessary to verify our results

Purpose. The purpose of this study is toevaluate the clinical and radiologic results after high flexiontotal knee arthroplasty, Lospa. ®. (Corentec Inc.) with 10mm cutting of posterior femoral condyle and LPS-Flex. ®. (Zimmer Inc.) with 12.5mm cutting of posterior femoral condyle.(Fig. 1). Materials and Methods. We prospectively compared 205 knees in 128 patients who underwent arthroplasty usingLospa. ®. (groupA) and 63 knees in 48 patients who underwentarthroplasty using NexGen LPS-Flex. ®. (group B) from September 2010 to March 2012 at Department of Orthopaedic Surgery, Sun General Hospital (Daejeon, Korea). Mean follow-up period was 33 months(24–42) in group A and 33months(23–45) in group B, and mean age was 69.5 in group A, 70.4 in group B. The radiologic analysis included the change of mechanical axis deviation and femoro-tibial angle, implant position (α,β,γ,δ)(Fig 2). The clinical results were evaluated according to Hospital for special surgery (HSS), Knee society score (KSS), and range of motion. Results. Mechanicalaxis deviations were change in varusfrom 34.8 mm to 2.6 mm(P=0.02) in group A, and change in varusfrom 32.9mm to 3.1mm(P=0.03) in group B; no statistically significant difference was observed between them (P=0.12). Femoro-tibial angles were varus 4.3° to valgus 6.6°(P=0.02) in group A, and varus 3.9° to valgus 5.7°(P=0.03) in group B;no statistically significant difference was observed between them(P=0.27). Implant positions were α=96.3°, β=90.7°, γ=1.0°, δ=88.2° in group A, and α=97.1°, β=90.3°, γ=1.5°, δ=88.9° in group B; no statistical significance in implant position was observed between the two groups (P=0.23 in α, P=0.19 in β, P=0.14 in γ, P=0.15 in δ). Mean HSS improved from 48.5 to 93.6 (P=0.02) in group A, and from 51.5 to 89.7(P=0.03) in group B; no statistical significal difference was observed between the two groups(P=0.12). Mean KSS improved from 55.1 to 93.4(P=0.03) in group A, and from 48.2 to 92.2(P=0.02) in group B; no statistical significal difference was observed between the two groups(P=0.12). Range of motion improved from 106.4°to 123.2°(P=0.01) in group A, and from 105.0° to 125.0° (P=0.03) in group B; no statistical significal difference was observed between the two groups(P=0.16). Conclusions. Lospa. ®. total knee arthroplasty showed excellent earlyradiologic, clinical results and no statistically significant difference in the results was observed between Lospa. ®. and LPS-Flex. ®.

INTRODUCTION. The specific factors affecting wear of the ultrahigh molecular weight polyethylene (UHMWPE) tibial component of total knee replacements (TKR) are poorly understood. One recent study demonstrated that lower conforming inserts produced less wear in knee simulators. The purpose of this study is to investigate the effect of insert conformity and design on articular surface wear of postmortem retrieved UHMWPE tibial inserts. METHODS. Nineteen NexGen cruciate-retaining (NexGen CR) and twenty-five NexGen posterior-stabilized (NexGen PS) (Zimmer) UHWMPE tibial inserts were retrieved at postmortem from fifteen and eighteen patients respectively. Articular surfaces were scanned at 100×100μm using a coordinate measuring machine (SmartScope, OGP Inc.). Autonomous mathematical reconstruction of the original surface was used to calculate volume loss and linear penetration maps of the medial and lateral plateaus. Wear rates for the medial, lateral and total articular surface were calculated as the slope of the linear regression line of volume loss against implantation time. Volume loss due to creep was estimated as the regression intercept. Student t-tests were used to check for significant. RESULTS. The NexGen CR and NexGen PS patient groups were approximately the same age at time of implantation (mean±SD: 72.1±9.9 and 68.7±8.8 years respectively, p=0.260) and implantation times were not significantly different (8.7±3.1 and 9.1±3.7 years, p=0.670). Both groups showed high variability in wear scars. No significant difference in wear rates on the total surface (mean±SE: 11.89±5.01 mm. 3. /year vs. 11.09±4.18 mm. 3. /year, p=0.905). However, NexGen CR components showed significantly higher volume loss due to creep than NexGen PS components (70.22±47.07 mm. 3. vs. 31.30±41.15 mm. 3. , p=0.007). These results were reflected on the medial and lateral sides, with no significant differences in wear rates on the medial side (p=0.856) or lateral side (p=0.633) and higher volume losses due to creep associated with the NexGen CR components. While NexGen CR and NexGen PS showed a near equal mean percentage of volume loss on the medial side (CR: 52.4±11.7%, PS: 52.5±11.6%), a paired t-test showed that NexGen PS components showed a higher volume loss on the medial side (p=0.056), NexGen CR components did not (p=0.404). DISCUSSION. The combination of higher conformity and more kinematic constraint in NexGen CR components may create larger contact areas with higher stresses, leading to higher volume loss due to creep observed in this study. However, these factors did not produce increased wear rates in the population. Constrained components may maintain more loading on medial side and limit sliding distance on lateral side, causing more wear medially. Total wear rates were very similar and resembled the previously reported rate of 12.9 ± 5.97 mm. 3. /year for retrieved Miller-Galante II (Zimmer) components, which features a near flat articulating surface. These findings indicate that materials factors may be most important in producing wear and that higher conformity alone does not decrease wear. For any figures or tables, please contact authors directly

Introduction. Long term data on the survivorship of cemented total knee arthroplasty (TKA) has demonstrated excellent outcomes; however, with younger, more active patients, surgeons have a renewed interest in improved biologic fixation obtained from highly porous, cementless implants. Early designs of cementless total knees systems were fraught with high rates of failure for aseptic loosening, particularly on the tibial component. Prior studies have assessed the bone ingrowth extent for tibial tray designs reporting near 30% extent of bone ingrowth . (1,2). While these analyses were performed on implants that demonstrated unacceptably high rates of clinical failure, a paucity of data exists on the extent on bone ingrowth in contemporary implant designs with newer methods for manufacturing the porous surfaces. We sought to evaluate the extent of attached bone on retrieved cementless tibial trays to determine if patient demographics, device factors, or radiographic results correlate to the extent of bone ingrowth in these contemporary designs. Methods. Using our IRB approved retrieval database, 17 porous tibial trays were identified and separated into groups based on manufacturer: Zimmer Natural Knee (1), Zimmer NexGen (10), Stryker Triathlon (4) and Biomet Vanguard Regenerex (2). Differences in manufacturing methods for porous material designs were recorded. Patient demographics and reason for revision are described in Table 1. Radiographs were used to measure tibiofemoral alignment and the tibial mechanical axis alignment. Components were assessed using visual light microscopy and Photoshop to map bone ingrowth extent across the porous surface. ImageJ was used to threshold and calculate values for bone, scratched metal, and available surface for bone ingrowth (Fig. 1). Percent extent was determined as the bone ingrowth compared to the surface area excluding any scratched regions from explantation. Statistics were performed among tray designs as well as between the lateral and medial pegs, if designs had pegs available for bony ingrowth. Results. Mean bone ingrowth extent was 51.4% for the tibial tray for the entire cohort. Bone ingrowth extent was statistically greater in the Zimmer NexGen design (63.8%; p=.027) compared to the other three designs (Table 2). Four sets of pegs were excluded from analysis due to lack of porous coatings or pegs having been removed at revision surgery. Across all designs, the medial peg had 45.2% ingrowth and the lateral peg had 66.1% ingrowth. The medial peg for the NexGen design had significantly less bone ingrowth compared to the lateral peg (58.7% vs. 75.4%; p=0.044). No significant differences were found in tibiofemoral alignment or tibial mechanical axis alignment between the implant groups. No significant differences were found among implants revised for aseptic loosening versus any other reason for revision (54% vs 30%; p=.18). Discussion. Our results demonstrate high rates of bone ingrowth extent in contemporary designs, further supporting porous design rationales and a role for additive manufacturing to form enhanced porosity. We plan on exploring staining techniques to confirm our visual inspection. Contemporary designs have shown successful rates for improved longevity for cementless total knee systems. For any figures or tables, please contact the authors directly

Introduction. Ideally, standardized wear testing protocols replicate the in vivo motions and forces of TKR patients. In a previous study with 30 TKR patients, two distinct in vivo gait patterns emerged, one characterized as having low anteroposterior (AP-L) motion and the other high anteroposterior (AP-H) motion. The aim of this study was to determine the effect of the two in vivo-determined gait patterns on total and backside insert wear in comparison with the ISO standard 14243-3. In order to differentiate and accurately quantify topside and backside wear, a novel technique was employed where different lanthanide tracers are incorporated into the polyethylene during manufacture. Materials and Methods. Components from the Zimmer NexGen CR Knee Replacement System were used. Europium (Eu) and Gadolinium (Gd)-stearates were mechanically mixed with GUR1050 UHMWPE resin to obtain two tracer-UHMWPE resins containing 49.1±1.5 ppm Eu and 68.8±1.6 ppm Gd, respectively. 12 grams of the Eu-doped resin was placed on the bottom, 10 grams of virgin GUR1050 resin was placed in the middle, and 10 grams of Gd-doped resin was placed on the top to mold NexGen CR tibial inserts. The backside was then machined to interlock with the tibial baseplate. The minimum insert thickness was 10 mm. All inserts were packaged in nitrogen and gamma sterilized. The wear test was conducted on a 4-station knee simulator in displacement-control mode. Simulator input was obtained from ISO 14243-3 and from gait of 30 NexGen TKR subjects, previously categorized into low (AP-L) and high (AP-H) anteroposterior motion groups. Per station, each insert was sequentially subjected to ISO, AP-L, AP-H motion for 2 Mc at 1 Hz. Subsequently, the ISO profile was repeated. Tibial inserts were weighed and lubricant samples were taken after every 0.5 Mc interval. Knowing the Eu and Gd concentrations from ICP-MS analysis, and normalizing those to the concentrations in the polyethylene inserts, the localized (Eu – backside; Gd – topside) wear was calculated. Wear particle analysis was conducted following established protocols. Results. For all tested liners (n=4 + soak) during the three tested motion profiles, the chemically calculated wear correlated closely with the gravimetrically determined wear (R. 2. »0.8), with slopes not different from 1. Both in vivo motion groups displayed higher wear rates than the ISO group following the order of the AP motion amplitudes (Figure). Backside wear for ISO constituted 2.76% ± 0.90% (mean ± SE) of the total wear, increasing significantly to 15.8 ± 3.2% for AP-L and further increasing to 19.3 ± 0.95% for AP-H (p<.001). The mean wear particle sizes were under 200 nm for all three motion patterns, being largest for the AP-H gait protocol (Table). Discussion. Both in vivo motion groups displayed higher wear rates than the group tested per ISO standard 14243-3. Interestingly backside wear was affected the most and increased 4.5 to 6-fold over ISO. Testing for the proportion of backside wear across various activities of daily living may therefore be an important consideration in evaluating knee prostheses wear and could be facilitated by this new tracer technology. For any figures or tables, please contact the authors directly

Introduction. Automated identification of arthroplasty implants could aid in pre-operative planning and is a task which could be facilitated through artificial intelligence (AI) and deep learning. The purpose of this study was to develop and test the performance of a deep learning system (DLS) for automated identification and classification of knee arthroplasty (KA) on radiographs. Methods. We collected 237 AP knee radiographs with equal proportions of native knees, total KA (TKA), and unicompartmental KA (UKA), as well as 274 radiographs with equal proportions of Smith & Nephew Journey and Zimmer NexGen TKAs. Data augmentation was used to increase the number of images available for DLS development. These images were used to train, validate, and test deep convolutional neural networks (DCNN) to 1) detect the presence of TKA; 2) differentiate between TKA and UKA; and 3) differentiate between the 2 TKA models. Receiver operating characteristic (ROC) curves were generated with area under the curve (AUC) calculated to assess test performance. Results. The DCNNs trained to detect KA and to distinguish between TKA and UKA both achieved AUC of 1. In both cases, heatmap analysis demonstrated appropriate emphasis of the KA components in decision-making. The DCNN trained to distinguish between the 2 TKA models also achieved AUC of 1. Heatmap analysis of this DCNN showed emphasis of specific unique features of the TKA model designs for decision making, such as the anterior flange shape of the Zimmer NexGen TKA (Figure 1) and the tibial baseplate/stem shape of the Smith & Nephew Journey TKA (Figure 2). Conclusion. DCNNs can accurately identify presence of TKA and distinguish between specific designs. The proof-of-concept of these DCNNs may set the foundation for DCNNs to identify other prosthesis models and prosthesis-related complications. For any figures or tables, please contact the authors directly

[Introduction]. One of the modern design total knee arthroplasty (TKA) system, the NexGen Legacy posterior-stabilized (LPS) Flex prosthesis, has been in use at our hospital since 2001. Between 2006 and 2011, NexGen LPS-Flex primary TKA were mainly performed in combination with a cemented short-keeled minimally invasive version tibial tray (MIS tibial component) instead of the traditional NexGen stemmed tibial tray. We observed some cases required early revision of isolated tibial component in primary TKA performed in this period. Therefore, our objectives were to report the series of this revision cases and to consider this failure mechanism. [Patients & Methods]. A total of 526 primary TKAs were performed using a NexGen LPS-Flex prosthesis and MIS tibial component during five-year period at our hospital. The mean age was 74 years at the time of the index procedure. We assessed revision rate of this tibial tray in this study and described clinical course of the revision cases. We also examined the clinical and radiographic features which could be associated with the failure. [Results]. The mean duration of follow-up was 2.5 years and there were 13 knees received tibial component revision during this period. Twelve knees were diagnosed with osteoarthritis and one knee with rheumatoid arthritis. The duration between primary TKA and revision averaged at 3.3 years, and the mean age at the second procedure was 67 years. TKAs were performed without applying the tibial central extension stem in all 13 knees, and thick polyethylene insert like 17 or 20 mm were selected for seven and 14 mm for five of 13 knees, that were the typical features on the primary TKA. Postoperative course of all 13 cases was uneventful and 10 of 13 knees achieved deep knee flexion over at 125 degrees. Prerevision radiographs showed characteristic pattern with tibial tray debonding at the cement-implant interface and subsidence into varus and flexion in all 13 knees. In all cases, intraoperative findings revealed a grossly loose tibial component with most of the cement mantle still attached to the bone. No case exhibited signs of macroscopic polyethylene wear and femoral component loosening. [Discussion]. The most common reason for failure of TKA is infection followed by implant loosening, polyethylene wear, and instability. Several studies document survival rates of over 90% up to 20 years with modern TKA designs using a cemented stemmed tibial component. Although failure of the tibial component was more prevalent in some early TKA designs, in recent years, failure of tibial fixation has been a rare cause of revision. Our experience with early aseptic loosening of this tibial component has suggested the low-profile design with no central stem as a cause for accelerated failure. Furthermore, other factors associated with increased this failure could include a thicker insert and postoperative achievement of high flexion

Introduction. Total knee arthroplasty is the standard treatment for advanced knee osteoarthritis. Patient-specific instrument (PSI)has been reported by several authors using different techniques produced by implant companies. The implant manufacturers produce PSI exclusively for their own knee implants and for easy straightforward cases. However, the PSI has become very expensive and unusable as a universal or an open platform. In addition, planning the implant is done by technicians and not by surgeons and needs long waiting time before surgery (6 weeks). Methods. We proposed a new technique which is a device and method for preparing a knee joint in a patient undergoing TKA surgery of any knee implant (prosthesis). The device is patient specific, based on a method comprised of image-based 3D preoperative planning (CT, MRI or computed X-ray) to design the templates (PSI) that are used to perform the knee surgery by converting them to physical templates using computer-aided manufacturing such as computer numerical control (CNC) or additive-manufacturing technologies. The device and method are used for preparing a knee joint in a universal and open-platform fashion for any currently available knee implant. Results. All patient-specific implants and any knee implant could be produced. The technique was applied on NExGen implant (Zimmer)on 21 patients, PFC implant (Depuy, J & J) on 5 patients, Scorpio NRG implant (Stryker) on 24 patients and SLK Evo implant (Implant International) on 81 patients. The >15 degrees varus gave a mean of 10.44 degrees in 56.67% of cases and the <15 degrees varus gave a mean of 24.04 degrees in 43.33% of cases. The total varus of 5–30 degrees gave a mean of 16.33 degrees in 90.9% of cases and the total valgus of 20–40 gave a mean of 25 degrees in 9.1% of cases. The fixed flexion deformity of < 20 degrees gave a mean of 9.4 degrees in 75.3% of cases while the fixed flexion deformity of >20 gave a mean of 31.87 degrees in 24.7% of cases. Discussion. The system is based on CT images, generic data of implant sizes, average bone geometry and standard TKA parameters for bone cutting, mechanical axis and rotation (e.g., zero-degree coronal cut, adjustable posterior slope, femoral flexion, epicondylar axis, no notching or overhang, etc.). The method of planning and completing virtual surgery of TKA includes several steps based on 3D reconstruction and segmentation of computed tomography (CT) or MRI scan data. The universal device and method are suitable to be used for any commercially and currently available knee implant. They are used for all on-shelf implants and all patient-specific instruments. The device is specifically designed for TKA and the planning is based on the 3D files of a universal TKA prosthesis. There are four standard sizes of the universal TKA prosthesis which were built depending on the average bone geometry. These 4 sizes are 55, 60, 65 and 70 mm. These sizes are consistent with the six most common implants available today: NexGen Zimmer, PFC Depuy, Sigma Knee, Triathlon Stryker, Vanguard Biomet, and Smith & Nephew Proflex. However, for extreme cases, one size above or below the maximum and minimum range can be used. The device has 2 parts: a femoral part and a tibial part, both of which are independent of any commercially available knee implant

Purpose. To evaluate the five year Radiostereometric Analysis (RSA) results of the NexGen LPS Trabecular Metal Tibial Monoblock component (TM) and the NexGen Option Stemmed cemented component (Cemented), (Zimmer, Warsaw IN). Method. 70 patients with osteoarthritis were included in a randomized series to receive either the TM implant or the cemented NG component. Surgery was performed by high volume arthoplasty specialists using standardized procedure. RSA exams were obtained postoperatively, at six months, one year, two years and five years. RSA outcomes were translations, rotations and maximum total point motion (MTPM) of the components. MTPM values were used to classify implants as ‘at risk’ or ‘stable’. Western Ontario and McMaster University Osteoarthritis Index (WOMAC) scores were gathered at all follow-ups. An analysis of variance was used to test for differences in age, body mass index (BMI), and subjective measures between implant groups. The Kruskal-Wallis test was used to investigate differences in maximum total point motion between implant groups. An analysis of variance was used to test for differences in translations and rotations between groups. Fishers exact test was used to investigate differences in proportions of implants found to be at risk between groups. Results. At the five year follow-up, 43 patients were able to be reached and were willing to participate in the follow-up exam. There were 25 in the trabecular metal group and 18 in the cemented group. There were no differences in subjective measures (WOMAC) between implant groups at any follow-up. At the five year follow-up there was no difference in MTPM between the cemented and trabecular metal groups (p=0.94) Compared to the cemented components, the trabecular metal tibial components had significantly higher subsidence than the cemented components (p=0.001). There were no other significant differences. The proportion of at risk components at five years was 2 of 16 (0.11, 95% CI, 0.03–0.33) in the cemented group and was 0 of 25 (0.0, 95% CI, 0.0–0.13) in the trabecular metal group (p=0.17). Conclusion. In the two year report on this cohort of patients, we indicated our uncertainty concerning the long term stability of the Trabecular Metal tibial implant due to the high initial migration seen in some cases. In this report we have seen stability of this implant out to five years and migrations in this period below the level of detection of our system in all cases. Given these results it is with increased confidence that we can state that this implant appears to achieve solid fixation despite high initial levels of migration

Introduction:. One of the important factors for success in TKA is to achieve proper stability of the knee joint. It is currently unknown that how much joint laxity exists in mid-range to deep knee flexion, postoperatively. We hypothesized that retaining the PCL or not during TKA has an influence on the postoperative joint laxity from mid-range to deep knee flexion. The purpose of this study was to investigate the postoperative coronal joint laxity throughout the full range of motion by the 3-dimensional in vivo analysis, both in PS and CR TKA. Methods:. We implanted 5 knees with a PS TKA using a NexGen LPS-flex and 5 knees with a CR TKA using a NexGen CR-flex. All of them were the osteoarthritis patients. We performed all operations with a measured resection technique. Four weeks after TKA, the valgus- and varus-stress radiographic assessments were performed at the five flexion angles from full extension to maximum flexion. The patients sat on the radiolucent chair with their lower legs hanging down. The examiner held their thigh, and a force of 50N was applied 30 cm distal to the tibiofemoral joint. The series of static fluoroscopic images via a flat panel detector were stored digitally. A 3-dimentional to 2-dimentional techniqueusing an automated shape-matching algorithm was employed to determine the relative 3-dimentional positions of the femoral component and tibial component in each fluoroscopic image (KneeMotion; LEXI, Tokyo). On the coronal plane of the tibial component, the angle between the tangent line of the condyles of the femoral component and the tibial plateau was measured as the joint laxity for valgus (α valgus) or varus (α varus). The flexion angle between the femoral component and tibial component was also measured. Results:. The total laxity (α valgus + α varus) tended to increase until deep knee flexion in PS TKA. While in CR TKA, the total laxity tended to increase until mid-range of knee flexion and then decreased until maximum flexion (Fig. 1). PS TKA: In varus stress, the mean tilting angles were 2.4, 3.6, 3.6, 4.1, 5.4 degrees at −2.3, 25.3, 42.2, 72.1, 97.1 degrees of knee flexion, respectively. The tilting angle measured at maximum flexion was significantly larger than that measured at full extension (p < 0.05) (Fig. 2). CR TKA: In valgus stress, the mean tilting angles were 0.8, 2.8, 2.8, 2.0, 0.6 degrees at −6.4, 24.1, 35.8, 67.7, 87.8 degrees of knee flexion, respectively. The tilting angles measured at full extension and maximum flexion were significantly smaller than that measured at 24.1 and 35.8 degrees of knee flexion (p < 0.05) (Fig. 3). Discussion:. In PS TKA, joint laxity for varus at maximum flexion was significantly larger than that at full extension. While in CR TKA, joint laxity for varus indicated no significant differences among at each flexion angle. Moreover, joint laxity for valgus at full extension and maximum flexion were significantly smaller than that at mid-range flexion in CR TKA. Retaining the PCL during TKA has a strong influence on the postoperative coronal joint laxity especially in deep knee flexion

Cementless total knee replacement (TKR) is at the present date a controversial topic. Aim of the study was to compare the effect on tibial periprosthetic bone mineral density (BMD) between different implant materials and designs. During the two-year period between January 2005 and December 2006, we analysed data of 45 patients who underwent consecutively cementless TKR (49 implants) at our Institution for primary osteoarthritis. Data was divided in 2 groups: A) 26 implants with tantalium tibial component (Zimmer NexGen Trabecular Metal. TM. Monoblock); B) 23 implants with porous titanium tibial component (Lima MultiGen. TM. ). Data was comparable per sex, age, BMI, post-op alignment, post-op KSS > 75, absence of major post-op complications. Standard AP x-rays were taken 4 months post-op and 8 years post-op. In order to quantify the reduction of BDM, we determined using ImageJ (an open source software) the Mean Grey Value (MGV) of a specific area on the 4 months- and 8 yrs-postop AP x-rays. Group A and Group B had an average MGV variation of, respectively, 11.79% and 10.51%; there was no statistically significant difference between the two groups. Reduction of BMD in a TKR is known to be a biomechanical response to load and it is conditioned by the alignment of the components and their design. Our study shows that the different materials (porous titanium vs. tantalium), in relation to the different implant design, have a similar effect on the surrounding bone. The overall results show a valid osseointegration in both group of patients

INTRODUCTION. Tibiofemoral contact at the base of the articular surface spine in posterior-stabilized total knee arthroplasty (TKA) implants can lead to spine fracture [1]. Revision TKA implants also have an articular surface spine to provide sufficient constraint when soft tissues are compromised. While some revision TKA designs have metal reinforcement in the articular surface spine, others rely solely on a polyethylene spine. This study used finite element analysis (FEA) to study the effect of metal reinforcement on stresses in the spine when subjected to posteriorly directed loading. METHODS. Two clinically successful Zimmer Biomet revision TKA designs were selected; NexGen LCCK with metal reinforcement and all-poly Vanguard SSK. The largest sizes were selected. FEA models consisted of the polyethylene articular surface and a CoCr femoral component; LCCK also included a CoCr metal reinforcement in the spine. A 7° and 0° tibial slope, as well as 3° and 0.7° femoral hyperextension, were used for the LCCK and SSK, respectively. A posteriorly directed load was applied to the spine through the femoral component (Figure 1). The base of the articular surface was constrained. The articular surfaces for both designs are made from different polyethylene materials. However, for the purpose of this study, to isolate the effect of material differences on stresses, both were modeled using conventional GUR1050 nonlinear polyethylene material properties. Femoral component and metal reinforcement were modeled using linear elastic CoCr properties. Additionally, the LCCK was reanalyzed by replacing the metal reinforcement component with polyethylene material, in order to isolate the effect of metal reinforcement for an otherwise equivalent design. Frictional sliding contact was modeled between the spine and femoral/metal reinforcement components. Nonlinear static analyses were performed using Ansys version 17 software and peak von mises stresses in the spine were compared. RESULTS. Peak von mises stresses were predicted towards the base of the anterior aspect of the spine in both designs (Figure 2). In LCCK, the high stresses were also predicted on the medial and lateral edges of the anterior spine, matching the tibiofemoral contact (Figure 3). The LCCK with metal reinforcement design predicted 14% and 31% lower stress than LCCK and SSK all-poly designs. DISCUSSION. Clinical reports of spine fracture in TKA highlight the need for further understanding of the biomechanics of spine loading. Here, through comparison of two clinically successful devices, the effect of multiple design factors was quantified. Inclusion of metal reinforcement in the spine, as well as differences in the conforming geometry between the femoral component and the articular surface, resulted in a 31% decrease in polyethylene stress for the LCCK as compared to the all-poly SSK; of which only 16% was attributed to the metal reinforcement. Further improvements to articular surface design, as well as polyethylene material advances, have the potential to result in all-poly designs with strength characteristics equivalent to or exceeding those of designs with metal reinforcement

Total knee arthroplasty has been the main treatment method among advanced osteoarthritis (OA) patients. The main post-operative evaluation considers the level of pain, stability and range of motion (ROM). The knee flexion level is one of the most important categories in the total knee arthroplasty patient's satisfaction in Asian countries due to consistent habits of floor-sitting, squating, kneeling and cross legged sitting. In this study, we discovered that the posterior capsular release enabled the further flexion angles by 14 degrees compared to the average ROM without posterior release group. Our objective was to increase the ROM using the conventional total knee arthroplasty by the posterior capsular release. Posterior capsular release is being used in order to manage the flexion contraction. Although the high flexion method extends the contact area during flexion by extending the posterior condyle by 2mm, the main problem has been the early femoral loosening. We searched for the method to get the deep knee flexion with the conventional knee prosthesis. 122 OA patients with less than preoperative 130 flexion that underwent conventional TKAs using Nexgen from January, 2014 to September, 2016 were reviewed. Posterior femoral osteophytes were removed as much as possible, but 74 cases were performed posterior capsular release, while 48 cases were not performed. After checking postoperative ROM after 6 months of operation, we compared 74 knees with a posterior capsular release and 48 knees without posterior capsular release. As a result, the average ROM in the posterior capsular release group was 132 degrees, but the average ROM without posterior release group is 118 degrees. No postoperative hyperextension was found when the adequate size of polyethylene (PE) thickness was utilized. Hence, the conventional TKA with a posterior capsular release showed satisfactory clinical outcomes in the deep knee flexion of Asians

Aim: To compare between the number of steps and instruments required for total knee arthroplasty (TKA) using 3 different techniques. The proposed techniques were conventional technique, conventional technique with patient-specific pin locators and CAOS technique using patient-specific templates (PST). Patients and methods: Zimmer/Nexgen was used as the standard implant and templating system for TKA. A Comparison was done on the number of steps and instruments required for TKA when performed with conventional technique, conventional technique with patient-specific pin locators and CAOS technique with patient-specific templates (PST) used as cutting guides. Results: The essential steps and instruments required for conventional TKA without surgical approach or bone exposure were average 70 steps with 183 different instruments; for conventional technique with patient-specific pin locators, they were average 20 steps with 40 instruments and two templates; for CAOS technique using PST, they were average 10 steps with two templates and 15 accessory instruments. CAOS PST technique required an average of 4 days for preoperative preparation and templates fabrication. Conclusion: CAOS technique using PST could make TKA less complicated in light of essential steps and instrumentation required. Although this technique required accurate preoperative preparation, it could offer less technical errors and shorter operative time compared to conventional TKA techniques. The errors’ rate for each technique was still depending on the surgeon's skills and training; however, CAOS technique with PST required shorter learning curve

Background. Constrained condylar knees are used infrequently but are successful for the treatment of the primary or revision knee with ligamentous instability and bony defect. The purpose of the present study is retrospectively analyze clinical and radiological outcome of primary and revision total knee arthroplasty with condylar constrained knee (CCK) prosthesis at a minimum of 5 years. Methods. Fourteen knees underwent total knee arthroplasty with CCK prosthesis, performed between 2003 and 2009. The average age of the patients at the time of the surgery was 71.4 years (range, 47 to 88 years). The reason for the operation was primary (osteoarthritis) in 2, revision due to aseptic loosening in 9 and infection after total knee arthroplasty in 4 knees. NexGen LCCK was used in all cases. The mean follow-up period was 91months (range, 60 to 128 month). Results. The mean Knee Society knee score and Knee Society functional score were 82.8 (range, 60 to 92) and 57.2 (range, 10 to 89) points at the time of the final follow-up. The mean knee extension and flexion angle were −3.3 (−20 to 0) and 99.2 (65 to 135) before the operation, and −1.7 (−5 to 0) and 103.2 (80 to 130) at the latest follow-up evaluation. In radiographic results, the mean of postoperative femorotibial angle (FTA) was 178° (range, 168 to 187). In one case, radiolucent line was present in Zone 1 to 4 of tibial component. There were one distal femur fracture and one dislocation of the femorotibial joint, with a rate of re-operation of 14.3%. In these two cases, the time from total knee arthroplasty to re-operation were 7 years and 2 years. There were no revisions for aseptic loosening, patella problems, or fractures. Kaplan-Meier survivorship analysis, with revision or other re-operation as the end point, revealed that the ten-year rate of survival of the components was 87.3%. Conclusions. Primary and revision total knee arthroplasty with use a constrained condylar knee prosthesis had reproducible clinical success at the mid-term follow-up

At the 2010 Effort congress Prof Hernigou of France stated that you never need to template knee x-rays as there is an absolute association with patients height and implant size. Templating of the knee for size is seldom done in clinical practice but could be handy when doing revision surgery where normal anatomy has been lost. This is however difficult with digital x-rays due to enlargement problems. With this in mind we retrospectively looked at the size of knee implants inserted to see if there was any relation with patient's height and also to see if this differs in male and female patients. Material:. 2084 IB II and NexGen knee replacements were reviewed from our database and implant size was correlated to patient height. Results:. Conclusion:. Patient length does not correlate to the AP size of the knee and cannot be used as a predictor of knee implant size

Introduction. Previous studies of CoCr alloy femoral components for total knee arthroplasty (TKA) have identified 3. rd. body abrasive wear, and apparent inflammatory cell induced corrosion (ICIC) [1] as potential damage mechanisms. The association between observed surface damage on the femoral condyle and metal ion release into the surrounding tissues is currently unclear. The purpose of this study was to investigate the damage on the bearing surface in TKA femoral components recovered at autopsy and compare the damage to the metal ion concentrations in the synovial fluid. Methods. 12 autopsy TKA CoCr femoral components were collected as part of a multi-institutional orthopedic implant retrieval program. The autopsy components included Depuy Synthes Sigma Mobile Bearing (n=1) and PFC (n=1), Stryker Triathlon (n=1) and Scorpio (n=3), and Zimmer Nexgen (n=4) and Natural Knee (n=2). Fluoro scans of all specimens prior to removal was carried out to assure no signs of osteolysis or aseptic loosening were present. Third-body abrasive wear of CoCr was evaluated using a semi-quantitative scoring method similar to the Hood method [2]. ICIC damage was reported as location of affected area and confirmed using a digital optical microscope with 4000X magnification. Synovial fluid was aspirated from the joint capsule prior to removal of the TKA device. The synovial fluid was spun at 1600 rpm for 20 minutes in a centrifuge with the cell pellet removed. The supernatant was analyzed in 1 mL quantities for ICP-MS (inductively coupled plasma mass spectrometry) by Huffman Hazen Laboratories. Data was expressed as ppb. Results. Mild to severe damage (Damage Score ≥ 2) was observed on 92% of the components in at least one quadrant, with no severe damage (Damage Score = 4) observed. ICIC damage was observed on three components in three different regions (the posterior lateral, anterior, and medial bearing surface). These observations were confirmed with digital optical microscopy, where we observed as interconnecting pits and indentations with a spiraling or trailing region, consistent with prior observation of ICIC in retrievals (Figure 1). Cobalt was detected in 7 cases, however the metal levels were not as high as levels observed in patients with a failed joint replacement (Table 1). There was no correlation between the metal ion concentration and the damage score on the CoCr femoral condyle. Discussion. This study documents the damage mechanics and associated metallic release into the synovial fluid of “well-functioning” TKA components retrieved at autopsy. It has been suggested that ICIC damage is actually damage from electrocautery during surgery. However, we observed ICIC damage on autopsy retrievals in which the use of electrocautery is unlikely. The damage mechanisms observed on the autopsy TKA components were similar but less severe compared to mechanisms observed in long-term TKA components from revision surgery [1]. More research is needed to better understand the metal release from CoCr femoral components and periprosthetic tissue reactions in TKA

Purpose. Analysis of the morphology of the distal femur, and by extension of the femoral components in total knee arthroplasty (TKA), has been related to the aspect ratio, which represents the width of the femur. Little is known about variations in trapezoidicity (i.e whether the femur is more rectangular or more trapezoidal). This study aimed to quantify additional morphological characteristics of the distal femur and identify anatomical features associated with higher risks of over- or under-sizing of components in TKA. Method. We analyzed the shape of 114 arthritic knees at the time of primary TKA using the pre-operative CT scans. The maximum AP dimension was measured. The mediolateral dimensions were measured on the theoretical distal resection slice at three levels: the posterior region (MLP), the central region (MLC) and the anterior region (MLA) (Fig 1). The ‘aspect’ ratio (MLC/AP) ratio quantified how wide or narrow the shape is. The ‘trapezoidicity’ ratio (MLP/MLA) ratio quantified how rectangular or trapezoidal the shape is. We also quantified the medial and lateral ‘narrowing angles’ in the anterior and central zones (α and β) (Fig 2). The post-operative prosthetic overhang was calculated from CT-scan. We compared the morphological characteristics with those of twelve TKA models scanned using a three-dimensional optical scanning machine (ATOS II, GOM mbH, Braunschweig, Germany) and its photogrammetric analysis software (TRITOP, GOM mbH, Braunschweig, Germany). Results. There were significant variations in both the aspect ratio (1.16±0.07; range 0.98–1.31) and the trapezoidicity ratio (1.21±0.08; range 1.06– 1.46). Femoral trapezoidicity was mostly due to an inward curve of the medial cortex. The multivariate analysis indicated that prosthetic overhang was correlated to the ‘aspect ratio’ (more overhang in narrow femurs, p=0.002), to the ‘trapezoidicity ratio’ (more overhang in trapezoidal femurs, p=0.002), and to the Tibio Femoral Angle (more overhang in valgus knees, p=0.035). The geometries of the twelve specimen components can be compared directly with the morphological findings of this study. Some components had excessively low trapezoidicity ratios (i.e. were too rectangular) such as DePuy LCS and Stryker Scorpio. Other designs had trapezoidicity ratios closer to anatomic values such as Zimmer Nexgen, Zimmer Persona, DePuy Attune and Smith and Nephew Journey (Fig 3). Several components had excessively low anterior lateral narrowing angle (αL) such as DePuy LCS, Stryker Scorpio. All had insufficiently low medial narrowing angles. Conclusion. This study shows that rectangular/trapezoidal variability of the distal femur cannot be ignored. Most of the femoral components, which were tested appeared to be excessively rectangular when compared with the bony contours of the distal femur. These findings suggest that the design of TKA should be more concerned with matching the trapezoidal/rectangular shape of the native femur

Background. Patellofemoral complications have dwindled with contemporary total knee designs that market anatomic trochlear grooves that intend to preserve normal patella kinematics. While most reports of patellofemoral complications address patella and its replacement approach, they do not focus on shape of trochlear grooves in different prostheses [1]. The purpose of this study was to characterize 3D geometry of trochlear grooves of contemporary total knee designs (NexGen, Genesis II, Logic, and Attune) defined in terms of sulcus angle and medial-lateral offset with respect to midline of femoral component in coronal view and to compare to those of native femurs derived from 20 osteoarthritic patient CT scans. Materials and Methods. Using 3D models of each implant and native femur, sulcus location and orientation were obtained by fitting a spline to connect sulcus points marked at 90°, 105°, 130°, and 145° of femoral flexion (Fig A). Implant reference plane orientations were established using inner facets of distal and posterior flanges. Reference planes of native femurs were defined using protocols developed by Eckhoff et al. [2] where coronal plane was defined using femoral posterior condyles and greater trochanter. In the coronal plane, a best fit line was used to measure sulcus angle and medial-lateral offset with respect to midline at the base of trochlear groove (Fig B). Results. With exception to Logic (0° sulcus angle & 0 mm offset), contemporary knee designs include high valgus angulations (4° to 18°) with laterally-biased offsets (3 to 5 mm). The native sulcus angle on average was slightly valgus, but varied significantly among the cohort (−0.2° ± 4.6°). Native trochlear groove offset was biased laterally (2.5 ± 1.7 mm). Discussion. We observed a considerable geometric deviation between native femur and implants in terms of sulcus angle while both geometries displayed comparable lateral bias at the base of trochlear groove. Similar to past studies by Iranpour et al. [4] and Feinstein et al. [5], a large variation in sulcus angle was observed among the selected native femurs with an average of small valgus angulation (Fig C). However, most contemporary trochlear grooves are biased towards higher valgus angulations. Retrieval and registry studies have shown that NexGen trochlear groove design (4° sulcus angle) has been shown to better accommodate natural patellas, which highlights that the differences among designs may be significant [5,6]. It remains unclear which features specifically translate to better patellafemoral outcomes, which is a merit for further study. Conflict of Interest: None. Figure A. Sulcus points defined at various flexion angles. Figure B. Best fit line to measure ML-offset and sulcus angle. Figure C. Sulcus angle comparison to past studies. For any figures or tables, please contact authors directly (see Info & Metrics tab above).

Generic walking profiles applied to mechanical knee simulators are the gold standard in wear testing of total knee replacements (TKRs). Recently, there was a change in the international standard (ISO) for knee wear testing (ISO 14243-3): the direction of motion in the anterior/posterior (AP) and internal/external (IE) directions were reversed. The effects of this change have not been investigated, therefore it is not known whether results generated by following this new standard can be compared to historical wear tests which used the old standard. Using a finite element analysis (FEA) model of a TKR in parallel with an energy based wear model and adaptive remeshing, we investigated differences in wear between the newest ISO standard developed in 2014, and the previous ISO standard developed in 2004. CAD models of a left sided NexGen Cruciate Retaining (CR) TKR (Zimmer, Warsaw, IN) were used to create the FEA model (Figure 1). The loads and motions specified by simulator standards ISO 14243-3(2004) and ISO 14243-3(2014) were applied to the model. Analyses were run using ABAQUS v6.13-2 Standard (Dassault Systèmes, Waltham, MA). 8 node hexahedral elements were used to model the UHMWPE component. The contact was modeled as penalty contact, with the friction coefficient set to 0.04 on the articular surface. The cobalt chromium molybdenum femoral component was modeled as a rigid surface, utilizing a mix of 2. nd. order quadrilaterals and tetrahedrons. Wear of the polyethylene (PE) component was predicted to 1,000,000 cycles using a previously published frictional energy-based wear model. The wear model, developed from data generated in wheel-on-flat tests, utilizes two parameters defining the frictional energy required to remove a unit volume of material both parallel (3.86E8 J/mm. 3. ) and perpendicular (3.55E7 J/mm. 3. ) to the primary polyethylene fibril direction. Primary fibril direction for the analysis was set to the AP direction. Wear for each simulation of a gait cycle was scaled to 500,000 cycles. Two gait cycles were simulated representing 1,000,000 cycles in total. Adaptive remeshing was driven by the wear model, with the mesh being updated every time increment to simulate material ablation. The time step size was variable with a maximum of 0.01s. The FEA predicted higher wear rates for the newest ISO standard (7.34mg/million cycles) compared to the previous standard (6.04mg/million cycles) (Figure 2). Comparing the predicted wear scars (Figure 3), the new version of the standard covered a larger percentage of the total articular surface, with wear being more spread out as opposed to localized. This is more similar to what is seen in patient retrievals. The results of the study suggest that major differences between the old and the new ISO standard exist and therefore historical wear results are not comparable to newly obtained results. In addition, this study demonstrates the utility of FEA in wear analysis, though the wear model needs further work and validation before it can be used as a supplement to simulator testing. Validation of the wear model against simulator tests and pin-on-disk experiments is currently underway. For figures/tables, please contact authors directly.