Background. Artificial total knee designs have revolutionized over time, yet 20% of the population still report dissatisfaction. The standard implants fail to replicate native knee kinematic functionality due to mismatch of condylar surfaces and non-anatomically placed implantation. (Daggett et al 2016; Saigo et al 2017). It is essential that the implant surface matches the native knee to prevent Instability and soft tissue impingement. Our goal is to use computational modeling to determine the ideal shapes and orientations of anatomically-shaped components and test the accuracy of fit of component surfaces. Methods. One hundred MRI scans of knees with early osteoarthritis were obtained from the NIH Osteoarthritis Initiative, converted into 3D meshes, and aligned via an anatomic coordinate system algorithm. Geomagic Design X software was used to determine the average anterior-posterior (AP) length. Each knee was then scaled in three dimensions to match the average AP length. Geomagic's least-squares algorithm was used to create an average surface model. This method was validated by generating a statistical shaped model using principal component analysis (PCA) to compare to the least square's method. The averaged knee surface was used to design component system sizing schemes of 1, 3, 5, and 7 (fig 1). A further fifty arthritic knees were modeled to test the accuracy of fit for all component sizing schemes. Standard deviation maps were created using Geomagic to analyze the error of fit of the implant surface compared to the native femur surface. Results. The average shape model derived from Principal Component Analysis had a discrepancy of 0.01mm and a standard deviation of 0.05mm when compared to Geomagic least squares. The bearing surfaces showed a very close fit within both models with minimal errors at the sides of the epicondylar line (fig 2). The surface components were lined up posteriorly and distally on the 50 femurs. Statistical Analysis of the mesh deviation maps between the femoral condylar surface and the components showed a decrease in deviation with a larger number of sizes reducing from 1.5 mm for a 1-size system to 0.88 mm for a 7-size system (table 1). The femoral components of a 5 or 7-size system showed the best fit less than 1mm. The main mismatch was on the superior patella flange, with maximum projection or undercut of 2 millimeters. Discussion and Conclusion. The study showed an approach to total knee design and technique for a more accurate reproduction of a normal knee. A 5 to 7 size system was sufficient, but with two widths for each size to avoid overhang. Components based on the average anatomic shapes were an accurate fit on the bearing surfaces, but surgery to 1-millimeter accuracy was needed. The results showed that an accurate match of the femoral bearing surfaces could be achieved to better than 1 millimeter if the component geometry was based on that of the average femur. For any figures or tables, please contact the authors directly

Knee arthroplasty with a rotating hinge knee (RHK) prosthesis has become an important clinical treatment option for knee revisions and primary patients with severe varus or valgus deformities and instable ligaments. The rotational axle constraints the anterior-posterior shear and varus-valgus moments, but currently used polyethylene bushings may fail in the mid-term due to insufficient creep and wear resistance of the material. Due to that carbon-fibre-reinforced (CFR) PEEK as an alternativ bushing material with enhanced creep, wear and fatigue behaviour has been introduced in a RHK design [Grupp 2011, Giurea 2014]. The objective of our study was to compare results from the pre-clinical biotribological characterisation to ex vivo findings on a series of retrieved implants. In vitro wear simulation according to ISO 14243-1 was performed on rotating hinge knee devices (EnduRo® Aesculap, Germany) made out of cobalt-chromium and of a ZrN multi-layer ceramic coating for 5 million cycles. The mobile gliding surfaces were made out of polyethylene (GUR 1020, β-irradiated 30 ± 2 kGy). For the bushings of the rotational and flexion axles and the flanges a new bearing material based on CFR-PEEK with 30% PAN fiber content was used. Analysis of 12 retrieved EnduRo. ®. RHK systems in cobalt-chromium and ZrN multi-layer in regard to. -. loosening torques in comparison with initial fastening torques. -. Optical, DSLR camera and stereo light microscope analysis. -. distinction between different wear modes and classification with a modified HOOD-score. -. SEM & EDX of representative samples. -. surface roughness and depth profilometry. with a focus on the four CFR-PEEK components integrated in the EnduRo. ®. RHK design. For the rotating hinge knee design with flexion bushing and flanges out of CFR-PEEK the volumetric wear rates were 2.3 ± 0.48 mm. 3. /million cycles (cobalt-chromium) and 0.21 ± 0.02 mm. 3. /million cycles (ZrN multi-layer), a 10.9-fold reduction (p = 0.0016). The UHMWPE and CFR-PEEK particles were comparable in size and morphology and predominantly in submicron size [5]. The biological response to representative sub-micron sized CFR-PEEK particles has been demonstrated in vivo based on the leucoyte-endothelian-cell interactions in the synovia of a murine intra-articular knee model by Utzschneider 2010. Schwiesau 2013 extracted the frequency of daily activities in hip and knee replacement patients from literature and estimated an average of 1.76 million gait cycles per year. Thus, the 5 million cycles of in vitro wear testing reflect a mean in vivo service life of 2.9 years, which fits to the time in vivo of 12–60 months of the retrieved RHK devices. The in vitro surface articulation pattern of the wear simulation tests are comparable to findings on retrieved CFR-PEEK components for both types of articulations – cobalt-chromium and ZrN multi-layer coating. For the rotating hinge knee design the findings on retrieved implants demonstrate the high suitability of CFR-PEEK as a biomaterial for highly loaded bearings, such as RHK bushings and flanges in articulation to cobalt-chromium and to a ZrN multi-layer coating

The aim of this study was to evaluate passive kinematics of a mobile-bearing, ultracongruent (UC) total knee design compared with a mobile-bearing, posterior stabilised (PS) design intraoperatively using navigation system. Thirty-four knees of 24 patients which had undergone total knee arthroplasty with UC prosthesis (E-motion. ®. , Aesculap, Tuttlingen, Germany) for primary osteoarthritis and fifteen knees of 14 patients with PS prosthesis (E-motion. ®. ) were included in this study. Thirty-one female and seven male patients were included and the mean age was 70.4 years. Patients were followed up for 7.26 months (6 to 12 months). Intraoperative kinematics including valgus/varus rotation, internal/external rotation, and anterior/posterior translation was assessed from 10° to 120° of passive flexion before and after total knee replacement using a surgical navigation system (Orthopilot. ®. , Aesculap). The range of motion (ROM) was measured preoperatively and at the final follow up. The tibiofemoral alignment in 10° flexion changed from varus 5.85° to valgus 0.38° in UC group and changed from varus 7.45° to valgus 1.08° in PS group (p> 0.05), the magnitude of varus rotation during flexion was 0.01° in UC group and 4.08° in PS group (p< 0.05). PS knee showed the tendency to slight varus alignment during flexion but UC knee showed the tendency toward valgus alignment fter midflexion. The mean internal rotation during flexion was 10.3° in UC group and 13.2° in PS group (p> 0.05). The translation of the femur was 4.99mm posteriorly in UC group and 3.24mm posteriorly in PS group at 120° flexion (p> 0.05). The maximum flexion angle at the final follow up was 123° in UC group and 118° in PS group (p> 0.05). Total knee arthroplasty with high flexion PS prosthesis showed good ROM and satisfactory early clinical results. UC total knee design showed less varus rotation during flexion, more valgus pattern in higher flexion angle than PS design, similar internal rotation angle and pattern, and similar posterior translation at 120° flexion with PS design

Total knee arthroplasty with a rotating hinge knee with carbon-fibre-reinforced (CFR)-PEEK as an alternative bushing material with enhanced creep, wear and fatigue behaviour has been clinically established [1-4]. The objective of our study was to compare results from in vitro biotribological characterisation to ex vivo findings on a retrievals.

A modified in vitro wear simulation based on ISO 14243-1 was performed for 5 million cycles on rotating hinge knee (RHK) designs (EnduRo®) out of cobalt-chromium and ZrN-multilayer ceramic coating. The rotational & flexion axles-bushings and the flanges are made of CFR-PEEK with 30% polyacrylonitrile fibre content.

Analysis of 12 retrieved EnduRo® RHK systems in cobalt-chromium and ZrN-multilayer in regard to loosening torques, microscopic surface analysis, distinction between different wear modes and classification with a modified HOOD-score has been performed.

For the RHK design with the polyethylene gliding surface and bushings and flanges made out of CFR-PEEK, a cumulative volumetric wear was measured to be 12.9±3.95 mm³ in articulation to cobalt-chromium and 1.3±0.21 mm³ to ZrN-multilayer coating - a significant 9.9-fold decrease (p=0.0072).

For the CFR-PEEK flexion bushing and flanges the volumetric wear rates were 2.3±0.48 mm³/million cycles (cobalt-chromium) and 0.21±0.02 mm³/million cycles (ZrN-multilayer) (p=0.0016). The 5 million cycles of in vitro wear testing reflect a mean in vivo service life of 2.9 years, which is in accordance to the time in vivo of 12–60 months of the retrieved RHK components [5]. The main wear modes were comparable between retrievals and in vitro specimens, whereby the size of affected area on the retrieved components showed a higher variation.

For the EnduRo® RHK design the findings on retrieved implants demonstrate the high suitability of CFR-PEEK as a biomaterial for highly loaded bearings, such as RHK bushings and flanges in articulation to cobalt-chromium and to a ZrN-multilayer coating.

A total knee design has been developed to support high flexion requirements of post-total knee replacement lifestyles. The extent of flexion, following total knee replacement, is influenced by relative femoral tibial kinematics, posterior knee soft tissue impingement, patella and patellar tendon tracking, preoperative knee flexion, and postoperative physical therapy. A new implant design incorporates features to prevent posterior tibial displacement in high flexion, improved conformity of the femoral/tibial articular surface contact to 155 degrees of flexion, greater femoral/tibial articular surface contact area in high flexion, and a shortened patellar tendon pathway. The requirement for tibial internal-external rotation during some knee flexion activity is accommodated by a rotating tibial poly-ethylene option within the implant system. Laboratory tests indicate the achievement of greater articular surface contact in high flexion conditions through extending the posterior femoral condyle curvature and accommodating the tibial polyethylene articular surface. Joint simulator testing indicates improved wear performance of the high flexion design. A prospective controlled multicenter clinical trial has been initiated to evaluate this high flexion implant design along with surgical techniques and post-surgery physical therapy developed to support patient achievement of high knee flexion following total knee arthroplasty

A new hinge knee system (LEGION HINGE, Smith & Nephew, Memphis, TN) was designed to treat gross knee instability resulting from loss of collateral ligament function, femoral and/or tibial bone loss, or from comminuted fractures of the proximal tibia or distal femur. The knee system is offered with an insert that guides the motion of the implant for kinematic improvement. The purpose of this study was to evaluate kinematic and wear performance of this novel hinge knee replacement system. The kinematics and kinetics of the Guided Motion (GM) hinge knee were assessed for a deep knee bend using a numerical lower leg simulator. Measurements of A/P translation and I/E rotation were compared to 3D MRI data of healthy weight bearing knees and measurements of M/L patella shear forces were compared to a standard primary knee implant. Three GM knee systems were tested for wear performance. All metal components were fabricated from cobalt chrome except for the Ti-6Al-4V insert locking screw. All plastic components were fabricated from UHMWPE. Wear testing was conducted on an AMTI 6-station force controlled knee simulator for approximately 5 million cycles under ISO 14243-1 load/motion profiles and soft tissue constraints. Simulation results showed that up to 130° of flexion the anterior/posteror (A/P) translation and internal/external (I/E) rotation followed a similar path over the flexion range compared to the MRI data. The magnitude of A/P translation at 130° was 9.5 mm for the GM design compared to 15.7 mm for the MRI data. The magnitude of I/E rotation at 130° was 18° for the GM design compared to 20.8° for the MRI data. The GM design showed a maximum M/L patella shear force of 456.8 N compared to 1152.4 N for a standard primary knee design over the flexion range. All constructs successfully completed wear testing and were fully functional with no issues for binding of the mating parts. All polyethylene components showed only burnishing on the articulating surfaces. The volumetric wear rate of polyethylene components was 17.54±1.24 mm3/Mcycle. The volumetric wear rate of the metal components (excluding femoral and tibial tray) was 0.045±0.01 mm3/Mcycle. Testing showed the GM design has A/P and I/E kinematics that are similar to those seen in a normal healthy knee and good patella tracking as evidenced by the low M/L patella shear forces. The wear rate of the polyethylene parts was within the range of wear rates published in the literature for primary knee designs (up to 35.8 mm3/Mcycle). The low metal wear rate indicates that fretting and corrosion of the components was minimal. We conclude the GM design more closely replicates the kinematics of the natural knee without compromising the wear characteristics. This could lead to better outcomes for the patient population that requires a hinge knee implant

INTRODUCTION

Most total knees today are CR or PS, with lateral and medial condyles similar in shape. There is excellent durability, but a shortfall in functional outcomes compared with normals, evidenced by abnormal contact points and gait kinematics, and paradoxical sliding. However unicondylar, medial pivot, or bicruciate retaining, are preferred by patients, ascribed to AP stability or retention of anatomic structures (Pritchett; Zuiderbaan). Recently, Guided Motion knees have been shown to more closely reproduce anatomic kinematics (Walker; Willing; Amiri; Lin; Zumbrunn). As a design approach we proposed Design Criteria: reproduce the function of each anatomic stabilizing structure with bearing surfaces on the lateral and medial sides and intercondylar; resected cruciates because this is surgically preferred; avoid a cam-post because of central femur bone removal, soft tissue entrapment, noises, and damage (Pritchett; Nunley). Our hypothesis was that these criteria could produce a Guided Motion design with normal kinematics.

Aims

The outcomes of total knee arthroplasty (TKA) depend on many factors. The impact of implant design on patient-reported outcomes is unknown. Our goal was to evaluate the patient-reported outcomes and satisfaction after primary TKA in patients with osteoarthritis undergoing primary TKA using five different brands of posterior-stabilized implant.

Introduction: When introducing new joint replacement designs, it is difficult to predict with any certainty the clinical performance of the new design. Using roentgen stereophotogrammetric analysis (RSA) to evaluate the first two years of follow-up may serve as a predictor of late mechanical loosening for both hip and knee prostheses. This randomized study was designed to evaluate the performance of the new Triathlon total knee system and compare the results to its predecessor design, the Duracon total knee system.

Methods: Sixty patients were consecutively randomized to receive either a Duracon (30 patients) or Triathlon total knee (30 patients). All components were cemented, and the posterior Cruciate Retaining version was used for both systems. The study was approved by the Ethical Committee for Lund University. All patients met the inclusion criteria. The mean age was 66 years (Duracon) vs 67 years (Triathlon). The BMI was 29 for both groups. The left knee was operated on in 15 vs 18 patients for the Duracon and for the Triathlon group. There were no statistically significant differences between the demographics for the two groups, except for the number of Ahlbäcks grade III OA, 20 (Duracon) vs 28 (Triathlon). The mean duration of surgery was 64 minutes (Duracon) vs 67 (Triathlon). The hospital stay was 5 days for both groups. The patients were followed up postoperatively at 3, 12 and 24 months. The principal evaluation tool was RSA to measure migration. The clinical results were evaluated using KOOS and KSS.

Results: There were no significant differences in rotation or translation for the three coordinal axes. Neither were there any significant differences in the Maximal Total Point Motion (MTPM) during the 2-year follow-up The MTPM for the Duracon and Triathlon groups respectively was 0.5±0.5 vs 0.4±0.3 mm at 3 months, 0.6±0.4 vs 0.6±0.5 mm at 1 year, and 0.8.±5 vs 0.6±0.7 mm at 2 years. There were no significant differences in the clinical results between the groups when using the KSS and the KOOS.

Discussion: The results of this study suggest that the new Triathlon total knee system is at least clinically equivalent to the Duracon total knee system. There were no significant differences in the RSA 2-year follow-up data nor in the clinical data (p< 0.05), which suggests the Triathlon knee system may replicate the excellent long-term clinical results achieved by the Duracon knee system.

Objectives

The objective of this study was to compare the early migration characteristics and functional outcome of the Triathlon cemented knee prosthesis with its predecessor, the Duracon cemented knee prosthesis (both Stryker).

Lateral retinacular release (LRR) may be necessary to balance the patellofemoral articulation in primary total knee arthroplasty (TKA). However, lateral retinacular release may be associated with an increased risk of patellar necrosis, loosening, perioperative bleeding, and pain.

Additionally, the need for lateral retinacular release may herald a more significant problem with implant positioning, rotation, and balance. The purpose of this study is to report the lateral retinacular release rate with a “patella friendly” femoral TKA design, and to identify if a less invasive approach is associated with reduced need for lateral retinacular release.

A retrospective review of our database identified 4667 primary TKA performed by two surgeons between October 2002 and January 2009. Beginning in 2002, a less invasive approach has been used in over 95% of primary TKA. Also beginning in 2002, the authors began using a new TKA design with a more swept back patellofemoral articulation (Vanguard Complete Knee System; Biomet). During the first two years of the study, the authors also used the Maxim Complete Knee System (Biomet). We previously reported a lateral retinacular release rate associated with the Maxim of 22%. There were 555 Maxim and 4112 Vanguard TKA performed. Lateral retinacular release with Maxim TKA was 12.8% (71/555), significantly less than that previously reported for the same implant design using a standard approach. Lateral retinacular release for Vanguard TKA was 1.8% (72/4112), significantly less than that with the Maxim TKA using either a standard or less invasive approach (p< 0.005).

Implant design, surgical technique, and a less invasive exposure combine to significantly reduce the need for lateral retinacular release in primary TKA.

Introduction: Recent knee prosthesis designs postulate to allow more flexion of the knee without increasing the contact stress on the polyethylene inlay. The study’s purpose was to compare the tibiofemoral contact stress of four different inlay types of a new “high flexion knee prosthesis system under dynamic, physiologic loading conditions in an in vitro test. Thereby, the cruciate retaining and posterior stabilizing designs were compared.

Material and Methods: The TriathlonTM system was implanted into 5 knees of fresh frozen human specimens. The prosthesis system is available with a mobile bearing (MCR) or fixed bearing inlay (FCR). In addition, the posterior stabilized design was although tested in the same manner (MPS=mobile bearing and FPS=fixed bearing inlay). After implantation, specimens were mounted for biomechanical testing in a knee simulator. The test mimicked both the speed and resulting moment exerted during a lower limb isokinetic extension test in a range of tibial motion from 120 degrees flexion to full knee extension. The quadriceps force cylinder was force-controlled provided a constant torque on the lower limb of 31 Nm whereby forces of up to 1500 N were recorded. Inlay motion was measured using an ultrasonic tracking system (CMS 100TM, Zebris GmbH; Isny, Germany). The tibiofemoral peak contact stress was measured using resistive ink, 0.1-mm-thin pressure sensors (Tekscan, Boston), measuring 572 points per compartment at 10 Hz.

Results: Average maximum peak contact stress was 18.8 (+/−6.6 MPa) at 11.5° flexion for the medial inlay (MCR) and 23 MPa (+/−11.7 MPa) at 119.5 deg for the lateral inlay (MCR). For the FCR we measured 23 MPa (+/−9,6 MPa, medial) at 67.5° and 19.7 MPa (+/−8.2 MPa, lateral) at 119.9° knee flexion. The average maximum contact stress on the MPS inlay was 19 MPa (+/− 12.6 MPa, medial) at 7.5° and 20 MPa (+/− 13.4 MPa) at 120°. For the FPS we measured 20.8 MPa (+/−13.1 MPa, medial) at 40.6° and 19 MPa (+/−11.6 MPa, lateral) at 120° knee flexion.

The maximal rotation recorded for the inlay centers was 1.6 ± 1.2 mm at 1.2° knee flexion and 4.3 ± 3.3 mm at 1.3° for the MPS design.

Discussion: This in vitro study characterizes the movement of the mobile bearing inlays of the TriathlonTM system on the tibial baseplate under simulated physiologic loading. With the dynamic ultrasonic tracking device the range of motion and internal/external rotation movement can be accurately determined. The results of this study correlated qualitatively to radiographic measurements. Contact pressures seem not to exceed the maximum contact stress of UHMWPE significantly even at high flexion angles up to 120°. The posterior stabilized design showed no significant lower maximum contact stresses than the cruciate retaining design.

Introduction: This study addresses the long term results of 1225 uncomplicated primary total knee arthroplasties performed between 1986 and 1995, using one design with various tibial fixation methods.

Methods: 1225 primary total knees were performed using a press fit total condylar cruciate retaining design. 108 cases were eliminated because of death and 171 due to lack of follow up leaving a group of 946 knees. Mean time insitu is 9.2 years. 500 knees had both the tray and stem cemented, 374 had only the tray cemented, and 72 used no cement. Both clinical and radiographic Knee Society Scores were tabulated preoperatively and annually thereafter. The SF-36 has been recorded both pre and postoperatively since 1993.

Results: Overall revision rates for the cemented, tray only and non-cemented groups were 1.0%, 3.4% and 12.5%, respectively. A combined 20 cases had the tibial component revised due to polywear and osteolysis with 0.6% from the cemented group, 2.4% from the tray only group and 11.1% from the tray only group. The joint portion of the Knee Society score was comparable for the cemented and tray only groups (88.9 and 88.3, respectively) but only 80.9 for the non-cemented group.

Discussion and conclusion: Using a component design that meets the needs of the majority of patients regardless of bone quality has proven to be successful and cost effective for this institution. The authors believe these excellent results and low revision rate for loosening indicate this design has much to offer with its flexibility of tibial fixation.

Aims: The purpose of this report is to present the short-term clinical performance of total knee arthroplasties performed with the Scorpio+ posteriorly stabilized mobile bearing knee. Methods: 100 Scorpio+ knees were implanted in 96 patients consecutively by the same surgeon and evaluated at one year of follow-up. All patients were assessed clinically using the IKS Score, Western Ontario McMaster Score (WOMAC), a chair rise evaluation6 and radiographically with long leg radiographs, standard A/P, lateral and patellar skyline views. Results: At one year of follow-up the average Range of Motion was 123° with an IKS Score averaging 191, an average knee score of 94, an average functional knee score of 97, and an average WOMAC score of 92. Furthermore, 95 out of 96 patients were able to arise from a chair without using their arms at 1 year of follow-up.

Radiographically no radiolucent lines were visible and all patellar components were centered. Conclusions: Patients with the Scorpio+ MBK demonstrated satisfactory clinical outcomes especially regarding overall stability, range of motion (average flexion 123°) and extensor mechanism function with 98% of patients being able to arise from a chair without the use of their arms at three months of follow-up.

Aims. Wear of the polyethylene (PE) tibial insert of total knee arthroplasty (TKA) increases the risk of revision surgery with a significant cost burden on the healthcare system. This study quantifies wear performance of tibial inserts in a large and diverse series of retrieved TKAs to evaluate the effect of factors related to the patient, knee design, and bearing material on tibial insert wear performance. Methods. An institutional review board-approved retrieval archive was surveyed for modular PE tibial inserts over a range of in vivo duration (mean 58 months (0 to 290)). Five knee designs, totalling 1,585 devices, were studied. Insert wear was estimated from measured thickness change using a previously published method. Linear regression statistical analyses were used to test association of 12 patient and implant design variables with calculated wear rate. Results. Five patient-specific variables and seven implant-specific variables were evaluated for significant association with lower insert wear rate. Six were significant when controlling for other factors: greater patient age, female sex, shorter duration in vivo, polished tray, highly cross-linked PE (HXLPE), and constrained knee design. Conclusion. This study confirmed that knee wear rate increased with duration in vivo. Older patients and females had significantly lower wear rates. Polished modular tibial tray surfaces, HXLPE, and constrained TKA designs were device design factors associated with significantly reduced wear rate. Cite this article: Bone Joint J 2021;103-B(11):1695–1701

Literature debates whether fluid aspirates for suspected PJI should undergo prolonged incubation for cultures. We looked at sensitivity and specificity of 14-day cultures, compared to 7-days, for aspirates from prosthetic hips and knees. Design and methods. Conducted at a quaternary referral centre for PJIs from Jan 2017 to July 2019. Suspected PJIs who underwent aspiration, incubated 14 days and later surgical intervention with minimum three tissue samples were included. Results. 176 aspirates were included. This is an increased number compared to our historic figures (average 88 Vs 48 pts/yr). 47 patients had fluid and tissue positive (true positive), 20 fluid +ive but tissue -ive (false positive), 98 fluid and tissue -ive (true negative) and 15 fluid negative but tissue +ive (False negative). Thus, sensitivity 76%, specificity 83%, positive predictive value70% and negative predictive value 87%. Of 88 positive aspirates, only 75% were within 7-day cultures. Low virulence organisms as Propionibacterium acnes and coagulase negative staph were grown later. Of 48 with only one tissue sample positive, 38 were culture-negative on aspiration and 6 grew different organisms on aspirate and tissues. Also, as many were cultured later, it suggests contamination. Conclusion. Increased numbers reflect quaternary referral nature of institution and increasing PJI load. Modest drop in sensitivity and specificity of 14-day cultures compared to 7-day(84 and 85% respectively) is due to higher false negatives. Contamination contributes to false-ive as more tissue samples become positive (there were 1076 tissue samples due to multiple sampling Vs 176 aspirates). Higher tissue yield may also be because they are more representative. Effect of antibiotic use between samples cannot be determined. Organism profile suggest14-day culture produces more contaminant growth despite a well-equipped microbiology lab with laminar airflow for subcultures. Caution in interpreting 14-day results in diagnosis of PJI of Hip and Knee is advised

The purpose of this study was to examine the influence of weight-bearing on the measurement of in vivo wear of total knee replacements using model-based RSA at 1 and 2 years following surgery. Model-based RSA radiographs were collected for 106 patients who underwent primary TKR at a single institution. Supine RSA radiographs were obtained post-operatively and at 6-, 12-, and 24-months. Standing (weight-bearing) RSA radiographs were obtained at 12-months (n=45) and 24-months (n=48). All patients received the same knee design with a fixed, conventional PE insert of either a cruciate retaining or posterior stabilized design. Ethics approval for this study was obtained. In order to assess in vivo wear, a highly accurate 3-dimensional virtual model of each in vivo TKA was developed. Coordinate data from RSA radiographs (mbRSA v3.41, RSACore) were applied to digital implant models to reconstruct each patient's replaced knee joint in a virtual environment (Geomagic Studio, 3D Systems). Wear was assessed volumetrically (digital model overlap) on medial and lateral condyles separately, across each follow-up. Annual rate of wear was calculated for each patient as the slope of the linear best fit between wear and time-point. The influence of weight-bearing was assessed as the difference in annual wear rate between standing and supine exams. Age, BMI, and Oxford-12 knee improvement were measured against wear rates to determine correlations. Weight bearing wear measurement was most consistent and prevalent in the medial condyle with 35% negative wear rates for the lateral condyle. For the medial condyle, standing exams revealed higher mean wear rates at 1 and 2 years, supine, 16.3 mm3/yr (SD: 27.8) and 11.2 mm3/yr (SD: 18.5) versus standing, 51.3 mm3/yr (SD: 55.9) and 32.7 mm3/yr (SD: 31.7). The addition of weight-bearing increased the measured volume of wear for 78% of patients at 1 year (Avg: 32.4 mm3/yr) and 71% of patients at 2 years (Avg: 48.9 mm3/yr). There were no significant (95% CI) correlations between patient demographics and wear rates. Volumetric, weight-bearing wear measurement of TKR using model-based RSA determined an average of 33 mm3/yr at 2 years post-surgery for a modern, non-cross-linked polyethylene bearing. This value is comparable to wear rates obtained from retrieved TKRs. Weight-bearing exams produced better wear data with fewer negative wear rates and reduced variance. Limitations of this study include: supine patient imaging performed at post-op, no knee flexion performed, unknown patient activity level, and inability to distinguish wear from plastic creep or deformation under load. Strengths of this study include: large sample size of a single TKR system, linear regression of wear measurements and no requirement for implanted RSA beads with this method. Based on these results, in vivo volumetric wear of total knee replacement polyethylene can be reliably measured using model-based RSA and weight-bearing examinations in the short- to mid–term. Further work is needed to validate the accuracy of the measurements in vivo

Objectives. The purpose of this study was to evaluate the impact of multi-radius (MR, n=20) versus gradually reducing radius (GR, n=18) knee design on the kinematics and kinetics of the knee during level ground walking one year after total knee arthroplasty. Materials and Methods. Thirty-eight knees with end-stage knee osteoarthritis were examined before and one year after total knee arthroplasty. The groups consisted of subjects who had undergone total knee arthroplasty with a representative MR designed implant (B Braun-Aesculap Vega. ®. Knee System) and a representative GR designed implant (Depuy Attune. ®. Knee System) (Figure 1). The kinematic and kinetic parameters of knee varus angle, first peak knee adduction moment, sagittal plane knee excursion and extensor moment were evaluated during gait, as well as the spatiotemporal gait outcomes of walking speed, stride length, cadence, step length, the percentage of stance phase. Comparisons of preoperative and postoperative outcomes were done by the paired t-test. Independent t-test was also done to compare the postoperative outcomes of MR designed implant and GR designed implant. Results. In spatiotemporal parameters of GR implant group, there was an increase in walking speed, stride length and cadence (all p<0.05) and no change in step length and the percentage of stance phase postoperatively. GR implant group showed large reductions in varus angle and adduction moment (all p<0.001), a significant increase in extensor moment (p=0.01), and a small reduction in sagittal plane excursion (p=0.04) after surgery. In comparison of two groups at one year after surgery, there were no significant differences of all spatiotemporal, kinematic and kinetic parameters between two groups except varus angle. GR implant group showed more reduction in varus angle than MR implant group (p=0.01). Conclusions. Total knee arthroplasty performed with gradually reducing radius knee design reduces frontal plane loading patterns of knee varus angle and adduction moment and provided improvement in spatiotemporal parameters. Post-operatively there were no statistical differences between the MR implant group and the GR implant group in any of the kinematic and kinetic measures except knee varus angle during level ground walking

Ligament releases are necessary for contemporary non-conforming femoral-tibial articulations. Most total knee arthroplasty prostheses are designed to be non-conforming at the articulation between the femoral and tibial components. This design is chosen on the arthroplasty principle that “constraint causes loosening” and conforming surfaces have been considered constrained. To provide stability the ligaments are adjusted so that tension in the ligament can provide stability for the total knee replacement. Ligament releases are NOT necessary for contemporary conforming femoral-tibial articulations. Through the majority of the range of motion, the normal human knee is not stabilised by ligament tension. Rather, it is the geometrical conformity of the femur and tibia, especially on the medial side, that provides stability. The ligaments are present and ready to restrain the knee from excess varus-valgus or anterior-posterior loads. In a knee design that is congruent, ligaments may be left intact as in the normal knee, ready to provide restraint but not necessarily to provide stability except when excess loads are applied to the knee. When designing and using the ADVANCE Medial Pivot total knee, the author has left ligaments in the toe-region of the stress-strain curve rather than releasing and tensioning the ligaments. Patient satisfaction survey data at routine follow-up visits for patients at 7–15 years after arthroplasty with this type of reconstruction indicate high satisfaction despite medial and lateral opening (on valgus and varus stress) that would be considered “mid-flexion instability” for non-conforming joints that require careful ligament releases and tensioning

Purpose. The purpose of this study was to examine the influence of weight-bearing on the measurement of in vivo wear of total knee replacements using model-based RSA at 1 and 2 years following surgery. Methods. Model-based RSA radiographs were collected for 106 patients who underwent primary TKR at a single institution. Supine RSA radiographs were obtained post-operatively and at 6-, 12-, and 24-months. Standing (weight-bearing) RSA radiographs were obtained at 12-months (n=45) and 24-months (n=48). All patients received the same knee design with a fixed, conventional PE insert of either a cruciate retaining or posterior stabilized design. Ethics approval for this study was obtained. In order to assess in vivo wear, a highly accurate 3-dimensional virtual model of each in vivoTKA was developed. Coordinate data from RSA radiographs (mbRSA v3.41, RSACore) were applied to digital implant models to reconstruct each patient's replaced knee joint in a virtual environment (Geomagic Studio, 3D Systems). Wear was assessed volumetrically (digital model overlap) on medial and lateral condyles separately, across each follow-up. Annual rate of wear was calculated for each patient as the slope of the linear best fit between wear and time-point. The influence of weight-bearing was assessed as the difference in annual wear rate between standing and supine exams. Age, BMI, and Oxford-12 knee improvement were measured against wear rates to determine correlations. Results. Weight bearing wear measurement was most consistent and prevalent in the medial condyle with 0–4% of calculated wear rates being negative compared to 29–39% negative wear rates for the lateral condyle. For the medial condyle, standing exams revealed higher mean wear rates at 1 and 2 years; supine, 16.3 mm. 3. /yr (SD: 27.8) and 11.2 mm. 3. /yr (SD: 18.5) versus standing, 51.3 mm. 3. /yr (SD: 55.9) and 32.7 mm. 3. /yr (SD: 31.7). The addition of weight-bearing increased the measured volume of wear for 78% of patients at 1 year (Avg: 32.4 mm. 3. /yr) and 71% of patients at 2 years (Avg: 48.9 mm. 3. /yr). There were no significant (95% CI) correlations between patient demographics and wear rates. Discussion and Conclusion. This study demonstrated TKA wear to occur at a rate of approximately 10 mm. 3. /year and 39 mm. 3. /year in patients imaged supine versus standing, respectively, averaged over 2 years of clinical follow-up. In an effort to eliminate the effect of PE creep and deformation, wear was also calculated between 12 and 24 months as 9.3 mm. 3. (standing examinations), This value is comparable to wear rates obtained from retrieved TKRs. Weight-bearing exams produced better wear data with fewer negative wear rates and reduced variance. Limitations of this study include: supine patient imaging performed at post-op, no knee flexion performed, and unknown patient activity level. Strengths of this study include: large sample size of a single TKR system, linear regression of wear measurements and no requirement for implanted RSA beads with this method. Based on these results, in vivo volumetric wear of total knee replacement polyethylene can be reliably measured using model-based RSA and weight-bearing examinations in the short- to mid–term. For any figures or tables, please contact authors directly