Background. Total Hip Arthroplasty (THA) has long been the standard treatment for cases in which non-surgical alternatives have failed to improve pain and function in hip osteoarthritis (OA) patients. Outcomes from THA have improved over time with better surgical techniques and improved implant designs. While conventional neck-sacrificing implants have been associated with favorable outcomes, there is evidence to suggest biomechanical advantages of newer, femoral neck-preserving short-stem implants, including the Corin MiniHip. However, there is a still a gap of knowledge regarding the potential benefits of the MiniHip stem over conventional neck-sacrificing stems in regards to patient-reported outcomes (PROs). In this study, we investigated the differences between a neck-sacrificing stem design and neck-preserving short-stem design (MiniHip, Corin Inc.) arthroplasty concerning PROs, and considering the known features of the short stem design, we hypothesized that MiniHip THA would be associated with improved PROs in comparison to a neck-sacrificing implant system. We further sought to investigate gender effects related to MiniHip or conventional stem surgery. Methods. Neck-sacrificing implant patients (n=90, age 57±7.9 years, female=58, male=32) and a matched (matching criteria: follow-up period, BMI, age) cohort group of MiniHip patients (n=105, age 55.16±9.88 years, female: 25, male: 80) reported both pre-operative and post-operative Hip disability and Osteoarthritis Outcome Scores (HOOS) at a minimum interval of 6 months post-operatively and up to three years postoperatively. We applied MANCOVA analysis to compare patient-reported outcome subscores from each group using follow-up period as a covariate and employing gender as an additional grouping factor to evaluate gender effects. Statistical significance was set at α=0.05 and Bonferroni corrections were applied to account for multiple comparisons. Results. There was a main effect of time, showing that all HOOS subscores of both groups increased significantly after surgery (p<0.001). There was a main effect of surgery for subscores Symptoms (p=0.038), ADL (p=0.046), and Sports and Recreation (p=0.039). There was a gender effect only for the subscore Symptoms (p=0.007). There were significant time by surgery interactions for HOOS subscores Symptoms (p=0.002), Pain (p=.009), Sports and Recreation (p=0.004), and QOL (p<0.001) subscores. We also observed a significant time by gender interaction effect for all HOOS subscores (p<0.001). Discussion. The interaction effects regarding most HOOS subscores and surgery/implant type indicate an advantage of MiniHip surgery regarding post-operative reported outcomes. The observed results may be due to previously described improved physiological loading and native hip structure preservation with neck-preserving short-stem designs. While longer-term studies are required for further investigation, evidence suggests the MiniHip may provide a significant benefit to primary THA patients. The additional gender/time interaction effect observed in our study highlights the necessity to consider potential sex differences regarding both the potential/expected improvement in PROs from THA and the requirement to account for such differences when designing osteoarthritis outcome studies based on PROs

Background

Recent studies indicate the benefits of total hip arthroplasty (THA) by using femoral neck-preserving short-stem implants (March et al 1999). These benefits rely on the preservation of native hip structure and improved physiological loading.

However, further investigation is needed to compare the outcome of these implants versus the conventional neck-sacrificing stems particularly assessed by patient-reported outcomes (PROs). In this study, we have investigated the differences in PROs between a neck-sacrificing stem design and neck-preserving short stem design (MiniHip, Corin Inc.). We hypothesized higher PROs outcome in patients who received treatment by using neck-preserving implants.

Stress shielding of the proximal femur occurs in stemmed implants. Resurfacing implant does not invade the intramedullary region. We studied the stress patterns in conventional and nonstemmed designs. Methods. FE model geometry was based on standard femur from the international Society of Biomechanics Mesh Repository. Loading simulated for one- legged stance with body weight of 826 N. 2 regions were defined, R1 (40 mm from tip of head) and R2 41 mm–150 mm) of the intramedullary part of the stemmed model's interface with bone. 2 different loading conditions bending and torsion were compared for stress and strain. The FE model was solved with ANSYS version 6.1 on a single processor NT station. Results. With conventional implants, stem shields cortical bone from being loaded. In nonstemmed implants, Von Misses stress contours show a similar distribution as intact bone, transferring loads to the cortical shell but with higher stresses and a maximum displacement of 17.39% higher than that of intact bone. 15–23 mm proximal to R2 and around 110 mm, region of the stem tip, there were higher stress and strain concentrations. Conclusion. Based on simulations, nonstemmed implants provide more physiological loading compared to conventional implants though stress shielding increases in region of the stem in resurfacing implant

Introduction. PEEK-OPTIMA™ has been considered as an alternative to cobalt chrome in the femoral component of total knee replacements. Whole joint wear simulation studies of both the tibiofemoral and patellofemoral joints carried out to date have shown an equivalent wear rate of UHMWPE tibial and patella components against PEEK and cobalt chrome (CoCr) femoral components. In this study, the influence of third body wear on UHMWPE-on-PEEK was investigated, tests on UHMWPE-on-CoCr were carried out in parallel to compare PEEK to a conventional femoral component material. Methods. Wear simulation was carried out in simple geometry using a 6-station multi-directional pin-on-plate simulator. 5 scratches were created on each PEEK and CoCr plate perpendicular to the direction of the wear test using a diamond stylus to produce scratches with a geometry similar to that observed in retrieved CoCr femoral components. To investigate the influence of scratch lip height on wear, scratches of approximately 1, 2 and 4µm lip height were created. Wear simulation of GUR 1020 UHMWPE pins (conventional, non-sterile) against the plates was carried out for 1 million cycles (MC) using 17g/l bovine serum as a lubricant using kinematic conditions to replicate the average contact pressure and cross-shear in a total knee replacement. Wear of UHMWPE pins was measured gravimetrically and the surface topography of the plates assessed using a contacting Form Talysurf. Wear factors of the pins against the scratched plates were compared to unscratched controls (0µm lip height). Minimum n=3 for each condition and statistical analysis carried out using ANOVA with significance taken at p<0.05. Results. For the control tests (0µm lip height), the wear factor of UHMWPE pins was similar (p=0.64) against PEEK and CoCr plates. Against CoCr, with an increasing lip height, an exponential increase in wear factor of UHMWPE pins was observed; for PEEK, with increasing lip height, the wear factor did not show an exponential increase. When articulated against the largest scratches, 4µm, the wear factor of UHMWPE was significantly higher against CoCr than PEEK (p=0.01). At the conclusion of the study, on the PEEK plates, a polishing effect of the pin against the plates was observed and in the area of the wear test, the lip height of the scratches was lower than pre-test values; for the CoCr plates, no change in lip height was measured after 1MC wear simulation. Conclusion. The exponential relationship between scratch lip height in CoCr and wear of UHMWPE has previously been described. However, the trend in the wear of UHMWPE was different when articulating against scratched PEEK compared to CoCr, with a significantly higher wear factor of UHMWPE against CoCr than PEEK at a scratch lip height of 4µm. This study suggests that the third body wear behaviour of this all-polymer knee replacement will be different to that of conventional implant materials

Background. Use of a robotic tool to perform surgery introduces a risk of unexpected soft tissue damage due to the lack of tactile feedback for the surgeon. Early experience with robotics in total hip and knee replacement surgery reported having to abort the procedure in 18–34 percent of cases due to inability to complete preoperative planning, hardware and soft tissue issues, registration issues, as well as concerns over actual and potential soft tissue damage. These damages to the soft tissues resulted in significant morbidity to the patient, negating all the desired advantages of precision and reproducibility with robotic assisted surgery. The risk of soft tissue damage can be mitigated by haptic software prohibiting the cutting tip from striking vital soft tissues and by the surgeon making sure there is a clear workspace path for the cutting tool. This robotic total knee system with a semi-active haptic guided technique was approved by the FDA on 8/5/2015 and commercialized in August of 2016. One year clinical results have not been reported to date. Objective. To review an initial and consecutive series of robotic total knee arthroplasties for safety in regard to avoidance of known or delayed soft tissue injuries and the necessity to abort the robotic assisted procedure and resort to the use of conventional implantation. Report the clinical outcomes with robotic total knee replacement at or beyond one year to demonstrate satisfactory to excellent performance. Methods. The initial consecutive series of 100 robotic total knee replacements using a semi-active haptic guided system including 34 from the initial IDE series in 2014 and those performed after commercial approval beginning in 2016 were reviewed. Pre- operative planning utilizing CT determined the implant placement and boundaries and thus the limit of excursion from any part of the end effector saw tip. Self-retaining retractors were also utilized. Operative reports, 2, 6, and 12 week, and yearly follow-up visit reports were reviewed for any evidence of inadvertent injury to the medial collateral ligament, patellar tendon, or a neurovascular structure from the cutting tool. Operative notes were also reviewed to determine if the robotic procedure was partially or completely aborted due to any issue. Knee Society and Functional scores were recorded from pre-operative and yearly. Results. No cases were unable to be completed robotically. No case had evidence for acute or delayed injury to the medial collateral ligament, patellar tendon, or neurovascular structure. The average follow-up for this series was 1.54 years. Average pre- operative Knee Society and Functional Scores improved from 44.7 and 50 to 98.1 and 87.8 at one year follow-up, 93.8 and 83.1 at two year follow-up, 98.5 and 87.7 at three year follow-up, and 99 and 85 at four year follow-up. Conclusions. A semi-active haptic guided robotic system is a safe and reliable method to perform total knee replacement surgery. Preliminary short-term outcomes data shows excellent clinical and functional results

Introduction. A previous computational study on an all-polymer PEEK-on-UHMWPE total knee replacement implant showed improved periprosthetic bone loading, compared to a conventional implant [1]. That study used a simulated gait cycle to determine distal loading, but a patella was not included. Substantial distal decrease of bone remodeling stimulus was found, in accordance with previous reports [2], but it was not consistent with other clinical and post-mortem DEXA results, which found the largest loss of bone stock in the anterior region [3,4]. As patellofemoral forces are relatively low during gait compared to squatting, we simulated a deep squat, expecting that a high-demand activity would provide similar indications of bone loss as literature [3,4]. Consequently, we applied both high tibiofemoral and patellofemoral loads, to provide more insight in the potential benefits of a new PEEK-Optima® femoral component on periprosthetic bone stock. Methods. We adopted a deep squat finite element model from Zelle et al. and included quasi-static deep flexion and load sharing at the posterior condyles [6]. A new implant design was inserted, with three variations in material properties: intact, CoCr and PEEK. The stiffness of the femoral elements was mapped from CT and applied to either the cut femur only (CoCr and PEEK) or the entire femoral construct (intact). The strain energy density (SED) was evaluated in the periprosthetic region as a measure for bone remodeling stimulus. To examine the effects of the entire exercise, SED values were integrated over all increments. Results. During squat the highest SED values were found at the intercondylar region, behind the posterior condyles and behind the anterior flange, extending further inward to the bone. Both the lateral and medial view of the periprosthetic region show markedly different SED patterns from the conventional CoCr implant. Higher values originating proximally extended to lower values in the anterodistal region (Figure 1). However, in the CoCr reconstruction these anterodistal patterns less prominent or even absent. In Figure 2, simulated DEXA images are presented showing the bone remodeling stimulus throughout the periprosthetic volume. Overall, the image for CoCr shows darker areas than PEEK and the reference, further corroborating the findings shown in Figure 1. Moreover, it is visible that the PEEK reconstruction had SED values similar to the reference in the femoral component region. Discussion. This study has corroborated that the influence of the patella in high-demanding tasks is of great importance to the anterior periprosthetic bone stock [4,5]. The loss of bone remodeling stimulus in the CoCr reconstruction is in accordance with literature findings [2–4]. The resemblance of PEEK to the intact reference suggests that the new PEEK-Optima® femoral component could largely retain the integrity of the periprosthetic bone

INTRODUCTION. Unicompartmental knee arthroplasty (UKA) is considered a highly successful procedure. However, complications and revisions may still occur, and some may be related to the operative technique. Computer assistance has been suggested to improve the accuracy of implantation of a UKA. The present study was designed to evaluate the long-term (more than 10 years) results of an UKA which was routinely implanted with help of a non-image based navigation system. MATERIAL AND METHODS. All patients operated on between 2004 and 2005 for implantation of a navigated UKA were included. Usual demographic and peri-operative items have been record. All patients were prospectively followed with clinical and radiological examination. All patients were contacted after the 10 year follow-up for repeat clinical and radiological examination (KSS, Oxford knee questionnaire and knee plain X-rays). Patients who did not return were interviewed by phone call. For patients lost of follow-up, family or general practitioner was contacted to obtain relevant information about prosthesis survival. Survival curve was plotted according to Kaplan-Meier. RESULTS. 57 UKAs were implanted during the study time-frame. Final follow-up (including death or revision) was obtained for 50 cases (88%). Clinical status after 10 years was obtained for 45 cases (80%). 4 prosthetic revisions were performed for mechanical reasons during the follow- up time (7%). The 10 year survival rate was 94%. No component was considered loose at the final radiographic evaluation. No polyethylene wear was detected at the final radiographic evaluation. DISCUSSION. This study confirms our initial hypothesis, namely quite satisfactory results of a navigated implanted UKA after more than 10 years. Navigation, whose precision is no longer to be demonstrated, probably contributed to the quality of the results. A more consistent anatomical reconstruction and ligamentous balance of the knee should lead to more consistent survival of the UKA. However, superiority of navigated UKA in comparison to conventional implanted UKA is difficult to prove because of the subtle differences expected in mostly underpowered studies. Longer term follow-up may be required

INTRODUCTION. Total knee arthroplasty (TKA) is considered a highly successful procedure. Survival rates of more than 90% after 10 years are generally reported. However, complications and revisions may still occur for many reasons, and some of them may be related to the operative technique. Computer assistance has been suggested to improve the accuracy of implantation of a TKA (Jenny 2005). Short term results are still controversial (Roberts 2015). However, few long term results have been documented (Song 2016). The present study was designed to evaluate the long-term (more than 10 years) results of a TKA which was routinely implanted with help of a non-image based navigation system. The 5- to 8-year of this specific TKA has already been documented (Jenny 2013). The hypothesis of this study will be that the 10 year survival rate of this TKA will be improved in comparison to historical papers when analyzing survival rates and knee function as evaluated by the Knee Society Score (KSS). MATERIAL AND METHODS. All patients operated on between 2001 and 2004 for implantation of a navigated TKA were eligible for this study. Usual demographic and peri-operative items have been record. All patients were prospectively followed with clinical and radiological examination. All patients were contacted after the 10 year follow-up for repeat clinical and radiological examination (KSS, Oxford knee questionnaire and knee plain X-rays). Patients who did not return were interviewed by phone call. For patients lost of follow-up, family or general practitioner was contacted to obtain relevant information about prosthesis survival. Survival curve was plotted according to Kaplan-Meier. RESULTS. 247 TKAs were implanted during the study time-frame. 225 cases had an optimal lower limb axis (HKA angle between 177° and 183°) after TKA (91%). Final follow-up (including death or revision) was obtained for 200 cases (81%). Clinical status after 10 years was obtained for 146 cases (59%) (KSS, 102 cases – Oxford questionnaire, 146 cases – radiologic evaluation, 94 cases). 4 prosthetic revisions were performed for mechanical reasons during the follow-up time (1%). The 10 year survival rate was 98%. The mean KSS was 188 points. The mean Oxford score was 55 points. No component was considered loose at the final radiographic evaluation. No polyethylene wear was detected at the final radiographic evaluation. DISCUSSION. This study confirms our initial hypothesis, namely quite satisfactory results of navigated implanted TKA after more than 10 years. Navigation, whose precision is no longer to be demonstrated, probably contributed to the quality of the results. A more consistent anatomical reconstruction and ligamentous balance of the knee should lead to more consistent survival of the TKA. Other authors did observe similar results (Baumbach 2016). However, superiority of navigated TKA in comparison to conventional implanted TKA is difficult to prove because of the subtle differences expected in mostly underpowered studies. Longer term follow-up may be required

Dislocation is a particular problem after total hip replacement in femoral neck fractures and elderly, especially female, patients. The increased rate of dislocation in this population is probably due to significant ligamentous laxity in these patients and poor coordination and proprioception. Another population of patients with increased propensity for dislocation is the revision hip replacement patient. Current dislocation rates in these patients can approach 10% with conventional implant systems. The Dual Mobility total hip system is composed of a cobalt chrome acetabular shell that has a grit blasted, beaded and/or hydroxyapatite coating to improve bone ingrowth. The polyethylene liner is highly crosslinked polyethylene and fits congruently into the cobalt chrome shell and acts like a large femoral head (usually > 40 mm). The femoral head attached to the trunnion is usually 28 mm. The femoral head snaps into the polyethylene liner to acts as a second protection against dislocation. Indications for the Dual Mobility socket are in the high risk for dislocation patient and particularly in elderly, female patients. It is also indicated in patients with neuromuscular disease who are at more risk to dislocate. To date 237 dual mobility cups have been performed with an average age of 79 and 207 of the procedures in women. The follow up extends to 5.6 years with an average of 3.5. There has been 1 dislocation which occurred after a traumatic event. There have been no mechanical failures, no infections and no other revisions in this series. Interprosthetic dislocation has been reported in long term follow up and there was, in this series, when reduction was performed on the only liner dislocation. Pain relief has been no different than conventional hip replacement and range of motion is unchanged as well

Dislocation is a particular problem after total hip replacement in femoral neck fractures and elderly especially female patients. The increased rate of dislocation in this population is probably due to significant ligamentous laxity in these patients and poor coordination and proprioception. Another population of patients with increased propensity for dislocation is the revision hip replacement patient. Current dislocation rates in these patients can approach 10% with conventional implant systems. The Dual Mobility total hip system is composed of a cobalt chrome acetabular shell with a grit blasted, beaded and/or hydroxyapatite coating to improve bone ingrowth. The polyethylene liner is highly cross-linked polyethylene and fits congruently into the cobalt chrome shell and acts like a large femoral head (usually >40mm). The femoral head attached to the trunnion is usually 28mm or 32mm. The femoral head snaps into the polyethylene liner to acts as a second protection against dislocation. Indications for the Dual Mobility socket are in the high risk for dislocation patient and particularly in elderly female patients. One hundred fifty-six patients with an average age of 79 have been performed to date with a maximum follow up to 4.2 years. To date there have been no mechanical or septic failures and no dislocations. Pain relief has been no different than conventional hip replacement and range of motion is unchanged as well. There have been reported cases of intraprosthetic dislocation but these have not occurred to date

Introduction. Conventional implant designs in total knee arthroplasty (TKA) are based on metal on UHMWPE bearing couples. Although this procedure is quite successful, early loosening is still a matter of concern. One of the causes for early failure is stress shielding, leading to loss of bone stock, periprosthetic bone fractures and eventually aseptic loosening of the component. The introduction of a polyetheretherketone (PEEK) on UHMWPE bearing couple could address this problem. With mechanical properties more similar to distal (cortical) bone it could allow stresses to be distributed more naturally in the distal femur. A potential adverse effect, however, is that the femoral component and the underlying cement mantle may be at risk of fracturing. Therefore, we analyzed the effect of a PEEK-Optima® femoral component on stress shielding and the integrity of the component and cement mantle, compared to a conventional Cobalt-Chromium (CoCr) alloy implant. Methods. We created a Finite Element (FE) model of a reconstructed knee in gait, based on the ISO-14243-1 standard. The model consisted of an existing cemented cruciate retaining TKA design implanted on a distal femur, and a tibial load applicator, which together with the bone cement layer and the tibial implant is referred to as the tibial construct. The knee flexion angle was controlled by the femoral construct, consisting of the femoral implant, the bone cement and the distal femur. The tibial construct was loaded with an axial force, anterior-posterior (AP) force and a rotational torque, representing the ground reaction force, soft tissue constraints and internal/external rotation of the tibia, respectively. The integrity of the femoral component and cement mantle were expressed as a percentage of their yield stress. Stress shielding in the periprosthetic femur was evaluated by the strain energy (density) in the bone and compared to a model replicating an intact knee joint. Results. Considering implant durability, the CoCr and PEEK-Optima® femoral components performed equally well, with peak stresses reaching only 12–18 percent of their respective yield stresses (Figure 1(A)). The bone cement experienced higher loads in the reconstruction with the PEEK-Optima® implant, but the principal stresses were within a safe range, with a maximum of 20 percent of the ultimate compressive load (Figure 1(B)). As anticipated, the more compliant polymer implant resulted in a strain energy magnitude and distribution similar to that of an intact knee (Figure 2,3), which could prevent the loss of bone stock on the longer term. Discussion. Our simulations indicate that the femoral implant and cement mantle are not at risk of failure during gait. Moreover, the hypothesis that stress shielding can be reduced by a polymer implant is corroborated by this model. ISO loads can be considered an underestimation and so we intend to expand the model with more comprehensive loading regimes, based on musculoskeletal simulations of gait as well as more arduous physical activities. We plan to include activities like squatting or stair ascending as they are likely to be more detrimental to the implant performance

Introduction. Significant reduction in the wear of current orthopaedic bearing materials has made it challenging to isolate wear debris from simulator lubricants. Ceramics such as silicon nitride (SiN), as well as ceramic-like surface coatings on metal substrates have been explored as potential alternatives to conventional implant materials. Current isolation methods were designed for isolating conventional metal, UHMWPE and ceramic wear debris. The objective of this study was to develop methodology for isolation and characterisation of modern ceramic or ceramic-like coating particles and metal wear particles from serum lubricants under ultra-low wearing conditions. Sodium polytungstate (SPT) was used as a novel density gradient medium due to its properties, such as high water solubility, the fact that it is non-toxic and acts as a protein denaturant, coupled with a large density range of 1.1–3.0 g/cm3 in water. Methods. SiN nanoparticles (<50nm nanopowder, Sigma-Aldrich) and clinically relevant cobalt-chromium wear debris were added to 25% (v/v) bovine serum lubricant at concentrations of 0.03 and 0.3 mm3/ million cycles. The particles were isolated by a newly developed method using SPT gradients. The sample volume was reduced by centrifuging the lubricant at 160,000 g for 3 h at 20°C. Then, re-suspended pellet was digested twice with 0.5 mg/ml proteinse K for 18 hours at 50°C in the presence of 0.5% (w/v) SDS. Particles were then isolated from partially hydrolysed proteins by density gradient ultracentrifugation at 270,000 g for 4 h using SPT gradients [Figure 1]. At the end of centrifugation, particles were pelleted at the bottom of the centrifuge tube, leaving protein fragments and other impurities suspended higher up the tube. Isolated particles were then washed with pyrogen free water, dispersed by sonication and filtered through 15 nm polycarbonate membrane filters for SEM and EDX analysis. Results and Discussion. The morphology and size distribution of the SiN and cobalt-chromium particles was not altered after isolation [Figure 2] [Figure 3]. The mode size of the SiN particles was 30–40 nm, while the mode size of cobalt-chromium particles was 10–20 nm [Figure 3]. Unlike current isolation methods, the present study developed a highly sensitive method which uses cost effective commercially available reagents and components. Furthermore, the particles are recovered in solution and can be readily analysed using commercial size analysers, prior to use in cell studies. This study also confirmed the aggregation characteristics of silicon nitride particles in aqueous medium as observed in previous studies. The above method may also be used to isolate wear debris of materials that have density higher than 1.6 g/cm3. This includes the majority of ceramics, metals and ceramic-like coatings used in TJR components such as alumina, zirconia toughened alumina, titanium, chromium nitride coating, titanium nitride coating and chromium carbon nitride coating. Conclusions. The new isolation method successfully isolated silicon nitride nanoparticles and cobalt-chromium wear debris from serum lubricant at ultra-low concentrations of 0.03 mm3/million cycles. Acknowledgements. The research leading to these results has received funding from the European Union's Seventh Framework Programme (FP7/2007-2013) under grant agreement no. GA-310477 LifeLongJoints

INTRODUCTION. Postoperative functional limitations after Total Knee Arthroplasty (TKA) are caused, in part, by a mismatch between a patient's natural anatomy and conventional “off-the-shelf” implants. To address this, we propose a new concept combining off-the-shelf femur and tibia implants with custom polyethylene tibial inserts designed to account for a patient's unique anatomy. Our goal in this study was to use knee specific computational modeling to determine the neutral path of motion and laxity of an intact knee under axial compression and shear forces through full flexion and compare intact motion against the same knee implanted with a conventional off-the-shelf vs. a custom tibial insert. METHODS. 3D models of a healthy knee joint were acquired from an open development repository funded by the National Institute of Biomedical Imagining and Bioengineering (Harris et al., 2016). The knee model was virtually implanted with conventional (off-the-shelf) posterior cruciate retaining (CR) components including the femoral component, tibial tray, and a conventional insert. A custom CR tibial insert was designed taking into account native articular geometry and compatibility with placement of the off-the-shelf femoral/tibial tray. Bone, cartilage and implant models were imported into ANSYS Workbench. Ligaments were calibrated using data from in-vitro experimental tests (Harris et al., 2016). The following load conditions were applied to the femur: 20 N axial compression (neutral path), 20 N axial compression with 80 N anterior shear force, and 20 N axial compression with 80 N posterior shear force. Simultaneously for each loading condition, the knee was flexed from 0 – 120 degrees. A circular axis system was used to describe the motion of the femur relative to the tibia. RESULTS. For the intact case, neutral path was characterized by greater posterior femoral displacement on the lateral side than on the medial side, especially in early flexion. Neutral path of the custom insert was closer to intact condition than the conventional insert. Overall AP laxity was similar between intact and implanted models except at 30 degrees where increased laxity occurred posteriorly for the implanted models, likely due to resection of the anterior cruciate ligament (ACL) as part of the TKA procedure. For intact and implanted models, AP laxity significantly decreased at the higher flexion angles. DISCUSSION. Our findings indicate that motion with a custom tibial insert was closer to intact than the conventional design. Nonetheless, custom articular surface alone may not fully reproduce intact motion due to limitations such as resection of the ACL, and such custom inserts may benefit from guiding features such as a cam, post, or retention of the native ACL to more closely reproduce normal knee function. We did not simulate specific activities of daily living. Increasing the magnitudes of compression and shear forces would not change the neutral path of motion, although, a reduction in laxity would be expected

Introduction:. Acetabular component orientation has been linked to hip stability as well as bearing mechanics such as wear. Previous studies have demonstrated wide variations of cup placement in hip arthroplasty using conventional implantation techniques which rely upon either anatomic landmarks or the use of commercial positioning guides. Enabling technologies such as navigation have been used to improve precision and accuracy. Newer technologies such as robotic guidance have been postulated to further improve accuracy. The goal of our study was to evaluate the clinical reproducibility of a consecutive series of haptically guided THR. Methods:. 119 patients at 4 centers were enrolled. All patients had preoperative CT scans for the purpose of planning cup placement in lateral opening and version using proprietary software (Mako, Ft. Lauderdale, FL). All procedures were performed using a posterolateral approach. Following bone registration, acetabular preparation and component position is performed using haptic guidance. Final implant postion is ascertained by obtaining 5 points about the rim of the acetabular component and recorded. At 6 weeks, all patients had AP and cross-table lateral radiographs which were then analyzed for cup abduction and anteversion using the Hip Analysis Suite software. The goal was to determine the variability between desired preoperative plan, intraoperative measurement and postoperative results. Results:. Of the 119 hips replaced, 9 hips were excluded due to problems using the Hip Suite software leaving 110 hips for analysis. As seen in Table 1., the mean cup inclination was planned for 40.0 degrees. Intraoperative recorded inclination was 39.9 degrees and using the Martell software, 40.4 degrees. Planned cup anteversion was 18.7 degrees, with intraoperative measurement of 18.6 degrees and postoperative Hip Suite analysis 21.5 degrees. There was no significant difference between any of these measurements. Conclusion:. The use of a haptically guided robot to prepare and implant an acetabular component during total hip arthroplasty is both precise and accurate based upon this multicentered study. While further research determining optimal cup position is needed, these results suggest that the ability to achieve desired position is possible utilizing this enabling technology

Introduction:. Large diameter femoral heads have been used successfully to prevent dislocation after Total Hip Arthroplasty (THA). However, recent studies show that the peripheral region of contemporary femoral heads can directly impinge against the native soft-tissues, particularly the iliopsoas, leading to activity limiting anterior hip pain. This is because the spherical articular surface of contemporary prosthesis overhangs beyond that of the native anatomy (Fig. 1). The goal of this research was to develop an anatomically shaped, soft-tissue friendly large diameter femoral head that retains the benefits of contemporary implants. Methods:. Various Anatomically Contoured femoral Head (ACH) designs were constructed, wherein the articular surface extending from the pole to a theta (θ) angle, matched that of contemporary implants (Fig. 2). However, the articular surface in the peripheral region was moved inward towards the femoral head center, thereby reducing material that could impinge on the soft-tissues (Fig. 1 and Fig. 2). Finite element analysis was used to determine the femoroacetabular contact area under peak in vivo loads during different activities. Dynamic simulations were used to determine jump distance prior to posterior dislocation under different dislocation modes. Published data was used to compare the implant articular geometry to native anatomy (Fig. 3). These analyses were used to optimize the soft-tissue relief, while retaining the load bearing contact area, and the dislocation resistance of conventional implants. Results:. The resulting ACH prosthesis retained the large diameter profile of contemporary implants over an approximately hemispherical portion (Fig. 2). Beyond this, the peripheral articular surface was composed of smaller convex radii. With this design, the jump distance under posterior and anterior dislocation modes, and the femoroacetabular contact area under loads corresponding to walking, deep knee bend and chair sit, remained identical to that of contemporary implants. Additionally, while contemporary prosthesis extended beyond the native articular surface in the distal-medial and proximal-lateral regions (shaded grey), the ACH implant remained within the margins of the native anatomy (Fig. 3). Conclusion:. A novel large diameter anatomically contoured femoral head prosthesis was developed, to mitigate the soft-tissue impingement with contemporary prosthesis. The ACH retained the large diameter profile of contemporary implants over a hemispherical portion. However, in the peripheral region, the ACH had a smaller profile to reduce soft-tissue impingement

INTRODUCTION. Polyethylene wear is one of the reasons for failure of total knee replacement (TKR). There are several reasons for wear, and the femoro-tibial contact area is an important factor. Mobile bearing, highly congruent prostheses might be more resistant to polyethylene wear than fixed bearing, incongruent prostheses. We evaluated the 5- to 8-year experience of three university departments by using an original system with following highlights: implantation with a navigation system, extended congruency up to 90° of flexion, floating polyethylene component with non-limited movements of rotation, antero-posterior translation and medio-lateral translation. MATERIAL. 347 patients have been operated on in the three participating departments with this new prosthesis system between 2001 and 2004, and have been prospectively followed with clinical and radiologic examination with a minimal follow-up time of 5 years. There were 246 women and 101 men, with a mean age of 67 years. METHODS. Clinical and functional results have been analyzed according to the Knee Society scoring system. Accuracy of implantation has been assessed on post-operative long leg antero-posterior and lateral X-rays. Survival rate up to 8 years has been calculated according to Kaplan and Meier, with mechanical revision or any revision as end-points. RESULTS. Complete patient history was obtained by 319 cases (92%). The mean clinical score was 93 points. The mean pain score was 47 points. The mean flexion angle was 118°. The mean functional score was 87 points. An optimal correction of the coronal femoro-tibial axis was obtained in 94% of the cases. Survival rate after 8 years was 98.8% for mechanical revisions and 95.5% for all revisions. DISCUSSION-CONCLUSION. We confirmed the influence of the navigation system on the accuracy of implantation. The clinical and functional results after 5 to 8 years are in line with the better results of the current literature after conventional implantation of non-congruent prostheses. 5- to 8-year survival rate is comparable to the current standards. The influence of the design on polyethylene wear will need a longer follow-up. SUMMARY. The 5- to 8-year results of this floating platform, high congruent prosthesis, are comparable to the best standard of the current literature

Polyethylene wear is one of the reasons for failure of total knee replacement (TKR). There are several reasons for wear, and the femoro-tibial contact area is an important factor. Mobile bearing, highly congruent prostheses might be more resistant to polyethylene wear than fixed bearing, incongruent prostheses. We evaluated the five- to eight-year experience of three university departments by using an original system with following highlights: implantation with a navigation system, extended congruency up to 90° of flexion, floating polyethylene component with non-limited movements of rotation, antero-posterior translation and medio-lateral translation. 347 patients have been operated on in the three participating departments with this new prosthesis system between 2001 and 2004, and have been prospectively followed with clinical and radiologic examination with a minimal follow-up time of five years. There were 246 women and 101 men, with a mean age of 67 years. Clinical and functional results have been analyzed according to the Knee Society scoring system. Accuracy of implantation has been assessed on post-operative long leg antero-posterior and lateral X-rays. Survival rate up to eight years has been calculated according to Kaplan and Meier, with mechanical revision or any revision as end-points. Complete patient history was obtained by 319 cases (92%). The mean clinical score was 93 points. The mean pain score was 47 points. The mean flexion angle was 118°. The mean functional score was 87 points. An optimal correction of the coronal femoro-tibial axis was obtained in 94% of the cases. Survival rate after eight years was 98.8% for mechanical revisions and 95.5% for all revisions. We confirmed the influence of the navigation system on the accuracy of implantation. The clinical and functional results after five to eight years are in line with the better results of the current literature after conventional implantation of non-congruent prostheses. The survival rate is comparable to the current standards. The influence of the design on polyethylene wear will need a longer follow-up

There is still want of evidence in the current literature of any significant improvement in clinical outcome when comparing computer-assisted total knee arthroplasty (CA-TKA) with conventional implantation. Analysis of alignment and of component orientation have shown both significant and non-significant differences between the two methods. Not much work has been reported on clinical evidence of stability of the joint. We compared computer-assisted and conventional surgery for TKA at 5.4 years follow-up for patients with varus osteoarthritic knees with deformity of more than 15∗. Our goal was to assess clinical outcome, stability and restoration of normal limb alignment. We used CT and Cine video X ray techniques to analysize our results in Computer navigated and conventional TKRs. A three dimentional CT scan of the whole extremity was performed and evaluation was done in three planes; saggital, coronal and transverse views. CT scan was done between 10 to 14 days postoperative. Mean deviations in the mechanical axis, femoral and tibial plateau angles, and in transverse view, the trans-epicondylar axis vs posterior condylar axis were measured. The prospective randomized study comprised of 98 patients with surgery done on knees, one side navigated and other side conventional. Mean deviation in the mechanical axis was 2.2∗ in conventional knees and 1.8∗ in navigated knees. In 5 % of cases retinacular release was needed and CT analysis showed TEA in deviation of more than 2 ∗ in these cases. We analysed intraoperative data (surgical time and intraoperative complications), postoperative complications, lower limb alignment, radiographic complication on X-ray imaging, and clinical outcome throughknee and function score, range of motion and joint stability. Our results showed that CAS had greater consistency and accuracy in implant placement and stability of joint in full extension and 90∗ flexion. In the coronal view, 93.3% in the CAS group had better outcomes compared with EM (73.4%). In the sagittal axis, 90.0% CAS also had better outcomes compared with EM (63.3%). Computer-navigated total knee arthroplasty helps increase accuracy and reduce “outliers” for implant placement

Summary:. Smaller increments in the antero-posterior dimensions of femoral components allows significant improvements in balancing of the knee after TKA with restoration of more normal soft-tissue stability. Introduction:. The soft-tissue stability of the knee after TKA is often compromised by the fact that only a finite set of implantable component sizes is available to match bony anatomy. While this could be overcome with custom components, a more practical solution is a set of femoral components with smaller increments in the antero-posterior (AP) dimension. However, this results in a larger assortment of sizes of both implants and trial components. This study was performed to determine whether smaller increments in the AP sizing of knee prostheses would lead to real benefits in restoration of normal knee function and stability after TKA. Methods:. Specimen-specific computer models of 5 cadaveric knees were created through reconstruction of computer tomography scans and co-registered magnetic resonance images. Modeled elements simulating all mechanically significant soft-tissue structures were incorporated in each model and calibrated through multi-axial robotic testing of each cadaveric specimen. The usage of the specimens was approved by the local ethics commission. A contemporary design of posterior-stabilized TKA was virtually implanted in each knee, based on in-vitro reference implantations performed by an orthopedic surgeon. The effect of implant sizing was evaluated by evaluating the change in laxity of each knee after varying the AP size of the femoral component by +/− 2 mm, and then by +/− 1 mm. This corresponded to the change between sizes of a conventional implant system with 4 mm increments vs. an alternative sizing scheme with increments of only 2 mm. For each implant selection, the laxity of the TKA at 0°, 30°, 60°, 90° and 120° of flexion was predicted in response to varus-valgus (v/v) moments of +/− 10 Nm, internal-external (int/ext) torques of +/− 6 Nm and AP shear loads of +/− 100 N under a compressive load of 44N. Results:. When the femoral component was down-sized by 2 mm (4 mm increment system), knee laxity at 90° of flexion increased by 3.1° in v/v (range: 2.7°–3.5°), 7.1° in int/ext rotation (range: 6.4°–8.6°) and 3.7 mm in AP translation (range: 2.1–6.3 mm). Up-sizing caused each component of knee laxity to decrease by a similar amount (Figure 1). When the increments in femoral component sizing were reduced to 2 mm, each component of knee laxity was reduced by approximately 50% (v/v: 1.5°; int/ext rotation: 3.6°, and 2.0 mm AP translation; all p < 0.05). In extension, no relevant changes in knee laxity were detected. Discussion and Conclusion:. This study demonstrates that the use of femoral components with 2 mm AP increments allows much closer approximation of the normal laxity characteristics of the knee. This may enable surgeons to improve ligament balancing and the creation of a knee that feels more natural after joint replacement

Introduction. Large diameter femoral heads provide increased range-of-motion and reduced dislocation rates compared to smaller diameter femoral heads. However, several recent studies have reported that contemporary large head prostheses can directly impinge against the local soft tissues leading to anterior hip pain. To address this we developed a novel Anatomically Contoured large diameter femoral Head (ACH) that maintains the profile of a large diameter femoral head over a hemispherical portion and then contours inward the distal profile of the head for soft-tissue relief. We hypothesized that the distal contouring of the ACH articular surface would not affect contact area. The impact of component placement, femoral head to acetabular liner radial clearance, and joint loading during different activities was investigated. Methods. A finite element model was used to assess the femoroacetabular contact area of a 36 mm diameter conventional head and a 36 mm ACH (Fig. 1). It included a rigid acetabular shell, plastically deformable UHMWPE acetabular liner, rigid femoral head and rigid femoral stem. The femoral stem was placed at 0°, 10° and 20° of anteversion. The acetabular shell and liner were placed in 20°, 40° and 60° of abduction and 0°, 20° and 40° of anteversion. The femoral head to acetabular liner radial clearances modeled were 0.06 mm, 0.13 mm and 0.5 mm. Three loading cases corresponding to peak in vivo loads during walking, chair sit and deep-knee bend were analyzed (Fig. 2). This allowed a range of component positions and maximum joint loads to be studied. Results. Under all tested conditions there was no difference between the two implants (Fig. 3). The contact area for both prosthesis depended on the radial clearance between the head and liner. The conventional head contact area (standard deviation) in mm. 2. for 0.5 mm, 0.13 mm and 0.06 mm of radial clearance was 230.5 (70.2), 419.8 (48.7) and 575.4 (60.1) respectively. Similarly, for the ACH these were 230.5 (70.4), 420.1 (48.7) and 575.9 (59.4). The average data for a head and radial clearance combination included all component placements and load conditions completed. A student T-Test (p = 0.05) confirmed that the ACH had the same contact area as the conventional head for all radial clearances. Conclusion. This study showed that, as intended, an anatomically contoured large diameter femoral head designed to provide soft-tissue relief maintained the load bearing articular contact area of a conventional implant. The novel ACH prosthesis could mitigate the risk of soft-tissue impingement with contemporary large head implants while retaining their benefits of additional stability and range-of-motion