Introduction. Bone mineral density (BMD) is correlated with component migration and aseptic loosening after total knee arthroplasty (TKA). Older implant designs have demonstrated BMD loss up to 23% in the first 6 months after TKA, and continued to BMD decline at an average of 5% per year for as long as 2 years after TKA. The impact of component design and fixation method on BMD loss after TKA in modern implant designs has not been fully elucidated. The purpose of this study is to determine the effect of tibial tray thickness and fixation method (cemented versus cementless) on BMD loss patterns of the proximal tibia in two different modern TKA implant systems. Methods. A prospective, nonrandomized, single center study of patients undergoing primary TKA by one of two surgeons was performed with four study cohorts: cemented DePuy Attune, cementless DePuy Attune, cemented Stryker Triathlon, cementless Stryker Triathlon. Target sample size was 80, with 20 per cohort based on adhoc power analysis. Exclusion criteria included: age over 75, BMI >40, inflammatory arthritis, previous knee surgery involving the femur, tibia or tibial bone, and diagnosis of osteopenia/osteoporosis. Implant fixation type was based on surgeon intraoperative assessment of patient bone quality. Demographic data was collected preoperatively. Dual Energy X-ray Absorptiometry (DEXA) Bone Density Monitoring was performed at 6 weeks and one year postoperatively. Bone mineral density was calculated from the DEXA scans for 4 zones for the tibia relative to the keel or central peg: anterior, posterior, medial and lateral. Results were reported as BMD at 1 year postoperatively as a percentage of BMD at 6 weeks postoperatively. Results. 81 knees with complete DEXA studies at 6 weeks and 1 year postoperatively were available for analysis. The mean (SD) age at the time of surgery was 65.4 years (6.1), with 39 men and 42 women and a mean (SD) BMI of 31.2 kg/m. 2. (4.7). The patients who received cementless implants were significantly younger with a mean (SD) age of 62.1 (6.0) than those who received cemented implants with a mean age of 69.1 (3.7) (p < 0.05). There was no difference in age between implant type (p > 0.05). There was no difference in BMI or gender distribution between implant types or fixation type (p > 0.05). There was no significant difference in mean BMD loss between 6 weeks and 1 year postoperatively between the cemented and cementless Triathlon in any zone, between the cemented Triathlon and Attune in any zone, the cementless Triathlon and Attune in any zone, and the cemented and cementless attune in the lateral, anterior and posterior proximal tibia (p > 0.05). There was significantly more BMD loss seen in the medial tibia in the cemented (BMD at 1 year 88% of BMD at 6 weeks) than cementless (BMD at 1 year 103% of BMD at 6 weeks) Attune (p = 0.043). Conclusion. BMD loss at 1 year postoperatively versus 6 weeks postoperatively after TKA with two modern implant designs is not significantly affected by tibial tray thickness. BMD loss was unaffected by fixation type for the Stryker Triathlon, but was significant less for the cementless DePuy Attune than the cemented version

Proper restoration of posterior condylar offset during TKA has been shown to be important to maximize range of motion and minimize flexion instability. However, there is little information as to the importance of restoration of mid-sagittal femoral geometry. There is controversy as to whether a TKA prosthesis should have a single radius or multiple radii of curvature. The purpose of this study is to evaluate the effectiveness of a multi-radius femoral component at restoring mid sagittal femoral offset. A consecutive series of 100 TKAs with digital preoperative and postoperative radiographs and standardized radiographic markers were analyzed. There were 71 female and 29 male knees with mean age of 59 years. All TKAs were performed by a single surgeon using a multi-radius femoral component design. The distal femoral resection was set to resect 10 mm from the distal femoral condyle and a posterior referencing system was used to size the femoral component. Using radiographic perfect lateral projections of the knees, a line was drawn along the posterior femoral shaft and another parallel line down the anterior femoral shaft. A 3rd line was then drawn parallel to the posterior shaft at the furthest point posterior on the condyle. A 4th line was drawn parallel to the anterior shaft at the furthest point anterior on the femur. 90 degree angles were constructed to create a grid in the anterior and posterior directions, similar to a previously reported technique. Finally, 45 degree angle lines were created in the grid to assess mid flexion dimensions [Fig-1 and 2]. The percent change in posterior condylar offset (PCO), anterior femoral offset (AFO), mid femoral anterior offset (MAFO) and mid femoral posterior offset (MFPO) were calculated. The mean reproduction of the mid-anterior femoral offset and mid-posterior femoral offset were 101.1% [range 56.5%–167.5%] and 96.8% [range 54.9%–149.0%] of preoperative measurements respectively. The average restoration of posterior offset and anterior offset were 92.8% [range 49.0%–129.8%] and 115.3% of preoperative measurements [range 35.7%–400.0%] respectively. When the posterior condylar offset was restored to within 10% of the native anatomy, the MPFO restoration more closely resembled normal anatomy (103.0% vs. 93.9%, p = 0.005). When the postoperative posterior condylar offset was decreased greater than 20%, both the MAFO (90.1% vs. 104.5%, p = 0.004) and MPFO (78.5% vs. 102.9%, p < 0.001) decreased compared to the native knee. There was no relationship between restoration of the PCO and the MAFO correction (104.6% vs. 99.4%, p = 0.213). Finally, there was no correlation between restoration of anterior femoral offset within 10% of normal and the restoration of mid sagittal femoral offset; 98.0% vs 102.0% for MAFO (p = 0.320) and 98.7% vs 96.3% for MPFO (p = 0.569). A modern multi-radius condylar knee design is capable of reproducing the mid-sagittal geometry of the preoperative knee. However, the restoration of mid sagittal offset is largely dependent on the restoration of the posterior condylar offset. Intraoperative adjustments in anterior and posterior femoral resections can have significant impact in the ability of the implant to reproduce mid-sagittal femoral anatomy

Introduction: ROM after TKA can be influenced by multi-factors such as preoperative range of motion, body habitus, implant design, intraoperative surgical technique, and postoperative rehabilitation. Recently many implant manufacturers have made modifications to traditional total knee designs to improved maximal knee flexion and range of motion. Some posterior cruciate ligament (PCL) stabilized total knee prostheses that incorporate design features intended to improve knee kinematics in high flexion were introduced and the use of these prostheses has attracted attention. Recently in the cruciate retaining (CR) prosthesis, high-flexion knee (CR-Flex) and gender-specified prosthesis were designed to allow a greater and safer flexion after TKA. The aim of this study was to evaluate the effect of cruciate retaining typed different femoral component design on knee range of motion using a computerized navigation system. Materials & method: 30 patients who underwent primary TKA because of primary osteoarthritis were included. EM navigation system was used in all cases. After tibia and femoral cutting using standard CR cutting block, standard fixed bearing CR knee (NexGen CR, Zimmer, Warsaw, IN) trial was inserted. If surgeon is satisfactory with alignment, stability and ligament balancing, the maximal knee extension and flexion was recorded using gravity by navigation system. Then, high-flexion fixed bearing CR knees(NexGen CR-Flex and Gender solution NexGen CR-Flex knee, Zimmer, Warsaw, IN) trial was inserted after additional posterior cutting. The maximal knee extension and flexion was evaluated exactly same way. Results: Preoperative mean varus deformity was 10.52°. The mean flexion contracture was 7.52±6.81° and further flexion 129.9±7.94°. The average intraoperative maximal flexion of NexGen CR was 133.5±5.35° (125–146°) and that of hyper-flexion design were 135.5±5.77°(125–147°) in Nexgen CR-Flex and 136.1±5.76°(126–146°) in Gender knee. All knees showed greater than 125° of flexion regardless of the implant design. All knees can achieve physiologic leg alignment and nearly full extension of the knee after operation. Conclusion: Hyper flexion designs showed subtle increase in mean maximal flexion and overall range of motion of the knee compared with the standard design, when it measured using navigation system intraoperatively. But clinically, it is not certain that these differences can lead to significant improvement of range of motion

Purpose

To review prospectively collected data on patients undergoing primary total hip arthroplasty utilizing two different cementless acetabular components.

To review prospectively collected data on patients undergoing primary total hip arthroplasty utilizing two different cementless acetabular components.

All patients undergoing primary total hip replacement surgery at our institution are entered prospectively into a database which includes history and physical examination, radiology, WOMAC and SF-36 scores. The patients are re-examined, re-x-rayed and re-scored at 3 months, 6 months and 1 year after surgery and yearly thereafter.

Using this database we are able to identify patients who have undergone total hip replacement using one of two geometric variants of the acetabular component. The first design is hemispherical and the second design has a peripheral rim expansion designed to increase initial press-fit stability.

Five hundred and twenty-seven consecutive primary total hip replacements were identified using either of the geometric variants of the acetabular component. Results at a mean of 7 years revealed a 95.6% survivorship with no significant difference between the two component designs with revision for aseptic loosening as the end point. Functional scores between the two groups of patients also demonstrated no statistically significant difference.

Radiologic assessment, however, showed a difference between the two designs. The hemispherical design which matches the reamer line-to-line had 80% complete osseointegration on final radiologic review while the second design with a peripheral rim expansion had only 57% complete osseointegration. This was statistically significant. The peripherally expanded components also had a greater number of screws inserted at the time of surgery, felt by us to be a reflection of initial surgeon dissatisfaction with component stability at the time of insertion of the component.

The difference in screw numbers was also statistically significant. This study demonstrates that a hemispherical design with line-to-line contact between the acetabular component surface and the acetabular bone is statistically superior in terms of bone ingrowth and probably statistically superior in terms of initial press-fit stability when compared to a peripherally expanded component.

Peripherally expanded components appear to offer no advantage over hemispherical components in terms of clinical outcome and are statistically inferior to hemispherical components in radiologic parameters at 7 years follow-up.

Purpose

To review prospectively collected data on patients undergoing primary total hip arthroplasty utilizing two different cementless acetabular components.

This is a report on the first 100 THR patients treated with an off the shelf version of a novel “Lateral Flare” femoral component. A prior published report has documented the up to 19 year follow up of custom fabricated stems of an identical design concept as being successful in patients < 55 years of age.

HHS, radiographic measure of bone morphology, implant stability and densitometric measure of bone response after THR with an off the shelf version, “Revelation Lateral Flare”, femoral component, confirm excellent bone preservation and implant stability with this design concept. DEXA analysis of a 20 consecutive patient subset of these 100 patients, documented preservation of more than 95% of proximal femoral bone stock in Gruen zone 1 and 102% of total bone stock in Gruen zones 1–7. Implant stability measurement documented < 0.5mm of subsidence in spite of patients being permitted immediate post-operative full weight bearing activity.

These findings support reasonable optimism for expectation of successful long term results being achievable with the use of an off the shelf version of the “Lateral Flare” design concept, in young, high demand patients suffering with early onset osteoarthrosis of the hip.

Background

There is paucity of data concerning the morphological dimensions of the distal part of the femur and the proximal part of the tibia in Indian population. The objective of this study was to analyse the exact anatomic data collected from patients undergoing total knee arthroplasty.

Objectives. Unicompartmental knee replacement (UKR) is a conservative option for degenerative disease, with mobile (Oxford UKR) and fixed bearing (Physica ZUK) the most commonly used devices. The primary reasons for revising UKRs include disease progression (36.9%), loosening (31.7%), and pain (7.5%). Loosening typically occurs due to osteolysis caused by wear particles from the polyethylene (PE) inserts. There is limited published literature which has quantified volumetric material loss from the PE inserts of cemented fixed-bearing UKRs. This study aimed to quantify bearing wear and backside deformation of these PE components. Design and Methods. At our national retrieval centre, we measured changes volumetric bearing wear and backside deformation of 31 explanted fixed-bearing Physica ZUK UKR PE inserts using a peer-reviewed methodology based on coordinate measuring machine analysis. These explants had been revised for any indication [Females (19) and Males (12)]. The location of the wear scars was identified and mapped. We compared the volumetric wear from the bearing surface with contemporary total knee replacement (TKR) inserts. Results. The median (IQR) total volumetric wear of the UKR PEs [96(50-152) mm. 3. ] was significantly higher (p<0.001) than contemporary TKR PEs [40 (24-83) mm. 3. ]. The median (IQR) total volumetric wear of the PEs in males [148(122-200) mm. 3. ] was significantly higher(p=0.016) than in females [56(61-119) mm. 3. ]. The wear scars were situated in the anterior third in 61% of cases, with 26% located posteriorly. Examination of the PE backside surfaces exhibited damage in the area directly inferior to the bearing surface wear scar in the majority of cases. Conclusion. In conclusion, this study highlights significant PE wear of Physica ZUK UKR inserts, with higher wear rates compared to contemporary TKR inserts, particularly in males

The fixation of articular fractures, with many small osteochondral fragments, is a challenging unmet need where a bone adhesive would be a useful adjunct to standard treatments. Whilst there are no such adhesives in current clinical use, preclinical animal models have demonstrated good healing of bone in unloaded models using an adhesive based on phosphoserine modified calcium phosphate cement (PM-CPC). An ex-vivo human bone core model has shown that this adhesive bonds freshly harvested human bone. To confirm this adhesive is capable of supporting loaded osteochondral fragments a porcine model has been developed initially ex-vivo on the path to an in-vivo study. In this model bone cores, harvested from the medial knee condyle, are glued in place with the adhesive. In-vivo adjacent pairs of bone cores would be replaced with adhesive and a control with conventional pin fixation respectively. As osteochondral bone fragments have both bone and cartilage components, this suggested a dual adhesive strategy in which components designed for each tissue type are used. This concept has been explored in an ex-vivo porcine pilot study presented herewith. At the subchondral bone level, the PM-CPC was used. At the cartilage level, a second adhesive, a methacrylated phosphoserine containing hyaluronic acid (MePHa) hydrogel designed specifically for soft tissues was applied. This is a challenging model as both adhesives have to be used simultaneously in a wet field. The pilot showed that once the subchondral component is glued in place, the PM-CPC adhesive intruding into the cartilage gap can be removed before applying the cartilage adhesive. This enabled the MePHa adhesive to be injected between the cut cartilage edges and subsequently light-cured. This two-stage gluing method is demanding and an in-vivo pilot is necessary to perfect and prove the operative technique. Acknowledgements: The human bone core project was partially financed by Innovation Fund of Västra Götaland Region, Sweden. The MePHa hydrogel work was supported by a Swiss National Fund grant # CR23I3_159301

Introduction. Retrieval investigations have shown that cracking or rim failure of polyethylene hip liners may occur at the superior aspect of the liner, in the area that engages the locking ring of the shell. 1. Failure could occur due to acetabular liner/stem impingement and/or improper cup position. Other contributing factors may include high body mass index, patient activity and design characteristics such as polyethylene material properties, thin liner rim geometry and cup rim design. Currently no standard multi-axis simulator methodology exists for high angle rim fatigue testing, although tests have been developed using static uniaxial load frames. 2. The purpose of this study was to develop a technique to create a clinically relevant rim crack/fracture event on a 4-axis hip simulator, and to understand the contribution of component design and loading and motion parameters. Method. A method for creating rim fracture in vitro was developed to evaluate implant design features and polyethylene liner materials. Liners were secured into acetabular shells, fixtured in resin mounted at a 55° (in vitro; 65° in vivo) inclination to ensure high load/stress was at the area of interest. Ranges of kinematic and maximum applied load profiles were investigated (parameters summarized in Table 1). Testing was conducted on an AMTI 12-station hip simulator for 0.25–1.0 million cycles or until fracture (lubrication maintained with lithium grease). At completion, liners were cleaned and examined for crack propagation/fracture. Inspection of the impingement site on the opposite rim was also analyzed. Additional assessments included liner disassociation/rock out, deformation of characteristics such as anti-rotation devices and microscopic inspection of high-stress regions. Results/Discussion. This study summarizes testing on hip wear simulators to create rim cracking/fracture in vitro. Results indicate that cup/stem angles must be controlled to ensure contact areas are reproducible, and therefore on a multi-station machine (i.e. AMTI), only one test station can/should be run at a time to ensure repeatability. Component design characteristics, such as head size and liner material had a marked effect on the results. It is noted that the kinematics, load and cycle count must be adjusted per the component design to create rim fracture in the high-risk region. Finite element analysis modeling may help identify the high-stress region(s) prior to simulator testing. Deformation of the rim opposite the fracture region (rim/taper impingement) was observed due to the high angle of inclination combined with the abduction/adduction angles. Conclusion. Rim fractures similar in location and morphology to those seen in retrieval studies can be created using a multi-axis hip simulator in vitro. It is noted, however, that the factors presented in this study must be considered and controlled to assure a repeatable method, as the differences in component design investigated and simulator inputs were seen significantly affect the outcome. This study was limited and did not attempt to reproduce rim damage seen in all implant retrievals (e.g. lateralized liners, high offset implants, etc.). These design inputs are being investigated and will be reported upon in the future. For any figures or tables, please contact the authors directly

The 10 year survivorship of THR is generally over 95%. However, the incidence of revision is usually higher in year one. The most common reason being dislocation which at least in part is driven by inadequate range of motion (ROM) leading to impingement, subluxation and ultimately dislocation which is more frequently posterior. ROM is affected by patient activity, bone and component geometry, and component placement. To reduce the incidence of dislocation, supported by registry data, there has been an increase in the use of so-called ‘lipped’ liners. Whilst this increases joint stability, the theoretical ROM is reduced. The aim of this study was to investigate the effect of lip placement on impingement. A rigid body geometric model was incorporated into a CT scan hemi-pelvis and femur, with a clinically available THR virtually implanted. Kinematic activity data associated with dislocation was applied, comprising of five posterior and two anterior dislocation risk activities, resulting from anterior and posterior impingement respectively. Cup inclination and anteversion was varied (30°-70°, 0°-50° respectively) to simulate extremes of clinical outcomes. The apex position of a ‘lipped’ liner was rotated from the superior position, anteriorly and posteriorly in steps of 45°. Incidence and location of implant and bone impingement was recorded in 5346 cases generated. A liner with the lip placed superior increased the occurrence of implant-implant impingement compared with a neutral liner. Rotation of the lip from superior reduced this incidence. This effect was more marked with posterior rotation which after 90° reduced anterior impingement to levels similar to a neutral liner. Complete inversion of the lipped liner reduced impingement, but this and anterior rotation both negate its function – additional stability. This study comprises one bone geometry and component design and one set of activity profiles. Nevertheless, it indicates that appropriate lip placement can minimise the likelihood of impingement for a range of daily activities whilst still providing additional joint stability

Introduction. Cementless TKA offers the potential for strong fixation through biologic fixation technology as compared to cemented TKA where fixation is achieved through mechanical integration of the cement. Few mid-term results are available for newer cementless TKA designs that have used additive manufacturing (3-D printing) for component design. The purpose of this study is to present minimum 5-year clinical outcomes and implant survivorship of a specific cementless TKA using a novel 3-D printed tibial baseplate. Methods. This is a single institution registry review of the prospectively obtained data on 296 cementless TKA using a novel 3-D printed tibial baseplate with minimum 5-year follow-up. Outcomes were determined by comparing pre- and post-operative Knee Injury and Osteoarthritis Outcome Score for Joint Replacement (KOOS JR) scores and pre- and post-operative 12 item Veterans RAND/Short Form Health Survey (VR/SF-12). Aseptic loosening as well as revision for any reason were the endpoints used to determine survivorship at 5 years. Results. At minimum 5-year follow-up, the KOOS JR score improved from 34.88 pre-operatively to 84.29 post-operatively (p-values = 0.0001), the VR/SF-12 scores improved from PH − 31.98 pre-operatively to 42.80 post-operatively (p-values = 0.0001) and the MH − 37.24 pre-operatively to 55.16 post-operatively (p-value = 0.0001). Eleven revisions were performed for an overall revision rate of 2.94% - including 5 PJI (1.34%), 3 loosening (0.80%), 1 instability (0.27%), 2 pain (0.53%). The overall 5-year survivorship was 97.1% and survivorship for aseptic loosening as the endpoint was 98.40%. The survivorship of the 3-D printed porous tibial component was 99.2%. Conclusion. This 3-D printed tibial baseplate and cementless total knee system shows excellent survivorship at 5-year follow-up. The design of this implant and the ability to obtain cementless fixation offers promise for excellent long-term durability

Introduction. The purpose of this study was to evaluate the long term changes in bone mineral density (BMD) following implantation of a low-modulus composite femoral component designed to closely match the stiffness of the proximal femur and minimize stress shielding. Specifically, we asked: 1) How does BMD in the proximal femur change with time and with Gruen zone location; 2) Does BMD in the proximal femur stabilize after two years of implantation?. Methods. We retrospectively reviewed a subgroup of sixteen patients who had preoperative and postoperative DEXA scans in an FDA multi-center prospective trial of this composite stem. Five of these sixteen patients returned for long-term DEXA scans at a mean 22.0 years post-op (range 21.2–22.6 years). BMD in the 7 Gruen zones at final follow-up was compared to immediate post-operative and 2-year follow-up values. Percentage change was calculated and change in BMD was plotted against time from immediate post-operative measurements to each subsequent follow-up. Results. At the time of last follow-up, all stems were well fixed with signs of extensive osteointegration. There were no mechanical implant failures. In Gruen zone 1, patients underwent an overall decrease or little change in BMD, though one patient experienced a notable increase from initial post-op to the latest follow-up. The overall mean (+ SD) annual percent change in BMD in Gruen zone 1 was −0.31% ± 1.09%. When considering the change from the two-year DEXA scan to latest follow-up, two patients demonstrated a decrease in BMD and three patients demonstrated an increase in BMD in Gruen zone 1. All patients demonstrated progressive increase in BMD in Gruen zones 2, 3, 4, 5, and 6 from the initial post-op scan until last follow-up with mean annual percent changes ranging from 0.59% ± 0.50% in Gruen zone 6 to 2.78% ± 2.49% in Gruen zone 3. In our cohort, BMD progressively decreased with time in Gruen zone 7 for all patients with a mean decrease of 1.78% + 0.38% annually from the time of the initial post-op DEXA scan until last follow-up. This was consistent with prior reports with shorter term follow-up. Conclusions. Despite the extensively porous coated design of this stem and concerns about distal fixation and related stress shielding, we observed consistent DEXA scan evidence of increases in BMD in Gruen zones 2–6 and limitation of decreases in BMD exclusively to zone 7 and to a lesser extent zone 1. This is unlike reported results with several other extensively porous coated and proximally porous coated implants designed to obtain proximal fixation. These increases in BMD occurred despite the potential age-related decreases in BMD in the proximal femur that one would anticipate over the mean 22-year follow-up in this study. Clearly, “normal” physiologic loading of bone after THA is determined by a complex interaction between location of ingrowth, location and extent of endosteal contact of the implant in the proximal femur, stiffness of the stem and other implant design and patient related factors. The long-term observations of this study suggest that effective loading of the proximal femur occurs with this low-modulus stem and that this concept may have a role in the future of THA

Aims. The incidence of thigh pain with the short stem varies widely across different studies. We aimed to evaluate the incidence and characteristics of post-operative thigh pain after using a particular bladed short stem and its potential risk factors. Patients and Methods. We respectively reviewed 199 consecutive patients who underwent unilateral total hip replacement using the Tri-lock stem from 2013–2016, of which 168 patients were successfully followed up with minimum two year clinical follow-up. All information about thigh pain and pre- and postoperative HHS score were gathered and all preoperative and immediate postoperative radiographs were available for review. Any complications were recorded. Results. Of the 168 patients, 34 (20.2%) patients reported thigh pain at a mean 3.1 years after surgery. Of these, 2 (5.9%) reported severe pain (NRS 5 or more). The pain was persistent (from surgery to final follow-up) in 13 patients (38.2%) and subsided within 2 years in 10 cases (29.4%). The most common site of pain was the lateral thigh (70.6%). The HHS improved from a mean 54.2 points preoperatively to 79.8 postoperatively. In 123 cases with radiographs at more than 2 years follow-up, all femoral stems were well-fixed and no revision surgery was needed at the latest. BMI and CFI were found to be independent risk factors for thigh pain after using this particular stem component. Conclusions. The incidence of thigh pain in Chinese THA patients with a bladed short stem component design is as high as 20%. Among them, nearly 40% will have some disruption in sleep or daily life. More than one-third of the cases of thigh pain were persistent. A larger BMI and patients with a funnel-type morphology of the femoral canal are independent risk factors for thigh pain in the setting of this particular stem component

Introduction. Patellar resurfacing during Total Knee Arthroplasty (TKA) is controversial. Problems unique to patellar resurfacing may be influenced by available patellar component design. These issues include; over-stuffing (the creation of a composite patellar-prosthesis thickness greater than the native patella) that may contribute to reduced range of motion; and over-resection of the native patellar bone that may contribute to post-operative fracture. Prosthesis design may play a role in contributing to these problems. Component diameter and thickness are quite variable from one manufacturer to another and little information has been previously published about optimal component dimensions. This anatomic study was performed to define the native patellar anatomy of patients undergoing TKA, in order to guide future component design. Methods. This retrospective, IRB approved study reviewed 797 Caucasian knees that underwent primary TKA by a single surgeon. Data recorded for each patient included: gender; patellar thickness before and after resurfacing, and the size of the component that provided the greatest patellar coverage without any overhang. The residual patellar bone thickness after resection was also calculated. Results. Mean (SD) native patellar thickness was 25.24 mm (2.11) in males, versus 22.13 mm (1.89) in females (P = <0.001). 84 of 483 females (17 %) had a native patellar thickness less than or equal to 20 mm. Only 3 male patients had a native patellar thickness less than or equal to 20 mm (1%). 374 females (78%) could only accommodate a round patellar button less than or equal to 32 mm. Conclusions. These findings suggest that patellar component design can be improved for Caucasian female patients. Round components between 26 and 32 mm that measure no more than 7 mm thick would be required to avoid systematic over-stuffing or over-resection of the native patellar in female patients. Most contemporary knee systems do not meet these needs

INTRODUCTION. Dislocation is a major complication post total hip replacement (THR) and a common cause for revision. Jameson et al (2012) studied 35,000 cemented Exeter (Stryker) THRs demonstrating the risk of revision was significantly influenced by the acetabular component design. This led 3 surgeons in a single hospital group to make a mass move from using the hooded Exeter Low Profile (LP) cup to the better performing Contemporary Flanged (CF) component. The purpose of this study was to show whether this change was associated with a fall in dislocation rates. PATIENTS/MATERIALS & METHODS. Locally held National Joint Registry data between 2010 and 2015 was used to ascertain implants used in all primary THRs by 3 experienced high volume surgeons. This was linked to local Hospital Episode Statistics to identify patients who had undergone closed or open reduction of a dislocated hip replacement in theatre. RESULTS. From January 2010 to March 2015 there were 611 primary THRs using the LP cup and 790 primary THRs using the CF, after the surgeons had switched. Between the two groups there was no significant difference in age, ASA grade, BMI, approach, grade of first surgeon or grade of assistant. The dislocation rate of the LP was 2.64%, CF 0.71% (p=0.003). After adjustment for co-variables the odds risk ratio of dislocating with a LP compared to a CF cup was 3.5 (95% CIs 1.3–9.2, p=0.01). The trust wide dislocation rate has dropped from 2.5% in 2010 to 0.8% in 2015. DISCUSSION. Rate of dislocation was significantly influenced by acetabular component design. The absence of a hood in the flanged cup may allow easier positioning; the hood in itself may also act as an impingement site causing dislocation. CONCLUSION. This project demonstrates a significant improvement in local services after implementing a change based on a national clinical audit

Background. Despite growing interest in direct anterior approach total hip arthroplasty, perioperative femoral fracture and early aseptic loosening are increasingly recognized complications. Previous research has documented the role of surgeon experience in association with these femoral complications. The purpose of this study was to explore the relationship between femoral component design and early periprosthetic femoral complications. Methods. This was an extension of previous work with an updated patient cohort of 5090 consecutive direct anterior primary total hip arthroplasties at a single institution with a single-taper, wedge femoral stem with 4 variants involving length and geometry: Group 1) full length, standard profile; Group 2) full length, reduced distal profile; Group 3) short length, standard profile; and Group 4) short length, reduced distal profile. Records were reviewed retrospectively for the incidence of early periprosthetic fracture or aseptic loosening and analyzed with regard to patient demographics and femoral stem type. Results. There were 42 (0.83%) periprosthetic femur complications observed in the early postoperative period. Increased age (p<0.001) and female gender (p=0.023) were significantly associated with incidence of femoral complications in univariate analysis, while age maintained this significant relationship in multivariate analysis (P<0.001). There was a trend toward increased complication rate in patients receiving a short stem with full profile taper (1.27%, p=0.0539). Conclusion. Despite an overall low rate of femoral complications after direct anterior total hip arthroplasty, the risk is increased in elderly patients and females. Furthermore, femoral stem design may portend an elevated risk of these complications

Background. Medical advances and an ageing population mean that more people than ever rely on artificial joints. In the past years, shoulder joint replacement has developed rapidly and the numbers of shoulder prostheses implanted increased dramatically. Wear is one of the main contributors to the failure of shoulder implants. It is therefore important to measure the wear properties of the articulating surfaces within the joint in vitro. Investigation of wear characteristics through a comprehensive range of motion using a sophisticated shoulder simulator would reveal the durability of the material, the performance of component design and the safety analyses of prostheses. The purpose of the work was to develop and validate a multi-station shoulder simulator, which could accurately simulate physiological gleno-humeral forces and displacements during activities of daily living. Materials and Methods. Imperial shoulder simulator was designed with six articulating stations and one loaded soak control station for anatomical shoulder system wear simulation. It gives an adduction-abduction (AA) range of-15° to 55°, flexion-extension (FE) range of −90° to 90° and internal external rotation (IER) range of 15° to −90°. The rotations are applied simultaneously to the humeral implants by using stepper motors with integral position encoders. Axial and shear loadings to each glenoid implant were applied using pneumatic cylinders. Force controlled translations were recorded using load cells and LVDTs, and a data acquisition system. Pneumatic cylinders were also installed to work to counterbalance weights during the motion of adduction-abduction. All bearing pairs are within isolated and sealed test chambers to prevent loss of fluid through evaporation, and cross contamination of third body wear (as recommended in F1714-96). The simulator is controlled by LabVIEW program allowing to reproduce shoulder activities of daily living. Results. A commissioning trial was conducted when shoulder implants were subject to rotational and translational motions and loading to replicate the ‘combing’ activity of daily living. The motion ranges were typically 5° to 15° in AA, 15° to 80° in FE, and −30° to −20° in IER with applied loads from 60 to 440 N, principally along the medio-lateral direction. The waveform was at frequency of 1 Hz. The activity was loaded at 250,000 cycles around 3 full days, when test and control specimens should be cleaned, measured and then re-installed into the simulator. The results from kinematic and kinetic inputs and outputs were obtained from the trial study. Discussion. A multi-station shoulder simulator was successfully developed, which is capable of reproducing typical activities of daily living by applying physiological patterns of motion and load. The performance of the simulator was validated in the commissioning trial, which leads to evaluation of novel implant designs

Introduction. The metal-backed patella was originally designed to address shortcomings found with cemented, all-polyethylene patellae. However, complications relating to an all-polyethylene patella were reported to account for up to half of all knee revisions. At the same time, good fixation with bone ingrowth was observed in both titanium and cobalt chromium porous-coated patellae. The advantages provided by using a metal-backed patella, such as uniform load sharing, decreased polyethylene deformation, and potential for biological fixation, may be unjustly outweighed by the fear of patellar component failure; high rates of failure have not been inherent to all metal-backed patella designs. Over the past decade, we have used a metal-backed patella design with excellent results that may be due largely to the design features of the component. Also, we believe there are certain selection criteria that should be strictly adhered to when implanting metal-backed patellae. Correct selection criteria and improved component design strongly indicate the use of press-fit metal-backed patellae. Methods. This single-center study was designed to conduct clinical and independent radiographic review of primary metal-backed, press-fit patella patients with a minimum five-year follow-up. Potential patients were recruited from a group of existing metal-backed patella patients within the principal investigator's medical practice. All patients recruited for this study were required to have undergone primary knee replacement surgery at least five years prior to clinical and radiographic evaluation. Patients were included if they had a diagnosis of noninflammatory degenerative joint disease. Patients with a BMI >40 were excluded from this study. Radiographic analysis was conducted by an independent reviewer according to the current Knee Society Total Knee Arthroplasty Roentgenographic Evaluation and Scoring System. Any radiographs that the reviewer deemed questionable were shown to a second independent orthopaedic surgeon for review, comment, and validation of observations. Kaplan-Meier survivorship was determined for all metal-backed patellae. For survival analysis, only knees with radiographic data were included (74 knees). KSS, WOMAC, and SF-36 scores were calculated also. Results. Seventy-four patients (88 knees) were enrolled in the study, 31 women (41.2%) and 43 men (58.1%). At the time of surgery, the average age was 59.7 years (range, 40–86 years), and the average BMI was 30.6 (range, 19.1–39.6). The breakdown of patients who completed the study and those who were lost to follow-up is shown in Table 1. One metal-backed patella was revised at 49 months for loosening at the bone/implant interface. Survivorship of the metal-backed patellae at minimum five-year follow-up was estimated to be 93.95% with bounds of 73.61% and 98.74%. No radiolucencies greater than 1 mm were observed in any radiographs (Fig. 1), with the exception of the one revision case. Conclusion. Our experience with this metal-backed patella design has been excellent. Failure does not occur due to dissociation of the plastic. As the porous coating is almost under constant compression, biological fixation is assured in most instances, as confirmed by our minimum five-year radiological results. Improved component design and adherence to the correct patient selection criteria absolutely indicate the use of press-fit metal-backed patellae