Aims. We aimed to examine the long-term mechanical survivorship, describe the modes of all-cause failure, and identify risk factors for mechanical failure of all-polyethylene tibial components in endoprosthetic reconstruction. Methods. This is a retrospective database review of consecutive endoprosthetic reconstructions performed for oncological indications between 1980 and 2019. Patients with all-polyethylene tibial components were isolated and analyzed for revision for mechanical failure. Outcomes included survival of the all-polyethylene tibial component, revision surgery categorized according to the Henderson Failure Mode Classification, and complications and functional outcome, as assessed by the Musculoskeletal Tumor Society (MSTS) score at the final follow-up. Results. A total of 278 patients were identified with 289 all-polyethylene tibial components. Mechanical survival was 98.4%, 91.1%, and 85.2% at five, ten and 15 years, respectively. A total of 15 mechanical failures were identified at the final follow-up. Of the 13 all-polyethylene tibial components used for revision of a previous tibial component, five (38.5%) failed mechanically. Younger patients (< 18 years vs > 18 years; p = 0.005) and those used as revision components (p < 0.001) had significantly increased rates of failure. Multivariate logistic regression modelling showed revision status to be a positive risk factor for failure (odds ratio (OR) 19.498, 95% confidence interval (CI) 4.598 to 82.676) and increasing age was a negative risk factor for failure (OR 0.927, 95% CI 0.872 to 0.987). Age-stratified risk analysis showed that age > 24 years was no longer a statistically significant risk factor for failure. The final mean MSTS score for all patients was 89% (8.5% to 100.0%). Conclusion. The long-term mechanical survivorship of all-polyethylene tibial components when used for tumour endoprostheses was excellent. Tumour surgeons should consider using these components for their durability and the secondary benefits of reduced cost and ease of removal and revision. However, caution should be taken when using all-polyethylene tibial components in the revision setting as a significantly higher rate of mechanical failure was seen in this group of patients. Cite this article: Bone Joint J. 2020;102-B(2):170–176

Background. Total knee arthroplasty (TKA) overall is a very reliable, durable procedure. Biomechanical studies have suggested superior stress distribution in metal-backed tibial trays, however, these results have not been universally observed clinically. Currently, there is a paucity of information examining the survival and outcomes of all-polyethylene tibial components. Methods. We reviewed 31,939 patients undergoing a primary TKA over a 43-year period (1970–2013). There were 28,224 (88%) metal-backed and 3,715 (12%) all-polyethylene tibial components. The metal-backed and all-polyethylene groups had comparable demographics with respect to sex distribution (57% female for both), mean age (67 vs. 71 years), and mean BMI (31.6 vs. 31.1). Mean follow-up was 7 years (maximum 40 years). Results. The purpose of this investigation was to analyze the outcomes of all-polyethylene compared to metal-backed components in TKA and to determine: (1) is there a difference in overall survival? All-polyethylene tibial components had improved survivorship (P<0.0001) and metal-backed tibias were at increased risk of revision (HR 3.41, P<0.0001); (2) Does body mass index (BMI) or age have an effect on survival of all-polyethylene compared to metal-backed tibial components? All-polyethylene tibias had improved survival (P<0.01) in all age groups except in patients 85 years or greater, where there was no difference (P=0.16). All-polyethylene tibial components had improved survival (P<0.005) for all BMIs except in the morbidly obese (BMI ≥40) where there was no difference (P=0.20); (3) Is there an increased risk of post-operative infection? Metal-backed tibial components were found to have an increased risk of infection (HR 1.60, P=0.003); (4) Is there a difference in the rate of reoperation and post-operative complications? Metal-backed tibial components were found to have an increased risk of reoperation (HR 1.84, P<0.0001). Conclusions. The use of all-polyethylene tibias should be considered for the majority of patients, regardless of age and BMI

The role of modular tibial implants in total knee replacement is not fully defined. We performed a prospective randomised controlled clinical trial using radiostereophotogrammetric analysis to compare the performance of an all-polyethylene tibia with a metal-backed cruciate-retaining condylar design, PFC-∑ total knee replacement for up to 24 months. There were 51 patients who were randomised into two treatment groups. There were 10 subsequent withdrawals, leaving 21 all-polyethylene and 20 metal-backed tibial implants. No patient was lost to follow-up. There were no significant demographic differences between the groups. At two years one metal-backed implant showed migration > 1 mm, but no polyethylene implant reached this level. There was a significant increase in the SF-12 and Oxford knee scores after operation in both groups. In an uncomplicated primary total knee replacement the all-polyethylene PFC-∑ tibial prosthesis showed no statistical difference in migration from that of the metal-backed counterpart. There was no difference in the clinical results as assessed by the SF-12, the Oxford knee score, alignment or range of movement at 24 months, although these assessment measures were not statistically powered in this study

Implant selection in TKA remains highly variable. Surgeons consider pre-operative deformity, patient factors such as BMI and bone quality, surgical experience, retention or substitution for the PCL, type of articulation and polyethylene, cost, and fixation with or without cement. We have most frequently implanted the same implant for the majority of patients. This is based on the fact that multiple large series of TKAs have demonstrated that the most durable TKAs have been non-modular metal-backed tibial components, retention of the PCL, with a cemented all-polyethylene patellar component. Polymer wear must be addressed for long-term durability. One method for reducing polyethylene wear is eliminating modularity between a metal-backed tray and the articular bearing surface. This can be done with a metal-backed implant as with the IB-1, AGC, Vanguard Mono-lock, or with elimination of the metal backing via a one piece all-polyethylene tibial component. The all-polyethylene implants appear design and patient sensitive. We observed higher clinical failure rates in a flat-on-flat design. Other authors have observed improved survivorship with coronal dishing of the articular surfaces which centralises osseous stresses. All-polyethylene implants have promise in the future but require proven design and fixation design features

We report the outcome of the flangeless, cemented all-polyethylene Exeter acetabular component at a mean of 14.6 years (10 to 17) after operation. Of the 263 hips in 243 patients, 122 prostheses are still in situ; 112 patients (119 hips) have died, 18 hips have been revised, and three patients (four hips) were lost to follow-up. Radiographs at the final review were available for 110 of the 122 surviving hips. There were acetabular radiolucent lines in 54 hips (49%). Two acetabular components had migrated but neither patient required revision. The Kaplan-Meier survivorship at 15 years with 61 hips at risk with revision for any cause as the endpoint was 89.9% (95% confidence interval (CI) 84.6 to 95.2) and for aseptic loosening of the acetabular component or lysis 91.7% (95% CI 86.6 to 96.8). In 210 hips with a diagnosis of primary osteoarthritis, survivorship with revision for any cause as the endpoint was 93.2% (95% CI 88.1 to 98.3), and for aseptic loosening of the acetabular component 95.0% (95% CI 90.3 to 99.7). The cemented all-polyethylene Exeter acetabular component has an excellent long-term survivorship

Aims. The tibial component of total knee arthroplasty can either be an all-polyethylene (AP) implant or a metal-backed (MB) implant. This study aims to compare the five-year functional outcomes of AP tibial components to MB components in patients aged over 70 years. Secondary aims are to compare quality of life, implant survivorship, and cost-effectiveness. Methods. A group of 130 patients who had received an AP tibial component were matched for demographic factors of age, BMI, American Society of Anesthesiologists (ASA) grade, sex, and preoperative Knee Society Score (KSS) to create a comparison group of 130 patients who received a MB tibial component. Functional outcome was assessed prospectively by KSS, quality of life by 12-Item Short-Form Health Survey questionnaire (SF-12), and range of motion (ROM), and implant survivorships were compared. The SF six-dimension (6D) was used to calculate the incremental cost effectiveness ratio (ICER) for AP compared to MB tibial components using quality-adjusted life year methodology. Results. The AP group had a mean KSS-Knee of 83.4 (standard deviation (SD) 19.2) and the MB group a mean of 84.9 (SD 18.2; p = 0.631), while mean KSS-Function was 75.4 (SD 15.3) and 73.2 (SD 16.2 p = 0.472), respectively. The mental (44.3 vs 45.1; p = 0.464) and physical (44.8 vs 44.9; p = 0.893) dimensions of the SF-12 and ROM (97.9° vs 99.7°; p = 0.444) were not different between the groups. Implant survivorship at five years were 99.2% and 97.7% (p = 0.321). The AP group had a greater SF-6D gain of 0.145 compared to the MB group, with an associated cost saving of £406, which resulted in a negative ICER of -£406/0.145 = -£2,800. Therefore, the AP tibial component was dominant, being a more effective and less expensive intervention. Conclusion. There were no differences in functional outcomes or survivorship at five years between AP and MB tibial components in patients aged 70 years and older, however the AP component was shown to be more cost-effective. In the UK, only 1.4% of all total knee arthroplasties use an AP component; even a modest increase in usage nationally could lead to significant financial savings. Cite this article: Bone Jt Open 2022;3(12):969–976

Objectives. Up to 40% of unicompartmental knee arthroplasty (UKA) revisions are performed for unexplained pain which may be caused by elevated proximal tibial bone strain. This study investigates the effect of tibial component metal backing and polyethylene thickness on bone strain in a cemented fixed-bearing medial UKA using a finite element model (FEM) validated experimentally by digital image correlation (DIC) and acoustic emission (AE). Materials and Methods. A total of ten composite tibias implanted with all-polyethylene (AP) and metal-backed (MB) tibial components were loaded to 2500 N. Cortical strain was measured using DIC and cancellous microdamage using AE. FEMs were created and validated and polyethylene thickness varied from 6 mm to 10 mm. The volume of cancellous bone exposed to < -3000 µε (pathological loading) and < -7000 µε (yield point) minimum principal (compressive) microstrain and > 3000 µε and > 7000 µε maximum principal (tensile) microstrain was computed. Results. Experimental AE data and the FEM volume of cancellous bone with compressive strain < -3000 µε correlated strongly: R = 0.947, R. 2. = 0.847, percentage error 12.5% (p < 0.001). DIC and FEM data correlated: R = 0.838, R. 2. = 0.702, percentage error 4.5% (p < 0.001). FEM strain patterns included MB lateral edge concentrations; AP concentrations at keel, peg and at the region of load application. Cancellous strains were higher in AP implants at all loads: 2.2- (10 mm) to 3.2-times (6 mm) the volume of cancellous bone compressively strained < -7000 µε. Conclusion. AP tibial components display greater volumes of pathologically overstrained cancellous bone than MB implants of the same geometry. Increasing AP thickness does not overcome these pathological forces and comes at the cost of greater bone resection. Cite this article: C. E. H. Scott, M. J. Eaton, R. W. Nutton, F. A. Wade, S. L. Evans, P. Pankaj. Metal-backed versus all-polyethylene unicompartmental knee arthroplasty: Proximal tibial strain in an experimentally validated finite element model. Bone Joint Res 2017;6:22–30. DOI:10.1302/2046-3758.61.BJR-2016-0142.R1

We report the results of a prospective randomised controlled clinical trial assessing the radiosterophotogrametric analysis (RSA), clinical and radiological performance of a metal backed and an all-polyethylene tibial cruciate retaining, condylar design, PFC-TKA up to twenty four months. 65 patients were recruited, of which 41 patients were randomised. There were 20 metal backed and 21 all-polyethylene. None were lost to follow-up. There were no significant inter-group demographic differences. We found a significant increase in SF-12 and Oxford knee scores after surgery in both groups. No significant difference was found between the groups in the RSA, SF-12, Oxford Knee score, radiological alignment and range of movement at 6, 12 or 24 months. At 2 years one metal backed implant showed translational migration > 1mm. No all polyethylene implant migrated > 1mm. Further analysis identified possible progressive subsidence of the metal backed implants compared to all-polyethylene implants, although the magnitude of this difference was very small. We conclude that in the uncomplicated primary total knee arthroplasty, all polyethylene PFC-_ tibial prostheses had equivalent performance to the metal backed counterpart, using RSA as the primary assessment instrument at 24 months. We found no differences between the two designs as assessed by the secondary instruments: SF-12, Oxford knee score, alignment and range of movement at 24 months. Should half of all primary total knee replacements performed in the UK receive an all-polyethylene tibial implant, the estimated annual cost saving would be 21 million pounds per annum

Objectives. All Polyethylene Tibial components in Total Knee Arthroplasty have been in use for some years, studies showing equivalent results to Total Knee Arthroplasty (TKA) with metal-backed Tibial components at 10 years have shown no significant difference between the two on radiostereometric analysis and revision rates[1]. Post operative patient outcome data using standard metal-backed Tibial components is widely reported in the literature. This study is looking at patient outcomes following All-polyethylene tibial component TKA. We hypothesize that using standard patient outcome measures, an improvement comparable with that expected for metal-backed tibial component TKA will be shown with All-polyethylene tibial component TKA. Methods. Between August 2006 and August 2008, 229 all-polyethylene tibial component TKA were implanted at the elective orthopedic unit. The choice of implant was entirely dependent on surgeon's preference. Of the 229 patient's, 225 details were available for review, 27 did not wish to take part in the study and 1 patient died a year following surgery of an unrelated illness. The remaining 197 patients agreed to take part in the study. The patient's were contacted either in person or over the telephone and asked to completed questionnaires for standard knee scoring. These included: the Oxford Knee Score (OKS), the WOMAC Score and the SF-12 Score, both pre-operatively and post operatively. Results. All three Scoring systems used showed an overall improvement post-operatively, as would be reasonably be expected. The results for the OKS, WOMAC and SF-12 all showed an improvement comparable with that expected for metal-backed tibial component TKA. Conclusions. Total Knee Arthroplasty using an all-polyethylene tibial component has been shown with these early results to be a reasonable alternative to metal-backed options offering some advantages. [1,2]

Introduction. The precise indications for tibial component metal backing and modularity remain controversial in routine primary total knee arthroplasty. This is particularly true in elderly patients where the perceived benefits of metal backing such as load redistribution and the reduction of polyethylene strain may be clinically less relevant. The cost implications for choosing a metal-backed design over an all-polyethylene design may exceed USD500 per primary knee arthroplasty case. Methods. A prospective randomised clinical trial was carried out at the QEII Health Sciences Centre, Halifax, Nova Scotia, to compare modular metal-backed versus an all-polyethylene tibial component. Outcome measures included clinical range of motion, radiographs, survivorship, Knee Society Clinical Rating System, WOMAC and SF-12. Results. 116 patients requesting primary knee arthroplasty were recruited and randomised between the Smith & Nephew Genesis I non-modular (57) and modular (59) tibial designs between September 1995 and August 1997. At 10 years clinical follow-up, 4 implant revisions or intention-to-revise decisions were recorded in the metal-tray/modular group of which 2 were for aseptic tibial component loosening. 2 implant revisions in the all-polyethylene non-modular group were recorded, neither of which were for tibial component loosening. At 5, 7 and 10 year review; the KSCRS, WOMAC and SF12 scores were similar in both groups. As most patients randomised were over seventy years of age, this impacted significantly on the numbers available for longer term review and data was analysed by comparing pre- and post-operative scores for individual patients. Conclusion. There was no difference in performance between the all-polyethylene tibial component and the metal-backed tibial component. The case for using the all-polyethylene tibia in elderly patients is justified on both clinical efficacy and cost-containment grounds

Purpose:. Glenoid loosening persists as a common cause of anatomic total shoulder arthroplasty (TSA) failure. Considering radiographic evidence of loosening as an endpoint, TSA has a reported survivorship of only 51.5% at 10 years. Component loosening may be related to cementation and it is postulated that poor cement penetration and heat-induced necrosis may partially be responsible. There is a growing interest among surgeons to minimize or abandon cement fixation and rely on biologic fixation to the polyethylene for long-term fixation. De Wilde et al. reported promising early clinical and radiographic results using a pegged, all-polyethylene ingrowth glenoid design implanted without cement. The goal of this study was to compare glenoid micromotion in an all-polyethylene, centrally fluted pegged glenoid using 3 cement fixation techniques. Materials and Methods:. Glenoid components (Anchor Peg Glenoid, Depuy Orthopaedics, Warsaw, IN, USA) (Figure 1) were implanted in polyurethane foam testing blocks with 3 different fixation methods (n = 5 per group). Group I glenoids were implanted with interference fit fixation with no added cement. Group II was implanted with a hybrid fixation, where only the peripheral pegs were cemented. Group III glenoids were fully cemented for implantation. Glenoid loosening was characterized according to ASTM Standard F-2028. The glenoid component and a 44 mm humeral head were mounted to a materials testing frame (858 Mini Bionix II, MTS Crop., Eden Prairie, MN, USA) with a 750N applied joint compressive force (Figure 1). A humeral head subluxation displacement of ± 0.5 mm was experimentally calculated as a value that simulates glenoid rim loading that may occur at higher load activities. For characterization of glenoid loosening, the humeral head was cycled 50,000 times along the superior-inferior glenoid axis, simulating approximately 5 years of device service. Glenoid distraction, compression, and superior-inferior glenoid migration were recorded with two differential variable reluctance transducers fixed to the glenoid prosthesis. Results:. All glenoid components completed the 50,000 cycles of humeral head translation successfully. With respect to glenoid distraction (Figure 2), interference fit fixation had significantly greater distraction compared to both hybrid and fully cemented fixation (p < 0.001). Hybrid fixation also displayed significantly higher distraction compared to fully cemented fixation (p < 0.001). In terms of glenoid compression (Figure 2), hybrid cementation had significantly greater compression compared to both interference-fit and fully cemented fixation (p < 0.001). Discussion:. This is the first biomechanics study comparing glenoid micromotion of a centrally fluted, pegged component using 3 different fixation techniques. Of all fixation methods, the fully cemented components displayed the least amount of motion in all parameters. Hybrid fixation exhibited lower distraction, higher compression, and comparable translation compared to interference-fit fixation. Results may indicate the differences in early motion and suggest little to no advantage of peripheral peg cementation over no cement with respect to initial fixation. Future studies are warranted to further evaluate interference-fit fixation as a viable option for implantation of a central fluted, all-polyethylene glenoid component

Background and Purpose:. Modularity of the tibial component in total knee arthroplasties (TKA) has many surgical benefits. It also reduces inventory related expenses but increases implant cost. The resulting locking mechanism micromotion that leads to non-articular microwear and has been an accepted consequence of modularity. The purpose of this study is to evaluate the risk of revision (all-cause and aseptic) of a monoblock all-polyethylene tibial component compared to a fixed bearing modular tibial construct with the same articular geometry while adjusting for potential confounders in a community based sample of primary TKAs. In addition, younger and older patient specific risk of revision was evaluated. Method:. A retrospective analysis of prospectively collected data from a Total Joint Replacement Registry (TJRR) was conducted. All 27,657 primary TKAs enrolled between 2001 and 2010 performed for any diagnosis with the same implant from a single manufacturer were included in the study. Patient characteristics, as well as surgeon, hospital, procedure, and implant characteristics were compared by the main exposure of interest, i.e. the type of tibial prosthesis (monoblock all-polyethylene vs. metal-backed modular). The main endpoints of the study were all-cause and aseptic revisions only. Descriptive statistics and Cox-regression models were employed. Hazard ratios (HR) and 95% confidence intervals (CI) are provided. Results:. The cohort consisted of 2,306 (8.3%) monoblock all-polyethylene tibial component TKAs and 25,351 (91.7%) modular metal-backed components. No gender, diagnosis or diabetic status differences were noted between the monoblock and modular cohorts. Patients with monoblock tibias were older (71.8 vs. 68.1 yrs, p < 0.001) and had a lower body mass index (30.1 vs. 31.6 kg/m2, p < 0.001). The median follow up time of the cohort was 2.9 years (interquartile range 1.2–5.1 years), during which 22 (0.95%) monoblock arthroplasties and 550 (2.17%) modular arthroplasties were revised. The all-cause revision rate/100 years of follow-up for monoblock and modular cohorts was 0.30 and 0.65, respectively. Their aseptic revision rate/100 of follow-up was 0.18 and 0.35, respectively. In adjusted overall models, the risk of all-cause revision (HR = 0.51, 95% CI 0.33–0.78, p = 0.002) and aseptic revision (HR = 0.59, 95% CI 0.29–1.19, p = 0.139) was lower in the monoblock cohort compared to the modular cohort. In adjusted models of patients 65 years and older, the risk of all-cause revision is 0.59 (95% CI 0.35–0.99, p = 0.045) in the monoblock cohort compared to modular cohort. In adjusted models of patients younger than 65 years old, the risk of all-cause revision (HR = 0.26, 95% CI 0.10–0.72, p = 0.010) and aseptic revision (HR = 0.27, 95% CI 0.11–0.65, p = 0.003) were lower in the monoblock compared to the modular cohort. Conclusion:. For our entire cohort of 27,567 primary fixed bearing TKAs, monoblock all-polyethylene tibial components had a 49% lower risk of revision for all-causes and a 41% lower risk of aseptic revision when compared to modular metal-backed tibial constructs. For patients younger than 65 years old, the all-polyethylene component had a 74% lower risk of all-cause revision and a 73% lower risk of aseptic revisions when compared to modular tibial constructs

Purpose: The purpose of this work was to report mid-term results of a series of 162 total knee prostheses with an all-polyethylene plateau. Material and methods: Between 1989 and 1995, 162 posterior stabilised cemented HLS2 total knee prostheses with an all-polyethylene plateau were implanted during first intention arthroplasties performed by the same surgeon. 142 prostheses were reviewed at more than one year, three patients died, and 17 were lost to follow-up (10%). Clinical results were assessed with the IKS criteria. Complete x-ray data included pangonograms. Mean follow-up was 4.5 years. Results: Ninety-six percent of the patients were satisfied or very satisfied and 95% had no pain or mild pain. Mean flexion was 114°. The mean postoperative knee score was 81/100 and mean function score was 64/100. Radiographic findings showed the good position of the implants with mean AFT at 178.6°, mean AFm at 89.1° and mean ATm at 89°. There were eight failures (4.9%) requiring replacement of a component, two for frontal laxity, three for patellar fracture, one for infection, one for aseptic loosening, and one for an oversized tibial plateau. Two revision procedures were performed without implant replacement, one for pain (biopsy) and one for arthrolysis. Discussion: These 162 prostheses with an all-polyethyl-ene plateau were retained among a consecutive series of 893 HLS prostheses. We compared the present results with those of the metal-backed prostheses implanted in this series and with data in the literature. We found a significant correlation between the presence of tibial lucent lines and postoperative alignment defects, explained by the type of tibial component, in these 162 all-polyethyl-ene plateau prostheses. These lucent lines did not progress with time and had no clinical consequence. Conclusion: Clinial and radiological results with total knee prostheses with an all-polyethylene plateau, i.e. without metal backing, were very good in this series. We analysed our experience in comparison with the literature, focusing on the advantages and disadvantages of these two types of components

25–40% of unicompartmental knee replacement (UKR) revisions are performed for unexplained pain possibly secondary to elevated proximal tibial bone strain. This study investigates the effect of tibial component metal backing and polyethylene thickness on cancellous bone strain in a finite element model (FEM) of a cemented fixed bearing medial UKR, validated using previously published acoustic emission data (AE). FEMs of composite tibiae implanted with an all-polyethylene tibial component (AP) and a metal backed one (MB) were created. Polyethylene of thickness 6–10mm in 2mm increments was loaded to a medial load of 2500N. The volume of cancellous bone exposed to <−3000 (pathological overloading) and <−7000 (failure limit) minimum principal (compressive) microstrain (µ∊) and >3000 and >7000 maximum principal (tensile) microstrain was measured. Linear regression analysis showed good correlation between measured AE hits and volume of cancellous bone elements with compressive strain <−3000µ∊: correlation coefficients (R= 0.947, R2 = 0.847), standard error of the estimate (12.6 AE hits) and percentage error (12.5%) (p<0.001). AP implants displayed greater cancellous bone strains than MB implants for all strain variables at all loads. Patterns of strain differed between implants: MB concentrations at the lateral edge; AP concentrations at the keel, peg and at the region of load application. AP implants had 2.2 (10mm) to 3.2 (6mm) times the volume of cancellous bone compressively strained <−7000µ∊ than the MB implants. Altering MB polyethylene insert thickness had no effect. We advocate using caution with all-polyethylene UKR implants especially in large or active patients where loads are higher

Background: Cemented and cementless fixations of acetabular components in total hip arthroplasty are routine practice with inherent advantages and disadvantages. The aim of our prospective randomized study was to compare the clinical and radiographic results of cementless porous-coated cobalt chromium acetabular component with cemented all-polyethylene acetabular component in total hip arthroplasty. Methods: Three hundred patients were randomized to receive a cementless hemispherical cobalt chromium porous-coated no-hole acetabular component (group 1) or cemented all-polyethylene acetabular component (group 2) with an identical cemented femoral stem and 28mm cobalt-chromium head. Patients were evaluated clinically with Harris Hip Scores (HHS) and radiographically. Analysis of both intention-to-treat groups was performed. Results: Group 1 had 128 patients (55 male, 73 female) with average age of 70.3 years. Group 2 had 147 patients (63 male, 84 female) with average age of 71.2 years. Average follow-up was 9.5 years (1.03–13.23). The median follow-up was 10 years. 25 patients were excluded from analysis for reasons including unfit for surgery (2), operation cancelled (2), missing data (8) and non-study device (10). Average preoperative HHS improved from 34.4 and 34.5 to 80 and 82.5 postoperatively in group 1 and 2 respectively. There was no statistically significant difference between the average HHS of the two groups (p=0.449) at last follow-up. There were 7 revisions in group 1 [infection (2), cup migration (2), aseptic loosening (1), slipped cup (1) and fractured liner (1)]. 11 patients had revision in group 2 [aseptic loosening (8) and recurrent dislocations (3)]. Revision rate between the two groups was not statistically significant (p=0.465). 10-year survivorship was 93.8%; and 86.6%; for group 1 and 2 respectively. No statistically significant difference was noted for prognostic factors like gender (p=0.006), body mass index (p=0.433), age (p=0.657) and surgical approach (p=0.004) for the two groups. Prognostic factors like gender (male, p=0.006) and surgical approach (posterior, p=0.004) were noted to be significant but body mass index (p=0.433) and age (p=0.657) had no statistical significance. Bootstrapping analysis for the two groups (p-value calculations N=3000) showed a significant p-value for 19 and not significant p-value for 2981 calculations. 4 porous coated cups and 29 all-polyethylene cups had radiolucencies. None of the porous-coated cups had expansile osteolysis. Conclusions: The results from our study indicate that patients with a cemented all-polyethylene cup and cementless porous coated cup have similar long term outcomes. In patients over 75 years cemented cups have excellent results (100% survivorship at 10 years)

We studied the stability of cemented all-polyethylene keeled glenoid components by radiostereometric analysis (RSA) in 16 shoulders which had received a total shoulder replacement. There were 14 women (one bilateral) and one man with a mean age of 64 years. The diagnosis was osteoarthritis in eight and rheumatoid arthritis in seven. Two of the shoulders were excluded from the RSA study because of loosening of the tantalum markers. Three tantalum markers were inserted in the glenoid socket, two in the coracoid process and two in the acromion. The polyethylene keeled glenoid component was marked with three to five tantalum markers. Conventional radiological and RSA examinations were carried out at five to seven days, at four months and at one and two years after operation. Radiolucent lines were found in all except three shoulders. Migration was most pronounced in the distal direction and exceeded 1 mm in four shoulders. In ten shoulders rotation exceeded 2° in one or more axes with retroversion/anteversion being most common. No correlation was found between migration and the presence of radiolucencies on conventional radiographs

We studied the quality of fixation of the tibial component using radiostereometric analysis (RSA) in 40 patients who had undergone a cemented Freeman-Samuelson total knee arthroplasty. They were prospectively randomised to either a stemmed metal-backed (MB) or non-stemmed all-polyethylene (AP) tibial component. The articulating geometry of the implants was identical, as was the operative technique and the postoperative regime. The study showed no complications of fixation using AP tibial components, and the migration was the same as that of their metal-backed counterparts. There was no bony collapse or increased subsidence of any part of the tibial component or increased incidence of radiolucent lines in the knees with AP components. Most AP implants were stable between one and two years after surgery, a finding known to be of positive prognostic significance when predicting future aseptic loosening

Intro: There are few modern reports which document the results of all-polyethylene tibial components in younger, more active patients. The potential benefits of this design are the elimination of backside wear and lower implant cost than modular, metal-backed components. From January 1992 to the present, 56 TKRs were implanted in 41 patients less than 60 years of age at the time of index surgery using a cemented all-poly tibial component with a PS design. Indications included all patients with osteoarthritis or post-traumatic arthritis without significant tibial bone loss. All patientswere followed prospectively with clinical and radiographic criteria asdefined by the Knee Society. Patient Assessment Questionnaires were used to quantify patient satisfaction, pain, and activity levels. From January 1992 to the present, 56 TKRs were implanted in 41 patients less than 60 years of age at the time of index surgery using a cemented all-poly tibial component with a PS design. Indications included all patients with osteoarthritis or post-traumatic arthritis without significant tibial bone loss. All patientswere followed prospectively with clinical and radiographic criteria asdefined by the Knee Society. Patient Assessment Questionnaires were used to quantify patient satisfaction, pain, and activity levels. Discussion: Since the mid 1980s, modular, metal-backed tibial trays have dominated the TKR market based on finite-element analysis studies which demonstrated superior force distribution compared to conventional all-poly components. As a result, backside wear has become an emerging problem and refocused design efforts on unitized components. Our clinical experience indicates an all-poly tibial component fixed with cement provides excellent performance and survivorship even in younger, more active patients

We compared the rate of revision of two classes of primary anatomic shoulder arthroplasty, stemmed (aTSA) and stemless (sTSA) undertaken with cemented all polyethylene glenoid components.

A large national arthroplasty registry identified two cohort groups for comparison, aTSA and sTSA between 1^st January 2011 and 31^st December 2020. A sub-analysis from 1 January 2017 captured additional patient demographics. The cumulative percentage revision (CPR) was determined using Kaplan-Meier estimates of survivorship and hazard ratios (HR) from Cox proportional hazard models adjusted for age and gender.

Of the 7,533 aTSA procedures, the CPR at 8 years was 5.3% and for 2,567 sTSA procedures was 4.0%. There was no difference in the risk of revision between study groups (p=0.128).

There was an increased risk of revision for aTSA and sTSA undertaken with humeral head sizes <44mm (p=0.006 and p=0.002 respectively). Low mean surgeon volume (MSV) (<10 cases per annum) was a revision risk for aTSA (p=0.033) but not sTSA (p=0.926).

For primary diagnosis osteoarthritis since 2017, low MSV was associated with an increased revision risk for aTSA vs sTSA in the first year (p=0.048). Conversely, low MSV was associated with a decreased revision risk for sTSA in the first 6 months (p<0.001). Predominantly aTSA was revised for loosening (28.8%) and sTSA for instability/dislocation (40.6%).

Revision risk of aTSA and sTSA was associated with humeral head size and mean surgeon volume but not patient characteristics. Inexperienced shoulder arthroplasty surgeons experience lower early revision rates with sTSA in the setting of osteoarthritis. Revision of aTSA and sTSA occurred for differing reasons.

Abstract