Aims. The aim of this study was to analyze the prevalence of culture-negative periprosthetic joint infections (PJIs) when adequate methods of culture are used, and to evaluate the outcome in patients who were treated with antibiotics for a culture-negative PJI compared with those in whom antibiotics were withheld. Methods. A multicentre observational study was undertaken: 1,553 acute and 1,556 chronic PJIs, diagnosed between 2013 and 2018, were retrospectively analyzed. Culture-negative PJIs were diagnosed according to the Muskuloskeletal Infection Society (MSIS), International Consensus Meeting (ICM), and European Bone and Joint Society (EBJIS) definitions. The primary outcome was recurrent infection, and the secondary outcome was removal of the prosthetic components for any indication, both during a follow-up period of two years. Results. None of the acute PJIs and 70 of the chronic PJIs (4.7%) were culture-negative; a total of 36 culture-negative PJIs (51%) were treated with antibiotics, particularly those with histological signs of infection. After two years of follow-up, no recurrent infections occurred in patients in whom antibiotics were withheld. The requirement for removal of the components for any indication during follow-up was not significantly different in those who received antibiotics compared with those in whom antibiotics were withheld (7.1% vs 2.9%; p = 0.431). Conclusion. When adequate methods of culture are used, the incidence of culture-negative PJIs is low. In patients with culture-negative PJI, antibiotic treatment can probably be withheld if there are no histological signs of infection. In all other patients, diagnostic efforts should be made to identify the causative microorganism by means of serology or molecular techniques. Cite this article: Bone Joint J 2022;104-B(1):183–188

Aim. One of the most severe complications of primary total knee arthroplasty (TKA) is periprosthetic joint infection (PJI). Nowadays, the use of antibiotic-loaded cement for prevention of infection is still controversial. The aim of the present study is to evaluate the use of an antibiotic-loaded cement to reduce the infection rate in primary total knee arthroplasty. Method. Prospective randomized study, with 2893 cemented total knee arthroplasties performed between 2005 and 2010 in our institution. Two different groups were formed depending on which bone cement was used, without antibiotic (the control group) or loaded with erythromycin and colistin (the study group). All patients received the same systemic prophylactic antibiotics. The patients were followed for a minimum of twelve months. The rate of infection was analyzed according to the criteria of the Centers for Disease Control and Prevention (CDC). Results. In 1452 patients the prosthetic components were fixed using bone cement without antibiotic and in 1441 patients bone cement loaded with erythromycin and colistin was used. There were no differences between both groups in terms of demographic data (age, sex and BMI), either in operating time (p>0,05). The rate of infection was similar in both groups, being 2,0% (n=29) in the control group and 1,7% in the study group (p=0,58) at 8,7 years (SD 5,1) of follow up. In terms of prosthetic revision due to any cause (infected or aseptic), there wasn't differences between groups, performing a total of 61 revision arthroplasties in control group and 68 in study group (p>0,05). Moreover, we analyzed the erythromycin resistance rate, being no differences between both groups (p=0.6). Conclusions. The use of erythromycin and colistin-loaded bone cement in total knee arthroplasty did not lead to a decrease in the rate of infection when systemic prophylactic antibiotics were used, a finding that suggests that its use would not be indicated in the general population

Introduction. Robotics have been applied to total knee arthroplasty (TKA) to improve surgical precision in component placement and joint function restoration. The purpose of this study was to evaluate prosthetic component alignment in robotic arm-assisted (RA)-TKA performed with functional alignment and intraoperative fine-tuning, aiming for symmetric medial and lateral gaps in flexion/extension. It was hypothesized that functionally aligned RA-TKA the femoral and tibial cuts would be performed in line with the preoperative joint line orientation. Methods. Between September 2018 and January 2020, 81 RA cruciate retaining (CR) and posterior stabilized (PS) TKAs were performed at a single center. Preoperative radiographs were obtained, and measures were performed according to Paley's. Preoperatively, cuts were planned based on radiographic epiphyseal anatomies and respecting ±3° boundaries from neutral coronal alignment. Intraoperatively, the tibial and femoral cuts were modified based on the individual soft tissue-guided fine-tuning, aiming for symmetric medial and lateral gaps in flexion/extension. Robotic data were recorded. Results. A total of 56 RA-TKAs performed on varus knees were taken into account. On average, the tibial component was placed at 1.9° varus (SD 0.7) and 3.3° (SD 1.0) in the coronal and sagittal planes, respectively. The average femoral component alignment, based on the soft tissue tensioning with spoons, resulted as follows: 0.7° varus (SD 1.7) in the coronal plane and 1.8° (SD 2.1) of external rotation relative to surgical transepicondylar axis in the transverse plane. A statistically significant linear direct relationship was demonstrated between radiographic epiphyseal femoral and tibial coronal alignment and femoral (r=0.3, p<0.05) and tibial (r=0.3, p<0.01) coronal cuts, resepctively. Conclusion. Functionally aligned RA-TKA performed in varus knees, aiming for ligaments’ preservation and balanced flexion/extension gaps, provided joint line respecting femoral and tibial cuts on the coronal plane

Computer-assisted techniques in total knee replacement (TKR) have been introduced to improve bone cuts execution and relevant prosthesis components positioning. Although these have resulted in good surgical outcomes when compared to the conventional TKR technique, the surgical time increase and the use of additional invasive devices remain still critical. In order to cope with these issues, a new technology in TKR has been introduced also for positioning prosthetic components according to the natural lower-limb alignment. This technique is based on custom-fit cutting block derived from patient-specific lower-limb scan acquisition. The purpose of this study is to assess the accuracy of the custom-fit technology by means of a knee surgical navigation system, here used only as measurement system, and post-operative radiographic evaluations. Particularly, the performances of two different custom-fit cutting blocks realized from as many scan acquisitions have been here reported. Thirty patients affected by primary knee osteoarthritis were enrolled in this study. Fifteen patients were implanted with GMK® (Medacta-International, Castel San Pietro, CH) and as many patients with Journey® (Smith&Nephew, London, UK). Both TKR designs were implanted by using custom-fit blocks for bone cut executions provided by the same TKR manufacturers according to a pre-operative web planning approved by the surgeon. Particularly, the cutting block for the former design was built from CT scan acquisition of the hip, knee and ankle, whereas that for the latter design from MRI scans acquisition of the knee and X-ray lower-limb overview. A knee surgical navigation system (Stryker®-Leibinger, Freiburg, Germany) was used for recording intra-operative alignment of bone cuts as performed by means of the custom-fit cutting blocks and relevant component positioning. Prosthetic components alignments were also assessed post-operatively on X-ray images according to a shape-matching technique. The accuracy of the custom-fit blocks was evaluated through the comparison between pre-operative planning, and intra/post-operative data. Discrepancies above 3° and millimeters were considered as outliers. Within the patient cohort, nine cases were fully analyzed at the moment and here reported. Over them and except for one case, the discrepancy between pre-operative planned femoral/tibial resection level on the frontal plane and the corresponding measured intra-operatively was within 3 mm, being 5 mm in the worse case. Two outliers were observed for the corresponding femoral/tibial cut rotational alignment. Particularly, in one patient, the discrepancy in femoral cut alignment was of 8° in flexion and 6° in external rotation; in another patient this was of 4° in extension and 4° in external rotation in the femoral and tibial cut alignment, respectively. Post-operative radiographs evaluations for the final prosthetic components revealed that femoral/tibial alignment were within 3° in all cases, except for those patients that were already outliers. These preliminary results reveal the efficacy of the custom-fit cutting block for TKR. These were generally fitted properly and final prosthetic components were accurately placed, although some discrepancies were observed. This new technology seems to be a valid alternative to conventional and computer-assisted techniques. More consistent conclusions can be deduced after final evaluation of all patients

Background. The current use of a spherical prosthetic humeral head in total shoulder arthroplasty results in an imprecise restoration of the native geometry and improper placement of the center of rotation, maintained in a constant position, in comparison to the native head and regardless of glenoid component conformity. A radially-mismatched spherical head to allow gleno-humeral translation is a trade-off that decreases the contact area on the glenoid component, which may cause glenoid component wear. This finding suggests that the use of a non-spherical head with a more conforming glenoid component may reduce the risk of glenoid component wear by allowing gleno-humeral translation while increasing the contact area. A non-spherical prosthetic head more accurately replicates the head shape, rotational range of motion and gleno-humeral joint kinematics than a spherical prosthetic head, compared with the native humeral head. The combination of inversion of the bearing materials with the non-spherical configuration of the humeral head may thus decrease polyethylene wear. Aim of the present study is to evaluate in vitro wear behaviour of an all-polyethylene elliptical humeral head component against a metallic glenoid component in an anatomic configuration. Material and methods. The prosthetic components tested are from the Mirai. ®. Modular Shoulder System by Permedica S.p.A.. The prosthetic bearing components were tested in their anatomic configuration: the humeral head rubbing against the glenoid inlay, assembled over the glenoid base-plate. The glenoid insert is made of Ti6Al4V alloy coated with TiNbN. The glenoid insert, as the glenoid base-plate have the same shape which reproduce the native shape of the glenoid. Moreover, the glenoid insert has a concave articular surface described by two different radii on orthogonal planes. The vitamin E-blended UHMWPE humeral head is not spherical but elliptic-shaped with an articular surface described by two different profiles in sagittal and coronal plane. The component sizes combination tested have the greatest radial mismatches allowed between humeral head and glenoid insert. The test was performed up to 2.5 million of cycles applying a constant axial load of 756 N. Results. After 2.500.000 cycles the mean mass loss from the humeral head was 0.68 mg. The mean wear rate of the humeral head was 0.28 mg/Mc (SD 0.45 mg/Mc). The surface of the humeral heads showed an elliptical worn area with matt and polished areas with scratching. The surface of the TiNbN-coated glenoid insert counterparts did not show wear signs. Conclusion. The tested prosthetic humeral head has a non-spherical shape with an elliptical base and 2 different radii on sagittal and coronal plane. Also the tested glenoid insert has 2 different radii on sagittal and coronal planes. This components geometry leads to a radial mismatch between head and glenoid on sagittal and coronal planes. A different kinematics, allowing gleno-humeral translation while increasing the contact area, radial mismatch in different planes and the inversion of bearing materials may have a role in reducing component wear and may explain the extremely low wear rate found in the present study

Introduction. Functional outcomes of mechanically aligned (MA) total knee arthroplasty have plateaued. The aim of this study is to find an alternative technique for implant positioning that improves functional outcomes of TKA. Methods. We prospectively randomized 100 consecutive patients undergoing TKA into two groups: in the group A an intramedullary femoral guide and an extramedullary tibial guide were used with aim to obtain a neutral traditional mechanical alignment; in the group B an extramedullary femoral guide set on distal femoral condyles and an extramedullary tibial guide neutrally aligned were used to obtain an adaptation of the conventional MA technique. Patients were followed-up clinically with the Short Form Health Survey (SF-12), Oxford Knee Score (OKS) and Visual Analogue Score (VAS) questionnaires pre-operatively and then at 1 year post-operatively. Mechanical alignment was calculated on standing weight bearing Xray pre- and post-operatively. T-test was used to compare the results between groups. Results. Both groups showed an improvement of clinical scores. At 1 year of follow-up OKS and SF-12 were significantly higher in group B: 47,6 ±0.75 and 46.5 ±0.76 respectively; VAS was similar in both groups. Values of mechanical alignment changed from 6.45 ±8.45 to 0.25 ±0.91 for group A and from 6.8 ±7.94 to 2.5 ±4.7 for group B. Conclusion. This study shows that adjusted mechanical alignment (AMA) with a small under-correction of frontal deformity lead to improved functional scores following total knee replacement compared to conventional technique of neutral alignment. These results are satisfactory at short follow-up but long-term studies are needed to evaluate the difference in the rate of wear of the prosthetic components

Introduction. Protective hard coatings are appealing for several technological applications and even for orthopaedic implants and prosthetic devices. For what concerns the application to prosthetic components, coating of the surface of the metallic part with low-friction and low-wear materials has been proposed [1, 2]; at the same time, concerning use of ceramic materials in joint arthroplasty, zirconia-toughned-alumina (ZTA) ceramic material has shown high strength, fracture toughness, elasticity, hardness, and wear resistance [3, 4]. The purpose of this study was to directly deposit ZTA coatings by using a novel sputter-based electron deposition technique, namely Pulsed Plasma Deposition (PPD) [5]. Preliminary characterization of realized coatings from the point of view of morphology, wettability, adhesion and friction coefficients was performed. Materials and methods. PPD technique was used to deposit ZTA coatings; this technique is able to maintain the stoichiometry of the starting target. In this study we started from a cylindrical ZTA target (30 mm diameter × 5 mm thickness, 75% alumina / 25% zirconia) and followed the procedure described by Bianchi et al [5]. Characterization of morphology, micro-structure and chemistry of deposited coatings was performed by Scanning Electron Microscopy (SEM) equipped with Energy Dispersive X-ray Spectroscopy (EDS) and Atomic Force Microscope (AFM). Coating-substrate interface quality were investigated by micro-scratch tests. Measurement of the contact angle between a drop of 1 ml of ultrapure water and the surface of the sample was performed to estimate the degree of wetting. A ZTA-coated stainless steel ball (AISI 420, 3 mm radius) was coupled against medical grade UHMWPE to evaluate the friction of the proposed coupling in preliminary ball-on-disk tribological tests. Results. Coatings up to several microns thick have been deposited by PPD. Deposited ZTA films exhibited a smooth nanostructured surface. Mechanical tests showed a well-adherent films were deposited. In particular, scratch tests assessed a good interface adhesion: first formation of cracking in the coating during testing was reported at about 0.8 N. Hydrophobic behavior of the coating was revealed by contact angles (average contact angle 116° ± 2°), probably due to the nano-roughness of the coating itself. Good average friction coefficient ranging from 0.12 to 0.15 was showed by preliminary tribological tests carried out in deionized water after up to 10000 m tracks. Conclusions. The preliminary results of a novel approach aiming to drastically improve the performance of prosthetic couplings by introducing hard ceramic coating was presented. Showed results suggested the feasibility of pursuing this approach of realizing ZTA coatings by means of PPD technique. Further analyses on mechanical properties, nanoroughness and tribology are ongoing. Well-adherent ZTA films deposited directly on the prosthetic components surface would then allow a drastic improvement of the actual prosthetic behaviour

Aim. At present, a variety of clinical guidelines for treatment of periprosthetic joint infections (PJI) inevitably lead to a variety in outcomes by differing case management. Ideally a treatment algorithm should incorporate all components contributing to the decision-making process for a patient tailored solution in PJI. We aim to present a comprehensive and reproducible treatment algorithm based on a validated staging system, a thorough understanding of the host, the causative microbiome and implant complexity. Method. The diagnosis of a PJI was defined according to major and minor criteria following revised International Consensus Symposium algorithm. The validated McPherson staging system was used in our university hospital from January 2015 until January 2019 in referred PJI patients. Standardised preoperative and postoperative survey documents were completed in order to register data from the patient's medical, social and surgical history. The complexity of the infected implant was taken into consideration, including quantity of preceding procedures, residual bone stock, type of fixation, magnitude of prosthetic components and presence or absence of reconstructive options. Further, preoperatively obtained bacteriological information by means of arthrocentesis or tissue/bone biopsies was categorized according to the mono- or polybacterial nature and to the qualification of virulence and difficulties to treat. Social and professional history, financial impediments and patient's functional outcome wishes were included in the joint decision making. Results. We present our comprehensive PJI treatment algorithm. The ‘deTerminators’ we included are a validated staging system focused on the host, the amount of unsuccessful prior attempts, the difficult to treat character of the microbiome, the implant complexity, anatomical location and socioeconomic patient derived factors. Furthermore, we call for source control by minimally invasive means or late DAIR in complex case management combined with lifelong suppressive antibiotic therapy with maintenance of quality of life as the main outcome instead of curative intention. Conclusions. We present a comprehensive treatment algorithm based on an expanded McPherson staging system coupled with bundled clinical, technical, social and psychological data which should assist the surgeon and the patient to make informed choices. We hope that usage and testing of our algorithm in other centers could further demonstrate its usefulness

Background. The main reasons for hip prosthesis failure are aseptic loosening and periprosthetic joint infection (PJI). The real frequency of PJI is probably largely underestimated because of non-standardized definition criteria, diagnostic procedure, treatment algorithm and other confounders. Therefore, data from joint registries are not reflecting the frequency of PJI and can be misleading; particularly low-grade PJI can be frequently misdiagnosed as aseptic failure. Therefore, prospective clinical studies with standardized protocol, comprehensive diagnostic procedure and sufficient follow-up should be performed. Sonication of explanted prosthesis is highly sensitive for detection of biofilms on prosthetic surface and allows quantitative analysis of biofilm formation. We hypothesize that by using sonication, ceramic components (BIOLOX®delta, BIOLOX®forte) will show higher resistance against biofilm adhesion compared to polyethylene (PE) and metal (CoCrMo). Methods. In this prospective multicentre study (level of evidence: Ia), we included all consecutive adults ≥18 years of age, who underwent explantation of the hip prosthesis for infection or aseptic reason. Excluded were patients in whom part of the prosthetic components were retained. A standardized and comprehensive diagnostic algorithm was applied, including sonication of all removed prosthetic components for qualitative and quantitative microbiological analysis (ultrasound bath 40 kHz, 1 W/cm2, 1 min). Individual components (metal, PE, ceramic) were separately placed in sterile boxes for investigation. All patients were simultaneously included in the European Prosthetic joint infection cohort (EPJIC, . www.epjic.org. ) to ensure long-term follow-up. Results. Up to date, 79 patients were included, of whom 47 (60%) were diagnosed with aseptic failure and 32 (40%) with PJI. Mean age was 73 years (27–87 years), 32 (41%) were males. Table 1 summarizes the demographic characteristics. In 32 patients with PJI, most frequently isolated organisms were coagulase-negative staphylococci (n=12, 38%), Staphylococcus aureus (n=7, 22%) and Propionibacterium acnes (n=4, 13%), followed by enterococci (n=2; 6%) and gram-negative bacilli (n=2; 6%); 2 infections (6%) were polymicrobial and 3 were culture-negative (9%). Table 2 summarizes the microbiological results from sonication of removed components. Causative microorganism could be detected in sonication fluid from polyethylene in 100%, from metal in 92% and from ceramic in 69%. Significantly lower bacterial counts expressed as colony-forming units (CFU) were detected in sonication fluid from ceramic components (230 CFU/ml) than from PE (6’250 CFU/ml) and metal components (5’870 CFU / ml) (p < 0.01). Conclusions. These first results support the hypothesis that significantly less biofilm biomass is formed on ceramic surface, compared to PE and metal surfaces, potentially indicating higher ceramic “resistance” against bacterial adhesion. These findings should be confirmed with non-microbiological investigation such as imaging (fluorescent in situ hybridization, confocal laser scanning or electron microscopy). Furthermore, in 6 of 32 patients (19%) with PJI, an aseptic loosening was preoperatively suspected. Infection was found only by systematic application of an optimized diagnostic method, particularly sonication of the removed implant. Final study results are expected to be available by the end of 2016

Introduction. Protective hard coatings are appealing for several technological applications like solar cells, organic electronics, fuel cells, cutting tools and even for orthopaedic implants and prosthetic devices. At present for what concerns the application to prosthetic components, the coating of the surface of the metallic part with low-friction and low-wear materials has been proposed [1]. Concerning the use of ceramic materials in joint arthroplasty, zirconia-toughned-alumina (ZTA) reported high strength, fracture toughness, elasticity, hardness, and wear resistance [2]. The main goal of this study was to directly deposit ZTA coating by using a novel sputter-based electron deposition technique, namely Pulsed Plasma Deposition (PPD) [3]. The realized coatings have been preliminary characterized from the point of view of morphology, wettability, adhesion and friction coefficients. Materials and methods. ZTA coatings were deposited by PPD technique, which is able to maintain the stoichiometry of the starting target. In this case we started from a cylindrical ZTA target (30 mm diameter × 5 mm thickness, 75% alumina / 25% zirconia). The morphology, micro-structure and chemistry of deposited coatings were characterized by Scanning Electron Microscopy (SEM) equipped with Energy Dispersive X-ray Spectrosopy (EDS) and Atomic Force Microcscope (AFM). Coating-substrate interface quality were investigated by microscratch tests. The degree of wetting was estimated by measuring the contact angle between a drop of 1 ml of ultrapure water and the surface of the sample. Preliminary ball-on-disk tribological tests were carried out in air and deionized water coupling ZTA-coated stainless steel ball (AISI 420, 3 mm radius, grade 200) against medical grade UHMWPE to evaluate the friction of the proposed coupling. Results. Deposited ZTA films exhibited a smooth nanostructured surface. Coatings up to several microns thick have been deposited by PPD [Fig. 1 – SEM image (left) and cross section (right)]. Mechanical tests showed a well-adherent films were deposited. In particular, the good interface adhesion was assessed by scratch tests, reporting at about 0.8 N the first formation of cracking in the coating during testing. The contact angles revealed an hydrophobic behavior of the coating (average contact angle 116° ± 2°), probably due to the nano-roughness of the coating itself [Fig. 2 – Contact angle]. Preliminary tribological tests carried out in deionized water after up to 10000 m tracks showed good average friction coefficient ranging from 0.12 to 0.15 [Fig. 3 – Friction coefficient]. Conclusions. We have presented the preliminary results of a novel approach aiming to the drastically improve the performance of prosthetic couplings by introducing hard ceramic coating. The results showed suggested the feasibility of pursuing this approach of realizing ZTA coatings by means of PPD technique. Further analyese on mechanical properties, nano-roughness and tribology should be performed. Well-adherent ZTA films deposited directly on the surface of prosthetic components of a joint implant would then allow a drastic improvement of the actual prosthetic behaviour

INTRODUCTION. A preoperative planning for accurately predicting the size and alignment of the prosthetic components may allow to perform a precise, efficient and reproducible total knee replacement. The planning can be carried out using as a support digital radiographic images or CT images with three-dimensional reconstruction. Aim of this prospective study is to evaluate and compare the accuracy of two different types of pre-operative planning, in determining the size of the femoral and tibial component in total knee arthroplasty performed with Patient Specific Instrument (PSI). The two compared techniques were: digital radiography and “CT-Based”. MATERIALS AND METHODS. A prospective study was conducted to compare the accuracy in predicting the size of the prosthetic components in total knee replacement in 71 patients diagnosed with primary and symptomatic osteoarthritis of the knee. Inclusion criteria was “Easy Knee”: BMI ≤ 35, varus/valgus deviation ≤15° and residual flexion of the knee ≥ 90°. Pre-operatively all the patients underwent to the same standard protocol including digital radiographs with calibration and a CT scan. A dedicated IMPAX digital software (Agfa-Gevaert, NV, USA) was used to template the radiographs. The CT-based planning was performed on 3D reconstruction of CT scans of 3 joints: hip, knee and ankle, as established in standardised protocol to build up patient specific cutting mask (MyKnee, Medacta, Castel S. Pietro, Switzerland). All the surgeries were performed by 2 senior Authors (M.A and N.C.) using the same implant and the definitive component sizes implanted were registered and compared with the sizes suggested by both planning techniques considering also the range of error. Results analysis was carried out using nonparametric tests. RESULT. The planning of digital radiography indicates the correct size in 63% of the cases for the femoral component and 53% for the tibial. The accuracy reaches 90% for both components if we consider the maximum error of one size. CT-based planning reached an accuracy of 95% for the femur and 63% for the tibia considering the exact size. The accuracy reaches 100% for both components if considered the maximum error of a size using CT-based planning with a statistically lower range of error (p=0.04). DISCUSSION. The planning, regardless of the method of execution helps to plan the surgery. In our study the accuracy of the X-ray planning using dedicated software confirms the results obtained by other studies in the literature. Likewise the CT-based planning does provide significant more accurate data and the error is never more than one size. Further studies are needed even to evaluate any potential economical advantages in term of reducing hardware and sterilisation costs in the operating theatre despite more expensive exams

Total Knee Artroplasty (TKA) is becoming more and more popular, even in the younger active age group. In this age group however the results are not that reproducible as in the older age group. People are more limited in their activities of daily living and complain more about pain, stifness and swelling. At the end and in general the younger age group is less satisfied than the older patients. The last decade minimal invasive solutions with modified instruments, Gender Knees, the use of navigation in TKA, ligament-based techniques, fast rehab protocols etc have all been introduced to make the results of TKA better. These are all elements that indeed can make the patient better. However the most important on the short term and the long term is the use of the correct implant size and the correct implantation of the prosthetic components. Since January 2011 we routinely use patient specific instruments in TKA patients under 60y that are very active or in older less active patients with important anatomic malformations. A CT-based system that scans the hip-knee-ankle is used. The data are sent to an engineer and a digital proposal is sent back to the surgeon that can approve the different measurements performed. Once approved the patient specific cutting blocks are sent to the surgeon. In our department we use the Advance Medial Pivot Knee System as our standard knee system since its introduction thirteen years ago. Since then more than 2000 implantations have been performed. This experience has made it possible to critically evaluate the patient specific cutting block technique. The first results are very satisfying. During surgery less ligamentous releases had to be performed, there was in all cases an optimal patellofemoral tracking without any release, there was less blood loss and surgery time was decreased. At all times during surgery we were very satisfied how we could verify all surgical steps and this is in our opinion very important. During the first postoperative days the patients experienced less pain (routine VAS recorded), there was a faster return to full ROM and patients asked to go home earlier. After two months patients are routinely followed up and they undergo a clinical and radiographic exam. All prosthetic components were implanted the way we had planned it. The overall axes were restored and up till now no complications were noticed. All patients experienced a fast recovery with full ROM at 2 months, no complaints about pain or swelling and very interestingly no residual intra-articular swelling which is often seen in these active and younger patient group. Patients are also asked to fill in a patient-based outcome measurements (KOOS) questionnaire. In our opinion it is a very easy and promising system for the experienced surgeon. Younger and less experienced surgeons however should be warned that they cannot blindly trust the system. We surgeons have to control what the engineer has proposed before and during surgery

Aim. The purpose of this single center study was to analyze the robustness and thoroughness of debridement and irrigation in first stage procedures for periprosthetic joint infections in which the latter had been confirmed by fulfilling the PJI criteria produced by the musculoskeletal infection society. Method. After introduction of ‘a clean phase’ concept in our center, we developed a method of using new instrumentation sets and waterproof cover sheets as well as sets of gloves and aprons after thorough debridement followed by copious irrigation under a splash sheet, once the prosthetic components were removed during which several (6 to 8) tissue biopsies and cultures were harvested. ‘Clean phase’ tissue specimens ad random were again obtained and cultured and compared with ‘dirty phase’ cultures and sonication results. Our zero hypothesis was that we were not able to entirely eradicate bacterial colonization. We tested this hypothesis during a period of 18 months in a consecutive series of first stage revisions for PJI at our center after introduction of the clean phase concept. Results. We were able to reject our zero hypothesis in that ‘clean phase’ tissue cultures were either negative or that they did not match ‘dirty phase’ tissue cultures suggestive of bacterial contamination. Descriptive statistical analysis was utilized. Conclusion. Our findings suggest that our procedures and methods of debridement and irrigation in first stage PJI revision procedures are robust and thorough. Further investigation is required to determine whether ‘clean phase’ culture negativity is matching with a successful outcome in the run up and after the second stage revision procedure

Excellent outcomes following total hip arthroplasty require both optimal soft-tissue management and precise planning and placement of prosthetic components. The use of detailed and dynamic three-dimensional surgical plans combined with smart mechanical instruments for component placement facilitates precise and efficient surgery. Interest in these technologies has increased recently as surgeons and institutions are now responsible for poor outcomes in a growing percentage of the patient population. Cloud-based, patient-specific planning allows the surgeon to review and refine and execute surgical plans efficiently (HipXpert System, Surgical Planning Associates, Boston, MA). The surgical plans include cup size, cup orientation, stem size, head length, femoral anteversion, and planned change in leg length and offset, all in relation to the patients bony anatomy in 3D and multiplanar views. The associated smart tool is adjusted specifically for that patient and when docked, provides orientation information to the surgeon. The system has been proven to be robust, with repeated studies showing accurate cup placement in 100% of cases including by an independent study. This compares to a recent study of robotic methods that 88% of inclination and 84% for anteversion and to even greater inaccuracy of conventional surgery. Cloud-based 3D planning combined with smart mechanical navigation of cup placement offers the optimum combination of accuracy, speed, and simplicity for solving the ubiquitous problems of component sizing, orientation, and version, offset, and leg length correction. Knowledge of component sizing pre-operatively can facility inventory management and allows the surgery team to better anticipate the surgeon's goals during the procedure

Aims

Safety concerns surrounding osseointegration are a significant barrier to replacing socket prosthesis as the standard of care following limb amputation. While implanted osseointegrated prostheses traditionally occur in two stages, a one-stage approach has emerged. Currently, there is no existing comparison of the outcomes of these different approaches. To address safety concerns, this study sought to determine whether a one-stage osseointegration procedure is associated with fewer adverse events than the two-staged approach.

Purpose. Failure resulting from a recurrent infection in total knee arthroplasty (TKA) is a challenging problem. Knee arthrodesis is one treatment option, however fusion is not always successful, as there is huge bone defect. The authors reports a new arthrodesis technique that uses a bundle of flexible intramedullary rods and an antibiotic-loaded cement spacer. Methods. There were 13 cases of arthrodesis due to recurrent periprosthetic joint infection, which were performed by the first author (WS Cho) at Asan Medical Center in Seoul from 2005 to 2014. All previous prosthetic components were removed and cement was thoroughly excised using a small osteotome. Two stage operation was done in most of cases. After thorough debridement, antibiotics loaded cement was inserted in first stage, flexible intramedullary rods were inserted retrogradely in the femoral side with the knee in flexion under fluoroscopy guidance. After filling the femoral intramedullary canal, the rods were then driven back securely into the tibial medullary canal. We aimed for as much rod length as possible to maximize stability. After 6 weeks of first stage operation, the rods of the femoral and tibial sides were arranged such that they overlapped and interdigitated to maximize mechanical strength, maintain the limb length and keep the rotational alignment. The interdigitating rod ends were tightly fixed using two (or three) cerclage wires. Antibiotic-loaded cement was filled into the knee joint space so that the cement is fit to the irregular contour of the femur and tibia, which was resulted from the severe bone loss. Postoperatively, patients were allowed to weight bear as tolerated. Results. The procedure was successful in every cases with no evidence of rod or cement failure at least 1 year follow up. Also there was no recurrence of infection. Conclusion. Although this simple method was not for bony union, the authors could achieve stable knee joint without recurrence of infection

Expectations for ceramic-on-metal (COM) bearings included (i) optimal lubrication due to smoother ceramic heads (ii), reduction of metal ions due to elimination of CoCr heads, and (iii) ‘differential hardness’ reducing adhesive wear and squeaking (Firkins 2001, Williams 2007). Additional benefits included (iv) use of heads larger than for ceramic-on-ceramic (COC), (v) reduction in taper corrosion and (vi) simulator studies clearly demonstrated metal ions and wear both reduced compared to MOM (Firkins 2001, Williams 2007, Ishida 2007). However, contemporary ‘3rd body wear’ paradigms focused only on metal debris size range 0.025–0.035um (Firkins 2001). Thus, neglected was the effect of hip impingement, provoking release of large metal particles sized 20–200um (Clarke 2013). In this study, we compared COM retrievals using hypotheses that adverse COM cases would demonstrate a combination of (a) steeply inclined cups, (b) liner “edge-loading”, (c) Ti6Al4V contamination on ceramic, and (d) evidence of 3rd-body CoCr wear by large particles. As a case example, this 51-year old female had her metal-polyethylene (MPE) bearing revised to COM in June 2011. She reported no symptoms 1-year post-op, but scans revealed a palpable mass in the inguinal region of left hip. By March 2013 the patient reported mild pain in her hip, which progressed to severe by April 2014. Scans showed a solid and cystic iliopsoas bursitis while cup position had changed from 43o to 73o inclination. Revision was performed in June 2014, her joint tissues were found extensively stained due to metal contamination, and histology described formation of a large pseudotumor. Analysis of retrieved components was by interferometry, SEM and EDS. Detailed maps were made of wear areas in heads and cups and volumetric wear was determined by CMM techniques. This adverse COM example revealed large diametral mismatch (595um) compared to COM controls (75–115um). The ceramic head had a broad polar stripe of CoCr contamination, roughness 0.1–0.3um high. Equatorial ceramic areas showed arrays of thin metal smears that demonstrated elemental Ti and Al. The CoCr liner revealed wear area into cup rim, as “edge loading”, and also featured a focal rim-defect over 18o circumferential arc. Liner scratches were 20um wide and larger, and wear-rate of CoCr liner averaged approximately 50mm3 per year. In contrast, ceramic head had minimal wear. Our study highlights the underappreciated risk of impingement by metallic prosthetic components. Prior studies of ceramic heads showed black metallic smears. With COM we can anticipate that the broad polar smear will be CoCr alloy (wear of liner on head). However, Ti6Al4V smearing on ceramic heads is a notable signpost indicating impingement by the Ti6Al4V acetabular shell. The femoral neck (Ti6Al4V: CoCr), may also be damaged. Release of large metal particles, 1500-times larger than prior predictions, provoke a particularly adverse ‘3rd body wear’ (Halim, 2015). Such cases confirm our four hypotheses, that COM bearings will then fail in a way similar to MOM. In contrast, COC bearings are immune to such impingement and 3rd-body metal damage

BACKGROUND. Early dislocation is a foremost complication of total hip arthroplasty through a postero-lateral approach. The extra-articular impingement of the anterior part of the great trochanter with ileum bone, with or without soft tissue interposition is a well recognized but underestimated etiopathogenetic cause reported in literature. In this retrospective study through the assessment of clinical and radiographic follow-up at a minimum of six months, the effectiveness of an antero- longitudinal osteotomy of the great trochanter for early dislocation prevention is evaluated. MATERIALS AND METHODS. 209 patients (48.3% males and 51,7% females) underwent a total hip arthroplasty from June 2011 to September 2015, with surgery being performed by the same surgeon. A modified posterolateral approach was used according to the tissue-sparing criteria, in all the cases an anterior longitudinal osteotomy of the great trochanter has been performed at 90° to the antiversion angle of the implant and aligned posteriorly with the prosthesis. All the patients underwent a clinical and radiological follow up at one, three, and six months. RESULTS. In this study, only one patient reported dislocation of THA. One patient suffered from a wound infection which was subsequently treated with antibiotics and had complete remission. All patients demonstrated a fast recovery of ROM and walking, starting from pre-op Harris Hip Score 42.24pts and obtaining a score of 81.52pts at three months, and 92.03 at six months post-op. After surgery and during the follow up period, there were no trochanteric fractures detected. DISCUSSION. The correct positioning of the implants, the head diameter, offset, soft tissues repair, absence of impingement, and patients compliance are all elements that define the prosthetic stability. Literature shows and incidence of primary total hip arthroplasty dislocation between 0.80% to 10%. The incidence of dislocation reported in a preliminary study in our Institute is 0.48%, demonstrating the effectiveness of the trochanteric osteotomy. CONCLUSIONS. The osteotomy of the great trochanter is an effective surgical technique used to decrease the anterior impingement and early dislocation incidence. It is particularly effective on patients with good compliance and correctly implanted prosthetic components

Background and aim. A significant reduction in wear using Durasul highly cross-linked polyethylene (PE) versus Sulene polyethylene (sterilized with nitrogen) at 5 and 10 years have been reported previously. We ask if the improvement observed at the earlier follow-up continues at 15 years. Methods. Between 1999 and 2001, 90 hips underwent surgery using the same cementless cup and stem: 45 received Allofit cups with a Sulene-PE liner and 45 Allofit cups with a Durasul-PE liner, both associated with an Alloclassic stem (28 mm metallic femoral head). 66 hips of this prospective comparative study were available over a minimum follow-up of 15 years. Linear femoral head penetration was estimated digitally at 6 weeks, at 6 and 12 months and annually thereafter, using the Dorr method, given the nonspherical cup shape. All radiographs were evaluated by the same author, who was not involved in surgery. Results. 2 hips in the Sulene group showed proximal femoral osteolysis, one of these was revised for stem loosening at 12 years. There was no loosening of any other prosthetic component. Femoral head penetration in the one year postoperative radiographs was 0.23 mm (range, 0.08–0.23) for the Sulene group and 0.10 mm (0.04–0.11) for the Durasul group (p<0.001). The mean yearly linear femoral head penetration was 68.8 % lower for the Durasul group: 0.020+0.018 mm for the Durasul and 0.062+0.051 mm/year for the Sulene group (p<0.001). Mean linear femoral head penetration at 15 years was 64.5 % less in the Durasul group (0.394+0.27 mm) than in the Sulene group (1.108+0.78 mm)(p=0.001). Conclusions. There is a significant reduction in yearly linear femoral head penetration with the Durasul-PE. Confirmation that this reduction will result in less osteolysis requires continued follow-up studies

The infected joint arthroplasty continues to be a very challenging problem. No test has 100% diagnostic accuracy for PPI and the treating surgeon must correlate the clinical and radiographic presentation with a combination of blood tests, synovial fluid analysis, microbiological and histopathological evaluation of periprosthetic tissue and intra-operative inspection to reach a definitive diagnosis. Diagnosis should begin with a high index of suspicion for new onset of pain or symptoms in well-functioning joints. Plain radiographs may identify osteolysis or early signs of implant failure and should be promptly investigated further for PPI. Peripheral blood ESR and CRP remain the most widely used next step for the diagnosis of PPI. Both these tests are widely available, inexpensive, and have a rapid turnaround time in laboratories. The results should be interpreted with caution due to their relative lack of specificity. The sensitivity and specificity values for CRP are approximately 88 and 74%, respectively; while that of ESR is slightly lower at 75 and 70%, respectively. The combined ESR and CRP tests are 96% sensitive for ruling out PPI but the specificity of this combination is as low as 56%. Advanced imaging modalities may be used as a part of the diagnostic algorithm. However, they require expert interpretation and are limited by availability and high costs. When available they have high sensitivity and specificity but their routine use is not recommended and indications have to be individualised in the light of clinical presentation. In the presence of high clinical suspicion, the clinician should plan synovial fluid analysis. This provides a synovial fluid white cell count with differential cell count, specimen for culture and possibility of analyzing other synovial fluid markers. It is important to note that failed metal-on-metal hip arthroplasties can give a falsely elevated synovial fluid cell count when using automated cell counters. This can be overcome by manually counting cell numbers. Synovial fluid should be directly into blood culture bottles, and antibiotics should be withheld at least 2 weeks prior to aspiration, whenever possible. Cultures also help establish the organism, virulence and sensitivities that help plan subsequent treatment algorithm. Periprosthetic tissue biopsy provides valuable information in microbiological diagnosis and workup of PPI. Routine use of gram staining is not recommended due to poor sensitivity. However, frozen section may have some role especially when performed by a skilled pathologist. Tissue culture remains the gold standard for diagnosis despite false-positive and false-negative results. Whenever possible multiple samples should be obtained to aid interpretation. A threshold of 2 to 3 positive specimens yielding indistinguishable microorganisms has been recommended to improve sensitivity. Acute inflammation, evidenced by neutrophilic infiltrate on fixed or frozen tissue, is suggestive of PPI and is defined as the presence of at least 5 neutrophils per high-powered field, in at least 5 separate microscopic fields. Sonication of removed prosthetic components is used to dislodge the biofilm and the associated bacteria from the surface of the implant. The fluid surrounding the implant can be used for culture or analysis. PCR testing: Synovial fluid aspirate, periprosthetic tissue or sonicate fluid may be subject to molecular diagnosis to amplify genetic material and improve microbiological diagnosis of PPI. This technique has shown increased sensitivity in patients who had received antibiotics within 14 days before implant removal. Results have to carefully interpreted with due consideration for possibility of false positive results