7% of adolescent idiopathic scoliosis (AIS) patients also present with a pars defect. To date, there are no available data on the results of fusion ending proximal to a spondylolysis in the setting of AIS. The aim of this study was to analyze the outcomes of posterior spinal fusion (PSF) in this patient cohort, to investigate if maintaining the lytic segment unfused represents a safe option. Retrospective review of all patients who received PSF for AIS, presented with a spondylolysis or spondylolisthesis and had a min. 2-years follow-up. Demographic data, instrumented levels and preoperative radiographic data were collected. Mechanical complications, coronal or sagittal parameters, amount of slippage and pain levels were evaluated. Data from 22 patients were available (age 14.4 ± 2.5 years), 18 Lenke 1–2 and four Lenke 3–6. Five patients (24%) had an isthmic spondylolisthesis, all Meyerding I. The mean preoperative Cobb angle of the instrumented curves was 58 ± 13°. For 18 patients the lowest instrumented vertebra (LIV) was the last touched vertebra (LTV); for two LIV was distal to the LTV; for two, LIV was one level proximal to the LTV. The number of segments between the LIV and the lytic vertebra ranged from 1 to 6. At the last follow-up, no complications were observed. The residual curve below the instrumentation measured 8.5 ± 6.4°, the lordosis below the instrumented levels was 51.4 ± 13°. The magnitude of the isthmic spondylolisthesis remained constant for all included patients. Three patients reported minimal occasional low back pain. The LTV can be safely used as LIV when performing PSF for the management of AIS in patients with L5 spondylolysis

Aim. Prosthetic joint replacement is more commonly done in the elderly group of patients due to an increase pathology related to joint degeneration that comes with age. In this age group is also more frequent having underling condition that may predispose to a prosthetic joint infection. Also, the pharmacological intervention in those patients may play an important role as a risk factor for infection after joint replacement surgery. The use of oral anticoagulants seems to be particularly increased in elderly patients but there aren't enough data published to support an association between prosthetic joint infection and the use of oral anticoagulants. Identifying risk factors in elderly patients age >75 years old with a special focus on the oral anticoagulation therapy is the aim of the study. Methods. In a retrospective study from 2011 till 2018 all the patients >75 years old with knee and hip replacement surgery have been review looking for acute prosthetic infection and risk factors that may be predispose to it. Patients with previous surgery or any other mechanical complication that needed intervention on the same area have been excluded. Results. A total of 1220 patients have been included (801 knee replacement surgery and 419 hip replacement surgery). The mean age was 79.5 ± 3.44 years and most of the patients were women (72,6%). The infection rate was 2,5%. Several factors have been identified to be associated with acute infection. (Table.1.). The patients receiving oral anticoagulants had an increased risk of infection (OR 3.63 (1.60–7.74), p=0.002). Conclusions. Even all the risk factors associated with risk infection have been described previously, the relevant aspect is the increased risk of prosthetic joint infection in patients receiving oral anticoagulants

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. Methods. A comprehensive electronic search and quantitative data analysis from eligible studies were performed. Inclusion criteria were adults with a limb amputation managed with a one- or two-stage osseointegration procedure with follow-up reporting of complications. Results. A total of 19 studies were included: four one-stage, 14 two-stage, and one article with both one- and two-stage groups. Superficial infection was the most common complication (one-stage: 38% vs two-stage: 52%). There was a notable difference in the incidence of osteomyelitis (one-stage: nil vs two-stage: 10%) and implant failure (one-stage: 1% vs two-stage: 9%). Fracture incidence was equivocal (one-stage: 13% vs two-stage: 12%), and comparison of soft-tissue, stoma, and mechanical related complications was not possible. Conclusion. This review suggests that the one-stage approach is favourable compared to the two-stage, because the incidence of complications was slightly lower in the one-stage cohort, with a pertinent difference in the incidence of osteomyelitis and implant failure. Cite this article: Bone Jt Open 2023;4(7):539–550

The reconstruction of peri-acetabular defects after severe bone loss or pelvic resection for tumor is among the most challenging surgical intervention. The Lumic® prosthesis (Implantcast, Buxtehude, Germany) was first introduced in 2008 in an effort to reduce the mechanical complications encountered with the classic peri-acetabular reconstruction techniques and to improve functional outcomes. Few have evaluated the results associated with the use of this recent implant. A retrospective study from five Orthopedic Oncology Canadian centers was conducted. Every patient in whom a Lumic® endoprosthesis was used for reconstruction after peri-acetabular resection or severe bone loss with a minimal follow-up of three months was included. The charts were reviewed and data concerning patients’ demographics, peri-operative characteristics and post-operative complications was collected. Surgical and functional outcomes were also assessed. Sixteen patients, 11 males and five females, were included and were followed for 28 months [3 – 60]. Mean age was 55 [17–86], and mean BMI reached 28 [19.6 – 44]. Twelve patients (75%) had a Lumic® after a resection of a primary sarcoma, two following pelvic metastasis, one for a benign tumor and one after a comminuted acetabular fracture with bone loss. Twelve patients (75%) had their surgery performed in one stage whereas four had a planned two-stage procedure. Mean surgical time was 555 minutes [173-1230] and blood loss averaged 2100 mL [500-5000]. MSTS score mean was 60.3 preoperatively [37.1 – 97] and 54.3 postoperatively [17.1-88.6]. Five patients (31.3%) had a cemented Lumic® stem. All patients got the dual mobility bearing, and 10 patients (62.5%) had the largest acetabular cup implanted (60 mm). In seven of these 10 patients the silver coated implant was used to minimize risk of infection. Five patients (31.3%) underwent capsular reconstruction using a synthetic fabric aiming to reduce the dislocation risk. Five patients had per-operative complications (31.3%), four were minor and one was serious (comminuted iliac bone fracture requiring internal fixation). Four patients dislocated within a month post-operatively and one additional patient sustained a dislocation one year post-operatively. Eight patients (50%) had a post-operative surgical site infection. All four patients who had a two-stage surgery had an infection. Ten patients (62.5%) needed a reoperation (two for fabric insertion, five for wash-outs, and three for implant exchange/removal). One patient (6.3%) had a septic loosening three years after surgery. At the time of data collection, 13 patients (81.3%) were alive with nine free of disease. Silver coating was not found to reduce infection risk (p=0.2) and capsuloplasty did not prevent dislocation (p=1). These results are comparable to the sparse data published. Lumic® endoprosthesis is therefore shown to provide good functional outcomes and low rates of loosening on short to medium term follow-up. Infection and dislocation are common complications but we were unable to show benefits of capsuloplasty and of the use of silver coated implants. Larger series and longer follow-ups are needed

The reconstruction of peri-acetabular defects after severe bone loss or pelvic resection for tumor is among the most challenging surgical intervention. The Lumic® prosthesis (Implantcast, Buxtehude, Germany) was first introduced in 2008 in an effort to reduce the mechanical complications encountered with the classic peri-acetabular reconstruction techniques and to improve functional outcomes. Few have evaluated the results associated with the use of this recent implant. A retrospective study from five Orthopedic Oncology Canadian centers was conducted. Every patient in whom a Lumic® endoprosthesis was used for reconstruction after peri-acetabular resection or severe bone loss with a minimal follow-up of three months was included. The charts were reviewed and data concerning patients’ demographics, peri-operative characteristics and post-operative complications was collected. Surgical and functional outcomes were also assessed. Sixteen patients, 11 males and five females, were included and were followed for 28 months [3 – 60]. Mean age was 55 [17-86], and mean BMI reached 28 [19.6 – 44]. Twelve patients (75%) had a Lumic® after a resection of a primary sarcoma, two following pelvic metastasis, one for a benign tumor and one after a comminuted acetabular fracture with bone loss. Twelve patients (75%) had their surgery performed in one stage whereas four had a planned two-stage procedure. Mean surgical time was 555 minutes [173-1230] and blood loss averaged 2100 mL [500-5000]. MSTS score mean was 60.3 preoperatively [37.1 – 97] and 54.3 postoperatively [17.1-88.6]. Five patients (31.3%) had a cemented Lumic® stem. All patients got the dual mobility bearing, and 10 patients (62.5%) had the largest acetabular cup implanted (60 mm). In seven of these 10 patients the silver coated implant was used to minimize risk of infection. Five patients (31.3%) underwent capsular reconstruction using a synthetic fabric aiming to reduce the dislocation risk. Five patients had per-operative complications (31.3%), four were minor and one was serious (comminuted iliac bone fracture requiring internal fixation). Four patients dislocated within a month post-operatively and one additional patient sustained a dislocation one year post-operatively. Eight patients (50%) had a post-operative surgical site infection. All four patients who had a two-stage surgery had an infection. Ten patients (62.5%) needed a reoperation (two for fabric insertion, five for wash-outs, and three for implant exchange/removal). One patient (6.3%) had a septic loosening three years after surgery. At the time of data collection, 13 patients (81.3%) were alive with nine free of disease. Silver coating was not found to reduce infection risk (p=0.2) and capsuloplasty did not prevent dislocation (p=1). These results are comparable to the sparse data published. Lumic® endoprosthesis is therefore shown to provide good functional outcomes and low rates of loosening on short to medium term follow-up. Infection and dislocation are common complications but we were unable to show benefits of capsuloplasty and of the use of silver coated implants. Larger series and longer follow-ups are needed

Aim. Periprosthetic joint infections (PJI) are a severe complications after hip arthroplasty. The infections rate ranges from 0.7 to 1.3 depending on different reports. The aim of the present study is to evaluate the radiological and clinical outcome of patients that underwent two-stage revision for the treatment of periprosthetic joint infection of the hip when an extended trochanteric osteotomy (ETO) was necessary to remove the femoral stem. Methods. We retrospectively analyzed data from 84 patients that underwent two-stage revision of the hip between January 2006 and December 2010 at our institution. In forty-nine patients (Group A, 58.3%), the femoral stem was removed without an ETO, while in the remaining thirty-five patients (Group B, 41.7%) an ETO was necessary. In each case a metallic cerclage was used to closure of the flap. The average age for patients in group A was 64.3 years, while the average age in patients in group B was 66.4 years. The mean follow-up was respectively 117 months in group A and 122 months in group B. Eight patients died before the last follow-up, and data from six patients were incomplete. Complications, radiological and clinical outcome were. Mann Whitney U Test and Chi Square Test were used respectively to analyze continues and categorical variables. Cumulative survival of the implants was calculated for reinfection and mechanical complications with Kaplan-Meyer curves. Results. The mean follow-up was 118 months. The cumulative incidence of reinfection was 4.7% at 1 years and 10.7 at last follow-up. No statistically significant (p-value > 0.05) differences were observed in the two groups neither at 1 year nor at last follow up. The cumulative incidence of mechanical complication was 3.6% at 1 year and 8.3% at last follow-up. No statistically significant differences (p-value > 0.05) were observed in the two groups neither at 1 year nor at last follow up. All the patients had the healing of the ETO at six months (mean 11.4 weeks). The mean Harris Hip Score was 77.5. No statistically significant (p-value > 0.05) differences were observed in the two groups. Discussion. The results obtained in this retrospective study demonstrates that there is no difference in terms of reinfection-rate, mechanical complications and clinical outcome in patients that underwent two-stage revision with or without an ETO. In presence of a well-fixed femoral stem, performing an ETO could be helpful to expose the femoral canal facilitating the femoral stem's removal avoiding intra-operative femoral fracture

Introduction. Dual mobility (DM) total hip arthroplasty (THA) prostheses are designed to increase stability. In the setting of primary and revision THA, DM THA are used most frequently for dysplasia and instability diagnoses, respectively. As the use of DM THA continues to increase, with 8,031 cases logged in the American Joint Replacement Registry from 2012–2018, characterizing in vivo damage and clinical failure modes are important to report. Methods. Under IRB-approved implant retrieval protocol, 43 DM THA systems from 41 patients were included. Each DM THA component was macroscopically examined for standard damage modes. Clinically-relevant data, including patient demographics and surgical elements, were collected from medical records. Fretting and corrosion damage grading is planned, according to the Goldberg et al. classification system. Results. In this 43-retrieved implant series, there were 23 female and 17 male patients (n=1, unknown), with an average body mass index of 29 (range, 19–49), and average ages at index and revision of 63 years (range, 34–80) and 64 years (range, 38–88), respectively. The average duration of implantation was 12.9 months (range, 0.1–72.0). Reasons for revision included infection (n=11, 26%), mechanical complication (n=10, 23%), intraprosthetic dislocation (n=6, 14%), periprosthetic fracture (n=5, 12%), pain (n=4, 9%), acetabular-associated loosening (n=3, 7%), unknown (n=3, 7%), hematoma (n=2, 5%), leg length discrepancy (n=1, 2%), and inflammatory reaction (n=1, 2%); some cases included multiple reasons for revision. On articular surfaces, scratching was the most commonly observed damage mode on all components, with more than 40% of acetabular cup and femoral heads showing scratching damage (Figure 1A). Abrasion, burnishing, and pitting damage were also observed in more than 10% of acetabular cup and acetabular liner components; further, approximately 20% of polyethylene acetabular liners exhibited edge deformation damage. On backside surfaces, polyethylene acetabular liners showed the greatest damage, with more than 60% of components exhibiting abrasion, scratching, or pitting damage (Figure 1B). Conclusion. This series showed various reasons for revision as well as in vivo damage of retrieved DM systems following short-to-midterm implantation. Damage was observed on both articular and backside surfaces of the five components of DM THA. Modularity of DM THA prostheses may amplify rates of in vivo damage. Future studies are needed to confirm these results and clinical significance. For any figures or tables, please contact the authors directly

Despite the successful, durable results, concern remains for using TKA in patients with isolated patello-femoral OA, as it requires an extensive surgical exposure and bone resection, a long recovery time, and a potentially more complex revision than that required for a patient with a failed patello-femoral arthroplasty (PFA). PFA was introduced in the late 1970s. While PFA was successful in providing pain relief, the procedure did not gain widespread use because of initial design limitations that predisposed to PF maltracking, catching, and subluxation. The mechanical complications associated with first-generation PFA offset the potential advantages of maintaining the knee's native soft tissues and spurred efforts to improve implant design, and to refine surgical techniques and patient selection. Over the past two decades, second generation PFAs incorporated changes in implant design and instrumentation and have shown promising results when used in the properly selected patient population. In addition, with improved instrumentation and robotics, adequate implant alignment and rotation can be achieved in the majority of patients, including those with severe patellofemoral dysplasia. Our meta-analysis of TKA and PFA for the treatment of isolated patello-femoral OA showed that the rate of complications of patients undergoing PFA was 30% after a median follow up of 5.3 years, which is significantly higher than the 7% rate of complications in patients who underwent TKA. The most frequent type of complication associated with PFA was mechanical (including loosening and instability), which is consistent with the malalignment and maltracking-related failures previously reported. The incidence of re-operation after PFA (21%) was significantly higher than that seen after TKA (2%). The most frequent indication for re-operation after PFA was mechanical failure (7%), followed by progression of OA (6%), and persistent pain or stiffness (5%). The most common re-operations after PFA were conversion to TKA, revision of PFA components, lateral releases, open or arthroscopic debridement, manipulations under anesthesia, and bony and/or soft tissue extensor mechanism re-alignment procedures. In our study, 11% of patients treated with PFA underwent a revision arthroplasty, with 4% undergoing revision PFA and 7% undergoing conversion to TKA. Our comparison of patients who were treated with second-generation PFA designs versus TKA showed no difference in the rate of complications, re-operation, or revision arthroplasty. Additionally, length of follow-up did not significantly influence any of these outcomes when comparing second-generation PFA and TKA. These observations provide support for the use of current PFA designs. The mechanical complications and subsequent re-operations that affected first-generation PFA designs appear to be of less concern with proper patient selection, meticulous surgical technique, current implant designs and peri-operative care. While it is difficult to predict the survivorship of current PFA designs, it is our expectation that patient selection will continue to be a critical component in determining long-term results. The potential benefit of providing pain relief while preserving the tibiofemoral articulations makes PFA a promising treatment option

Introduction. The management of patients with open leg fracture in Ivory Coast does not meet the standards of developed countries due to socio-economic conditions, accessibility and organization of care. However, is this care problematic? Is it associated with more post-traumatic infection or mechanical complications and are these correlated with the delay for treatment and the method of treatment?. Material and Methods. This is a single-center prospective study conducted on between January 2018 and May 2018 at Bouaké University Hospital. The observed parameters included factors related to patient, fracture and treatment conditions and were correlated with the rates of complications by multivariate analysis. Results. Fractures, mostly comminuted (69.8%), occurred following a road accident (93%). The series has 30 Gustilo 1 and 2 fractures and 13 Gustilo 3 fractures. The average delay before surgery was 26.6 ± 8.1 hours. Fracture stabilization required the use of a cast, an external fixator or an unlocked nail in 27, 10 and 6 cases, respectively. Complications developed in 28 patients (65%), including 17 malunions and 22 postoperative infections. 11 infections were controlled but 8 developed chronic osteomyelitis and 3 septic non-unions. Uncomplicated union was observed in only 15 cases and an acceptable functional outcome in only 16 cases. Gustilo Grade 3 fractures were associated with an increased risk of complication (p=0.02). The delay of management was not correlated with the appearance of a complication. In contrast, the use of plaster immobilization was significantly associated with an increased risk of complications and infection (p = 0.001). Conclusion. The management of open fractures in our conditions is associated with a high rate of complications and a satisfactory result in a small number of patients. More than the delay of management, the immobilization modalities by plaster and the insufficiency of this method of contention are correlated to the complications. The development of a National Health Care system covering the expenses for emergent treatment, including rapid transportation to hospitals and availability of external fixators at a lower cost would most probably contribute to a reduction of complications and infection. Keywords. Open fractures, developing countries, fixation, operative time

Total knee arthroplasty (TKA) is currently one of the most common elective surgical procedures in the United States. The increase in the proportion of younger patients in receipt of surgery, in concert with a dramatic rise in the incidence of obesity, has contributed to the on-going, exponential increase in the number of arthroplasties performed annually. Despite materials advances for implants, the U.S. revision burden has remained static for the last decade. According to the 2013 CMS MEDPAR file the typical CMS reimbursement falls far short of costs incurred by the hospital, resulting in an average net loss of revenue of $9,539; and over 90% of hospitals lose money for every revision case performed. Today, approximately 5% of all primaries performed will result in an early revision (< 3 years). In order to understand ways with which to mitigate the incidence of early revision due to mechanical complications, a multicentric group of sensor-assisted patients was follow-up out to 3 years. In this study, 278 sensor-assisted patients were followed out to 3 years. The intraoperative devices used in this study contain microsensors and a processing unit. Kinetic and center of load location data are projected, in real-time, to a screen. Because of the wireless nature of the intraoperative sensors, the patella can be reduced, and kinematic data can be evaluated through the range of motion. For each patient, the soft-tissue envelope was balanced to within a mediolateral differential of 15 lbf., through the ROM, as per the suggestion of previously reported literature. The average patient profile indicates: age = 69.7 years, BMI = 30.4, gender distribution = 36% male/64% female. Any adverse event within the 3-year follow-up interval was captured. By 3 years, 1 patient in this population has required revision surgeon due to mechanical complicatons. Overall adverse events included: pain in hip (3), pain in contralateral knee (2), wound drainage (3), DVT (1), death (1), stiffness in operative knee (2), infection (3), global pain (2), back pain (2). Based on the average reported number of early revisions that occur in the U.S. (5% of primaries), it was anticipated for this patient group to require approximately 13 revisions by the 3-year follow-up interval. Using 2013 CMS MEDPAR data, these 13 revisions would have resulted in $124,007 cost-to-hospital. However, only 1 revision (0.4%) was observered, therefore $114,468 in additional costs were spared for the aggregate of participating hospitals. This data suggests that the incorporation of kinetic sensors in TKA may assist the surgeon in achieving soft-tissue balance and thereby avoiding adverse mechanical complications that require surgical intervention

Patients with neuromuscular disease and imbalance present a particularly challenging clinical situation for the orthopaedic hip surgeon. The cause of the neuromuscular imbalance may be intrinsic or extrinsic. Intrinsic disorders include those in which the hip is in development, such as cerebral palsy, polio, CVA, and other spinal cord injuries and disease. This can result in subluxation and dislocation of the hip in growing children, and subsequent pain, and difficulty in sitting and perineal care. Extrinsic factors involve previously stable hips and play a secondary role in the development of osteoarthritis and contractures in later life. Examples of extrinsic factors are Parkinson's disease, dyskinesis, athetosis, and multiple sclerosis. Goals of treatment in adults with pain and dysfunction in the setting of neuromuscular imbalance are to treat contractures and to perform salvage procedures to improve function and eliminate pain. Treatment of patients with neuromuscular imbalance may include resection arthroplasty (Girdlestone), arthrodesis, or total hip arthroplasty. Resection arthroplasty is typically reserved for patients that are non-ambulatory, or hips that are felt to be so unstable that arthroplasty would definitely fail due to instability. In modern times arthrodesis has limited use as it negatively impacts function and self-care in patients with neuromuscular disorders. Total hip arthroplasty has the ability to treat pain, relieve contractures, and provide improved function. Due to the increased risk of instability, special considerations must be made during primary total hip arthroplasty in this patient cohort. Risk of instability may be addressed by surgical approach, head size, or use of alternative bearing constructs. Posterior approach may have increased risk of posterior dislocation in this patient group, particularly if a posterior capsular repair is not possible due to the flexion contractures and sitting position in many patients. Surgeons familiar with the approaches may utilise the anterolateral or direct anterior approach judicially. Release of the adductors may be performed in conjunction with primary total hip arthroplasty to help with post-operative range of motion and to decrease risk of instability. In a standard bearing, the selected head size should be the largest that can be utilised for the particular cup size. Rigorous testing of intra-operative impingement, component rotation, and instability is required. If instability cannot be adequately addressed by a standard bearing, the next option is a dual mobility bearing. Multiple studies have shown improved stability with the use of these bearings, but they are also at risk for instability, intraprosthetic dislocation, and fretting and corrosion of the modular connections. Another option is a constrained liner. However, this results in reduced range of motion, and an increased risk for mechanical complications of the construct. The use of a constrained liner in a primary situation should be limited to the most severe instability cases, and the patient should be counseled with the associated risks. If total hip arthroplasty results in repeated instability, revision surgery or Girdlestone arthroplasty may be considered

Aim. Femoral or tibial massive bone defects (AORI F2B-F3 / T2B-T3) are common in septic total knee replacement. Different surgical techniques are described in literature. In our study we show clinical and radiological results associated with the use of tantalum metaphyseal cones in the management of cavitary bone defects in two-stage complex knee revision. Method. Since 2010 we have implanted 70 tantalum metaphyseal cones associated with constrained or semiconstrained knee prostheses in 47 patients. The indication for revision was periprosthetic knee infection (43 cases, 91.5%) or septic knee arthritis (4 patients, 8.5%) with massive bone defect. All cases underwent a two-stage procedure. Patients were screened for main demographic and surgical data. Clinical and radiological analysis was performed in the preoperative and at 3,6 months, 1 years and each year thereafter in the postoperative. The mean follow-up was 31.1 months ± 18.8. No dropout was observed. Results. Objective and subjective functional scores (KSS, OKS) showed a statistically significant improvement from the preoperative to last follow-up (p <0.001). All cones but one (98.6%) showed radiological osteointegration. We did not find any cone-related intraoperative or postoperative mechanical complication with a 100% survival rate when we consider aseptic loosening as cause of revision. Six non progressive radiolucencies were observed. Two septic failures (4.3%) with implant and cone removal were reported. Conclusions. The ideal treatment for cavitary bone defects in two-stage TKA septic revision is still unclear. The use of metaphyseal tantalum cones showed excellent clinical and radiographic results with a low rate of related complications. The main finding of our study is the cone-related infection rate (2.9%) in this particular series of patients. This data is comparable or better than other previous report about this topic with unhomogeneous cohort of patients

Aim. The diagnosis of peri-prosthetic infection is sometimes difficult to assess, and there is no universal diagnostic test. The recommendations currently accepted include several diagnostic criteria, and are based mainly on the results of deep bacteriological samples, which only provide the diagnosis after surgery. A predictive score of the infection might improve the peri-operative management before repeat surgery after total hip arthroplasty (THA). The goal of this study was to attempt defining a composite score using conventional clinical, radiological and biological data that can be used to predict the positive and negative diagnosis of peri-prosthetic infection before repeat surgery after THA. The tested hypothesis was that the score thus defined allowed an accurate differentiation between infected and non-infected cases in more than 75% of the cases. Method. 104 cases of repeat surgery for any cause after THA were analyzed retrospectively: 61 cases of infection and 43 cases without infection. There were 54 men and 50 women, with a mean age of 70 ± 12 years (range, 30 to 90 years). A univariate analysis looked for individual discriminant factors between infected and uninfected case file records. A multivariate analysis integrated these factors concomitantly. A composite score was defined, and its diagnostic effectiveness was assessed by the percentage of correctly classified cases and by sensitivity and specificity. Results. The score was defined with the following items which were individually weighted: body mass index (BMI), presence of diabetes (D, yes = 1, no = 0), mechanical complication (MC, yes = 1, no = 0), scar complication after THA implantation (SC, yes = 1, no = 0), fever (F, yes = 1, no = 0). The score was calculated as (0.09 × BMI) + (0.94 × D) − (1.34 × MC) + (17.55 × SC) + (1.22 × F) − 3.63. This composite score separated the infected (positive score) and non-infected (negative score) patients accurately in 78% of cases, with a sensitivity of 57% and a specificity of 93%. Conclusions. Subject to prospective validation, this score could be a significant help to define the medico-surgical strategy during a reoperation of the hip prosthesis for whatever reason. No funding from any part was received for the purpose of this study

Introduction. Few studies are published about total hip arthroplasties (THA) in Parkinson's disease as it is often considered as a contraindication for hip replacement. THA for fracture is reported as a high complication rate surgery. Regarding bone quality these cases are assimilated to elderly patients and cemented implants are generally preferred. However, due to the improved length and quality of life, we face more potential indications for joint replacement. The aim of this study is to report our experience of cementless dual mobility implants for primary THAs for osteoarthrosis and THA revisions focusing on the risks and benefits of surgery. Material and methods. 65 THA were performed in 59 patients (34 men, 25 women, mean age 73 years, 55–79). Mean latest follow-up was 8,3 years (4–14). Indications were 42 primary THA (osteoarthrosis) and 21 revisions (11 recurrent dislocation, 6 acetabular PE wear, 4 femoral loosening). Surgical approach was always antero-lateral. All patients were implanted with the same dual mobility cementless cup. The same cementless corail-type stem was used for primary THA cases. All the cemenless implants were hydroxyapatite coated. The disability caused by the disease was classified according to Hoehn and Yahr. (19 stage 1, 21 stage 2,16 stage 3). Results. 2 patients were lost for follow-up before 2 years. general complications were 3 pulmonary infection, 7 urinary tract infection, 12 cognitive impairment and 2 sacral pressure ulcer. A post-op. wound infection (E Coli) required an early revision in 2 cases without secondary consequencies (7 and 9 years follow-up). We did not observe early or late THA dislocation except in one case at 9 years follow-up (intraprosthetic dislocation due to an increase of ilio psoas muscle retraction requiring a revision of the dual mobility mechanism). We did not observe loosening cases of the cementless cup. 4 patients fell and fractured the femur. The cementless cup was not affected. 10 patients died. Good to excellent pain relief was achieved in 53/57cases at 2 years and in 40/47 cases at latest follow-up. The progression of neurological disability was observed in most of cases. At the latest follow-up for the 47 remaining patients, we had 5 stage 1, 12 stage 2, 21 stage 3,9 stage 4. Discussion. According to literature infection and dislocation are the main concerns for THA in Parkinson patients. This study does not report any trauma cases; this may explain the rather good results on a mean follow-up to more than 8 years. Nevertheless progression of Parkinson's disease is the rule, with significant disability or even death (10 /57 cases). Cementless fixation is possible even on the acetabular side. The poor bone quality of these patients was not an argument against hydroxyapatite coated implants. Conclusion. THA in Parkinson's disease is a challenging surgery due to associated comorbidity. For all patients the functional status improved in the early follow-up and declined with the disease progression. Cementless dual mobility cups and femoral stems can be used with a very low rate of mechanical complication

INTRODUCTION. The diagnosis of peri-prosthetic infection may be difficult. But this diagnosis can guide antibiotic prophylaxis and implementation of intraoperative bacteriological samples. The hypothesis of this study was that a composite score using clinical, radiological and biological data could be used for positive and negative diagnostic of infection before reoperation on prosthetic hip or knee. MATERIAL. 200 reoperations on hip and knee arthroplasty for any cause were analyzed retrospectively. 100 cases concerned infected cases, while the diagnosis of infection was excluded in the other 100 cases. METHODS. Different criteria were collected: previous surgery of the operated joint, clinical, biological and radiological signs. Univariate analysis investigated the discriminating factors of infected and non infected cases. Multivariate analysis integrated concomitantly these factors. A composite score was defined, and its diagnostic efficacy was assessed by the percentage of the total variance explained by the score, by the percentage of correctly classified cases and by the sensitivity and specificity. RESULTS. The univariate and multivariate analyzes have isolated the following significant factors: body mass index, diabetes, prosthetic mechanical complication, fever, existence of a wound defect. The composite score so defined allows separating the infected and non infected patients accurately in 78% of cases, with a sensitivity of 57% and a specificity of 93%. DISCUSSION. The composite score defined predicts infection or no infection in the prosthetic joint before reoperation with good efficiency. This score could be a significant help to define the medical and surgical strategy in a prosthetic hip or knee reoperation for whatever reason. CONCLUSION. A prospective study is needed to confirm definitively the contribution of this score

Introduction. The reconstruction of the knee in growing children considers many options and the chosen solution is often patient (or surgeon) based. Megaprostheses represent a reliable solution but quite expensive in the non-invasive growing version and not free from complications. In an Italian reference center for Bone and Soft tissue sarcomas, following the experience of Rizzoli Institute in Bologna, we performed the reconstruction with a resurfaced allograft for the distal femur or the proximal tibia in selected patients. The aim of the study is to confirm the reliability of this technique and to identify its potential advantages and indications. Methods. Among 60 children below 16 years old with bone sarcomas (39 osteosarcomas, 21 Ewing's sarcomas, age range 4–16) treated since 2007, 35 cases were around the hip and the knee. 7 pediatric knees (age range 5–12 ys) with the tumor involving the epiphysis were reconstructed using a resurfaced allograft for distal femur (2) or proximal tibia (6) leaving intact the other half of the joint. Functional outcome (MSTS score), complication rate, and oncologic follow up were evaluated. Results. Oncologic follow up has been regularly conducted (range 2–9 years). No patient died of disease or developed a local recurrence. Two patients are alive with stable lung disease. Mean MSTS score was 32. No complications such as delayed union at the junction allograft-host bone, segmental deformities, fractures of the allograft, or infection have been observed. No prosthesis-related complications occurred. One limb length discrepancy with secondary scoliosis and 2 requiring a contralateral epiphysiodesis were also observed. Conclusions. In children older than 12 years old and with an expected lower limb discrepancy within 5 cm an adult megaprostheses eventually oversized is the gold standard; in children younger than 6 years old with an expected limb discrepancy longer than 10 cm the big choice is between an amputation (conventional or rotantionplasty) or a temporary reconstruction for the future implant of a growing megaprostheses. In the range 6–12 years old with an expected limb length discrepancy of 5–10 cm one of the options is the resurfaced allograft. It has been found a reliable solution in our case series with an excellent functional result probably derived from the capsule and ligaments reconstruction. Applying this protocol we observed a low mechanical-implant related complication rate. Comparing our results to Literature data of other techniques (induced membrane technique, distraction epiphysiolisis, custom-made or growing prostheses) we observed a lower reintervention rate. It is not possible to evaluate the infection rate among the different techniques used because of the low number of cases. A revision with a conventional first implant or revision total knee arthroplasty is always feasible reducing mechanical complications from megaprostheses. Further studies with longer follow up are mandatory to obtain an international consensus on reconstructive techniques in children with bone sarcomas around the knee

Utilising the (ACS-NSQIP) database, we aimed to evaluate the impact of resident level of training on surgical outcome following (TKA) and to compare the US and Canadian health care training system in regards to 30 days postoperative complications and readmission rates. Using the (CPT) codes we selected from the 2011 and 2012 NSQIP database elective primary TKA with the resident surgeon involved. Of these, all cases with a primary diagnosis code of infection, fracture, mechanical complication, or malignancy and all cases with incomplete or incongruous demographic information were excluded. We also eliminated all the cases with the Attending not present. A total of 2513 cases were included in the study. The cases were stratified into three groups according to the postgraduate level of training {PGY 1 to 3 (junior resident), PGY 4 to 5 (senior resident), and fellow}. Univariate analysis of all patient demographics, comorbidities, intra and postoperative variables, length of surgery, hospital stay and 30 days readmission rates were conducted in order to identify differences between the groups. A standard student's t test was used for continuous variables while the ChiSquared was used for categorical variables. Multivariable logistic regression models were created to assess the independent effect of the resident level of training on the 30 days major complication and re-admission rates while controlling for all other variables. We identified, 854 (34%) TKAs with junior residents, 1013 (40%) TKAs with senior residents and 646 (26%) TKAs with fellows' participation. Junior residents had a significant (p<0.0001) longer operative time (107±36 minutes) compared with senior residents and fellows. Length of hospital stay was longer in the fellow group probably because of their involvement in more complicated cases. Additionally, an increased number of blood transfusion was observed for the cases performed with involvement of senior residents when compared with the other two groups. However, no significant difference in complications was observed across training levels. When comparing US (2074 TKAs) versus Canada (423 TKAs) cases, we found that fellow contribution to TKA surgeries is higher in Canada. The occurrence of pulmonary embolism and pneumonia was three times higher in Canada cases, while blood transfusion was more frequent in US. Increased operative time, ASA class, age, diabetes, percutaneous cardiac intervention, and steroid use were all independent risk factors for complications following primary TKA. However, no significant difference was observed between the two groups with regards to major complications suggesting no difference between Canadian and American training system in regards to post operative complication. Our results support previous study study indicating that involvement of residents did not affect the surgical outcome within 30 days when compared to cases with no resident involvement. Our study suggests that resident level does not independently increase the risk of short term complications and support continuing involvement of junior trainees in TKA

Introduction. Dislocation due to suboptimal cup positioning is a devastating complication in the early phase after total hip arthroplasty. Malpositioning can also result in other mechanical complications like subluxation, edge loading, increased debris, surface damage or squeaking in ceramic-on-ceramic hips. Preventing at least some of these complications in younger and more active patients is of paramount interest for the individual patient and for the society since optimized component orientation is an important determinant to reduce such risks and to further increase longevity of the implant. This study reports on two new surgical instruments that help the orthopedic surgeon to manually place both components within the optimized combined safe-zone (cSafe-Zone). Material and Methods. More than 900 minimal-invasive total hip arthroplasties (MIS-THA) have been performed between 2007 and 2015 in our institution using the minimal-invasive direct anterior approach (DAA) on an orthopedic table with foot holder. Cups were implanted applying the “stem-first” surgical technique i.e. the prosthetic stem dictates the orientation of the socket depending on the prosthesis design. A system-specific trial head which indicates the prosthesis-specific relative orientation of cup and stem and a modified cup impactor were used to finally seat the definitive acetabular socket manually during trial stem reduction while fully visually controlling the optimal orientation of the cup during impaction. This surgical technique drives both components into their optimal relative positions according to the combined version and the combined safe-zone concept in total hip arthroplasty. Results. Both new instruments, femoral trial head as well as the modified cup impactor, provide an easy way to manually control the optimal placement of the acetabular socket during impaction intraoperatively. The combined safe-zone is clearly indicated and the inverse interrelationship of stem and cup anteversion is ideally reflected by this simple mechanical system. In patients operated on with the “stem-first” technique the components were placed in the new cSafe-Zone in 94% of the cases and no squeaking or prosthetic impingement did occur in any of these patients. One early dislocation did occur and was treated by closed reduction. Conclusion. Stem-first technique using trial head-controlled impaction with a modified cup impactor is ideally suited for the minimal-invasive direct anterior approach in total hip arthroplasty to control the placement of both prosthetic components. It assists the surgeon in aligning the cup and the stem according to the cSafe-Zone in order to get the intended range of movement (iROM)

Component placement and the individual's functional posture play key roles in mechanical complications and hip dysfunction after total hip arthroplasty (THA). The challenge is how to measure these. X-rays lack accuracy and CT scans increase radiation dose. A newer imaging modality, EOSTM, acquires low-dose, simultaneous, perpendicular anteroposterior and lateral views while providing a global view of the patient in a functional standing or sitting position, leading to a 3D reconstruction for parameter calculation. The purpose of the present study was to develop an approach using the EOS system to compare patients with good versus poor results after THA and to report our preliminary experiences using this technique. A total of 35 patients were studied: 17 with good results after THA (G-THA), 18 with poor results (P-THA). The patients were operated on or referred for follow-up to a single expert surgeon, between 2001 and 2011, with a minimum follow-up of at least two years. Acetabular cup orientation differed significantly between groups. Acetabular version relative to the coronal plane was lower in P-THA (32°±12°) compared to G-THA (40°±9°) (p=0.02). There was a strong trend towards acetabular cup inclination relative to the APP being higher in P-THA (45°±9°, compared to 39°±7°; p=0.07). Proportions of P-THA vs. G-THA patients with cup orientation values higher or lower than 1 SD from the overall mean differed significantly and substantially between groups. All revision cases had a least four values outside 1 SD, including acetabular cup orientation, sagittal pelvic tilt, sacral slope, femoral offset and neck-shaft angle. This is the first study to our knowledge to provide acetabular, pelvic and femoral parameters for these two groups and the first to provide evidence that a collection of high/low parameters may together contribute to a poor result. The results show the importance of acetabular component placement, in both inclination and version and the importance of looking at individuals, not just groups, to identify potential causes for pain and functional issues. With the EOS system, a large cohort of individuals can be studied in the functional position relatively quickly and at low dose. This could lead to patient-specific guidelines for THA planning and execution

Several risk factors can and should be addressed during first stage or spacer implantation surgery in order to minimize complications. Technical aspects as well as practical tips and pearls to overcome common nuisances such as spacer instability or femoral and acetabular bone loss will be discussed and shown with pictures. Total joint arthroplasty (TJA) is one of the most successful procedures in orthopaedics and excellent results are expected in virtually all cases. Periprosthetic joint infection (PJI) though unusual, is one of the most frequent and challenging complications after TJA. It is the third most common cause of revision in total hip replacement, responsible for up to 15% of all cases. In the past few years several improvements have been made in the management of an infected total hip prosthesis. Nevertheless it remains a challenging problem for the orthopaedic surgeon. Although numerous studies report favourable outcomes after one-stage revision surgery, two-stage has traditionally been considered as the gold standard for management of chronic infection. Two-stage exchange consists of debridement, resection of infected implants and usually temporary placement of an antibiotic-impregnated cement spacer before reimplantation of a new prosthesis. Spacers can be classified as static or articulating. The goals of using an articulating antibiotic loaded cement spacer are two-fold: to enhance the clearance of infection by local antibiotic therapy and dead-space management while maintaining joint function during treatment thus improving the functional outcome at reimplantation. Still, hip spacer implantation is not innocuous and there are several possible complications. Going forward, one must consider not just eradicating infection but also the importance of restoring function. In this regard using a mobile spacer adds an element of physiologic motion that both increases patient comfort between stages and facilitates re-implantation surgery. Conversely, mechanical complications are one of the major consequences of this preference. Be that as it may there are ways to minimize these problems. It is the surgeon responsibility to optimize mechanical circumstances as much as possible. I would like to thank Dr. Ricardo Sousa for his help with this work