Introduction. Ultra-high molecular weight polyethylene (UHMWPE) is the sole polymeric material currently used for weight- bearing surfaces in total joint replacement. However, the wear of UHMWPE in the human body after total joint replacement causes serious clinical and biomechanical reactions. Therefore, the wear phenomenon of UHMWPE is now recognized as one of the major factors restricting the longevity of artificial joints. In order to minimize the wear of UHMWPE and to improve the longevity of artificial joints, it is necessary to clarify the factors influencing the wear mechanism of UHMWPE. Materials and Methods. In a previous study (Cho et al., 2016), it was found that roundness (out-of-roundness) of the retrieved UHMWPE acetabular cup liner [Figure 1(a)] had a tendency to increase with increasing roundness of the retrieved metal femoral head [Figure 1(b)]. It appears that roundness of the femoral head contributes to increase of wear of the polyethylene liners. We focused on the roundness of femoral head as a factor influencing the wear of polyethylene liner in hip prosthesis. In this study, further roundness measurements for 5 retrieved metal femoral heads were performed by using a coordinate measuring machine. The elasto-plastic contact analyses between femoral head and polyethylene liner using the finite element method (FEM) were also performed in order to investigate the influence of femoral head roundness on the mechanical state and wear of polyethylene liner in hip prosthesis. Results. The range of roundness of the 5 retrieved metal femoral heads measured in this study was 14.50∼44.70 µm. Two examples of the results of FEM contact analyses are shown in Figure 2. Figure 2(a) is the results of the repeated contact analysis between femoral head and polyethylene liner under constant axial loading of 1000 N. Figure 2(b) is the results of the repeated contact analysis between femoral head and polyethylene liner under hip joint loading during normal gait. These figures show the distribution of the contact stress (von Mises equivalent stress) in the polyethylene liner. The graph in Figure 3 shows the changes in the maximum contact stress in the polyethylene liner with the flexion/extension angle of femoral head. Discussion and Conclusions. As the results of a series of the FEM contact analyses, it was found that repeated high contact stresses which exceed the yield stress of UHMWPE caused by roundness of the metal femoral head occurred in the polyethylene liner as shown in Figures 2 and 3. It was also found that the magnitude and amplitude of the repeated contact stresses had a tendency to increase with increasing roundness of the femoral head and axial loading applied to the femoral head. The results of this analytical study suggest that the roundness (out-of- roundness) of the femoral head is associated with accelerating and/or increasing wear of the UHMWPE acetabular cup liner in a hip prosthesis after total hip replacement. For any figures or tables, please contact authors directly

Introduction. Ultra-high molecular weight polyethylene (UHMWPE) is the sole polymeric material currently used for weight- bearing surfaces in total joint replacement. However, the wear of UHMWPE and the polyethylene wear debris generated in the human body after total joint replacement cause serious clinical and biomechanical reactions. Therefore, the wear phenomenon of UHMWPE in total joint replacement is now recognized as one of the major factors restricting the longevity of these implants. In order to minimize the wear of UHMWPE and to improve the longevity of artificial joints, it is necessary to clarify the factors influencing the wear mechanism of UHMWPE. Materials and Methods. The wear and/or failure characteristics of 33 retrieved UHMWPE acetabular cup liners of hip prostheses were examined in this study. The retrieved liners had an average in vivo duration of 193.8 months (75 to 290 months). Several examples of the retrieved liners are shown in Figure 1. The elasto-plastic contact analyses between metal femoral neck and polyethylene liner and between metal femoral head and polyethylene liner using the finite element method (FEM) were also performed in order to investigate the factors influencing the wear and/or failure mechanism of the polyethylene liner in hip prosthesis. Results. In the examination of the retrieved polyethylene liners, the generation of component impingement was observed in 24 cases of the 33 retrieved liners (72.7%) as shown in Figures 1(a) and (b). In addition, the generation of cold flow into the screw holes in the metal acetabular cup was observed in 27 cases of the 33 retrieved liners (81.8%) as shown in Figures 1(c) and (d). Several examples of the results of the FEM contact analyses are shown in Figure 2. In the simulation of the component impingement, it was found that high contact stresses which exceed the yield stress of UHMWPE and considerable plastic strains occurred in the rim of the polyethylene liner as shown in Figures 2(a) and (b). In the simulation of the cold flow, it was found that the stress concentration near the edge of screw hole has significant influence on the states of contact stresses and plastic strains in the surface and undersurface (backside) of the polyethylene liner as shown in Figures 2(c) and (d). Discussion and Conclusions. In this study, we focused on the impingement between the metal femoral neck and the polyethylene liner and the cold flow into the screw holes on the backside of the polyethylene liner as the factors influencing the wear and/or failure of the UHMWPE acetabular cup liner in hip prosthesis. The results of these retrieval and analytical studies confirmed that the component impingement and the cold flow into the screw holes contribute to increase of wear and/or failure of the polyethylene liner. Therefore, it is necessary to improve resistance to the component impingement and the cold flow in order to decrease the wear and/or failure of the UHMWPE acetabular cup liner and to increase the longevity of hip prosthesis. For any figures or tables, please contact authors directly

Introduction. Ultra-high molecular weight polyethylene (UHMWPE) is the sole polymeric material currently used for weight- bearing surfaces in total joint replacement. However, the wear of UHMWPE in knee and hip prostheses after total joint replacement is one of the major restriction factors on the longevity of these implants. In order to minimize the wear of UHMWPE and to improve the longevity of artificial joints, it is necessary to clarify the factors influencing the wear of UHMWPE. A number of studies have investigated the factors influencing the wear of UHMWPE acetabular cup liner in hip prosthesis. Most of these studies, however, have focused on the main articulating surfaces between the femoral head and the polyethylene liner. Materials and Methods. In a previous study (Cho et al., 2016), the generations of cold flow into the screw holes in the metal acetabular cup were observed on the backside of the retrieved UHMWPE acetabular cup liners as shown in Figure 1. We focused on the screw holes in the metal acetabular cup (Figure 2) as a factor influencing the wear behavior of polyethylene liner in hip prosthesis. In this study, computer simulations of the generation of cold flow into the screw holes were performed using the finite element method (FEM) in order to investigate the influence of the screw holes in the metal acetabular cup on the mechanical state and wear behavior of polyethylene liner in hip prosthesis. Results. An example of the results of the FEM simulations performed in this study is shown in Figure 3. In the region which the cold flow into the screw holes occurred, it was found that locally high contact stresses which exceed the yield stress of UHMWPE and considerable plastic strains were generated throughout the overall thickness between the backside and top surface of the polyethylene liners. On the contrary, in the case of the polyethylene liner combined with the metal acetabular cup without screw hole, although the regions of high contact stress and high plastic strain had a tendency to be limited around contact surface compared with those of the combination with screw holes, the values of contact stress and plastic strain were lower than the combination with screw holes. Discussion and Conclusions. The results of this study suggest that the cold flow generated by the existence of the screw holes in the metal acetabular cup of hip prosthesis reduces the wear resistance of the UHMWPE acetabular cup liner. It would appear that the cold flow into the screw holes contributes to structural weakening of the UHMWPE and reduction of the polyethylene thickness, thus increase of internal stresses and plastic strains in and around the regions of cold flow. Therefore, it is required that improvement of the screw holes in the metal acetabular cup and/or improvement of fixation method of the metal acetabular cup to a pelvis in order to enhance the wear resistance of the polyethylene liner. For any figures or tables, please contact authors directly

The accurate differentiation of aseptic loosening from periprosthetic infection in the painful hip prosthesis is a major clinical challenge. FDG-PET imaging has shown great promise in various clinical settings for detection of infection. This prospective study was designed to determine the efficacy of FDG-PET imaging in the assessment of patients with painful hip prosthesis. One hundred and thirteen patients with 127 painful hip prostheses were evaluated by FDG-PET. Approximately 60 minutes after the intravenous administration of FDG images of the lower extremities were acquired using a dedicated PET machine. FDG-PET images were interpreted by experienced nuclear medicine physicians. Images were considered positive for infection if PET demonstrated increased FDG activity at the bone-prosthesis interface of the femoral component of the prosthesis. Surgical findings, histopathology, and clinical follow-up served as the “gold standard”. FDG-PET was positive for infection in 35 hips and negative in 92 hips. Among 35 positive PET studies, 28 were proven to be infected by surgical and histopathology findings as well as follow-up tests. Of 92 hip prostheses with negative FDG-PET findings, 87 were proven to be aseptic. The sensitivity, specificity, positive and negative predictive values for FDG-PET were 0.85 (28/33), 0.93 (87/94), 0.80 (28/35), and 0.95 (87/92), respectively. The overall accuracy of FDG-PET in this clinical setting was 90.5% (115/127). The results demonstrate that FDG-PET is a highly accurate diagnostic test for differentiating infected from non-infected painful hip prosthesis. Therefore, FDG-PET imaging is considered the study of choice in the evaluation of patients with suspected hip prosthesis infection

Background: Revision total hip replacement is challenging when there is severe proximal bone loss. The Kent hip femoral prosthesis – a distally locked femoral stem – was designed to overcome this difficulty, however no study to date has assessed its durability. Methods: We independently reviewed the results of 105 Kent Hip Prostheses used at one hospital between 1987 and 2000. The indication for revision was aseptic loosening in 64, periprosthetic fracture in 19, septic loosening in 4, and severe bony deformity in 14. In the remaining 4 cases, a Kent hip prosthesis was inserted in the presence of metastatic tumour in the proximal femur to enable mobilisation. A functional evaluation of these patients using the Oxford Hip Score and a survival analysis of the stems was performed. Results: The mean duration of follow-up was 5.3 years (range 20 months to 15 years). The mean time to full weight bearing following surgery was 4 days and mean hospital stay was 13 days. Almost all patients experienced substantial improvement in hip related pain and disability (as measured by the Oxford Hip Score). 12 stems required further revision. Taking removal of the stem for any cause as the end point, cumulative survival at 15 years was 88%. Conclusions: Cumulative survival rates for the Kent hip femoral prosthesis compare favourably with other revision stems used where there is severe proximal bone loss. It enables early full weight bearing and hospital discharge, resulting in a low post-operative medical complication rate. However the need for continuing follow-up remains, since the rate of complications such as locking screw fracture, aseptic loosening, and periprosthetic fracture, may increase in the future

The Huckstep ( Bbraun Medical) interlocking hip prosthesis has been used in the Sheffield Lower Limb Arthroplasty Unit in cases of complex primary and revision hip arthroplasty since 1996. We reviewed the outcomes in cases performed prior to October 2001. Eighty cases were identified. Of these, eight died within one year of surgery, four of which were in the peri operative period. A further thirteen were lost to follow up in the first year due to medical deterioration, move from area or refusal to attend. The remaining 57 patients had a mean time to follow up of 34 months (12–81m). As a primary prosthesis the Huckstep was used to allow corrective osteotomy. In revision cases it was employed to bypass periprosthetic fractures and fragile proximal femoral bone, in cases requiring extended trochanteric osteotomy to facilitate cement removal, and to enable use of bulk proximal femoral allograft. The use of the Huckstep was planned pre operatively in 67 cases and as a salvage option in 13.The design of the implant allowed a stable construct without the need for bone cement which could interpose and prevent bone healing or graft incorporation. It avoids problems incurred in pressurising cement or impaction grafting against fragile bone. Complications included infection requiring further surgery (5), dislocation (5), periprosthetic fracture (2), screw breakage (4), and mechanical failure (2). Eleven patients required further revision surgery. The apparently high complication rate reflects the complex nature of the surgery and the high degree of co morbidity in the elderly patient group. In conclusion, we have found the Huckstep hip prosthesis to be a useful option in cases of complex hip surgery. Whilst the long term outcome is as yet unknown, our short term results show it to have allowed healing of fractures, osteotomy sites and cortical defects, allograft incorporation and replenishing of bone stock, hence facilitating further arthroplasty surgery

Introduction. After total hip arthroplasty, dislocation is one of the most frequent serious early complications. This occurs in part due to impingement (catching and leverage of the neck-cup on the inlay/cup border). Impingement may also negatively impact long-term outcomes. Materials and Methods. A preliminary model for an optimised hip endoprosthesis system was developed to offer a mechanical solution to avoid impingement and dislocation. A computer-supported range of motion simulation using parameters of cup anteversion and inclination as well as torsion and CCD shaft angle was then performed to localise areas of anterior and posterior impingement of typical acetabular cups. Results. Through isolation of the two main trajectories of motion, and modifications with corresponding gaps to the inlay/cup areas as well as oppositional banking in the abduction/adduction plane, the combination of a snap-fit acetabular cup with reduced cup profile was the result: the “bidirectional total hip prosthesis.”. Under standardised parameters, the ranges of impingement for typical implants are not directly opposite one another (at 180°), but are found instead at an angle of 108.3°. Conclusion. Complications such as dislocation and impingement may possibly be avoided with the bidirectional total hip prosthesis. Typical implantation parameters yield an implant design with rotational asymmetry. [Fig. 1, 2]

Fracture of the femur in association with total hip arthroplasty is a challenging complication that has been well described. A variety of surgical treatment options have been reported. We present our experience of the Kent hip prosthesis in the management of periprosthetic femoral fractures. We reviewed all patients (46) who had a Kent hip inserted for a periprosthetic femoral fracture. This group consisted of 16 males and 30 females of average age 73 years (43–96 years) at the time of fracture. Follow up ranged from 2 to 85 months (average, 4 years). In 26 cases the primary prosthesis was a Charnley stem. Of the remaining cases the primary prostheses were as follows: 6 Austin Moore prostheses, 5 Howse, 4 Custom, 1 Exeter, 1 DHS, 1 Richards and 1 Thompson stem. There were 6 intraoperative fractures. Of the postoperative fractures forty-four were associated with a traumatic event. Time to fracture varied from 3 weeks to 20 years (average, 8 years). Prior to fracture 42 patients were living in their own home and 24 patients were mobile unaided. Twenty patients had pain prior to their fracture. The majority of patients were deemed ASA grade II or III. Thirty fractures were Johanssen type II, 14 type I, and 2 type III. At the time of surgery, 32 patients had a loose stem and/or cup. Operating time was on average 143 minutes (range, 65–235 minutes) and intraoperative transfusion requirements ranged from 0–7 units of packed red cells (average, 3 units). Duration of hospital stay was on average 23 days (range, 7–77 days). Two patients developed superficial wound infections, six patients dislocated their prosthesis and one patient developed a chronic wound sinus. In 34 cases fracture union was complete at latest review. Three patients required revision surgery for stem breakage and in 10 cases there was evidence of screw breakage. At latest review, of the 31 patients that could be contacted 18 are still resident in their own homes. Twenty-six patients require the use of a walking aid (most commonly one stick). Ten patients have ongoing pain in relation to their operated hip. In conclusion, we feel that the Kent hip prosthesis is a useful surgical option in the one-stage management of periprosthetic femoral fractures

We report the result of 46 patients (30 female, 16 male) with periprosthetic femoral fractures who underwent insertion of the Kent Hip Prosthesis. Average age was 73 years (range 43–96years) and follow-up ranged from one to seven years (average, 4 years). The primary implants involved were as follows: Charnley (26), Austin Moore (6), Howse (5), Custom (4), Exeter (1), DHS (1), Thompson (1) and Richards (1). Average time to fracture from insertion of the primary implant ranged from 3 weeks to 20 years (average, 8 years). Forty cases were post-primary implant fractures (38 traumatic, 2 atraumatic) and 6 occurred intraoperatively. Using the Johanssen classification there were 12 type I, 30 type II and two type III fractures. Of the 46 cases, prior to fracture, 42 were living in their own home, 24 were mobile unaided and 20 had thigh and/or groin pain. Thirty-two had a loose stem and/or cup assessed at the time of surgery. Operating time was on average 143 mins (65–235mins). At latest follow-up, 43 were living in their own home, 5 were walking unaided and 10 had ongoing pain. In 34 cases complete union was achieved. There were no cases on non-union. Three patients required revision surgery for broken stems. Three patients sustained wound infections and there were six posterior dislocations. All of the complications were treated satisfactorily. We conclude that the Kent Hip Prosthesis is a useful option in the management of periprosthetic femoral fractures

Introduction. This study reports outcomes of 35 revisions of a recalled metal-on-metal (MOM) monoblock prosthesis performed by a single surgeon. Methods. We prospectively collected data on all patients who underwent revision of a recalled metal-on-metal monoblock prosthesis between 2010 and 2015. Average follow-up was 2.5 years post-revision and 6.9 years post-primary procedure. We evaluated the cohort for age, BMI, gender, existence of medical comorbidities, and post-op complications. We compared pre and post-revision cup abduction angles, anteversion angles, combined angles, cup sizes, and Harris Hip Scores. Cobalt and chromium levels were followed throughout the study period for each patient. Results. Thirty-one patients underwent 35 revisions surgeries for pain, high metal ions, infection, aseptic loosening, failure of ingrowth, leg length discrepancy and/or pseudotumor. Two of these revisions were subsequently re-revised – one for continued pain and one for failure involving multiple dislocations, breakage of screws, and acetabular fracture. The survival rate for our revisions to date is 94.3%. Female patients comprised a majority of revisions (54%) despite comprising a minority (28%) of primary hip replacements using the studied prosthesis. Revised patients were an average of 51.8 years of age with a BMI of 31.07. Demographics are included on Table 1. There were five post-operative complications, including 2 infections, 2 dislocations, and one DVT. Cups were revised from a mean abduction angle of 47.5° in primary hips to 42.3° in revisions. Cups were revised from a mean of 53.4 to 57.8. Cobalt and chromium levels were followed in all patients and showed significant decrease after revision (Graph 1). Cobalt levels decreased from an average of 33.7 to 13.1 ng/mL while Chromium levels decreased from an average of 12.4 to 9.2 ng/mL. Harris Hip Scores increased significantly after revision (45.8 to 72.1). Conclusion. This study presents 35 revisions of a recalled monoblock hip prosthesis performed by a single surgeon at our institution from 2010 to 2015. To our knowledge, this is the largest single-surgeon study reported in the literature. Acetabular cups were revised to a lower average abduction angle. Patients have had significant improvements in Harris Hip Scores and significant decreases in Cobalt and Chromium levels after revisions. Our revision survival rate to date is 94.3% at an average of 2.5 years (range 2 weeks – 4.3 years). To view tables/figures, please contact authors directly

Previous scientific studies have highlighted how coupling is an important element affecting total hip arthroplasty's survival.

This study aims to evaluate whether metal-on-metal (MOM) coupling could be a statistically significant risk factor.

The data from the regional joint registry (Registro dell'Impiantologia Protesica Ortopedica, RIPO) was used for analysis. The data collection accuracy of this registry was 97.2% in 2017.

We retrospective evaluate all MOM total hip arthroplasties (THAs) implanted in our department between January 01st 2000 and December 31st 2011. We used a control group composed by all other prosthesis implanted in our Department in the same time lapse.

We registered 660 MOM THAs. Mean age of patients was 66.9 years. 603 patients have a >36mm head, while 78 a <36 mm one. Neck modularity was present in half of patients. 676 implants were cementless. We registered 69 revisions, especially due to aseptic mobilization (16 THAs), implant breakage (9 THAs) and periprosthetic fracture (6 THAs).

The MOM THAs overall Kaplan-Meier survival rate was 87.2 at 15 years, and the difference between MOM THAs and other implants two curves is statistically significant (p<0.05). Male sex is a significant risk factors. Further evaluations are in progress to establish the presence of any additional risk factors. We think weight and/or BMI may be included in this category.

Our study confirms the data currently present in the literature regarding a lower survival of metal-on-metal hip prostheses.

The male sex is a statistically significant risk factor (p<0.05), while age, head size and modularity of the prosthetic neck are not statistically significant (p>0.05).

Any new finds will be presented at the congress venue.

Nine cases of acetabular erosion following insertion of the Monk "hard top" hip prosthesis for subcapital fractures are presented. All of these patients had significant symptoms and represented 5% of the total group. In our experience acetabular erosion has proved to be a significant complication of the Monk "hard top" prosthesis

Elderly patients with a high mortality risk for revision surgery are severely handicapped by a loosened hip prosthesis. Loosening is mainly caused by particle-induced osteolysis leading to the formation of a synovium-like interface tissue. As an alternative to revision surgery we have investigated the possibility of removing the tissue using a gene therapy approach and thereafter stabilizing the prosthesis with percutaneous cement injection. First we demonstrated that transduction of interface cells with a gene coding for E.coli nitroreductase (NTR) resulted in a 60-fold increase in sensitivity to the prodrug CB1954 that is converted to a toxic metabolite by NTR. Given these in-vitro data, we explored if intra-articular administration of this adenoviral vector encoding NTR followed by the prodrug was able to kill sufficient tissue in-vivo to allow refixation of the prosthesis by cement. We report the first three patients from a phase 1 study of 12 patients with a loosened hip who are experiencing debilitating pain and have significant comorbidity. On day 1 the vector is injected into the hip joint and on day 3 the prodrug is injected. On day 10 three holes are drilled in the femur and one in the acetabulum. Biopsies are taken from the periprosthetic space and low viscosity cement (Osteopal, Biomet Merck, Sjöbo, Sweden) is injected under fluoroscopic guidance. The first three patients have been included in the study and five more are planned for treatment before June 2005. The patients are females of 86, 72, and 79 years old. There were no adverse effects from vector injection (3x10 exp 9 particles). Six hours after prodrug injection the patients experienced nausea, (WHO grade 1) a commonly reported reaction to this prodrug. There was vomiting in two patients. Hip pain increased, but this was anticipated as this therapy will increase prosthesis loosening. 16 ml of cement was subsequently injected into the periprosthetic space in the first patient and 18 ml in the second. The patients were ambulated the day after surgery. The first two patients have a follow-up of twelve and six weeks. There was no pain in the hip. The maximum walking distance had increased from 5 to 30 meters in the first patient. The current study is the first to use in vivo intra-articular adenoviral mediated gene transfer in a clinical setting. Our preliminary results suggest that gene therapy and cement injection for hip prosthesis refixation is clinically feasible

We report the clinical and operative details of seven cases of fracture of the femoral stem of the Ring TiMESH cementless hip prosthesis (two were cemented and five uncemented). Six fractures occurred in the proximal one-third of the stem and one at mid-stem. The failures are attributed mainly to two defects in stem design, the narrowness of the anteroposterior dimensions and the depth of the recess for the titanium mesh pads. Great difficulty was experienced in removing the osseo-integrated distal fragments of the broken stems

Aims: The authors report oncological and functional results after 15 acetabular reconstructions, followed tumor resection, with an original technique using homo-lateral proximal femoral autograft and total hip prosthesis. Material and method: The modiþed Musculoskeletal Tumor Society Score (MSTS) and the Toronto Extremity Salvage Score (TESS) were used for functional analysis. Functional results were available for only 10 patients who presented with a minimal of 2 years follow-up. Results: Fifteen consecutive patients, 9 men and 6 women with a median age of 50 years, were managed in our department for acetabular bone malignant tumor. The tumors involved the zones II in 5 patients, the zones II and III in 5 patients. The tumors included 10 chon-drosarcomas, 1 malignant þbrous histiocytoma, 1 radio-induced sarcoma, 1 myeloma and 2 metastasis. The mean follow-up was 31 months (Range, 12 to 50 months). Local recurrence occurred in 1 case and metastases in 3 cases. Three patients died of tumoral disease and one of intercurrent disease. Eight complications were observed: aseptic failure (n=1), obturator nerve damage (n=1), deep infection (n=4), skin necrosis (n=2), pros-thesis dislocations (n=1) and deep venous thrombosis (n=1). Five revision were performed. The mean MTS was 72% (range, 40 to 96%) and the mean TESS was 82.5% (range, 56 to 86%). Fusion occurred in all reconstructions and all patients recovered an active hip abduction and ßexion. Discussion: This original technique, using an autograft and a standard total hip prosthesis, is available for zone II and III acetabular reconstructions

A 70-year-old man with an uncemented metal-on-polyethylene total hip prosthesis underwent revision arthroplasty 33 months later because of pain, swelling and recurrent dislocation. There appeared to be corrosion and metal release from the prosthetic head, resulting in pseudotumour formation and severe local soft-tissue destruction. The corrosion occurred at the junction between the titanium-molybdenum-zirconium-iron taper and the cobalt-chrome-molybdenum head, but the mechanism was unproven

Radiographs are often used to determine the varus/ valgus alignment of the prosthesis in relation to the long axis of femur. This is usually considered to be one of the important parameters in predicting early mechanical failure of the total hip replacement. The measurements made by the University of Dundee X-Ray Analysis Software and skilled manual operators of the varus and valgus angulations of hip prosthesis in relation to the femoral shaft were compared for inter and intra-observer reliability. The manual measurements were carried out on the same randomly selected digitised images of 78 postoperative X-rays by two independent observers and by the same analysis software twice. The results of the study showed a very high agreement between the readings of the two methods (the largest difference was 0.6 degrees) and two observers (the largest difference being 0.08 degrees) indicating excellent intra and inter observer reliability. The lowest correlation was 0.82 and this was between software reading 1 of observer 1 and software reading 1 of observer 2. The highest correlation of 0.99 was between software reading 1 and software reading 2 for the same observer. The software analysed the x-rays with precision and accuracy and was much faster than manual measurement. A further benefit of the computerised method is an unskilled operator can be trained in 15 minutes to use the software

Because we encountered a high failure rate of the acetabular component of the uncemented, hydroxy-apatite coated, Omnifit total hip prosthesis (Osteonics corporation, Allendale, NJ, USA), we conducted a retrospective study of 418 consecutive total hip arthroplasties with a mean follow up of 60 months. The results of 418 hydroxy-apatite coated, uncemented Omnifit total hip arthroplasties, conducted between 1989 and 1996 were evaluated. Two different acetabulum cups were used: 145 screwcups with one central screwhole, and 273 press fit (PF) cups with several screwholes. The internal geometry of these cups and the fixation of the polyethylene insert in the metal cups were identical. In 339 arthroplasties a 32-mm femur-head was used, in 79 a 28-mm head. Patients’ records and x-rays were evaluated for clinical findings, polyethylene (PE) wear, acetabular and femoral osteolysis and findings during revision surgery. Revision surgery was performed in 73 patients, mainly because of symptomatic acetabular osteolysis (79%). Mean PE wear was 0.16 mm/year (0.19 mm in PF cups, 0.11 mm in screwcups). Acetabular osteolysis was found to be present in178 hips (70 screwcups and 108 PF cups). In both cupdesigns the osteolysis was mainly found around the screwholes of the metal cups. During revision surgery these osteolytic defects were a lot larger than suggested by x-ray imaging. In 22.6% of the hips osteolysis was also present in the proximal femur. Kaplan-Meier survival analysis showed, after 6 year follow up, a better survival for of the screwcup (96%, confidence interval 93–99%) than the PF cup (66%, 95%CI 56–77%). We hypothesized that this specific combination of metal cup and polyethylene insert -possibly due to an insufficient fitting- is responsible for the migration of polythylene wear particles through the screwholes in the metal cup, causing acetabular osteolysis and neces-satating revision surgery. For this reason we abandonned the use of this type of uncemented acetabular component

Introduction: One of the primary complications in total hip and knee arthroplasty is infection. One of the major risk factors for deep periprosthetic infection is wound infection. This alone is associated with a substantial morbidity-increase which, in turn, increases hospital admittance time and therefore adds significant costs to the healthcare system. The aim of this study is to determine whether contamination of instruments used during primary insertion of a prosthesis, can be considered an early indicator for the occurrence of prolonged wound discharge. Early antibiotic treatment could then prevent this and decrease hospital admittance time and costs to the health care system. Material and Methods: During 121 procedures, swabs were taken from the first unused broach at the beginning and at the end of the procedure. Removed material from the bone (acetabulum and femur in the hip joint; femur and tibia in case of the knee joint) was tested for contamination as well. During 50 procedures a control swab was taken. The patients on the ward were also monitored to find out whether prolonged wound discharge occurred and to see after how many days the patients were discharged. Results: In 46 cases (38%) at least one culture showed microbial growth. In the other 75, there was no growth at all. If one of the cultures is positive, there is a 52% risk of prolonged wound discharge. Ifall cultures are negative, this risk is reduced to 13% (Chi-square: PO.001). Patients with a positive peroperative culture have to remain in the hospital for an additional 2.4 days (T-test: P-0.001). Conclusion: Peroperative culturing during primary insertion of a knee or hip prosthesis, provides a reliable tool to predict postoperative duration of wound discharge and hospital-admittance time

Introduction. Total hip arthroplasty in young patients is still associated with high failure rates, especially at the acetabular side. Purpose of this study was to evaluate the long-term results of the Alloclassic cementless Zweymüller total hip prosthesis in patients younger than 50 years at the time of surgery. Methods. Between 1987 and 1994, 73 Zweymüller total hip arthroplasties with a titanium threaded cup were placed in 67 patients younger than 50 years. Mean age at surgery was 43 years (23–49 years). Patients were followed clinically with use of the HHS, revisions were determined and radiographs were analyzed. Kaplan-meier analysis was used to determine survival for different endpoints. Results. Three hips were revised for septic loosening, 3 cups for aseptic loosening and 1 hip because of periprosthetic fracture. Four patients (4 hips) died and 8 patients (9 hips) were lost to follow-up without any revision. 48 patients with 53 prostheses could be evaluated after a mean follow-up of 208 (170–253) months and the mean HHS was 90 (52–100). Cumulative survival analysis with endpoint revision for any reason was 89% (C.I. 85–93) at 17 years. With endpoint aseptic loosening, survival was 95% (C.I. 91–98) at 17 years. Conclusion. Alloclassic Zweymüller total hip arthroplasty with a titanium threaded cup showed good long-term results, even in this group of patients younger than 50 years

The ABG total hip prosthesis had been studied to prevent any kind of stress shielding and to allow the localization of the loads in the metaphiseal region of the femur. The aim of this study was to analize the effective behaviour of the loads in long-term implants and the possible correlations of those findings with the clinical situation of the patients. We considered 87 total hip arthroplasty implants executed from 1989 to 1995 and performed by using Anatomique Benoist Girard I uncemented prosthesis. The radiographical findings have been classified observing Engh’s stability criteria according to Gruen’s subdivision of the periprosthetic femoral zones. The radiographical analysis shows a higher presence of can cellous densification in Gruen’s zones 3 and 5 than the one found in zones 2 and 6. Furthermore the presence of a cortical reaction is more relevant in the distal zones.> Radiolucent lines are present in 16% of the cases in zone 4; their percentage in zones 3 and 5 decreases to 7.14% and 10.71%. Our study shows the certain presence of the stress shielding mechanism in long-term analysis and documents that the main region of late anchorage is the distal, not hydroxyapatite-coated, one.> The comparison with other similar studies shows the decrease of the presence of radiolucent lines in proximal femoral zones with the rise of the follow-up: it can be interpreted as the lesser presence of micro movements of the tip of the prosthesis due to the distalization of the anchorage

Purpose: The surgical approach is an essential element for precise reduction and rigid fixation of fractures of the acetabulum. In cases where the anterior column is mainly involved and total hip arthroplasty (THA) is indicated, classical approaches do not allow double assess to the anterior column necessary for reduction and fixation and to the femoral canal for insertion of the prosthesis. Combining Heuter’s anterior approach and Letournel’s ilio-femoral approach provides access to the anterior column and to the often associated posterior hemi-transverse fracture, while allowing insertion of the total hip prosthesis. Material and method: This combined approach was used for ten among 60 THA performed for fracture of the acetabulum. Seven were primary procedures and three were differed reconstruction procedures. Mean patient age was 60.6 years (range 50 – 85 years). Fracture types were: acetabular wall and anterior column (n=8), anterior column and posterior hemi-transverse (n=2). All fresh fractures exhibited major acetabular damage associated with fracture of the femoral neck. A hybrid THA was used for all cases after fixation of the fracture. The femoral heads were used as graft material for deficient anterior columns in two patients and as “piecemeal” grafts for the others. Results: Mean follow-up was 36 months (range 24–35 months). At last follow-up all fractures had healed and all acetabular components exhibited solid fixation with no sign of migration. The mean outer diameter of the ace-tabular components inserted was 56 mm (52–64) using a 2 mm press-fit and one screw. The only complication was one postoperative anterior dislocation. Pain relief and function were satisfactory in all patients at last follow-up with a Postel Merle d’Aubigné score of 16 (13–18). Discussion: This anterior surgical approach enables good access to the acetabular walls and anterior columns, allowing solid fixation and relatively easy THA. The Kocher-Langenbech approach is still better in case of posterior deficiency or when posterior fixation requires space for inserting an acetabular component. We reserve it for THA used to treat fresh fractures of the acetabulum with major damage to the acetabulum and/or the femoral head, with or without neck fracture in patients aged 55 years or more. For differed reconstruction, we also use this approach if the acetabular damage involves the anterior column

Introduction: Proximal bone resorption is a common problem after total hip arthroplasty. This has been attributed to stress shielding and has been reported to be more pronounced for cemented than for uncemented implants. Aim: To investigate the cortical strain distribution of a new proximal “fit and fill” cementless, titanium, femoral, hip prosthesis based on the SROM design. Methods: Strain gauges were mounted on five fresh-frozen cadaveric and five saw-bone femora and checked against a template for the prosthesis. The strain gauges were placed at four levels on the anterior, posterior, medial and lateral cortices corresponding to the Gruen zones. Two extra strain gauges were placed on the proximal posteromedial cortex. Loading was applied to the intact and reconstructed femora in the ISO 7206–4 orientation and single legged stance in an MTS servo-hydraulic testing machine. Data were analysed using analysis of variance. Results: The strain distributions following reconstruction and multi-axis loading (ISO 7206–4 orientation) approximated the strains in an intact femur in the diaphysis. The proximal posteromedial cortical strains were approximately 50% of those of the intact femur. Conclusions: The strains observed in the proximal femur following reconstruction in the present study are considerably higher than most others reported in the literature. A number of factors may contribute to the high proximal strains observed. This study has illustrated that geometric design and material selection along with surgical technique may allow for greater loading to proximal bone and enhance the long term integrity of this type of implant

Introduction: In case of massive bone defect, femoral stem revision may cause significant problems to the orthopaedic surgeons. The periprosthetic infection introduces a further element of complication which often leads to complex surgical strategies. The aim of this study was to assess the preliminary results of femoral revision with modular resection femoral stems in a selected group of patients with infected total hip arthroplasty and extensive bone defect. Materials and Methods: The study group included five patients (three women – two men) with an average age of 72 years (range 62–81 years). From 2006 to 2008 the patients underwent a prosthetic femoral revision with resection modular stems to treat a septic loosened primary hip prosthesis (one case) or revision hip prosthesis (four cases). The bacteria responsible for the infection were MRSE in three cases, MSSE and Str. Agalactie in one case, Proteus Mirabilis in one case. Three patients were treated in election for septic loosening of hip implant and two were admitted in our Department as emergency for a periproshtetic femoral fracture (Duncan type B3). In all the patients the femoral bone defect was grade III-B according to Paprosky classification of femoral bone deficiency. One patient with periproshtetic femoral fracture underwent a one-stage prosthetic revision and four patients sustained a two-stage prosthetic revision. In one patient a local flap was performed and Vaacum Assisted Therapy was applied in order to treat an associated loss of substance. The patients underwent periodical clinical controls in which the result has been evaluated by means of Merle-d’Aubigné hip score. Results: The follow-up period ranged from 10 to 28 months. We observed one case of recurrence of infection in the patient treated with a one-stage revision. At present, we did not observe signs of infection in the remaining four patients who underwent a two-stage revision. As for functional result, four patients walked with supports and one without them. No patient referred moderate or severe residual pain. Discussion: The preservation of bone stock is one of the most important goals in prosthetic revision procedures. In some circumstances the amount of femoral bone loss can be so wide to prevent the application of conventional or modular uncemented femoral stems. In these selected cases cemented modular resection femoral stems may represent the only available option for femoral reconstruction. In our clinical experience this solution offered altogether successful outcomes. In our opinion two-stage revision is the preferable surgical choice

INTRODUCTION

Ceramic-on-ceramic hip resurfacing offers a bone conserving treatment for more active patients without the potential metal ion risks associated with resurfacing devices. The Biolox Delta ceramic material has over 15 years of clinical history with low wear and good biocompatibility but has been limited previously in total hip replacement to 48mm diameter bearings [1]. Further increasing the diameter for resurfacing bearings and removing the metal shell to allow for direct fixation of the ceramic cup may increase the wear of this material and increase the risk of fracture.

Purpose: Fracture of the neck of the femur in elderly subjects is generally treated by arthroplasty, either using a total or intermediary hip prosthesis, but with a high risk of dislocation, estimated at about 10% in the literature. We investigated the contribution of a double mobile cup to lower this risk. Material and methods: This prospective study was conducted by several operators in the same university unit between 1998 and 2001. A total of 177 mobile prostheses were implanted in patients with fracture of the anatomic neck of the femur (n=145), the neck and trochanter (n=22), or pathologic fracture (n=4). For six patients, the prosthesis was implanted after failed osteosynthesis of a trochanteric fracture. The postero-lateral approach was used for 136 women and 41 men (age range 61 – 92 years) living at home (n=124), or in an institution with a high degree of independence (n=53). The femoral stem was cemented (n=115) or impacted (n=62). A double mobile cup was used in all cases. A chromium-cobalt/ polyethylene couple was used and head diameters were 28 mm (n=150) or 22.2 mm (n=27). We studied outcome and risk of dislocation one year after implantation. Results: There were six deaths during the postoperative period. Among the 171 patients, 134 were seen at two months, 108 at six months and 89 at one year: 39 were questioned to ascertain outcome. During the first postoperative year, there were 37 deaths; these patients were followed. Six patients were lost to follow-up. We had two cases of intraprosthetic dislocation related to a defect in the chromium-cobalt head retention of the polyethylene insert. These two cases required revision and were reported to material surveillance with corrective measures for the manufacturer. There were three true dislocations (2%): 1) a posterior dislocation on day 24 in a female patient presenting a fracture with impaction of the femoral stem; 2) a posterior dislocation on day 22 in a female patient in very poor general condition (severe cardiorespiratory failure, death at 48 hr); 3) one recurrent posterior dislocation related to major acetabular retroversion, revised at four months. Discussion and conclusion: The double-mobile cup appears to be a simple reproducible method for preventing dislocation of prostheses implanted for fracture of the neck of the femur

Purpose: Wear of prosthetic implants, especially the metal-polyethylene head-cup couple, and dissemination of wear particles throughout the organisms the dominant long-term complication of total hip arthroplasty. We determined serum concentrations of chromium, cobalt, nickel, and molybdenum in patients bearing a total hip prosthesis with a chromium-cobalt metal-poly-ethylene head-cup couple. The purpose of our work was first to compare the levels observed with those found in a control population and then to study variations in these levels as a function of clinical and radiological signs commonly searched for during the follow-up of patients with a total hip arthroplasty. Material and methods: During a period of 30 months, a total hip arthroplasty (PVL®) was implanted in 53 patients suffering from degenerative hip disease. Forty-eight patients were assessed at a minimum follow-up of 32 months with physical examination and standard x-rays as well as serum assay of the specified metals using mass spectrometry on whole blood samples. The control group was composed of 56 patients scheduled for total hip arthroplasty. Results: At a mean follow-up of 44 months, 17% of the patients had a fair or poor functional score and 37% had radiological signs suggestive of femoral stem loosening. There was a significant increase in the serum level of cobalt compared with the control group. This increase was greater in patients with radiological signs of loosening. Discussion: The metal-on-metal couple does not appear to be the only couple which increases serum metal levels. Serum metal assay could be a diagnostic tool useful for following patients with total hip prostheses

Introduction: “Spongiosa metal” this unique implant surface was introduced in 1982 by ESKA implants Germany. Pore size was between 800 and 1500 microns with an overall porosity of 60%. The pore depth of the interconnecting surface structure reached up to 3000 microns. The purpose of this retrospective study is to report the long term results of Spongiosa Metal I cement less total hip prosthesis in Japan. Materials and Methods: Between 1986 and end 1990 total 113 prostheses were implanted and consecutive 106 implants could be evaluated. The all evaluated prosthesis combined 28mm ceramic head and polyethylene inlay. Results: Average follow up period was 17 years. 2 cups and 1 stem were revised by aseptic loosening. 2 stem breakage and 7 ceramic head fracture were seen while following up. 85% of the patients had retained the original prostheses (cup, stem, ceramic head, and inlay). Survival rate was investigated by Kaplan-Meier method. Survival rate for the cup component was 95%, and for the stem component was 93%. Discussion: Main reason of the revision surgery was the ceramic head fracture (7 implants 6%). We thought that beating with the hammer when we install the ceramic head to the taper was one problem. On the other hand, few aseptic loosening was seen while following up. These results suggest that spongiosa metal system can bear for long term of use. Conclusion: 85% of the patients had retained the original prostheses average 17years following up period. Main reason for the revision surgery is ceramic head fracture. We are convinced with this spongiosa metal surface can bear long term of use

The Kent hip is a distally-locked femoral stem which was developed to address severe proximal bone loss, severe bony deformity and peri-prosthetic fracture.

We reviewed the results of 145 consecutive Kent hips implanted into 141 patients between 1987 and 2000. The indications for implantation were aseptic loosening (75 hips), septic loosening (two), peri-prosthetic and prosthetic fracture (37), severe bony deformity (24), and fracture through a proximal femoral metastasis (seven).

The median time to full weight-bearing after surgery was two days and the mean length of follow-up was 5.1 years (2 to 15). Further revisions were required for 13 femoral stems. With removal of the stem for any reason as an end-point, the cumulative survival at five, ten and 15 years was 93%, 89% and 77%, respectively. In patients aged ≥ 70 years, the cumulative survival at 15 years was 92%, compared with 68% in those aged < 70 years. Because of these findings, we recommend the use of interlocking stems in patients aged ≥ 70 years, particularly in those with a peri-prosthetic fracture, for whom alternative methods are limited. Outcome scores and survival data, compared with other systems, indicate that the Kent hip should be used with caution in younger patients.

SL-PLUS MIA stem (Smith & Nephew Orthopaedics AG) is a modified implant of Zweymuller type SL-PLUS standard stem (Smith & Nephew Orthopaedics AG). We constructed finite element (FE) models and analysed equivalent stresses in the femur. In addition, we measured bone mineral density (BMD) in the femur by dual-energy X-ray absorptiometry (DEXA) after THA. The purpose of this study was to investigate the equivalent stress and to compare the results of the FE analyses with changes in BMD after THA. Twenty-one patients (18 women and 3 men) who underwent primary cementless THA with SL-PLUS MIA or SL-PLUS formed the basis of this study. Eleven patients received SL-PLUS MIA and ten patients received SL-PLUS. Zones were defined according to Gruen's system (zones 1∼7). Computed-tomography (CT) images of the femur were taken before and at 1 week after THA. FE models of the femur and prosthesis were obtained from CT data by Mechanical Finder (Research Center of Computational Mechanics Inc., Tokyo, Japan), software that creates FE models showing individual bone shape and density distribution. Equivalent stresses were analysed in zones 1 to 7 and compared to the DEXA data. FE studies revealed that there was no significant difference in equivalent stress between SL-PLUS MIA and SL-PLUS. BMD was maintained after THA in zones 3, 4, and 5, whereas BMD decreased in zones 2, 6, and 7. In zone 1, BMD decreased in SL-PLUS MIA stem group by 14%, while BMD was maintained in SL-PLUS standard stem.

Introduction: The search for a gold standard uncemented hip prosthesis with long term results matching cemented Charnley implants continues. It has been suggested that biological fixation would reduce the incidence of aseptic loosening caused by cement and polyethylene particles. The ABG (Howmedica) is a titanium alloy stem with an anatomic design and a modular head option of vitallium or ceramic. The cup is hemispherical and is fully coated with hydroxyapatite while the stem is proximally coated for metaphyseal fixation. We present a prospective series of 100 Consecutive patients with an immediate term follow up. Methods: 100 patients who had an ABG prosthesis inserted between 1991 & 1996 were included in the study. All patients were operated upon by the senior author or under his direct supervision. Patients underwent a preoperative assessment including a detailed history, measurement of range of motion, Postel Merle D’Aubigne scoring and ADL assessment. Clinical and radiological review was Conducted at 3 months, 6 months, 1 year and then at yearly intervals. At each visit Patients were questioned regarding the presence of any thigh pain and Complications. All patients were clinically evaluated, Postel Merle D’Aubigne Score was obtained and ADL status assessed. AP and lateral radiographs were Taken and studied. Polyethylene wear was measured by using the Livermore Method. The Kaplan- Meier method was used to explore the survival pattern of the implants. Results: The mean age of the patients was 52 years (range 23–72). Follow up ranged from 3 To 8 years (mean 5 years ). The mean preoperative Postel Merle D’Aubigne score Was 7 ( range 0–14) and mean score at final follow-up was 17.7(range 15–18). Only 4 patients complained of thigh pain and most had dramatic and lasting improvement of the ADL status. Complications included 3 dislocations and 2 Superficial infections. Non progressive lucencies were noted in 6 stems and 2 cups. No stems were loose and one patient had a loose cup and is awaiting surgery. A high rate of superior polethylene wear of 0.2mm/year was identified in a Number of patients yet the survivorship was 99% after an average 5 year follow up. Conclusion: Our results demonstrate the efficacy and excellent medium term outcome of the ABG prosthesis. A higher rate of complications in the first 2 years reiterates the lesson that every surgeon has to complete a learning curve before being technically comfortable with a new prosthesis. Of concern was the high rate of superior polyethylene wear although this did not effect the survivorship

Purpose: A spacer can be used for two-phase replacement of an infected total hip prosthesis. The goal is to facilitate reimplantation by avoiding soft tissue retraction. Several types of spacers can be used. We searched for a spacer which avoids wear debris due to methacrylate friction against bone, delivers a local antibiotic, is easily removed, and does not worsen bone damage. Since 1995, we have used a Charnley Kerboull type prosthesis as a spacer. The purpose of the present study was to 1) verify the absence of spacer-related complications, 2) assess outcome in terms of cure of infection and improved function. Material and methods: We used 14 articulated spacers for two-phasee prosthesis replacement in nine men and five women, mean age 64 years. Erythrocyte sedimentation rate was 32 and C-reactive protein was 17. The mean Postel-Merle d’Aubigné (PMA) score was 3+5+2. All patients were reviewed at a minimum 37 months follow-up. Technique: The approach was generally a digastric trochanterotomy, associated with a more or less extensive femoral procedure (depending on the length of the plug to remove) to achieve removal of all implants and cement. A small-size polyethylene cup was inserted with cement delivering at least one antibiotic on a Surgicel bed to facilitate later extraction. A long small-diameter femoral stem was then inserted (bridging the femoral window) and blocked with cement, also on a Surgicel bed. Partial then total weight bearing was authorised between the phases. Results: There were no dislocations. All patients achieved total weight bearing between the two phases. The same germ identified at the first operation was also identified at the second in two patients, requiring prolonged antibiotic therapy. There was one septic failure, in a different patient. The mean PMA score was 5.7+5.8+5.2. Conclusion: This technique avoids methacrylate wear induced by classical spacers and does not modify polymorphonuclear chemotactism, facilitating the efficacy of medical treatment. Patient comfort is also improved between the two phases and muscle atrophy, which could compromise long-term function, is avoided

Total Hip Arthroplasty (THA) is a well-established, cost-effective treatment for improving function and alleviating pain in patients who have disabling hip disease with excellent long-term results. Based on the excellent results, there is an ongoing trend for THA to be performed in younger and more active patients, having higher physical demands on their new total joints.

Polyethylene (PE) wear and its biological consequences are one of the main causes of implant failure in THA. Macrophages phagocytise PE wear particles and this will result in osteolysis and loss of periprosthetic bone. The risk of these complications can be estimated in relation to the amount of volumetric wear based on two assumptions: that the number of PE particles dispersed in the peri-prosthetic tissues is controlled by the amount of PE wear; and that the development of osteolysis and the resulting aseptic loosening is triggered by these PE particles. Based on these assumptions, a model was developed to estimate the osteolysis-free life of a THA, depending on the Linear Wear Rate (LWR) and femoral head size of the PE bearing.

A review of the literature was conducted to provide an estimate of the radiologic osteolysis threshold based on the volumetric wear of the PE bearing. This review demonstrates that this radiologic osteolysis threshold is approximated 670 mm3 for conventional PE. The osteolysis-free life of the THA was estimated by simply dividing this threshold volume by the annual Volumetric Wear Rate (VWR) of the bearing. The annual VWR is basically controlled by two parameters: (1) annual LWR and (2) head size, and was calculated by using published formulae.

For 28 mm heads, following osteolysis-free life was determined in function of the annual LWR. LWR: 10 µm/y => 116.6 years / LWR: 25 µm/y => 46.6 years / LWR: 50 µm/y => 23.3 years / LWR: 100 µm/y => 11.6 years. For 40 mm heads, following osteolysis-free life was determined in function of the annual LWR. LWR: 10 µm/y => 57.1 years / LWR: 25 µm/y => 22.9 years / LWR: 50 µm/y => 11.4 years / LWR: 100 µm/y => 5.7 years.

The osteolysis-free life determined by this model is in good agreement with the clinical results of PE bearings having a 28 mm head size and demonstrates that extreme low LWRs are mandatory to assure a descent osteolysis-free life for THA (PE bearings) using large heads, such as 40 mm. For such head sizes, small variations of the LWR may have large impacts on the osteolysis-free life of the THA.

INTRODUCTION. Cementless Total Hip Replacement surgery is a well established procedure for relative young patients with severe hip disease. Excellent long term clinical results have been published on the performance of the femoral component. With growing clinical experience, our concern focused on excessive wear of the Ultra High Molecular Weight Polyethylene (UHMWPE) ringloc liner of the Mallory Head cementless Total Hip Prosthesis. After its introduction in our clinic in 1997, this implant is still in use without any modification. We were concerned that due to premature liner wear, the performance of this implant would not be compliant with the international guideline on implant survival (NICE guidelines: at 10 year follow up, 90% of all implants should still be in situ). Our objective was to establish the amount of liner wear in our first 200 MH implants. METHODS. Our first 200 patients consecutively treated with Mallory Head prostheses were followed up to obtain a recent digital image. Follow up was complete for 181 (90.5%) of our 200 patients. Ten had died and nine were not able or willing to come for follow up. The mean duration of follow up was 8.3 years (range: 8–13). The 181 recent digital images were classified as either excessive wear or no excessive wear by two independent orthopedic surgeons. Next, liner wear was measured in the 2D frontal plane using PolyWare Pro/3D Digital Version Rev 5.1 software (Draftware Developers, Conway, USA). A threshold for excessive liner wear was set at 0.2mm/year, according to literature. RESULTS. Using software for measuring PE wear, 46.7% of all patients had excessive UHMWPE wear (> 0.2mm/yr). There was no relation between the amount of wear and BMI, gender, component size or the acetabular inclination angle. Thirteen patients (6.5%) were revised. Nine of these revisions were for excessive liner wear or aseptic loosening (4.5%). For now, our series of cementless Mallory Head prostheses is compliant with the NICE guideline on implant survival. However, with the measured amount of wear we expect to see a significant increase in the number of revisions for liner wear in the near future. DISCUSSION. Our clinical observation of premature UHMWPE wear proved correct. The measured amount of UHMWPE wear is consistent with the few other studies published on this subject. Although we present a retrospective study, limiting the strength of our results, we have included a large group of patients with acceptable loss to follow up. It is unclear if the observed wear will lead to a sharp increase in the number of revisions within the next few years. Possibly, future revisions will be complicated by loss of acetabular bone stock following the pathofysiological reaction to wear particles. Our results can probably be generalised for any district hospital

Introduction: Unique spongiosa like surface structure was introduced in 1982 by ESKA implants Germany. It is called “Spongiosa-Metal I surface” The purpose of this retrospective study is to report and compare long term results of Spongiosa Metal I total hip prosthesis in Japan and Germany. Method: In Japan, between June 1986 and August 1990 total 113 prostheses were implanted and consecutive 106 implants could be evaluated. In Germany, between May 1983 and December 1985 total 209 prostheses were implanted and consecutive 165 implants could be evaluated. The all evaluated prosthesis combined ceramic head and polyethylene inlay. Results: In Japan, average follow up period was 17 years. 85% of the patients had retained the original prostheses (cup, stem, ceramic head, and inlay). Survival rate was investigated by Kaplan-Meier method. Survival rate for the cup component was 95%, and for the stem component was 93%. In Germany, average follow up period was 21.8 years. 88.5% of the patients had retained the original prosthesis. Survival rate for the cup component was 95%, and for the stem component was 85%. Discussion: Main reason of the revision surgery was the ceramic head fracture (7 implants 6%) in Japan and the stem component loosening (14 implants 8%) in Germany. There was no ceramic head fracture in Germany. We thought that beating with the hammer when we install the ceramic head to the taper was one problem. Stem loosening was seen in undersized stem component. On the other hand, survival rate for the cup component was 95% in Japan and Germany. This was good result in comparison with other reports about long term survival. Conclusion 85% of the patients had retained the original prostheses average 17years in Japan and 88.5% average 21.8 years in Germany. Main reason for the revision surgery is stem loosening and ceramic head fracture. Survival rate for the cup component was 95% in Japan and Germany. We are convinced with this spongiosa metal surface can bear long term use

Aims: The purpose of this study is to present our experience with the A.B.G.-I hip system after ten years follow-up. Methods: Prospective study about 162 hip prosthesis implanted from 1990 to 1992. We have assessed clinical and radiographic results immediately before surgery and at a minimum follow-up of ten years. Statistical analysis has been developed with S.P.S.S. Results: Sex distribution of the 162 initial prosthesis: 50.71% men and 49.29% women; affected side: right in 50.71%, left in 49.29%. First hip disease: rheumatoid arthritis in 7.48%, osteoarthritis in 77.57% and avascular necrosis in 14.95%. At this moment only 102 prosthesis continue on study: 8 revised (7.27%), 21 patients died (20.39%), 28 disappeared (17.18%) and 4 (2.45%) have not been considered. Clinical assessement let us be very satisþed, with a Merle DñAubigne score improving from 7.9 preoperative to 15.8 at ten years follow-up. Clinical results have been: excellent in 54.81%, good in 27.88% and bad in only 3.85%. Radiographic results are worse than expected: 84.11% of femoral stems developed some grade of stress shielding phenomenon and polyethylene inners wore excessively (mean value = 1.77 mm). The inßammatory response to polyethylene particles originated osteolytic lesions in 88.78% of femurs and 56.48% of periacetabular bones. Today 15.53% of patients in study are waiting for a revision. Conclusions: In spite of the very good clinical results, the radiographic assessement is very concerning. We think the þrst problem is the bad quality of polyethylene inner, that is responsible for grave osteolytic lesions

Aims

The aim of this study was to evaluate blood metal ion levels, leucocyte profiles, and serum cytokines in patients with a total hip arthroplasty (THA) involving modular dual-mobility components.

Background

The two-stage revision strategy has been claimed as being the “gold standard” for treating prosthetic joint infection. The one-stage revision strategy remains an attractive alternative option, however, its effectiveness in comparison to the two-stage strategy remains uncertain. A systematic review and meta-analysis was conducted to compare the effectiveness of one- and two-stage revision strategies to prevent re-infection after prosthetic hip infection.

Introduction

Post op cup anatomical and functional orientation is a key point in THP patients regarding instability and wear. Recently literature has been focused on the consequences of the transition from standing to sitting regarding anteversion, frontal and sagittal inclination. Pelvic incidence (PI) is now considered as a key parameter for the analysis of sagittal balance and sacral slope (SS) orientation. It's influence on THP biomechanics has been suggested. Interestingly, the potential impact of this morphological angle on cup implantation during surgery and the side effects on post op functional orientation have not been studied.

Our study explores this topic from a series of standing and sitting post-op EOS images

In the present study we describe the clinical results of the Scientific Hip Prosthesis® (SHP). With the goal of smoothening cement-bone interface stress peaks, the SHP was developed using shape optimization algorithms together with finite element modelling techniques. The resulting shape and cement stresses are seen in Figure 1. The introduction of the SHP prosthesis was performed in a stepwise fashion including a RSA study performed by Nivbrant et al¹. RSA studies for prosthetic types that are in long-term use are of great value in predicting the survivorship related to the migration rate and pattern for that specific type of prosthesis. If a stem in a patient shows a much higher migration rate than the typical one, the stem may be identified as at high-risk for early loosening. The study of Nivbrant et al¹ revealed unexpectedly high migration values and it was stated that the SHP stem was not the preferred stem to use despite the good Harris Hip Score and Pain score at two years follow-up.

In the present study the clinical results of a single surgeon study consisting of 171 hips with a follow-up of 5–12 years were evaluated. The mean follow-up was 8.2 years (5.0–12.0). The survival rate was 98.8% at ten years follow-up for aseptic loosening of the stem. The mean Harris Hip Score at 10 year follow-up was 89.2 ± 7.5. This study therefore indicates that a new prosthetic design may function clinically rather well, despite the relatively high migration rates which have been reported.

In case of a RSA study with a new prosthesis it may not be so evident what the expected “typical” migration rate or pattern is. So in order to predict early loosening the typical migration rate has to be known. Perhaps typical migration rates can be established using standardized cadaver migration experiments or computer simulation models techniques. Since these standardized tools are currently not available, the prediction of clinical survival of new prosthetic components remains a challenging task and the interpretation of migration rates with new designs should be considered with much caution.

Background

The worldwide withdrawal of the DePuy Articular Surface Replacement (ASR) device in both its resurfacing and total hip replacement (THR) form on 26 August 2010, after 93,000 were implanted worldwide, has had major implications. The 2010 National Joint Registry for England and Wales quoted figures of 12-13% failure at five years; however these figures may be an underestimate.

Purpose: Osteolysis is one of the important issues during the life of noncemented total hip arthroplasty (THA). The purpose of this study was to evaluate a series of 228 THA using an ABG-1 implant to determine the incidence of osteolysis and contributive factors.

Material and methods: This series of 228 THA using noncemented ABG-1 anatomic implants coated with hydroxyapatite was implanted in 210 patients, 116 women and 112 men, mean age 62.2 years. The indication was primary osteoarthritis (53.6%), primary necrosis (21.5%), posttraumatic osteoarthritis (11.8%), rheumatoid disease (8.3%) and hip dysplasia (4.8%). The bearings were, 200 zirconium-polyethylene (87.7%), 28 metal-polyethylene (12.3%). At mean 88.6 months follow-up, a minimum 60 months postoperatively, we reviewed 163 patients (37 patients died without revision, 28 (12.3%) were lost to follow-up, and 17 had undergone a revision procedure). We analyzed osteolysis on the digitalized radiograms using the Delee-Charnley classification to which we added a fourth retroacetabular zone. Polyethylene wear was measured with the Imagika(r) software using the method described by Martell.

Results: The 17 cup revisions (8.5%) were required for instability (4 pt), loosening (4 pt), osteolysis (4 pt), infection (3 pt), and limping (1 pt). Overall implant survival was 92.1%. Implant survival, considering loosening and osteolysis as failure, was 96.1%. Mean wear at last follow-up was 1.26 mm, for an annual average of 0.17 mm (0.04 – 0.69 mm/yr). Acetabular osteolysis was observed in 41.6% of cases, mainly in the Delee-Charnley zone 1, but was also found in all the other zones. The average surface area was an estimated 223 mm2. Possible factors favoring osteolysis were: aetiology, age, gender, activity level, body mass index, Charnley ABC classification, presence of preoperative acetabular defects, cup size, polyethylene insert thickness, position of the insert rim, cup inclination, complementary fixation, bearing type, polyethylene offset and wear. There was a statistically significant relationship between osteolysis and: the Charnley classification (p=0.012), presence of preoperative acetabular defects (p=0.0034), cup inclination angle (p=0.035), cup size (p=0.042), polyethylene thickness (p< 0.01), use of complementary fixation (p=0.048), and polyethylene wear (p=0.0011). Paradoxically, we did not find any relationship with gender, age, body mass index, and the other factors.

Discussion: This analysis demonstrated the determining causes of osteolysis: time, polyethylene thickness, polyethylene wear, the Zicronium-polyethylene bearing. Wear was probably not only the consequence of the Zicronium-polyethylene bearing but was also related to the quality of the polyethylene, and the instability of the insert. Diffuse osteolysis is favored by orifices in the first-generation cups which have been eliminated in the ABG-2 cups.

A consecutive series of 30 total hip replacements using a hydroxyapatite (HA)-coated, modular implant (Omnifit) was followed clinically and by roentgen stereophotogrammetric analysis for two years and compared with two control groups, one of 27 cemented Charnley sockets and one of 40 cemented Charnley stems.

Omnifit sockets with a central gap between the dome of the socket and the acetabular bone in the postoperative radiographs, migrated less than sockets without such gaps (p = 0.01). After adjustment for patient-related factors (age, gender and weight), no significant difference was found between the two prostheses with respect to micromotion and wear.

We conclude that the early fixation of the HA-coated Omnifit prosthesis compares with that of the cemented Charnley prosthesis.

We reviewed 82 primary arthroplasties (in 71 patients) in which cementless porous-coated hip prostheses were used. The mean age of the patients at operation was 52 years (24 to 86); they were followed up for an average of 62.1 months (60 to 66). The diagnosis was avascular necrosis of the femoral head in 35%, fracture of the femoral neck in 24%, primary osteoarthritis in 16% and miscellaneous in 25%. The average preoperative Harris hip score was 56.7 points and the average postoperative score was 83.3 points. Eight hips (10%) had component loosening; four had been revised and four were awaiting revision. In 27 hips (33%) there was a radiolucent line wider than 2 mm in zones 1 and 7. In 55 hips (67%) there was calcar resorption of more than 10 mm. Twenty patients (28%) complained of thigh pain although they had no radiographic evidence of loosening of a component. Factors that may have contributed to the poor clinical and radiographic results were: 1) inadequate surface area for bone ingrowth, particularly on the lateral aspect of the upper part of the prosthesis, 2) poor initial fit of the stem in the metaphysis, which resulted in cantilever motion of the proximal part of the stem about the well-fixed distal stem, and 3) the collar of the prosthesis, which prevented it from subsiding to a naturally stable position and caused damage to the calcar.

This abstract is currently withdrawn to allow an independent review of findings to take place.

Between January 1984 and January 1986, 131 porous-coated anatomic total hip replacements were performed in 119 consecutive patients. Of these, 100 patients (110 hips) who were alive at a minimum of 18 years after replacement were included in the study. The mean age of the patients at surgery was 48.4 years and that of surviving patients at the latest follow-up was 67.8 years. The mean duration of the clinical and radiological follow-up was 19.4 years (18 to 20).

The mean Harris hip score initially improved from 55 points before to 95 points at two years after operation, but subsequently decreased to 91 points after six years, 87 points after 11.2 years, and 85 points after 19.4 years. At the final follow-up, 23 hips (18%) of the entire cohort and 21% of survivors had undergone revision because of loosening or osteolysis of the acetabular component and eight hips (6%) of the entire cohort and 7% of survivors for loosening or osteolysis of the femoral component. Only four femoral components (4%) were revised for isolated aseptic loosening without osteolysis and two (2%) for recurrent dislocation. On the basis of these long-term results, the porous-coated anatomic femoral component survived for a minimum of 18 years after operation while the acetabular component was less durable. The findings identify the principles of uncemented joint replacement which can be applied to current practice.

Aim

The objective of this study was to evaluate the intermediate term clinical and radiological results of a new short stem hip implant.

After a few years from its introduction, the limits of the THA became evident, mainly due to high rates of mobilization for polyethylene wear and to the release of metal ions from MOM and MOP couplings.

Ceramic bearings were thus introduced in surgery to obtain lower levels of friction and wear.

These issues have now been well recognized by several studies, which show that ceramic-on-ceramic joint has the lowest wear rate among various articulations and that ceramic particles induce less macrophage reaction and decrease cytokine secretion, allowing to have little periprosthetic osteolysis.

After the first results in the late 70′s and early 80′s, the mechanical reliability was improved due to the manufacturers' efforts to reduce the ceramic fragility evolving average grain microstructure and lowering the degree of impurity.

Betterment and standardization of production have led to 3^rd generation alumina, Biolox Forte in 1994, that achieved a lower incidence of fracture.

The purpose of our study has been to assess long-term follow-up results of alumina-on-alumina 3^rd generation ceramic total hip cementless arthroplasty performed at our institution from January 1995 to December 2000.

We prospectively followed more than 200 patients operated of THA for primary or secondary hip osteoarthritis analyzing clinical and radiographs features.

In this period, the total hip replacement were performed by a single surgeon, who is the senior author (A.T.) in our Institution.

All patients were clinically examined to confirm the diagnosis and all of them were checked with a standard plain radiographs in two projections and, when necessary, the radiographic examination was completed by CT scans.

The same prosthesis was used in all patients, a 3^rd generation alumina COC articulation, composed of a hemispherical titanium alloy cup and a 28-mm alumina ceramic femoral head. The modular ceramic head was fixed to a 12/14 taper cone.

Proximally plasma-spray hydroxyapatite coated Ti alloy stems completes the implant features. Modular necks were used in retro or anteversion and varus or valgus offset, allowing changes in neck-shaft angle and giving a perfect intraoperative stability.

Clinical assessment was performed using the Merle-D'Aubigne and Postel hip score. Each patient was assessed before surgery, after 30 days, afterwards at 4 months and annually after surgery.

The mode of femoral component fixation was radiographically classified as bone ingrowth fixation, stable fibrous fixation or unstable fixation, according to the criteria Engh-Bobyn.

Osteolysis was evaluated on the femoral side at each Gruen zone. Osteolysis on the acetabular side was evaluated by DeLee and Chanley zone.

Our study has concluded that cementless modular hip arthroplasty with 3^rd generation ceramic-on-ceramic bearing, with a 13 to 18 years follow-up, shows an excellent survivorship, in particular for the very low volume release of microparticles during friction, which consequently reduction of cytokine release, thus diminishing the risk of periprosthetic osteolysis and loosening of implant components.

Introduction

This study reports outcomes of primary and revision total hip arthroplasties of a recalled metal-on-metal (MOM) monoblock prosthesis performed by a single surgeon.

In a frail elderly patient a pathological fracture of the femur at the lower end of a loose femoral stem was treated by the retrograde insertion of an intramedullary nail over the tip of the prosthesis.

A prospective, randomised and independently assessed trial of the Ring UPM total hip replacement showed that the quality of the early result was better if the femoral prosthesis was cemented than if it was not. More patients with cemented prostheses were painfree at four months (58% cemented:42% uncemented) and at one year (63% cemented:50% uncemented), but at two years pain relief was equal in both groups. At two years significantly more patients with cemented prostheses could walk without support (96% cemented:62% uncemented, p = 0.01 to 0.05). There is a need for more similar trials to compare the results of contemporary designs of cemented and uncemented total hip prostheses.

Hip implant retrieval analysis is the most important source of insight into the performance of new materials and designs of hip arthroplasties. Even the most rigorous in vitro testing will not accurately simulate the behavior of implant materials and new designs of prosthetic arthroplasties. Retrieval analysis has revealed such factors as the effects of gamma-in-air sterilisation of polyethylene, fatigue failure mechanisms of polymethylmethacrylate bone cement, fretting corrosion of Morse taper junctions, third body wear effects of both hard-on-hard and hard-on-soft bearing couples, and the effects of impingement of components on the full spectrum of bearing surfaces, none of which was predicted by pre-implantation in vitro testing of these materials and combinations. The temporal sequence of the retrieval process is approximately six years from first implantation through retrieval analysis, laboratory investigation, and publication of results, and thus, in addition to rigorous clinical evaluation, represents the true development and insight cycle for new designs and materials.

Customization makes it possible to fulfill design requirements during MIS-THA procedures, and has helped define the parameters of fit and fill. This study describes the results of using customization techniques to develop a femoral implant for utilization.

CT-based design criteria for femoral implants has-been developed and used for primary, cement-less, non-minimally invasive THA surgery. Over 1000 procedures performed with these devices have been associated with displaced femoral fractures, and have been revised for septic loosening. This study has 2 parts:

20 implants were designed and implanted with CT-based criteria that utilized the identical fit and fill standards of the custom implants previously established, but had short (< 115 mm), tapered stems;

The stem of these implants was shortened (95–115 mm) and tapered. Implants in both groups were inserted using a single incision, posterior-lateral MIS approach. Patients were followed clinically and radiographically for six months. Immediate full weightbearing and use of a single cane were encouraged.

The use of CT-based customization techniques is helpful for defining design criteria of femoral implants, but the instrumentation for inserting these implants must be adapted to the specific surgery. Customization also facilitates the design and evaluation of CAOS applications for inserting these MIS implants.

Early reports on revision total hip arthroplasty (RTHA) suggested that outcomes of this procedure are as good as those of primary total hip arthroplasty (THA). However, RTHA is associated with longer surgery time, greater blood loss and increased risk of complications (thromboembolism, nerve injury, periprosthetic fractures, recurrent hip dislocations and infections). Aseptic loosening after RTHA was reported in 36% of patients aged over 55 years within 4 years after revision. Infections were reported in 32% and complications during surgery in 23% of patients respectively. Unsatisfactory results of RTHA stimulate the search for alternative procedures. Girdlestone excision arthroplasty (GA) seems to be a good solution for older patients with high risk of complications related to a poor general condition.

Material and method Between 2000 and 2003 we operated 39 patients, 10 for septic (26%) and 29 aseptic (74%) loosening of their THA. All patients complained of painful limb aggravated by weight bearing and the severity of pain was the main indication for the surgery. Average survival time of previous THA was 9 year (range: 1 to 20). We assessed pain, walking distance and the need to use walking aids. The outcomes were measured according to the Harris Hip Scale. The patients had the GA performed. The procedure involved removing implant and bone cement and placing the major trochanter into bone acetabulum. If an infection was present, an antibiotic irrigation system was introduced. No cast or braces were used and walking was started 2–7 days after surgery, depending on patients general condition.

Results Good pain control was reported by 33 (85%) patients. The average Harris Hip Score changed from 25 points preoperatively to 53 at latest follow-up. Average limb shortening was 4 centimetres (range: 2 to 8). Walking aids (one or two crutches) were required by all patients. Eighteen (46%) patients walked more than 500 m, 12 (31%) patients walked 200–500 m and 9 (23%) patients walked less than 200 m, of whom one patient was wheelchair bound.

Infection ceased in 9 cases, 1 patient died because of complications related to chronic infection.

Discussion GA yields satisfactory results in patients who have to have their prostheses removed. It provides a mobile, painless joint. The disadvantages of GA are: limb shortening and unstable gait which requires the use of crutches. This procedure should be indicated for patients with high risk of complications due to poor general health, infection and/or massive loss of bone stock which render more invasive procedures impossible. GA is also advisable in patients with weak hip abductor muscles, when RTHA is associated with a high risk of recurrent hip dislocation. The Girdlestone arthroplasty is a satisfactory salvage procedure in most cases of failed THA, when the choice of reimplantation exposes the patient to a high risk of further failure.

We report the clinical outcome and survival of 100 total hip arthroplasties with Link RS cementless hip prostheses after a mean of 63 months (51 to 93). The average preoperative Merle d'Aubigne hip score was 9.4 points and the average score at the latest follow-up was 15.3 points. Thirteen prostheses have been revised and seven await revision. Survivorship analysis based on intention to revise showed only 68% survival at seven years (95% CI 53% to 81%). The survivals of femoral and acetabular components verified to be loose at surgery were 78% and 89% respectively at seven years. A number of other patients have pain and it seems likely that there will be substantial reduction in these survival figures in the future.

Seven hips with protrusio acetabuli which showed complete or partial resolution of the protrusion after replacement with Ring's prosthesis are reported. It is suggested that this prosthesis offers a simple and effective method of treating painful protrusion into the pelvis; it allows healing of the medial wall of the acetabulum while avoiding many of the hazards of other methods of treatment.

Sixty-five total hip arthroplastics were reinserted after sepsis around the hip, positive cultures being obtained from fifty-six. Although 65 per cent of patients still have their implant in position, only sixteen of sixty-five (25 per cent) show an excellent or good result on a Harris rating. Twenty-three of sixty-five (35 per cent) subsequently required an excision arthroplasty. The indications and contraindications for this procedure are given.

Purpose of the study: Hip resurfacing with a metal-on-metal bearing gives good mid-term clinical results. The design of the femoral piece has an effect on implant longevity, as does the vitality of the underlying cephalic bone. Computer-assisted surgery has been helpful in position the implant but the choice of the best position is still empirical. Prosthesis designers recommend valgus, but with too much there is a risk of a superolaterl notch which would weaken the neck. This leads the surgeon to use a larger femoral implant, and consequently to resect more acetabular bone. Anteversion is not evaluated. The purpose of this study was test mechanically different valgus/varus, anteversion/retroversion positions of the femoral implant.

Material and methods: We implanted 15 femurs made of resin which were geometrically and mechanically identical. The following angles were tested: varus/valgus (−10°, neutral, +10°, +20°) and ante/retroversion (−10°, neutram, +10). A valgus notch (+20° and +10°) and a varus notch (−10°) were simulated. The femurs thus prepared were tested with Instron 8874. Load at failure was noted as well as the type of fracture: distance from the fracture line to the greater trochanter (FGT). Student’s t test was applied.

Results: All of the femurs fractured at the neck. The fracture was closer to the implant (FGT: 11.0 mm) for the 20° valgus implantation (p< 0.05). The displacement was lesser with a valgus notch (mean 2.2 mm) then without a notch (mean 3.3 mm (p< 0.05). The varus notch had no effect. The failure load was lower for 20° valgus (1236 N, range 1117–1356N) then for the other angles (1664N, range 1142–2113 N) with near statistical significance (p=0.08). Retroversion had no effect. Anteversion allowed greater displacement (4.1 mm) and supported greater loading (1879 N) before failure.

Discussion: This study, unlike clinical studies, did not demonstrate any static mechanical superiority of the valgus position for the femoral piece. Another study on cadaver bones is planned for confirmation. Clinical studies reflect the vitality of the trabecular bone supporting the implant, a vitality which could be stimulated by the valgus position.

Mechanical wear and corrosion lead to the release of metal particulate debris and subsequent release of metal ions at the trunnion-taper surface. In order to quantify the amount of volume loss to ultimate locations in the surrounding joint space, finite element analysis of the modular head-stem junction is being carried out. The key purpose being to determine a set of optimum design changes that offer the least material loss at the taper-trunnion junction using optimization algorithms such as the gradient based local search (Sequential Quadratic Programming–SQP) and global search (Non-Dominated Sorting Genetic Algorithm-II–NSGA-II). In a broader sense, the principal goal is to work toward the minimization of wear debris produced in the hip joint, thereby resulting in a longer prosthetic lifetime.

A numerical approach that simulates wear in modular hip prostheses with due consideration to the taper-trunnion junction on metal-on-metal contacts is proposed. A quasi-static analysis is performed considering realistic loading stages in the gait cycle, and nonlinear contact analysis is to be employed. The technique incorporates a measured wear rate as an input to the finite element model. The simulation of wear is performed by progressively changing nodal coordinates to simulate the wear loss that occurs during surface interaction. The geometry of the worn surface is updated under gait loading. With a given geometry and gait loading, the linear and volumetric wear increases with the number of gait cycles. The continuous wear propagation is discretized and an approximation scheme known as surrogates is to be developed using Artificial Neural Networks (ANN) to reduce the expensive computational simulations during optimization.

The model is employed in the optimization schemes coded in MATLAB and linked to the finite element model developed in ANSYS batch mode. The objective function of the optimization problem is to minimize the volumetric wear at taper-trunnion interface under some constraints. By minimizing the volumetric wear, the chance of failure of modular hip implants is also minimized. The FE model developed to reproduce fretting wear is validated through in vitro wear simulations.

The important taper design variables considered to have impact on the fretting corrosion performance include; medial-lateral offset, neck length, taper head diameter, trunnion length and diameter, included angle for the head/neck tapers, angle of mismatch or variation in taper trunnion angle, etc. It is expected from clinical outcomes that increased offset and large taper diameter has serious implications in the fretting corrosion behavior primarily because these variables control the bending stresses and strains along the length of the taper. During cyclic loading of the taper, the higher the strain range, the higher will be the relative micromotion at the point of engagement between the stem and head tapers. This research is carried out with the objective to optimize the effects of these geometrical factors at the mating taper interfaces.

The developed models have great potentiality for accurate assessment of wear in a range of metal-on-metal (MoM) hip prostheses at the femoral head taper-trunnion junction while substantially reducing the wear and failure rate of prostheses.

Introduction: The non-cemented, extramedullary anchored Thrust Plate Prosthesis (TPP) was conceived as an implant for younger people with osteoarthrosis of the hip. The proximal part of the femur is loaded as physiologically as possible by transmitting the hip joint force directly to the cortex of the femoral neck, enabling the bone stock in the proximal femur to be preserved.

Materials and methods: We prospectively followed-up 102 hip replacements radiologically and clinically in 84 patients (63 men and 21 women) with a mean follow-up time of nine years (6–12 years). The mean age at operation was 54 years for the men and 47 years for the women.

Results: Four implants were revised: two because of an infection and two because of aseptic loosening. In 85 implants major contact was maintained between the thrust plate and bone, in ten implants partial contact prevailed, and in only three instances did the bone retract from the thrust plate so that a gap appeared. The average Harris hip score (HHS) increased from 51 points preoperatively to 96 points postoperatively.

Conclusions: Our long-term results with the TPP are similar to those for conventional prostheses of the stem type. The detected radiological changes normally take place in the first two years after implantation. After the prosthesis is osseointegrated aseptic loosening of the prosthesis is very unlikely. Bone remodelling underneath the thrust plate is in 85% of the cases as expected from the biomechanical principles. These long-term results confirm our encouraging medium-term observations. The TPP is a prosthesis of first choice when revision might be expected, as in the case of younger patients.

A modular neck allows to choose the offset of the femoral head and the degree of anti-retroversion, lateralization and varus-valgus intraoperatively. At the G. Pini Institute we have been using modular necks in custom prostheses since 1989. Excellent results in this application did open the way to a larger use in off-the-shelf prostheses. Modular necks can be now coupled with different stems, leaving the surgeon free to use the preferred prosthetic stem design. Modular necks have been implanted in more than 50,000 in the world. Medium term results in custom prosthesis and the experience in off-the-shelf non-cemented stems are presented, together with further improvements of this technology under study.

From 1989 to December 1999, 481 custom stems have been implanted. All patients but ten received modular necks. The prostheses were made of a titanium alloy and HA coated. 61 % of patients had dysplastic oxarthrosis. 372 implants performed between 1989 and 1996 were retrospectively evaluated. Data from off-the-shelf prosthesis, at a shorter follow-up, are also reported. Laboratory data showed that the use of an elliptical Morse cone of the neck reduced wear debris production to less than 1 mg/year. In custom implants, (mean follow-up: 7 years), we did not observe any thigh pain or radiological signs of osteolysis or fretting. Mean leg-length discrepancy was 2.8 cm pre-op and 0.3 cm post-operatively. Off-the-shelf implants also showed good clinical and radiological results. New design modular necks will increase the possible range of motion and provide more solutions for positioning the center of rotation. Modular neck is a safe and reliable solution to obtain the correct position of the center of rotation intra-operatively, without side effects. Applications in off-the-shelf prostheses allow to reduce costs while maintaining the advantages of this technology.

The increasing success rates of total hip replacements (THR) have led to a younger patient population with an increased probability for revision. The survival of revised components is improved by a good bone quality. This has led to an increased interest in bone preserving THR designs. A novel type of THR was developed of which the femoral component is cemented in the neck. The load carrying area of this prosthesis is reduced in comparison with conventional cemented implants. Whether an adequate stability can be achieved was biomechanically evaluated during simulated normal walking and chair rising. In addition, the failure behaviour was investigated.

Bone mineral density (BMD) was measured in 5 fresh frozen proximal human cadaver femora. The femoral heads were resected and a 20 mm diameter canal was created in the femoral necks. Bone cement was pressurised in this canal and the polished, taper-shaped prosthesis was subsequently introduced centrally. A servohydraulic testing machine was used to apply dynamic loads up to 1.8 kN to the prosthetic head. Radiostereophotogrammetric analysis was used to measure rotations and translations between prosthesis and bone. In addition, the constructions were loaded until failure in a displacement-controlled test.

During the dynamic experiments, the femoral necks did not fail, and no macroscopical damage was detected. The initial stability of the implant did not seem to be sensitive to bone quality. Maximal values were found for normal walking with a mean rotation of about 0.2 degrees and a mean translation of about 120 microns. These motions stabilised during testing. The failure loads in this study varied between 4.1 and 5.5 kN, higher failure loads were associated with higher BMD values. Most specimens showed subtrochanteric spiral fractures.

In conclusion, the stability of the prosthetic device may be adequate under dynamic, physiological loading conditions. The static failure loads were relatively low and require further optimisation of the prosthetic implant.

We examined the risk of thrombotic and major bleeding events in patients undergoing total hip and knee replacement (THR and TKR) treated with thromboprophylaxis, using nationwide population-based databases. We identified 83 756 primary procedures performed between 1997 and 2011. The outcomes were symptomatic venous thromboembolism (VTE), myocardial infarction (MI), stroke, death and major bleeding requiring hospitalisation within 90 days of surgery.

A total of 1114 (1.3%) and 483 (0.6%) patients experienced VTE and bleeding, respectively. The annual risk of VTE varied between 0.9% and 1.6%, and of bleeding between 0.4% and 0.8%. The risk of VTE and bleeding was unchanged over a 15-year period. A total of 0.7% of patients died within 90 days, with a decrease from 1% in 1997 to 0.6% in 2011 (p < 0.001). A high level of comorbidity and general anaesthesia were strong risk factors for both VTE and bleeding, with no difference between THR and TKR patients. The risk of both MI and stroke was 0.5%, which remained unchanged during the study period.

In this cohort study of patients undergoing THR and TKR patients in routine clinical practice, approximately 3% experienced VTE, MI, stroke or bleeding. These risks did not decline during the 15-year study period, but the risk of dying fell substantially.

Cite this article: Bone Joint J 2014;96-B:479–85.

We have followed up for a period of seven to nine years 100 consecutive arthroplasties of the hip in which an entirely HA-coated implant had been used.

The clinical results were excellent and bony incorporation was extensive in all components. No stem became loose or subsided but five cups were revised because of loosening after 3.8 to 5.5 years, having functioned painlessly and shown radiological ingrowth.

Revision procedures because of excessive polyethylene wear have been performed on 18 hips and are planned for six more. Two eroded metal backings with worn-through polyethylene were exchanged; six hips showed metallosis without polyethylene wear-through. There were two cases of granulomatous cysts in the groin and 66 hips had osteolysis located periarticularly, in the greater trochanter or in the acetabulum.

We enrolled 98 patients (107 hips) with a mean age of 47 years (SD 8.6) into a prospective study of the Madreporic Lord THR; 34 hips had primary and 73 secondary osteoarthritis.

After ten years, the survival rate using revision as the endpoint for failure was 70% (±9) for the cup and 98% (±0.3) for the stem. The combined clinical and radiological survival rates were 46% (±11) and 81% (±10), respectively. Osteoporosis due to stress-shielding was observed in the proximal femur. Hips with radiologically dense bone postoperatively showed the most pronounced bone loss.

We recommend continued radiological follow-up of patients with this type of implant to allow revision to be performed before there is severe bony destruction of the pelvis.

Summary Statement

Proximal femoral bony deficits present a surgical and biomechanical challenge to implant longevity in revision hip arthroplasty. This work finds comparable primary stability when a distally fixing tapered fluted stem was compared with a conical design in cadaveric tests.

Twenty-nine patients with thirty pseudarthroses after removal of infected total hip prostheses have been reviewed one to six years later. Six hips still had a discharging sinus. Complete removal of all cement was found to be essential for healing, and various points in the technique of its clearance have been made. In this respect radio-opaque cement was a great advantage, and lateral guttering of the femur was most effective. Compared with the situation before replacement considerable relief of pain was obtained in most patients but there was much less improvement in function.

The ABG stem (Anatomique Benoist Girard, How-medica) was realized of titanium alloy (TA6V) and it was designed to provide anchoring only at the femour’s metaphyseal portion. The long-term stability is achived by osteointegration of the implant at the metaphyseal region, which is coated with hydroxyapatite (HA) crystals. The plasma-sprayed HA coating has a tickness of 60 μm for the stem.

The current study presents radiographic outcomes of more than one hundred primary uncemented HA stems with a long-term follow-up. One hundred and eleven ABG hip arthroplasties were evaluated with a mean follow-up of 9.8 years. The radiographical findings have been classified observing Engh’s stability criteria according to Gruen’s subdivision of the periprosthetic femoral zones.

Dividing the hips into two different groups (in the first one the prosthesis implanted 11, 12 or 13 years ago and in the second one the prosthesis with a maximum age of 10 years) it’s possible to see as in the first group the radiolucent lines are quite reduced. Among the older prosthesis the percentage of radiolucent lines is 3.1% in zones 3 and 5 and 18.8% in zone 4. For what concerns the younger ones the percentage are 10.1% (zone 3), 21.5% (zone 4) and 15.2% (zone 5).

We believe that there is a load transfer from the metaphyseal to the metadiaphyseal portion of the femur without a worsening of the clinical outcomes. The absence of reactive lines and lucencies around the proximal HA-coated portion of the stem supports an excellent circumferential bony ingrowth in the metaphyseal area of the proximal femur. According to these percentages we can say that there’s less presence of radiolucency in the oldest prosthesis and it could be possible to argue that radiolucent lines tend to reduce along the time. This is probably due to the increase of the strength of the stem anchorage.

Purpose: We reviewed retrospectively 349 cases of infected total hip arthroplasty treated by prosthesis replacement. The surgical strategy, 127 single-stage procedures and 222 two-stage procedures, was determined by the surgeon on a case by case basis.

Material and methods: At least one positive sample during the clinical history was required for inclusion in the series. Results of all bacteriological samples collected pre- and intra-operatively were noted. Samples were considered reliable if obtained from a deep site (puncture, biopsy, intraoperative specimen) and non-reliable if obtained from any other site. We studied the agreement between preoperative and intraoperative samples, taking the intraoperative samples as the reference, in order to determine the effect of complete preoperative knowledge of the causal germ on the outcome of infection treatment at last follow-up.

Results: For single-stage replacement procedures, preoperative samples were reliable in 74 cases (58%) and non reliable in seven (6%); they were sterile or absent in 46 cases (36%). Intra-operative samples were positive in 103 cases (81%). Agreement between the preoperative and intraoperative samples was observed in 48 cases (38%). The rate of success was not different if the surgeon had or did not have reliable knowledge of the causal germ(s) preoperatively: successful treatment in 66 cases (89%) with knowledge and successful in 46 cases (87%) without knowledge. For two-stage procedures, preoperative samples were reliable in 155 cases (70%) and non-reliable in 15 (7%); they were sterile or absent in 52 cases (23%). Intraoperative samples were positive in 178 cases (80%). Agreement between preoperative and intraoperative samples was observed in 107 cases (48%). The rate of success was not different if the surgeon had or did not have reliable knowledge of the causal germ(s) preoperatively: successful treatment in 133 cases (86%) with knowledge and successful treatment in 56 cases (84%) without knowledge.

Conclusion: Reliable preoperative knowledge of the causal germ(s) did not affect the rate of success for single-stage or two-stage total hip arthroplasty replacement procedures. These findings do not corroborate the notion that it is absolutely necessary to recognise the germ(s) causing the infection before undertaking a single-stage replacement procedure.

The aim of this study is to review the relation of polyethylene wear in patients underwent Anatomic Medullary Locking total hip replacement with respect to the types of acetabulum used.

85 cementless primary AML joint replacements were performed in the 10 years period from 1988 to 1998. The average age at operation was 46.6 with a range from 22 to 63. Two different types of acetabulum design namely the Acetabulum Cup System (ACS) and Duraloc were used. 39 of them were followed up from 2 to 10 years with an average of 69 months. Xrays were performed at the review visit and the thickness of the insert was calculated. The cup abduction angle was measured and the size of the cup and initial insert thickness was also recorded. The findings were correlated and subjected to statistical analysis.

Our findings suggested that the wear of the ACS cup was significantly higher than that of the Duraloc cup. The size of the cup but not the age of the patient at the time of operation also affects the wear rate. It appears that wear rate started to accelerate from year 8 onwards. The risk is higher with cups of less than 50mm diameter

We conclude that it is advisable to review closely those patients with the ACS cup implanted. Revision surgery should be considered if eccentric wear started to be seen on Xray to avoid complicated procedure.

Infection of total hip replacement still is considered a devastating complication. One-stage revision, meaning complete removal of the implant and thorough debridement of the site together with the insertion of a new prosthesis during the same operation, is desirable because of improved rehabilitation of the patient and reduced costs. Although this method is known since more than 30 years it is not used widely yet because of several related risks: known methods rely on the use of antibiotic-loaded cement, which often has shown insufficient release of the added antibiotic. The carrier may even act as a bed for colonisation with selected bacteria. Osseous conditions presented during revisions prevent interconnection of the cement with the sclerotic bone. The toxic monomers of PMMA and heating during polymerisation causes necroses which may be origin of repeated loosening and new growth of bacteria. Filling the defects with cement provides unfavourable conditions in case of another revision, which has to be expected at a high percentage. To overcome these disadvantages uncemented techniques seem to be favourable.

After removal of the implants debridement is performed as in conventional septic surgery. After thorough cleaning and rinsing, bone voids are filled with bone graft using an impaction technique. We use allograft or xenograft bone that is free from antigenic material but intact structures of bone concerning collagen and mineral content. The bone is impregnated with high loads of antibiotic, using a specific incubation technique. There are two options of antibiotic impregnation: vancomycin (“V”) or tobramycin (“T”), the choice being dependent on the causative pathogen isolated. Combinations are possible in cases of mixed infections. The impregnation procedure guarantees high levels of antibiotics at the grafting site for several weeks during which the antibiotic is released into the surroundings. Systemic drug levels are usually undetectable. At the acetabular site we take care that the ground be sufficiently filled with antibiotic graft. Preferably an uncemented cup of hemispherical design is inserted. At the femoral site we prefer implants with a rectangular diameter. This design enables stable press fit contact with the shaft medially and laterally and leaves enough space for graft impaction at the posterior and anterior aspect of the endoprosthesis. Wounds are drained and closed immediately; rehabilitation is performed as after non-septic surgery.

Between 1998 and 2004 thirty-seven patients have been revised because of culture-proven infection of hip endoprosthesis. Causative pathogens were Coag.neg. staph (18x), S.aureus (11x), MRSA (4x), enterococci (9x) and other gram-positive pathogens (3x). In 6 hips gram-negative germs were found additionally. All hips could be followed up with a minimum of 2 years and a maximum of 8 years (mean: 4.1 years).

Wound healing was uneventful in all cases. Mean hospital stay was 16 days (10–32 days). Rehabilitation was in the range of uncomplicated primary THR in cases with short history of infection (up to 3 months) and prolonged in relation to duration of infection and amount of preceding surgery. In three hips there was recurrence of the infection, diagnosed between 6 and 12 weeks after surgery. In one of them the well-fixed stem had not been exchanged, in another one a technical error had occurred during impregnation of the bone graft. This one could be successfully re-operated using the same technique with appropriately impregnated bone graft, the other two were converted to a girdlestone situation. All other 32 hips showed no sign of infection until the last follow-up.

Bone processed in an adequate way represents an excellent carrier for vancomycin and tobramycin. With antibiotic graft compound eradication of pathogens, grafting of bony defects and re-insertion of an uncemented prosthesis may be accomplished in a single operation, making it an ideal tool in one stage non-cemented revision for infected total hip replacement. However, principles of septic surgery need to be observed. We now recommend removing even well-fixed prostheses and taking care, that we implant at least 50cc of well impregnated bone graft. Since the graft gradually is replaced by healthy own bone, improved conditions may be expected even in the case of another revision.

Introduction & Aims: A new femoral component for hip arthroplasty has been designed for a younger patient population. The design makes use of a higher femoral cut, which conserves bone stock, increasing options for future revision surgery. It uses the existing load bearing properties of the proximal femur, and therefore distributes load more evenly. The stem is longer than that of a resurfacing, so will be easier to insert at the correct orientation, minimising failure rates in inexperienced hands. The cross-sectional dimensions have been designed to produce torsional stability. The collar maximises the loading of the calcar, reducing stress resorption. The surface is hydroxyapatite coated and porous, which will produce a long-term biological fixation.

This project assessed the long-term stability of this design at different orientations, by measuring the change in surface strain distribution following its insertion.

Methods: Ten composite bones were coated in a Photoelastic material, positioned at a simplified single leg stance, and loaded at 2.3 KN. The surface strain was measured at one-centimetre intervals down the medial cortex. Then the prostheses were inserted into the bone at 135°, 145° and 125° to the femoral shaft, and the surface strains reread.

Results: The results were compared with an FEA model, and analysed statistically using the Wilcox signed rank test. The prosthesis inserted at 135° produced no significant difference in surface strain distribution compared with the intact bone.

Conclusions: This study suggests this stem design will be stable in the long term following insertion, and there were no areas of excessively high or low strain.

Cemented modular metal backed total hip prostheses have the theoretical advantage to allow different inlays to be used. Asymetric or snap inlays are some of the options. First attempts with this kind of implant failed due to PE quality. A novel implant has been specifically designed and constructed for the use of cement. In vitro testing has shown results equal to other cemented cups. Aim of this study is to investigate the first clinical results of this implant with special consideration to intraoperative complications, intraoperative change of inlays, postoperative complications and clinical results.

Patients and Methods: Study setup was prospective, location a university hospital, approval for this study was granted by the local ethical committee. Inclusion criteria were patients with a biological age over 70 years that suffered a recent fractured neck of femur with the general indication for arthroplasty. Exclusion criteria were the inability for full informed consent, ASA IV and current infection. Thirty patients were included in this study. Mean age was 78.6 years (55.1 to 88.6), 23 patients were female (77%). The mean BMI was 25.3 (17.5–41).

The implant under investigation was a cemented modular acetabular component (C-MIC, ESKA Implants, Germany). The inlays are manufactured of highly crosslinked polyethylene. The standard protocols regarding DVT prophylaxis and antibiosis for HHS and the Barthel index.

Results: Implantation of the C-MIC component was possible in all cases. In 1 case (3.3%) the inlay was changed and replaced by an asymmetrical anti-luxation inlay intraoperatively as there was a luxation tendency. There were no other intraoperative complications. There was no case of infection or significant hematoma. In 1 case there was a DVT of the lower leg diagnosed by ultrasound on day 21. The mean Barthel index preop. was determined with 96.5 of 100, the mean Harris Hip Score with 89. At 3 months F/U the Barthel index was mean 96.1, at 6 months 96. The Harris Hip Score at 3 months was mean 72 points (17 pts below the preoperative status), at 6 months mean 79 points (10 pts below preoperative status).

Discussion: The C-MIC acetabular component does not show increased complication rates when compared to published results of hemiarthroplasty. The Barthel index as an outcome measurement of mobility and activities of daily living showed a return to the preoperative level. The HHSshowed a satisfactory result at 12 weeks, it also showed that patients of a geriatric population have problems to regain their full hip function after a fractured neck-of-femur.

We can conclude that the C-MIC acetabular component is safe to use. Due to limitations of this study we are not able to state if THA is superior to hemiarthroplasty in geriatric patients.

In this meta-analysis we included 32 English-language articles published between January 1975 and June 2004 on the diagnostic performance of plain radiography, subtraction arthrography, nuclear arthrography and bone scintigraphy in detecting aseptic loosening of the femoral component, using criteria based on the Cochrane systematic review of screening and diagnostic tests.

The mean sensitivity and specificity were, respectively, 82% (95% confidence interval (CI) 76 to 87) and 81% (95% CI 73 to 87) for plain radiography and 85% (95% CI 75 to 91) and 83% (95% CI 75 to 89) for nuclear arthrography. Pooled sensitivity and specificity were, respectively, 86% (95% CI 74 to 93) and 85% (95% CI 77 to 91) for subtraction arthrography and 85% (95% CI 79 to 89) and 72% (95% CI 64 to 79) for bone scintigraphy. Although the diagnostic performance of the imaging techniques was not significantly different, plain radiography and bone scintigraphy are preferred for the assessment of a femoral component because of their efficacy and lower risk of patient morbidity.

Introduction: Hip dislocation remains a relevant complication of total hip arthroplasty.The implants position plays a major role, especially cup anteversion.It has been demonstrated that anteversion measured on CTscan depends on the pelvic position in a lying patient. This prospective study evaluates the influence of pelvic tilt according to standing and sitting positions.

Material and Methods: The radiological records of 328 consecutive asymptomatic patients with THP were analyzed. These were routine radiological controls of non cemented THP with metal back acetabular implants. All patients had AP and lateral radiographs in standing and sitting position and a “low-dose” CT scan of the pelvis in lying position.Patients were checked for the absence lower limb length discrepancy and lumbosacral junction abnormality.

All the measurements were done by two independent observers and averaged. From the standard radiographs, the sacral slope (SS), the acetabular frontal inclination (AFI), and the acetabular sagittal inclination (ASI) were measured in standing, sitting, and lying positions.

From the CT scan sections, the anatomical ante-version (AA) was measured in lying position on axial images according to Murray. The results were compared to a previously described protocol replicating standing and sitting positions: CTscan sections were oriented according to sacral slope.

Results: We confirmed that the anatomical anteversion (AA), the frontal inclination (FI), and the sagittal inclination (SI) were functional parameter which significantly varied between standing, sitting, and lying positions according to sacral slope variations.The acetabular parameters in lying position highly correlated to the one in standing position, while poorly correlated with sitting position. The difference between the lying and the sitting positions was about 10°, 25°, and 15° for the AA, the AFI, and the ASI respectively.Mean lying anteversion angle was 24.2° (SD6,9°).Posterior pelvic tilt in sitting position, (sacral slope decrease) was linked to anteversion increase (mean value 38,8° - SD 5,4°). Anterior pelvic tilt in standing position (sacral slope increase) was linked to lower anteversion (mean value 31,7° - SD5,6°).

Discussion and Conclusions: Our study confirms the interest CTscan sections oriented according to sacral slope.The strong correlation between lying and standing measurements suggests that classical CTscan protocol is relevant for standing anteversion. According to the poor correlation between lying and sitting positions, it is less contributive for the investigation of dislocations in sitting position.

The shape of the femoral canal is variable, infact more variable than most contemporary designs of femoral components would suggest or accommodate. Clinical and experimental studies of total hip replacement have demonstrated the need for a close geometric fit between the femoral component and the supporting bone for a durable implant fixation. In order to provide a basis for design and selection of femoral components in future, we undertook an anthropometric study of proximal femoral geometry on Indian specimens.

74 cadaveric femorae were studied to analyze the difference in the endosteal and periosteal geometry between Indian and Western population. Standard extra-cortical and endosteal dimensions were determined by direct measurements of radiographs. To enable comparison standard horizontal and vertical axis were established using the geometric center of lesser trochanter and the bisecting axis of the medullary canal at the level of the isthmus. Statistically significant differences were found for the following measurements: Femoral head offset, Width at lesser trochanter, Width at lesser trochanter-20mm, Proximal border of isthmus, Neck shaft angle.

Introduction

A new conservative hip stem has been designed to address the complex problem of total hip arthroplasty in the younger population.

Introduction

Revision surgery is generally recommended for recurrent dislocation following Total hip arthroplasty (THA). However, dislocation following revision THA continues to remain a problem with further dislocation rates upto 28% quoted in literature.

We present early results of one of the largest series in U.K. using dual mobility cemented acetabular cup for recurrent hip dislocation.

Cementless femoral fixation is the gold standard in revision hip arthroplasty. Distal fixation is achieved using either a cobalt chrome or titanium stem. The purpose of this study is to report the long-term survivorship and clinical outcome of a titanium, long-stemmed, load-bearing calcar-replacement femoral component from an independent centre.

Eighty-one patients (average seventy-four years, range thirty-five to ninety-one) underwent hip arthroplasty with the Mallory-Head calcar-replacement femoral component, by a single surgeon. There were thirty-eight males and forty-three females with fifty-four hips initially revised for aseptic loosening, thirteen for peri-prosthetic fracture, and five for infection as a two-stage procedure. The implant was used as a primary device in eight patients with deformed proximal femurs. At most-recent follow-up, radiographic analysis was conducted and clinical outcome scoring was assessed using the SF-12, Harris Hip Score, and WOMAC questionnaire for surviving patients. Complications were also reviewed.

At a mean follow-up of 7.4 years (range four to fifteen), eight patients have died. There was one deep infection, three DVT’s, and two dislocations in the perioperative period. Six femoral stems have ultimately required another revision surgery for aseptic loosening, two for infection, and 1 for implant fracture at a mean of 5.6 years after initial revision. Four patients required removal of the proximal trochanteric bolt due to breakage or loosening. Overall survival of the implant at five years is 95% (CI 0.87–0.98) and 87% (CI 0.72–0.94) at ten years.

The clinical outcome of the Mallory-Head calcar-replacement femoral revision stem is reported from an independent centre. Although the results are encouraging, it would appear that proximal load-bearing fixation with the calcar-replacement stem is not as reliable as distal fixation. The use of a trochanteric bolt was associated with fracture of the greater trochanter or need for a separate surgical procedure for removal. For this series, there was an overall 11% failure rate at a mean follow-up of 7.4 years. The mechanical failure rate is 7.4%. Our overall and mechanical failure rates are somewhat higher than those of the implant developers, who reported 94% overall survival, and a 1.9% mechanical failure rate at a mean follow-up of eleven years.

The neck is the firmer structure of the proximal femur designed to spread the stresses both in compression and tension towards the metadiaphisys and the greater trochanter. Therefore femural neck preserving in total hip arthroplasty allows an optimized stresses’ distribution to obtain both an optimal integration and a subsequent better bone remodelling. The solidity of the structure and the geometric architecture with a femural neck angle of 125° guarantee the maximum primary stability, especially torsional of the stem. At last femural neck retaining allows, when requested, the revision with a richer bone-stock. For the aforementioned reasons since 1979 I proposed the femural neck preservation making a short cementless stem named Biodinamica. From 1983 to 1996 I personally implanted 498 Biodinamica prostheses with very satisfactory results showing a long term survival of the 98% (f.up 13 to 17 years). In 1996 with Ing. Keller it has been created the C.F.P. stem with the T.O.P. acetabular cup as evolution of Biodinamica system. The improvements are critical: materials have changed (from Cr-Co-Mb to Ti alloy), coating and design too. We report clinical and radiographical results of 10 years of C.F.P. implants that showed a further improvement, not only about the prosthesis’ survival, but especially regarding their quality with a 91% excellent clinical outcome. In conclusion we report the 25 years experience retaining the femural neck in hip arthroplasty with Biodinamica (498) and after C.F.P. (445) of a complessive cases of 943 arthroplasty.

Purpose of the study: The purpose of this work was to compare the subjective and functional outcomes of patients with a large diameter total hip arthroplasty (LD-THA) or hip resurfacing (HR).

Material and methods: Forty-eight persons were assessed and double blind randomised to receive either LD-THA (n=24) or HR (n=24). The clinical and radiographic assessment and gait analysis were performed preoperatively and at three, six and 12 months postoperatively. Gait analysis was performed once in a third group of healthy adults (n=14) who served as controls.

Results: The two groups were comparable preoperatively regarding demongraphic and functional characteristics. Postoperatively, the two groups with prostheses exhibited very rapid recovery with normalization of test results compared with controls within three to six months. The clinical assessment, the analysis of postural balance, gait analysis and most of the specific tests were not different between the two groups with prostheses.

Conclusion: There was no remarkable difference in subjective or objective assessments between subjects with a LD-THA or HR. This suggests that the only potential advantage of HR is the preservation of femoral bone stock. Long-term HR implant survival will determine the reality of this benefit.

Purpose: Several studies have shown elevated levels of metal ions in blood of patients with metal-on-metal (MM) total hip arthroplasty (THA). To minimize wear, the elastohydrodynamic theory suggests wear reduction for larger diameter head bearings. This significant reduction in wear has been demonstrated in hip simulators for the 36 mm-head compared to the 28 mm-head prosthesis. However, the survival of larger head MM THAs and the levels of metal ions in the blood of patients having these implants are still to be determined.

Method: Fifty (50) patients (56 hips) who received a DePuy Ultamet™ MM hip bearing (40/44 mm-head) at our Institution between July 1st 2007 and August 31st 2008 were included in the study. Clinical and radiologic data were collected pre-operatively as well as at 6–8 weeks, 4–6 months, and 1 year postoperatively. Results were compared to those of subjects (65 patients, 71 hips) who received a 36 mm-head prosthesis. Cobalt (Co) and chromium (Cr) concentrations were measured at 1 year post-operatively in the blood of patients by ICP-MS. Since Co and Cr ions have the potential to induce irreversible biochemical damage to macromolecules, the levels of oxidative stress markers (total antioxidants and lipid peroxides) were measured in the plasma of these patients.

Results: At their 1-year post-operatively follow-ups, all patients were doing well and no sign of osteolysis was observed on X-rays. Harris Hip Score increased in both groups with a tendency to higher score in the 40–44 mm group compared to the 36 mm group. Activity score also increased in both groups after 1 year without statistical significant differences. Results also show that the levels of Co and Cr ions increased significantly in both groups compared to the Pre-OP control group. The levels of Co were also significantly higher in patients with large head arthroplasty (40 and 44 mm-head) compared to those of the 36 mm-head group (p=0.012). The levels of Cr were similar in both the large head and the 36 mm-head group (p=0.41). Finally, results show that there were no differences in the levels of total antioxidants and peroxides between the 40–44 mm group and the 36 mm group. Moreover, there was no increase in the level of these markers of oxidative stress compared to the Pre-OP control group.

Conclusion: The present study shows that at 1-year postoperatively, patients with large 40–44 mm-head THA had comparable clinical outcomes than those with 36 mm-head prosthesis. However, the levels of Co ions were significantly higher in these patients compared to patients with 36 mm-head THA. This suggests a higher health risk for these patients due to the presence of these ions. However, there were no effects on the levels of oxidative stress markers in the blood of these patients, suggesting that there is no increased risk at short-term. In conclusion, due to the high level of Co ions, longer follow-ups are required to conclusively determine the outcomes of the patients and the survivorship of these new bearings.

Aims: Infection of total hip replacement still is considered a devastating complication. One stage revision, meaning removal of implant and debris together with insertion of a new prosthesis during the same operation, reduces rehabilitation time and costs. To overcome the disadvantages of using cement, uncemented techniques seem to be favourable.

Methods: After removal of the implants debridement is performed as in conventional septic surgery. After thorough cleaning and rinsing, bone voids are filled with bone graft using an impaction technique. We use cancellous bone that is free from antigenic material but intact structures concerning collagen and mineral content. The bone is impregnated with high loads of antibiotic, using a proprietory incubation technique. There are two options of antibiotic impregnation: vancomycin or tobramycin. The impregnation procedure guarantees high levels of antibiotics at the grafting site for several weeks during which the antibiotic is released into the surrounding. Systemic drug levels usually are undetectable. Consequently an uncemented prosthesis is inserted. Wounds are drained and closed immediately, rehabilitation is performed as after non-septic surgery.

Between 1996 and 2003 35 patients have been revised because of culture proven infection of a hip endoprostheses. All hips could be followed with a minimum of 3months and a maximum of 6years.

Results: Wound healing was uneventful in all cases. Mean hospital stay was 16days (10–32days). In three hips there was recurrence of the infection, diagnosed between 6 and 12 weeks after surgery. One could be successfully re-operated using the same technique, the other two were converted to a girdlestone situation. All other 32 hips showed no sign of infection until the last follow up.

Conclusion: One stage non-cemented revision may provide an excellent solution for infected total hip replacement. However, several principles need to be observed. Bone processed in an adequate way represents an excellent carrier for vancomycin and tobramycin. Using an antibiotic graft compound eradication of pathogens, grafting of defects and re-insertion of an uncemented prosthesis may be accomplished in a one stage procedure. Since the graft gradually is replaced by healthy own bone, improved conditions may be expected even in the case of another revision.

Material and methods: Two series of 35 total hip arthroplasties (THA) implanted by the same surgeon using the posterior approach were compared. The first group underwent surgery in 1999 and the second in 2001. Ligation of the posterior medial circumflex artery was systematically performed in the second group. The same prosthesis was used in all cases: an omnicase stem and a Schuster (Centerpulse) or polyethylene cup. The series included cemented (n=37) and non-cemented (n=32) prostheses with one hybrid implant. We analysed retrospectively, intra- and postoperative bleeding, haematocrit before and just after surgery, and the number of packed red cell units transfused during and after surgery in order to determine the degree of intra- and postoperative bleeding. Statistical tests were applied.

Technique: Via the posterior approach, before sectioning the pelvitrochanteric muscles, the upper third of the fibres of the quadratus femoris muscle were dissociated. The artery runs upwardly and anterior toward the posterior border of the greater trochanter and is difficult to identify in the fatty tissue. Ligation is performed at this level with the satellite veins. Ligation decreases bleeding when the pelvitrochanteric muscles and the capsule are sectioned. Likewise, section of the femoral neck appears to be less haemorrhagic as is the preparation of the proximal greater trochanter.

Results: Intra- and postoperative bleed, expressed in ml, was significantly decreased by ligation of the posterior circumflex artery and its two satellite veins. Mean intraoperative bleeding was decreased by more than half. Six of the 35 patients who did not have ligation lost more than 600 cc blood during the operation. This degree of bleeding was not observed in the ligation group. The postoperative haematocrit was significantly higher in the ligation group and the difference in pre- and postoperative haematocrit was decreased 7-fold. Postoperative transfusion became exceptional. Finally, it is interesting to note that among the variables studied, mode of implant fixation did not affect blood loss.

Discussion: The conventional technique without ligation of the posterior circumflex artery does not always lead to significant bleeding. It is quite possible to perform such procedures with less than 200 cc blood loss. Use of posterior circumflex artery ligation leads to much more regular control of intraoperative bleeding, making autologous blood collection and postoperative transfusions unnecessary. The ligation is a simple procedure. Electric coagulation is generally insufficient for the calibre of these vessels and veins are not always accessible to effective coagulation. Intraoperative bleeding due to section of the circumflex artery is underevaluated due to the tension created by the forced internal rotation. Haemostasis after section is difficult due to retraction of the proximal segment under the muscles.

Introduction: The goal of the study was to determine the precision of a three-dimensional pre-operative planning tool using a specific software (HIP-PLAN^®) and an anatomic cementless neck-modular stem.

Method: 223 patients who underwent a primary total hip replacement had a CT Scan before and after surgery. A pre-operative three-dimensional planning based on the CT-scan was performed. A cementless cup and a neck-modular stem were used. A computational matching of the pre-operative and the post-operative CT-scans was performed in order to compare the values of the planned anteversions and the planned displacement of the hip rotation center to the post-operative values.

Results: The implanted component was the same as the one planned in 89% for the cup and 94% for the stem. For the mean femoral anteversion, there was no significant difference between the planned value (26.1° +/−11.8) and the post-operative value (26.9° +/−14.1). There was a poor correlation between the planned values and the actual ones for the acetabular cup anteversion (coefficient 0.17). The hip rotation center was restored with a precision of 0.73 mm +/3.5 horizontally and 1.2 mm +/−2 laterally. Limb length was restored with a precision of 0.3 mm +/−3.3 and the femoral off-set with a precision of 0.8 mm +/−3.1. There was no significant modification of the femoral off-set (0.07 p=0.7) which was restored or slightly increased in 93% of cases. Almost all the surgical difficulties were predicted

Conclusion: HIP-PLAN^® software is a reliable three-dimensional pre-operative planning tool which allows acurate prediction of components and hip anatomy.

We compared and quantified the modes of failure and patterns of wear of 11 Mittelmeier and 11 Ceraver-Ostal retrieved alumina-alumina hip prostheses with reference to the corresponding clinical and radiological histories.

Macroscopic wear was assessed using a three-dimensional co-ordinate measuring machine. Talysurf contacting profilometry was used to measure surface roughness on a microscopic scale and SEM to determine mechanisms of wear at the submicron level.

The components were classified into one of three categories of wear: low (no visible/measurable wear), stripe (elliptical wear stripe on the heads and larger worn areas on the cups) and severe (macroscopic wear, large volumes of material lost). Overall, the volumetric wear of the alumina-alumina prostheses was substantially less than the widely used metal and ceramic-on-polyethylene combinations. By identifying and eliminating the factors which accelerate wear, it is expected that the lifetime of these devices can be further increased.

Introduction: There have been concerns regarding early loosening of the Elite Plus implant. In addition, catastrophic failure has been reported with the Zirconia ceramic head in combination with Hylamer Ultra-High-Molecular-weight-polyethylene (UHMWPE) acetabular liner.

We reviewed all patients under the care of the senior author, who had undergone Elite Plus hip arthroplasty.

Methods: All patients are under regular review in a nurse-led clinic and complications recorded.

Pre and post-operative radiographs were assessed for adequacy of cementation and evidence of loosening.

Results: 197 patients (mean age 72 years) had undergone 225 Elite Plus total hip arthroplasties since 1996. An additional 21 patients had no radiographs or case notes available at the time of review – none of these are known to have failed.

Standard UHMWPE Ogee acetabular components were used in all cases. Thirty-six percent of heads were Zirconia. Mean survivorship of all implants 5 years 2 months.

The revision rate was 2.7%. Only one revision was performed for femoral component loosening.

At latest radiographic review all patients were asymptomatic. However, 31% of femoral components were possibly loose, 5% probably loose and none definitely loose using the Harris criteria. Thirty-four percent of acetabular components were possibly loose, 8% probably loose and 1% definitely loose using Charnley/DeLee criteria.

Discussion: Our results demonstrate satisfactory performance for this hip system. We have not found significant evidence of early failure with the Zirconia and Ogee combination.

A cement restrictor, high-viscosity cement and pressurisation were used as standard. Alternative cementation techniques may partially explain early failure seen in other series.

Purpose: Bone remodelling and osteolysis around total hip arthroplasty (THA) is a highly debated subject in the medical literature. Such bone behaviour is poorly understood around femoral stems used in revision THA. The main problem is to obtain an objective assessment of bone remodelling and bone reconstruction over time, reconstruction techniques being very variable. Conventional radiology is insufficient, but dual energy x-ray absorptiometry (DEXA) provides a means of following changes in the bone around first intention femoral stems.

Material and methods: We studied bone behaviour around revision femoral stems using the non-cemented “P.P. system”. This type of femoral stem is implanted after trochanter osteotomy to facilitate access and stimulate reconstruction. The series included 31 patients who underwent revision total hip arthroplasty. Follow-up examinations included standard radiographs and DEXA of the operated hips, the contralateral hip and the lumbar spine. Periprosthetic zones defined by Grüen were compared with the same zones in the contra-lateral femur. Mean follow-up was six years.

Results: The standard radiographs did not demonstrate any significant change in periprosthetic cortical thickness. The DEXA demonstrated a significant an average 19.97% reduction in bone density in zones 2, 3, 4, 5 and 6. There was no significant difference in zone 7 and an increase in zone 1 (torchanter osteotomy). These figures are to be compared with the variable thickness observed for first intention pros-theses even shortly after implantation.

Discussion: Our results are the first to our knowledge demonstrating the behaviour of bone around revision femoral stems.

Conclusion: Digastric trochanterotomy appears to be an effective means of stimulating reconstruction of the proximal femur. At equivalent follow-up, the quadrangular section of the revision P.P. stem is more favourable in terms of bone loss compared with first intention stems.

Computational modelling has the potential of becoming a useful tool in assessing revision risk on a patient-specific basis. However, there are many difficulties encountered in generating subject-specific computational models that have unknown influences on such predictions, e.g. accuracy of the anatomical geometry and material properties of the patient. This study compares the influence of these two patient-specific parameters on predictions of revision risk due to aseptic loosening.

First, X-rays from seventeen patients were processed using previously developed technique utilising rigid scaling of a generic femur to match selected dimensions from each patient’s post-operative X-ray and, then, the same set of 3D models was obtained by using an automated technique that generates 3D extra-cortical geometries from planar X-rays using a combination of 2D contour extraction and 3D warping of a generic model to match the extracted contour.

A cement and cement-metal interfacial damage accumulation algorithm developed previously was used. For each geometric set two types of simulations were performed. First, constant cortical and cancellous bone apparent Young’s moduli were assumed. A second set of simulations used age-dependent Young’s moduli for each bone type. Walking and stair-climbing activities were simulated. Resultant migration of the prostheses was used to indicate revision risk.

Factorial analysis has shown that the geometry has a larger influence on resultant migration magnitude for each case; however, unexpectedly, using more realistic geometry weakened the strength of predictions. This is most likely to be due ongoing mesh-induced contact problems.

Purpose of the study: Implantation of a total hip arthroplasty (THA) for major misalignment is a difficult procedure and few results have been published. In the 1950s to 1970s, supra-trochanteric osteotomy was proposed for sequelar osteoarthritis of congenital hip dislocation. Subsequent degradation 20 to 30 years later can lead to neo-osteoarthritis of the joint with an effect on hip alignment and overall balance between the knee and the spine. We present a prospective consecutive series of 60 THA performed from 1991 to 2003on hips with Milch and Schanz osteotomies.

Material and methods: The objective was to reconstruct an anatomic hip joint by femoral re-alignment de-osteotomy, inferior displacement of the hip joint to enable insertion of an implant with a correctly position center of rotation and normal muscle lever arms. The technique was novel because of the direct approach to the subtrochanteric angle. The step by step procedure enabled insertion of the prosthesis without trochanterotomy. Overall recovery was long, often 12 to 18 months. There were 47 patients 60 hips) with at least 18 months follow-up. None of the patients were lost to follow-up.

Results: Results were available for 54 hips (three deaths, six hips). Mean follow-up was eight years. Outcome was good (patient satisfaction, normal x-ray) for 77%. Twelve hips presented poor clinical and radiological results due to loosening and mobilization of the femoral implant with or without nonunion of the deosteotomy. Ten hips were revised at mean five years via a femoral access for insertion of a press-fit distally locked prosthesis with graft of the nonunion (with acetabular replacement in one hip). The outcome was good at last follow-up for nine of these hips. One repeated revision gave satisfactory results.

Discussion: The only factors of risk of failure were related to femoral re-alignment and absence of trochanterotomy. A lesser risk of nonunion was related to the technique used for osteotomy, osteosynthesis and grafting. The use of a non-cemented implant with a solid primary stability and in certain cases a custom-made implant can be discussed for selected patients.

Stress shielding of the proximal femur occurs in stemmed implants. Resurfacing implant does not invade the intramedullary region. We studied the stress patterns in conventional and nonstemmed designs.

Introduction. Advantages of ceramic materials for hip joint prosthesis are recognized to be high hardness, scratch resistance, improved wettability, lower friction and lower wear than CoCr surfaces. Recent studies suggest the use of ceramic femoral head reduce fretting corrosion at stem taper junction compared to metal-on-metal taper junction[1]. Continuous improvement of ceramic materials for orthopedic lead to the development of a resurfacing ceramic-on-ceramic hip joint prosthesis. The main differences of resurfacing heads respect to standard heads are their anatomical dimension and the empty shape suitable to cover the femoral bone and to connect with the resurfacing stem. Ceramic is essentially a brittle material and its strength is influenced by the minimum thickness in the stressed area. Ceramic resurfacing head minimum thickness is comparable with ceramic revision head already on the market. The aim of this study is to develop a mechanical pre-clinical analysis verification process for the newly developed system. Materials and methods. The empty shape of the ceramic resurfacing head may influence its strength in a crush loading scenario. Although this is not a physiological condition this test represents the most severe loading for a resurfacing head. Also comparative analysis can be done considering the yield point of conventional metal resurfacing heads reported by the FDA Center for Devices and Radiological Health. For this reason a static unsupported head strength test is performed by applying a compressive load perpendicular to the head axis along the equatorial plane[2](Fig.1). Resurfacing ceramic head made in ZTA is suitable both for a resurfacing stem and an adaptor to be coupled with a standard stem. Mechanical test was performed on worst case resurfacing head size both with resurfacing stem and standard stem based and on FE non linear analysis performed in ANSYS 17.2 according the following material properties: ZTA ceramic (modulus of elasticity E, Poisson ratio ν and density ρ of 348GPa, 0.23 and 4.25g/cm. 3. respectively), and Ti6Al4V (E=114GPa, ν=0.33 and ρ=4.43g/cm. 3. ). For comparison purposes unsupported test was performed on standard head Ø28#S both in Biolox®Delta and Biolox®Forte ceramic. At least three components were used for each test and the average values was compared with predicates[2]. Static compressive load was applied with MTS hydraulic actuators with load cell of 100kN. Results. FE analysis indicated the larger resurfacing head as the worst case size in the size range(Fig.2). Static unsupported head strength test was performed on resurfacing ceramic head Ø57 coupled both with resurfacing stem and standard stem, Biolox®Delta head Ø28#S, Biolox®Forte head Ø28#S and respectively reached a strength value of 53±7kN, 90±3kN, 78±27kN, 49±1kN. Equivalent test were reported in literature for DeltaSurf® Ø58 and BHR. TM. , and respectively reached a strength of 26kN and 5.6kN. Discussion and Conclusion. LIMA ceramic resurfacing head and Biolox Forte Ø28#S showed equivalent unsupported head burst strength. LIMA ceramic resurfacing head showed higher unsupported head burst strength respect to DeltaSurf® and BHR. TM. highlighting its potential in clinical use. For any figures or tables, please contact the authors directly

Purpose: The purpose of this study was to evaluate ten year outcome of the 28-mm head self-locking cemented Müller THA.

Material and methods: From May 1988 to May 1990, 187 second generation cemented prostheses were implanted via the transgluteal approach for osteoarthritis. The femoral implant was a straight Prostasul 10 implant with a 28-mm modular head and a gamma ray sterilised poly-ethylene cup. At ten years, for the 187 implants: 64 patients had died, 24 patients were contacted by telephone (all with implants in place) nine were lost to follow-up, and 90 implants in 82 patients were reviewed. The reviewed series included 42 women and 49 mean, mean age 65 years. Clinical outcome was noted with the Postel Merle d’Aubigné score (PMA). Radiographical assessment noted lucent lines, granulomas, migrations, wear, and ossification.

Results: Among the 187 implants, two patients required revision: one for infection and the other for posttraumatic dislocation. Among the 82 patients reviewed at ten years, the PMA score was 16.85 (92% good and very good results). Radiographically, the acetabulum showed nine lucent lines measuring greater than 1 mm and progressing between five and ten years, one migration, and two cases of migration as well as three cases of wear greater than 2 mm. Evaluation of the femur showed osteolysis in zone 3 and 4 in one hip and rarified bone in zone 7 in four. Linear penetration of the head in the cup was 0.08 mm/yr. Brooker stage 3 ossifications were found in 27% of the men and 14% of the women.

Discussion: The clinical results were comparable to other series of cemented prostheses. At ten years, potential loosenings were more frequent at the acetabular level with progressive lines always present at five years; and polyethylene wear that was not always associated with osteolysis or granuloma, while osteolysis and granulomas were always associated with wear greater than 2 mm. Furthermore, there was no anatomoclinical relationship and radiographic anomalies did not always have an effect on function. Prevention of ossifications appears to be important, particularly in men.

Total hip arthroplasty in adult patients with congenital high dislocation of the hip (DDH, Crowe type IV) presents many challenges. Various reconstruction methods including iliofemoral distraction lenghtening and custom made prosthesis have been reported but the standard technique for dealing with this problem is femoral shortening with a subtrochanteric osteotomy. There are many reports of different subtrochanteric osteotomy techniques with satisfactory results.

Since 1999, we have been using the same anatomic reconstruction principles with a proximally hydroxyapatite coated cementless stem. Surgical technique on the femoral side comprises a short oblique subtrochanteric osteotomy and excision of a segment as indicated for a safe reduction. This usually requires extensive soft tissue releases of the pelvifemoral muscles. Gluteus maximus, tensor fascia latae and adductors are routinely released. However, we don’t want to do any more release until it is absolutely necessary. Preserving the attachment of the abductors and iliopsoas are important for eventual functional outcome. They help stabilizing the joint, avoid limping and promote hip flexion during the initial swing phase of the gait and stair climbing. We never resect neither osteotomize the trochanters and, if a release is unavoidable, it is performed proximally. Thus, it is possible to preserve a complete segment of the proximal femur with a soft tissue envelope. This segment allows for better bone stock, prompt healing, reliable proximal fixation through the intact medial calcar and, avoids the complications of trochanteric osteotomy. With this technique we have not observed a femoral revision for any reason in 101 high dislocated hips (in 84 patents), since 1999. Compared with other techniques for arthroplasty in patients with developmental hip dysplasia, this surgical technique has a better functional outcome and a low prevalence of revision.

To evaluate the effect of this reconstruction on gait parameters we analyzed the gait cycle in 17 hips in 10 patients before and after the the total hip arthroplasty and compared it with the patients with hip arthroplasty due to primary osteoarthritis. Our aim is to determine the restoration of normal anatomy in DDH patients compared to the patients with total hip arthroplasty but a normal hip anatomy. As a result we have demon-strated that our technique restores normal gait parameters by improving walking speed, lengthening step-stride length, correcting hip and knee flexion and ankle equinus, improving hip and knee stiffness during gait and helps to restore normal gait parameters

BACKGROUND CONTEXT

Ceramic bearings are widely used in total hip arthroplasty (THR) along with metal and polyethylene bearings. There were several studies in past few years evaluating the advantage of one over the other. The young population with high activity levels has an increased risk of wear debris production at bearing surface and subsequent implant failure. Recently, interest and use of a ceramics with high wear resistance has been growing. Early reports on ceramic on ceramic THR have demonstrated excellent clinical and radiological results.

We report the long-term radiographic results of the total hip arthroplasty with use of the cementless porous coated Harris-Galante (H-G) stem. Seventy-five consecutive patients, eighty-eight hips formed the basis of this study. Fifty patients were male, twenty-five patients were female, and thirteen patients were bilateral. The mean age of patients at operation was 42 years. They were followed up for an average of thirteen years four months (ten years two months to fourteen years four months). The diagnosis was avascular necrosis of the femoral head in 49 cases, degenerative osteoarthritis in 32 cases. Clinical results were estimated by modified Harris hip score and thigh pain, and radiographic results by periodically checked plain X-ray film. The average Harris hip score increased from 60 points preoperatively to 83 points at the most recent follow-up examination. The hip pain score increased from 31 points to 41 points. Clinically severe thigh pain was observed in 3 cases (4%). In radiographic evaluation, subsidence more than 5mm was seen in 2 cases (2%). Periprosthetic osteolytic lesion was observed in 15 cases (17%), but the lesions do not influence stability of the stem. Femoral stem stability by Engh was stable in 72 cases, fibrous stable in 12 cases, unstable in 4 cases. Pedestal formation, cortical hypertrophy of the distal femur, and stress shielding was observed more than 40%. Subcollar resorption was identified in 29% and ectopic ossification in 15%. Revision of the femoral stem was needed in 4 cases for aseptic loosening. At 10 years probability of survival of the stem using Kaplan-Meyer method was 95.5%. Use of the cementless H-G stem yielded the excellent long-term outcome, but osteolysis and stress shielding would be the main problems to solve.