INTRODUCTION. Progressive polyethylene wear is associated with the occurrence of osteolysis, which can lead to component loosening and subsequent revision. Massive wear of the polyethylene liner may result in the penetration of the femoral head through the metal shell. Although metallosis after total hip arthroplasty has been well documented in the literature, extensive metallosis with polyethylene wear-through has been only sparsely described. The purpose of the present study was to assess clinical findings and the results of revision total hip arthroplasty in these cases. METHODS. We evaluated seven hips in five patients who underwent revision total hip arthroplasty because of metallosis with polyethylene wear-through. The average age of the patients at the time of hip revision was 70.1 years. There were granulomatous cysts surrounding the hip joint and osteolysis in the greater trochanter or in the acetabulum. Eroded metal shells with worn-through polyethylene were exchanged. Kerboull-type acetabular reinforcement device were used in five hips and GAP cup in two. Distal interlocking femoral stems were used in four hips and extensively porous-coated stems in two. All cases with osteolysis were in addition treated with bulk or morselized allograft bone. The mean duration of follow-up was 3 years. RESULTS. At the time of final follow-up evaluation, none of the hips showed osteolysis. Stable fixation of femoral and acetabular components was achieved in all cases. Bulk allograft bone was resorbed in two cases, but in all other cases grafted bones were united and improve bone stock. CONCLUSIONS.
Purpose: Although hip prosthesis heads made of titanium are no longer implanted to our knowledge, it is important to officially record the failures related to their use. Device monitoring experts can only prove the hazard resulting from these implants if results of human clinical series have clearly described the inconveniences. We found a rich body of literature dating from the end of the eighties that concluded that the rate of wear with the polyethylene lined titanium implants was very low but have found no paper describing the problems related to its use. We report this work to fill the gap. Material and methods: This prospective study included a consecutive series of the first 100 total hip prostheses using the ion-implanted titanium 22.2 mm head (NITRU-VID) implanted between January 30, 1990 and June 19, 1991. There were 45 men and 55 women, 55 right hips and 45 left hips implanted for primary degenerative disease in 92, dysplasia in two and congenital dislocation in six. Mean age at implantation was 60 years (28–82). The same operative technique was used for all patients using the same Atlas-PSM implant. Eleven patients died and six were lost to follow-up. Thus 83 ere retained for analysis with the Postel-Merle-d’Aubigné (PMA) score on the AP and lateral views of the hip. Kaplan-Meier survival curves were established. Results: Eleven patients underwent revision surgery for different causes, metallosis in seven. The delay to revision for metallosis was eight years in two, nine years in one and ten years in four. These cases of metallosis were expressed clinically by moderate pain and minimal radiographic signs: bone defect in the greater trochanter in seven, acetabular lines in three. Four cups loosened, none of the femur components. The diagnosis of metallosis was made at revision in five cases, and on the basis of hip biopsy in two.
There is no doubt that the future of limb lengthening lies with internal lengthening. Complication rates are reduced and patient satisfaction is increased. The evolution of internal lengthening peaked with the dual direction, easily inserted and externally controlled PRECICE Nail. It has excelled in performance in accuracy and satisfaction. Its versatility increased with smaller sizes and increased excursion. A field safety notice was issued was issued in October 2021 by the parent company NuVasive. The advice was monitoring of current cases and a hold on implantation until after a review of process. At the National Orthopaedic Hospital Cappagh we elected to remove all implanted nails and assess the nail integrity and physiological changes associated with implantation. All patients in who a retained Precice nail at the time of the field safety notice were identified. Patients and families were contacted to explain the issued safety notice from the company and explain that we would be scheduling them for nail removal. This was part of our standard care but we prioritised this group on our waiting list. Consent was obtained for nail removal but also for histological assessment of canal scrapings, blood ion level analysis and independent assessment of the retrieved nail by our academic collaborators at University College Dublin. Ion levels were then repeated at an interval post removal with consent.Introduction
Materials & Methods
Recent reports about the excellent clinical results of unicondylar knee arthroplasty (UKA; also known as unicompartmental knee arthroplasty), by the minimally invasive approach, have encouraged the adoption of the surgical technique. However, friction between metallic prosthetic components resulting from polyethylene wear may result in the development of metallosis and the use of metal implants has become a huge issue in the worlds recently. Here, we report a case in which a patient underwent UKA and developed metallosis in soft tissues and bone adjacent to an implanted artificial joint three years postoperatively.
We studied 12 patients (13 elbows) who underwent total elbow replacement (TER) using the Kudo Mk IV or V prosthesis between 1989 and 1997. There were eight females and four males (mean age: 61 years, range: 38–74 years). The diagnosis was Rheumatoid arthritis in 10 patients and osteoarthritis in two patients. In each patient the initial result was classified as either excellent or good. All these patients then reported the recurrence of severe pain at a mean of four years from the time of the primary operation. Radiographic examination demonstrated fracture of the humeral stem in 10 elbows and subluxation of the joint in three elbows. The fractured humeral components were exchanged for long stem components. The three subluxated elbows were found to have undergone delamination and loosening of the ulnar components which were revised. One of these required revision to a linked prosthesis due to bone loss. In each case metallosis was found involving principally the synovial tissues which were as far as possible excised. Each patient regained a similar range of movement to that following the primary arthroplasty but continues to experience episodes of pain requiring anti-inflammatory medication. This is in contrast to our patients requiring revision procedures for implant loosening or instability who have become pain free. We conclude that the development of metallosis complicating mechanical implant failure predisposes to persisting symptoms following revision arthroplasty and recommend that this should be undertaken sooner rather than later when mechanical failure is detected.
Between 1989 and 1993, 158 patients with a total of 187 damaged knees underwent TKA using AGC-S prosthesis (Biomet). Of these patients, six required revision surgeries due to metallosis. The average period from the first operation to the revision was 68.0 months (range: 41–97 months). In all six cases, the plain X-rays taken immediately before reoperation, showed sinking of the tibial component. The withdrawn implants showed severe abrasion of the polyethylene used in the posteromedial area. The percent share of the tibial component averaged 90.3% (range: 85.3–93.5%) on the anteroposterior view, and on the lateral view averaged 83.1% (range:76.9–94.0%). The tibial components used for AGC-S type TKA can be characterized by the presence of a rim. In some cases, however, the rim cannot be placed on the tibial cortex, and this obliges the surgeon to select smaller components, resulting in a smaller percent share of the tibial component. The tibial component can sink in such cases. The sinking of the tibial component probably leads to malalignment and joint instability. Furthermore the insert with a flat surface was likely to induce articular instability, thus enhancing the abrasion of the polyeth
Complete wear-out of Polyethylene (PE) liner results in severe metallosis following articulation of the artificial head with the acetabular metal shell. We postulated that an adverse response can be led to surrounding bone tissue and new implant after revision surgery because the amount of PE wear particle is substantial and the metal particles are infiltrated in this catastrophic condition. We evaluated clinical characteristics and the survival rate of revision total hip arthroplasty (THA) performed in patients with severe metallosis following failure of PE liner. Between January 1996 and August 2004, severe metallosis following complete wear-out of PE liner were identified during revision THA in 28 hips of 28 patients. One patient had died at 7 days after surgery and 3 patients could not be reached at 5 year follow-up. Twenty-four hips of 24 patients (average age, 47.5 years) were followed for at least 6.5 years (average, 11.3 years; range, 6.5–15.9 years) and were evaluated. The mean time interval between prior surgery and the index revision surgery was 9.6 years (range, 4.0–14.3 years). The indications for revision surgery were osteolysis around well-fixed cup and stem in 22 hips and osteolysis with aseptic loosening of the cup in 2 hips. Bubble sign was observed on preoperative radiograph in 10 hips. Total revision, cup revision, and solitary bearing change were performed in 13, 10, and one hip respectively. A cementless implant was used in 23 hips and acetabular reinforcement ring was used in one. Clinical evaluation was performed using Harris hip scores and Kaplan-Meier survival analysis was performed. Multivariate analysis was performed with age, gender, BMI, bone defect type, existence of bubble sign and type of revision surgery as variables to evaluate the association with osteolysis or loosening.Purpose
Materials and Methods
The risk of dislocation in large diameter metal on metal hip replacement is significantly lower than in standard THR. This is due to the increased primary arc, increased jump distance and possibly a suction effect. Our unit has performed over 1500 of these cases with an overall revision rate of <1%. We report a case series of dislocations in 5 large diameter metal on metal hips undertaken at our unit. All cases were reduced closed and investigated for cause of dislocation. Radiological investigation included plain film radiographs and CT to exclude component mal-position and MRI to document soft tissue deficiency. Metal ion levels were measured and microbiological investigation was undertaken.INTRODUCTION
METHOD
The advantages of large diameter metal on metal total hip arthroplasty (MoM THA) and hip resurfacing arthroplasty are decreased wear rate, preservation of bone stock, anatomical restoration and enhanced stability. Large amounts of metal wear particles and metal ions are released which may induce adverse reactions including local soft tissue toxicity, hypersensitivity reactions, bone loss and risk of carcinogenesis. Aseptic loosening can be the result of a peri-prosthetic osteolysis generated as a result of a biological response to particulate wear debris. No reports in the literature exist as to whether circulating levels of Chromium (Cr) and Cobalt (Co) decrease upon removal of a symptomatic large diameter MoM implant or whether levels remain high due to the effect of metal ions debris left behind in the soft tissues after revision surgery. Between June 2006 and June 2009 we undertook 44 revision surgeries of both large head MoM THAs (femoral head diameter 38mm) and metal-on-metal hip resurfacings for suspected metallosis. Mean time from original implant to revision was 4 years, 8 months (1yr 4mo–7yr 9mo). The mean follow up evaluation was 2 years and 2 months (1yr 2mo–4 years). Blood samples were taken for whole blood Cr and serum Co according to a recognised protocol and compared with reference levels indicated by the Medicines and Healthcare Regulatory Agency recommendation of less than 7ppb for Cr (130nM/L) and Co (119nM/L).INTRODUCTION
PATIENTS AND METHODS
We present two patients with swelling of the groin following metal-on-metal total hip replacement without radiological signs of component loosening. MRI in both patients showed a round shaped intrapelvic lesion ventral to the femoral head. During surgery we found cystic structures filled with fluid and necrotic masses. After resection the metal head and insert were changed to a ceramic head and a polyethylene insert. Although two different kinds of CoCrMo alloy were used in the metal-on-metal THR (Sikomet: low carbon content-Metasul: high carbon content) histopathological analysis in both cases showed typical morphological signs of hypersensetively determined inflammation. Despite the distinct soft tissue reaction bony component integration was unaffected. In our opinion open resecion of the cystic lesion and changing of the metal-on-metal articulation is the treatment of choice. As we do not have any reliable testing for clinical use to predict a hypersensitive reaction to metal wear after implantation of metal-on-metal THR this articulation surface should not be used in cases where allergy to metal is suspected.
The December 2013 Wrist &
Hand Roundup. 360 . looks at: Scapholunate instability; three-ligament tenodesis; Pronator quadratus; Proximal row carpectomy; FPL dysfunction after volar plate fixation; Locating the thenar branch of the median nerve;
Introduction. In revision surgery, detection of periprosthetic joint infection is of prime importance. Valuable preoperative and intraoperative diagnostic tests and tools are necessary. The classical standard procedures are puncture and bacteriology examination, frozen section intraoperative and powerfield micro analysis. Since autumn 2014 a new device for detection of periprosthetic joint infection is available, named Synovasure. It is a fast test for the detection of Alpha defensing, which plays a major role in the antimicrobial defence and only occurs in inflammatory processes. „The alpha-defensin test is an immunoassay that measures the concentration of the alpha-defensin peptide in human synovialfluid. A-Defensin is an antimicrobial peptide that is secreted into the synovial fluid by human cells in response to pathogenic presence” (Deirmengian C et al., CORR 2014). Summarized, the evidence of Alpha defensin indicates infection. It is produced by CD Diagnostics (Wynnewood, PA, USA) and merchandised by Zimmer (Warsaw, IL, USA). We are using Synovasure in daily routine at our department since September 2014. The aim of this conducted study is to present our first clinical experience and to report our results of the first 54 cases. Material and Methods. At our department Synovasure is standardly used in hip and knee revision surgery. Additionally an intraoperative frozen section and a standard bacteriology were performed. The explanted endprosthesis were sent to examination by sonification in order to gain culture of the sonification fluid and were further examined by Multiplex PCR. A pathologist with more than 15 years of experience conducted the frozen section. The results of Synovasure were matched with all above examinations in order to describe specifity and sensitivity of it. Results. A negative Synovasure Test during surgery and a negative PCR were observed in 3 patients, however, the bacterial culture was positive (after 14 days of breeding) as well as the Multiplex PCR. One patient had a negative frozen section and a negative culture but a positive PCR. Another patient with a high CRP level, all clinical signs of infection and a positive Synovasure Test, had 6 negative cultures. This patient suffered from a
Aim. A key of success in the treatment of prosthetic joint infection (PJI) is the proper diagnosis. There is a lack of diagnostic tools able to diagnose a PJI with high accuracy. Alpha-defensin has been proposed as possible solution but the available literature is still limited. This prospective study was carried out in order to determine (1) what is the sensitivity, the specificity, the positive and the negative predictive value of the Alpha-defensin immunoassay test in diagnosing PJI; (2) which clinical features may be responsible for false positive and false negative results?. Method. Preoperative aspiration was performed in patients presenting with a painful hip/knee arthroplasty.
Revision total knee arthroplasty (rTKA) is a technically challenging and costly procedure. It is well-documented that primary TKA (pTKA) have better survivorship than rTKA; however, we were unable to identify any studies explicitly investigating previous rTKA as a risk factor for failure following rTKA. The purpose of this study is to compare the outcomes following rTKA between patients undergoing index rTKA and those who had been previously revised. This retrospective, observational study reviewed patients who underwent unilateral, aseptic rTKA at an academic orthopaedic speciality hospital between June 2011 and April 2020 with > one-year of follow-up. Patients were dichotomized based on whether this was their first revision procedure or not. Patient demographics, surgical factors, postoperative outcomes, and re-revision rates were compared between the groups.Aims
Methods
Hip resurfacing remains a potentially valuable surgical procedure for appropriately-selected patients with optimised implant choices. However, concern regarding high early failure rates continues to undermine confidence in use. A large contributor to failure is adverse local tissue reactions around metal-on-metal (MoM) bearing surfaces. Such phenomena have been well-explored around MoM total hip arthroplasties, but comparable data in equivalent hip resurfacing procedures is lacking. In order to define genetic predisposition, we performed a case-control study investigating the role of human leucocyte antigen (HLA) genotype in the development of pseudotumours around MoM hip resurfacings. A matched case-control study was performed using the prospectively-collected database at the host institution. In all, 16 MoM hip resurfacing 'cases' were identified as having symptomatic periprosthetic pseudotumours on preoperative metal artefact reduction sequence (MARS) MRI, and were subsequently histologically confirmed as high-grade aseptic lymphocyte-dominated vasculitis-associated lesions (ALVALs) at revision surgery. ‘Controls’ were matched by implant type in the absence of evidence of pseudotumour. Blood samples from all cases and controls were collected prospectively for high resolution genetic a nalysis targeting 11 separate HLA loci. Statistical significance was set at 0.10 a priori to determine the association between HLA genotype and pseudotumour formation, given the small sample size.Aims
Methods
Controversy has existed for decades over the role of fretting-corrosion in modular CoCr heads used with stems of CoCr vs Ti6Al4V. Since retrieval data on taper performance remains scant, we report here an18-year survivorship of a Ti6Al4V: CoCr combination (APR design; Intermedics Inc). Unique to this study were the threaded profiles present on both stem and head tapers (Fig. 1). This female patient was revised for pain, osteolysis and recurrent hip dislocation at 17 years, 10 months. A prior MPE hip replacement performed for her severely dysplastic right hip had lasted 11 years. At this 2nd revision, the 28 mm CoCr head was found dislocated posteriorly and superiorly.