Fractures of the femoral component are well reported complications that present a challenging task in revision total hip arthroplasty. Albeit being uncommon, with an incidence of 0.23–11%, the consequences can be devastating. Its extraction being a demanding undertaking that is potentially detrimental to the remaining host bone. Several techniques have been described to address this complex issue prior to revision: drilling of the exposed part of the femoral stem and attaching a threaded extraction device, surface undercutting with an extraction device wedged in, femoral trephine techniques, creation of a femoral cortical window, an extended femoral osteotomy procedure, as well as extraction by means of retrograde nail impaction. Here we present the modified technique we employed in the revision of a failed cementless extensively porous coated femoral component that had fractured at the neck-stem interface. The proximal femoral component was visualized and an orthopedic burr and a femoral osteotome employed surrounding the component. Utilizing a Midas Rex® MR7 drill with its metal cutting attachment, a circular recess was created in the shoulder of the femoral component. This facilitated the application of the distal end of a universal slap hammer. The component was retrieved successfully with no associated bone loss negating the need for a femoral osteotomy.Background
Technique
Cement restrictors are used for maintaining good filling and pressurization of bone cement during hip and knee arthroplasties. The limitations of certain cement restrictors include the inability to accommodate for large medullary canals particularly in revision procedures. We describe a technique using SurgicelTM (Johnson & Johnson) and SPONGOSTAN™ (Johnson & Johnson) (Fig 1) to form a cement restrictor that can accommodate for large canal diameters and provide excellent pressurisation. The technique involves the application of SPONGOSTAN™ (Johnson & Johnson) foam onto a SurgicelTM (Johnson & Johnson) mesh which is then rolled onto the SPONGOSTAN™ foam forming a uniform cylindrical structure Figs 2,3. The diameter of the restrictor can be adjusted according to the desired femoral canal diameter through increasing the thickness of the SPONGOSTAN™ (Johnson & Johnson) foam. The restrictor is then inserted into the desired position in the medullary canal where it expands uniformly creating an effective restrictor and bone plug Fig 4. Bone cement is then applied and pressurisation commenced prior to the insertion of the implant Fig5. SPONGOSTAN™ is an absorbable haemostatic sponge intended for haemostatic use by applying to a bleeding surface. It consists of a sterile, water-insoluble, malleable, porcine gelatin absorbable sponge. Surgicel ™ is an absorbable hemostatic agent composed of oxidized regenerated cellulose. It is a sterile, absorbable knitted fabric that is flexible and adheres readily to bleeding surfaces. Both products are routinely used for their haemostatic properties in various surgical disciplines.Background
Technique
The development of new bearing surfaces for total joint replacement is constantly evolving. Oxidized zirconium (Oxinium) has been introduced for use in both total hip arthroplasty (THA) and total knee arthroplasty (TKA). The aetiology of wear is multifactorial and includes adhesive, abrasive, third-body and fatigue wear mechanisms. Oxinium femoral components have demonstrated clear improvements in wear characteristics in-vitro. The purpose of this prospective study was to evaluate the mid-term (minimum 5 year) clinical and radiographic results and survivorship of the Genesis II™ knee implant system using an Oxinium femoral component. Between January 2001 and December 2008, 382 Genesis II Oxinium (Smith & Nephew) primary total knee arthroplasties (TKA) (313 patients) were implanted at our institution. A comparison with a cohort of 317 patients (382 knees) who received a Genesis II knee implant using a ‘conventional’ cobalt-chrome (Co-Cr) femoral component was performed during the same time period. Prospective data was collected on all patients including demographics (age, BMI, diagnosis) as well as pre and postoperative clinical outcome scores (SF-12, WOMAC, and knee society clinical rating scores (KSCRS). Radiological analysis for evidence of osteolysis and loosening was performed in all patients. Comparisons were performed to determine differences between the Oxinium and Cobalt Chrome cohorts. Kaplan-Meier survival analysis was performed to show cumulative survival over time. Failure was defined as femoral component revision due to any cause.INTRODUCTION
METHODS
Total knee arthroplasty (TKA) has proven clinical success with reported longterm survivorship of 92% in the elderly population. Concerns regarding increased loosening rates and potential need for multiple revision surgeries in patients younger than 60 years have traditionally discouraged TKA in younger patients. The purpose of this study was to review the longterm clinical and radiographic results of patients under the age of 45 yrs who underwent a total knee replacement. A retrospective review of our institutional database was performed between January 1996 and December 2004 The criteria for inclusion in the study were as follows: age 45 years or younger at index arthroplasty, cemented condylar prosthesis, and a minimum follow-up of 9 years. A total of 39 consecutive primary cemented condylar knee arthroplasties in patients with end stage arthritis were performed in 36 patients who were 45 years or younger. The median length of followup was 13.6 years. There were 18 men and 21 women. The mean age was 40.6 years (range, 28–44). There were 23 right, 16 left, and 3 bilateral procedures. The mean body mass index was 31.2 kg/m2 Clinical and radiological evaluations were performed before surgery and at 6 weeks, 3 months, 1 year and every 2 years subsequently. Knee scores were calculated using the Knee Society Clinical Rating Scores (KSCRS), SF-12 and WOMAC scores to assess pre, and post-operative function. Postoperative anteroposterior and lateral views were assessed for femoral and tibial component position, alignment, and presence or progression of radiolucent lines at the bone-cement and prosthesis-cement interfaces Statistical analysis was performed using the 2-sample test or Wilcoxon rank sum test for comparison of continuous variables. Kaplan-Meier analysis of implant survival was performed with failure defined as femoral component revision due to any cause.Introduction
Materials and Methods
Porous metal surfaces have been a popular option for acetabular component fixation in total hip arthroplasty (THA). New THA component designs are introduced periodically with the expectation of better wear properties and survivorship. Since its approval for use in 2002 there have been few clinical outcome studies published on the Pinnacle acetabular cup system. We hypothesised that the hemispherical porous coated Pinnacle acetabular cup system with a range of cup options and bearing surfaces would give us predictably good fixation and survivorship at five years post implantation. A total of 1391 Pinnacle acetabular cups (De Puy, a Johnson & Johnson company, Warsaw IN) were implanted between the period March 2003 to August 2011 by four senior surgeons. There were a total of 29 patients requiring revision surgery. Of these revisions, 23 were excluded from the final analysis. Sixteen were for early infection requiring debridement of the hip joint and exchange of the modular liner and femoral head. Five patients sustained femoral peri-prosthetic fractures requiring further surgery with retention of the acetabular component in all cases. Of the remaining 8 revision cases, only 6 had more than two years follow-up. All patients had pre and post-operative Harris hip scores, WOMAC and SF-12 scores. All patients were assessed with serial radiographs immediately post-operatively, 3 months, 1 year, 2 years, every 2 years thereafter. Component migration and revisions (excluding infection and peri-prosthetic fractures) are reported as failures. Post-operative radiographs were evaluated for component migration. Kaplan-Meier survivorship curves were drawn to show survivorship for cup type and bearing type.Objectives
Materials and Methods
The development of new bearing surfaces for total joint replacement is constantly evolving. Oxidized zirconium (Oxinium) has been introduced for use in total hip arthroplasty (THA) and total knee arthroplasty (TKA). One of the most common causes of failure of THA is aseptic loosening secondary to polyethylene wear debris. The aetiology of wear is multifactorial and includes adhesive, abrasive, third-body and fatigue wear mechanisms. Oxidized zirconium is a relatively new material that features an oxidized ceramic surface chemically bonded to a hard metallic substrate. This material possesses the reduced polyethylene wear characteristics of a ceramic, without the increased risk of implant fracture While short-term results of oxidized zirconium in THA have been reported, there have been no reports on retrieved highly cross linked PE articulating with Oxinium headsObjectives: The purpose of this study was to compare matched pairs of retrieved highly cross-linked polyethylene (XLPE) acetabular liners with OxZr and CoCr articulation. The liners were examined for evidence of wear damage, including articular surface damage, impingement, screw-hole creep, and rim cracksIntroduction
Objectives
To determine the relative contributions of bilateral versus unilateral femoral shaft fracture plus injuries in other body regions to mortality after injury. A retrospective analysis of the prospectively recorded Trauma Registry data (TARN) from 1989 to 2003.Background
Study design
Both fractures healed and the patient is currently pain free and mobile with walking aids.
Bilateral peri-prosthetic stress fractures following total hip replacements have not been previously reported.