Purpose. The results of ceramic-on-ceramic (CoC) bearing surfaces in primary total hip arthroplasty (THA) were well known. However, it was not known in revision THA. The purpose of this study is to report the results of revision THA with ceramic
Background. The anatomy of the human knee is very different than the tibiofemoral surface geometry of most modern total knee replacements (TKRs). Many TKRs are designed with simplified articulating surfaces that are mediolaterally symmetrical, resulting in non-natural patterns of motion of the knee joint [1]. Recent orthopaedic trends portray a shift away from basic tibiofemoral geometry towards designs which better replicate natural knee kinematics by adding constraint to the medial condyle and decreasing constraint on the lateral condyle [2]. A recent design concept has paired this theory with the concept of guided kinematic motion throughout the flexion range [3]. The purpose of this study was to validate the kinematic pattern of motion of the surface-guided knee concept through in vitro, mechanical testing. Methods. Prototypes of the surface-guided knee implant were manufactured using cobalt chromium alloy (femoral component) and ultra-high molecular weight polyethylene (tibial component). The prototypes were installed in a force-controlled knee wear simulator (AMTI, Watertown, MA) to assess kinematic behavior of the tibiofemoral
Introduction. Mobility at insert-tray
A ceramic is currently considered as the most ideal
Introduction. There is interest in minimally invasive solutions that reduce osteoarthritic symptoms and restore joint mobility in the early stages of cartilage degeneration or damage. The aim of the present study was to evaluate the Biolox®delta alumina-zirconia composite as a counterface for
Purpose. This study was undertaken to assess the result of total hip arthroplasty (THA) performed for fused hips. Patients and Methods. Twenty nine patients (31 hips), aged 21 to 70 years (average 46 years), underwent THA conversion surgery and were followed for an average of 4.6 years (2.4-12.0 years). There were 23 cases of spontaneous fusion and 8 case of surgical fusion. The causes of joint fusion were tuberculosis in 6 hips, childhood coxitis in 13, ankylosing spondylitis in 6 and childhood trauma in 4. Modified two incision technique was used in 9 hips and in 22 hips, the surgery was performed through a posterolateral approach combined with anterior capsulotomy through gluteus medius and tensor fasica lata interval. In 1 case, greater trochanter osteotomy was done. All acetabular components were inserted at the true acetabulum and the
Purpose. Hip arthroplasty is a good treatment option for displaced femoral neck fracture in elderly patients. However, neuromuscular disease such as cerebral infarction or hemorrhage can be a concerning problem for THA since dislocation after operation can frequently occur. The purpose of this prospective study was to evaluate the functional results of modified minimally invasive (MI) two-incision total hip arthroplasty (THA) with the use of large-diameter (>38mm) metal-on-metal
Introduction. Large head total hip arthroplasty (THA) reduces dislocation rates and provides a theooretically larger range of motion. We hypothesised that this would translate into greater improvement in functional scores when compared to 28mm metal-on-polyethylene THA at 5 years. We believe ours to be the first in vivo comparison study. Methods. A multi-surgeon case-control study in a District General Hospital. The study group consisted of 427 patients with 452 hips, the 38mm uncemented metal-on-metal
The authors modified the original minimally invasive (MI) two-incision total hip arthroplasty (THA) technique and used large-diameter (32mm, 36mm) ceramic-on-ceramic
Introduction. Several devices based upon the dual mobility (DM) concept have recently been FDA approved. However, little is available on the efficiency of current DM on THA instability prevention, and on specific complications. The aim of this retrospective study was to report on the minimal 5-year follow-up results of a cementless DM socket. Methods. Between January 2000 and June 2002, 168 primary consecutive non selected THAs were performed in 92 females and 76 males. The average age at surgery was 67.3 years. A single DM socket design was used (Tregor, Aston Medical, France) consisting of a Ti-sprayed and HA-coated CoCr shell with a highly polished inner surface articulating with a mobile intermediate polyethylene component. The opening diameter of the mobile insert was 6% smaller than that of the femoral head. In 115 hips, the modular femoral head completely covered the Morse taper, whereas a long-neck option leaved the base of the Morse taper uncovered in the remaining 53 hips. Results. At the minimum 5-year follow-up, 119 patients were still alive and had not been revised at a mean of 7.2 years (5-8.9 years), 4 hips were revised for dislocation between the femoral head and the mobile insert (intra-prosthetic dislocation) at a mean of 5.9 years, 22 patients were deceased, and 23 patients were lost to follow-up. Intra-prosthetic dislocation occurred in 4 of the 53 hips (7.5%) with an incompletely covered Morse taper, whereas no dislocation were reported in the remaining 115 hips (p = 0.009). Discussion and Conclusion. A current cementless DM socket was highly effective in the prevention of dislocation following primary THA. However, fatigue damage and wear of the mobile insert at the capturing area can lead to intra-prosthetic dislocation requiring revision. Surgeons should be aware of this specific complication and efforts should be made to avoid aggressive contact at the femoral neck to mobile insert
Introduction. The National Joint Registry of England, Wales, Northern Ireland, and the Isle of Man (NJR) monitors the performance of primary total hip arthroplasty (THA) implants and summarizes usage and outcomes for specific hip systems. The objectives of this study were to 1) determine if survivorship for the PROCOTYL® L acetabular cup, a hemispherical press-fit cup coated with hydroxyapatite and a metal on XLPE
Metal-on-metal bearings (MoM), in both a total hip and resurfacing application, saw an increase in global utilization in the last decade. This peaked in 2008 in the US, with approximately 35% of bearings being hard-on-hard (metal-on-metal or ceramic-on-ceramic). Beginning in 2008, reports in the orthopaedic literature began to surface regrading local soft tissue reactions and hypersensitivity to metal-on-metal bearings. A major implant manufacturer recalled a resurfacing device in 2010 after national joint registries demonstrated higher than expected revision rates. Patients with painful metal-on-metal bearings presenting to the orthopaedic surgeon are a difficult diagnostic challenge. The surgeon must go back to basic principles, perform a complete history and physical exam, obtain serial radiographs and basic bloodwork (ESR, CRP) to rule out common causes of pain and determine if the pain is, or is not, related to the bearing. The Asymptomatic MoM Arthroplasty: Patients will present for either routine followup, or because of concerns regarding their bearing. It is important to emphasise that at this point the vast majority of patients with a MoM bearing are indeed asymptomatic and their bearings are performing well. The surgeon must take into account: a) which specific implant are they dealing with and what is its track record; b) what is the cup position; c) when to perform metal ion testing; d) when to perform further soft tissue imaging (MARS MRI, Ultrasound); e) when to discuss possible surgery. A simple algorithm for both painless and painful MoM Arthroplasties has been developed and will be presented.
The present clinico-radiographical study evaluated the long term performance of a Ti-Al-V alloy cementless modular press-fit cups (Fitek™) having, on the outer surface, an oriented multilayer titanium mesh (Sulmesh™) with 65% tridimensional porosity and 2 fins applied to the outer surface. Fins were initially designed for anti-rotatory purposes but showed to give an excellent initial mechanical stability. Thus, in the following years, we have designed 2 other cups having 8 fins and ceramic insert. In this paper we compare the design and the results obtained with these 3 cups. We have reviewed the first 100 consecutive FITEK cups implanted in 92 patients with an average FU of 9,7 years (range 9-11 years). Results were evaluated with the Harris score. We had 86 Excellent, 10 Good, 2 Fair and 2 Poor. In this series we always used 28 mm heads. Dysplastic patients showed inferior results compared to arthritics patients in different parameters, as pain, limp, ROM (p < 0.05), putting socks and shoes (p < 0.05). Radiographically, our cups were implanted in a fairly horizontal position (36.5° an average). At the last FU radiolucent lines were present in 14 % of the cases, never progressive. In no case we found a change of position of the cup, and in this series no revision was necessary. Between 2005 and 2008 we have implanted 140 consecutive Delta Fins cups with ceramic-on-ceramic
Total Knee Arthroplasty has proven to be a successful procedure for improving pain and function. Long-term studies have shown survivorship to be 90% or greater at 20 years. Most patients in those studies were over 60 years old. There has been a large increase in patients under 60 years old who are undergoing knee arthroplasty. Younger patients have much greater demands on the artificial articular surfaces. The average 55 year old is likely to perform two to three time as many gait cycles as the average 65 or 70 year old. Long-term studies demonstrate that polyethylene wear is a major cause of long-term failure. Newer bearing materials such as cross-linked polyethylenes show promise in reducing wear in THA and more recently in TKA. Femoral component material can significantly influence wear. Studies reveal that Oxidised Zirconium (OxZr) has been shown to significantly reduce polyethylene wear in knee simulators. The ceramic surface has greater lubricity and is harder. We have examined the Extending longevity of TKA requires improved materials to reduced wear. To optimise this, bearing surfaces must be coupled with improvements in both tibial polyethylene and femoral component materials.
Theoretically, improved material properties of new alumina matrix composite (AMC) material, Delta ceramics, are expected to decrease concerns associated with pure alumina ceramics and allow manufacturing thinner liners and consequent larger heads. However, limited short-term clinical results are available and mid-term results of these effects are unclear. (1) Does AMC material decrease the rate of ceramic fracture and noise, concerns of previous-generation ceramics, following change of material properties? (2) Does the possible use of larger heads consequent to manufacturing thinner liners decrease dislocation rate and affect inguinal pain? (3) Do any other complications associated with the use of AMC ceramics occur?Background
Questions/Purposes
Total knee arthroplasty with a rotating hinge knee with carbon-fibre-reinforced (CFR)-PEEK as an alternative bushing material with enhanced creep, wear and fatigue behaviour has been clinically established [1-4]. The objective of our study was to compare results from in vitro biotribological characterisation to ex vivo findings on a retrievals. A modified in vitro wear simulation based on ISO 14243-1 was performed for 5 million cycles on rotating hinge knee (RHK) designs (EnduRo®) out of cobalt-chromium and ZrN-multilayer ceramic coating. The rotational & flexion axles-bushings and the flanges are made of CFR-PEEK with 30% polyacrylonitrile fibre content. Analysis of 12 retrieved EnduRo® RHK systems in cobalt-chromium and ZrN-multilayer in regard to loosening torques, microscopic surface analysis, distinction between different wear modes and classification with a modified HOOD-score has been performed. For the RHK design with the polyethylene gliding surface and bushings and flanges made out of CFR-PEEK, a cumulative volumetric wear was measured to be 12.9±3.95 mm. 3. in
Introduction. Instability continues to be the number one reason for revision in primary total hip arthroplasty (THA). Commonly, impingement precedes dislocation, inducing a levering out the prosthetic head from the liner. Impingement can be prosthetic, bony or soft tissue, depending on component positioning and anatomy. The aim of this virtual study was to investigate whether bony or prosthetic impingement occurred first in well positioned THAs, with the hip placed in deep flexion and hyperextension. Methods. Twenty-three patients requiring THA were planned for a TriFit/Trinity ceramic-on-poly cementless construct using the OPS. TM. dynamic planning software (Corin, UK). The cups were sized to best fit the anatomy, medialised to sit on the acetabular fossa and orientated at 45° inclination and 25° anteversion when standing. Femoral components and head lengths were then positioned to reproduce the native anteversion and match the contralateral leg length and offset. The planned constructs were flexed and internally rotated until anterior impingement occurred in deep flexion [Fig. 1]. The type (bony or prosthetic), and location, of impingement was then recorded. Similarly, the hips were extended and externally rotated until posterior impingement occurred, and the type and location of impingement recorded [Fig. 2]. Patients with minimal pre-operative osteophyte were selected as a best-case scenario for bony impingement. Results. 6/23 (26%) patients were planned with only a 32mm
Aim. Prosthetic joint infections pose a major clinical challenge. Developing novel material surface technologies for orthopedic implants that prevent bacterial adhesion and biofilm formation is essential. Antimicrobial coatings applicable to articulating implant surfaces are limited, due to the
Total hip arthroplasty (THA) is effective, reproducible, and durable in the treatment of hip joint arthritis. While improvements in polyethylene materials have significantly reduced wear rates and osteolysis, aseptic loosening of implants remains one of the leading causes of revision THA. Additionally, fears of dislocation and instability have driven the increase in the utilization of larger diameter femoral heads in primary THA which can lead to increased wear when coupled with a polyethylene
Introduction. Shoulder arthoplasty has increased in the last years and its main goal is to relieve pain and restore function. Shoulder prosthesis enters in the market without any type of pre-clinical tests. Within this paper we present study experimental and computational tests as pre-clinical testing to evaluate total shoulder arthoplasty performance. Materials and methods. An in vitro experimental simulator was designed to characterize experimentally the intact and implanted shoulder glenoid