We report a systematic review and meta-analysis
of the peer-reviewed literature focusing on metal sensitivity testing
in patients undergoing total joint replacement (TJR). Our purpose
was to assess the risk of developing metal hypersensitivity post-operatively
and its relationship with outcome and to investigate the advantages
of performing hypersensitivity testing. We undertook a comprehensive search of the citations quoted in
PubMed and EMBASE: 22 articles (comprising 3634 patients) met the
inclusion criteria. The frequency of positive tests increased after
TJR, especially in patients with implant failure or a metal-on-metal
coupling. The probability of developing a metal allergy was higher
post-operatively (odds ratio (OR) 1.52 (95% confidence interval
(CI) 1.06 to 2.31)), and the risk was further increased when failed
implants were compared with stable TJRs (OR 2.76 (95% CI 1.14 to
6.70)). Hypersensitivity testing was not able to discriminate between
stable and failed TJRs, as its predictive value was not statistically
proven. However, it is generally thought that hypersensitivity testing
should be performed in patients with a history of metal allergy
and in failed TJRs, especially with metal-on-metal implants and
when the cause of the loosening is doubtful.
Since July 2008 we are experimenting a new cup with iliac screw fixation, developed on the idea of Ring and Mc Minn. Iliac fixation is permitted by a polar screw of large diameter, coated by HA, which allows a compression to bone and a firm primary stability. Moreover it's possible to increase primary stability with further smaller peripherals screws. We present this new cup and report the preliminary results. Since July 2008 to April 2010, 51 cups were implanted. The diagnosis was aseptic loosening in 36 cases, septic loosening treated by two-stage revision in 7, hip congenital dislocation in 5, one case of post-traumatic osteoarthritis, one case of instability due to cup malposition and a case was an outcome of Girdlestone resection arthroplasty. Mean age was of 66 years (31-90).INTRODUCTION
MATERIALS AND METHOD
Ceramic-on-ceramic bearing is an attractive alternative to metal-on-polyethylene bearing due to the unique tri-bological advantages of alumina. However, despite the long-term satisfactory results obtained so far in the vast majority of patients, failure may occur in a few cases. Clinical, radiographic, laboratory and microbiological data of 30 consecutive subjects with failed alumina-on-alumina total hip arthroplasties (THA) were analyzed to define if foreign body reaction to wear debris may be responsible for periprosthetic bone resorption, as in conventional metal-to-polyethylene bearings. In all cases, clinical and radiographical material was reviewed, retrieved implants were examined, and histology of periprosthetic tissues was analyzed. Massive osteolysis was never observed. Apart from 5 five patients for which revision surgery was necessary due to the occurrence of late infection, in all other cases failure had occurred due to secondary implant instability (as in the case of screwed sockets, 19 cases) or to malpositioning of the implant (5 cases). One patient suffered from chronic dislocation. In the vast majority of cases, ceramic wear debris was absent or scarce, and did not induce any tissue reaction. In a few cases with severe wear, debris was evident in clusters of perivascular macrophages, notably in the absence of foreign body multinucleated cells, confirming the excellent biocompatibility of ceramics. These findings indicate that wear debris and peri-prostetic bone resorption were the effect rather than the cause of failure, differently from revised metal-on-polyethylene bearings, in which foreign body cell reaction is the main pathogenetic mechanism of failure. On the contrary, mechanical problems, due to incorrect surgical technique or to inadequate prosthetic design, may cause instability of the implant, in turn resulting in wear debris production and moderate if any biological reaction.
We investigated the role of ion release in the assessment of fixation of the implant after total knee replacement and hypothesised that ion monitoring could be a useful parameter in the diagnosis of prosthetic loosening. We enrolled 59 patients with unilateral procedures and measured their serum aluminium, titanium, chromium and cobalt ion levels, blinded to the clinical and radiological outcome which was considered to be the reference standard. The cut-off levels for detection of the ions were obtained by measuring the levels in 41 healthy blood donors who had no implants. Based on the clinical and radiological evaluation the patients were divided into two groups with either stable (n = 24) or loosened (n = 35) implants. A significant increase in the mean level of Cr ions was seen in the group with failed implants (p = 0.001). The diagnostic accuracy was 71% providing strong evidence of failure when the level of Cr ions exceeded the cut-off value. The possibility of distinguishing loosening from other causes of failure was demonstrated by the higher diagnostic accuracy of 83%, when considering only patients with failure attributable to loosening. Measurement of the serum level of Cr ions may be of value for detecting failure due to loosening when the diagnosis is in doubt. The other metal ions studies did not have any diagnostic value.
The use of monoblock tapered stems has shown very good results in hip revision surgery, particularly in case of severe proximal femur bone deficiency. However a too valgus neck, a short offset, may result in a high risk of dislocation. In addiction monoblock stems make the control of limb length difficult, and potentially increase the risk of subsidence or intraoperative fracture. Different types of modular tapered stems with distal fixation have been developed to allow a more user-friendly restoration of limb-lenght discrepancy and an indipendent proximal control of offset and anti-retroversion. We assessed 64 hip revisions performed on 63 patients (mean age 62 years). Indication for treatment was: aseptic loosening (42 cases) septic loosening (18 cases) and periprosthetic fracture (4 cases). According to Paprosky classification, femoral defects were staged as type I (2 cases), type II (20 cases), type IIIA (25 cases) and type IIIB (13 cases); periprosthetic fractures were all type B2 according to the Vancouver classification. In all cases we used a Restoration® Modular (Striker, Orthopaedics) cone-conical uncemented stem implanted by a lateral approach, with a trans-femoral osteotomy in 19 cases. A preventive cerclage cable was used in 10 patients in case of very thin cortex. We used the minimum size stem in most of the cases. Mean follow-up was 20 months (range 6–36). Short-term complications included hip dislocation (1 case), recurrent infection (1 case), stem subsidence >
5 mm (1 case). Mean Harris Hip Score improved from 43 to 81.9 (t test p<
0.0005), while limb lenght discrepancy improved in 97% of cases with symmetry in 76%. The use of modular revision stems is an effective alternative in hip revision surgery that ensures good primary stability, while modularity enables the implant to be tailored to the patient, allowing restoration of the limb length and correct muscular balancing.
Replacing a fused or ankylosed hip with a prosthesis has several advantages. It reduces the pain in the lumbar-sacral spine and the ipsilateral knee. It gives a better range of movement and leg length is restored. In this study we present our experience of 50 cases of total hip arthroplasty in fused or ankylosed hips. Aetio-pathogenesis was rhizomelic spondylitis in 35 cases, sequelae of cox it is in 2, posttraumatic in 4, Ankylosis in 6, and fusion in 3. For clinical assessment we used the Merle D’Aubignè score, and for radiographic evaluation we used the Gruen method of area subdivision Of the 50 prosthesis implanted, 3 were removed due to aseptic loosening. The other were the radiographically stable after an average follow-up of 12 years. Preoperative clinical scores were: pain (2.9), range of motion (2.5), and walking (2.1). At the latest exam the scores were: pain (5.5), motion (4.6), walking (4.5). Preoperative leg shortening was 3.5 cm, whereas at the latest exam it was 0.9 cm. Lumbalgia decreased notably in 62%. Total hip arthroplasty may have advantages over fusion on one hand, but on the other it is technically more difficult and gives results that are inferior to common indications. It is therefore important to assess patients (time of fusion, age of patient, residual muscular function) preoperatively to obtain good results.
The Gpsystem Medacta vision system is composed of an infrared camera that produces and receives infrared rays reflected by almost 3 reflectors mounted on different rigid body devices (F=femoral, T=tibial, G=guide), in order to determine its position with an error lower than 0.35mm. Data received from this vision system are than elaborated by the Cinetique Gpsystem Version 1.0 system in order to determine the correct cutting guide positioning both for the femur and the tibia. The cutting guide is moved on different planes by 5 electric engines applied on 5 no ending screws. The first step of this system is determining, with the F and the T rigid bodies, patient’s lower limb kinematic in order to evaluate its mechanical axis, its flexion-extension range of movement and its pathological deviations. The second step is evaluating anatomical landmarks to find out the correct degrees of tibial and femoral cuts: these landmarks are the medial and lateral tibial glena, the distal femoral condyles, the posterior femoral condyles, the anterior femoral cortex, the tibial tuberosity, the Whiteside line and the epycondilar axis (each anatomical landmark is identified by multiple points in order to decrease possible errors). The third step is applying the cutting guide and the Grigid body on the femoral clamp in order to estimate the correct level for the tibial cut than, once the tibial osteotomy is done the vision system controls its correct execution and the soft tissue balancing of the knee. The fourth step is calculating with the Gpsystem the correct orientation of the femoral cutting guide and checking its positioning and cutting execution. The last step is applying the test-prosthesis verifying the mechanical axis of the knee and than assembling the definitive prosthesis. Since now we have applied 10 Cinetique knee prosthesis with the Medacta computer navigation system with good results and good positioning of the prosthesis Medacta computer navigation system for Cinetique knee arthroplasty is innovative for its simple cutting guide and movement device both in their hardware than in their way of using and for a simpler software interface; these characteristics allows faster surgeon technique learning, shortening of surgical time and a better prosthesis positioning.
Girdlestone’s arthroplasty is often used to treat septic loosening of hip prostheses. Although this operation provides goodresults with regards to pain and loosening, it causes instability and in the hip and limb shortening that force the patient to use walking aids. From 1990 to 1999 we treated ten cases of revisionhip arthroplasty after Girdlestone’s arthroplasty. Girdleston e’sarthroplasty was carried out in all cases due to sepsis in the previousimplant. Preoperatively all patients underwent granulocyte-labeledscintigraphy. For clinical evaluation we used the Merle D’Aubignè score. From 1990 to 1999 we treated ten cases of revisionhip arthroplasty after Girdlestone’s arthroplasty. Girdleston e’sarthroplasty was carried out in all cases due to sepsis in the previousimplant. Preoperatively all patients underwent granulocyte-labeledscintigraphy. For clinical evaluation we used the Merle D’Aubignè score. Girdlestone’s arthroplasty is very effective for treating septic loosening of hip prostheses, but it causes severe walking impediment. Revision surgery restores limb length and walking. Patients that undergo this treatment should be checked for residual sepsis, which may jeopardize the operation. Currently we are experimenting with spacers with antibiotics and our initial results are promising.
Compromised patellar bone stock poses significant the chnical problems in primary and revision knee arthroplasty. In these situations, traditional approaches have included: non resurfacing, patellectomy, patellar bone grafting, ‘Gull-Wing’ osteotomy. A new material (Trabecular Metal) fabricated using a tantalum metal and vapor deposition techhnique that create a metallic strut configuration with 80%porosity, and physical and mechanical properties similar to bone has been introduced. The authors studied the short-term results following patellar resurfacing using trabecular metal patella in primary and revision total knee arhroplasty (TKA). Nine patients undergoing primary (2 cases) or revision (7 cases) TKA with the use of a trabecular metal patella were evaluated at a mean of 16 months follow-up. All patients had marked patellar bone deficiency precluding resurfacing with a standard cemented patellar button. The all polyethylene patela was cemented into the trabecular metal base and the remaining patella bone stock; additional fixation was provided by # 2 non absorbable sutures through the peripheral holes on the metal shell. Revision TKA may be complicated by severe patellar bone loss that preclude implantantion of a standard cemented patellar component. Several options including patellectomy, non resurfacing and osteotomy or grafting of remaining bony shell have been proposed. It is rare in primary knee arthroplasty that the patella has been so eroded that resurfacing is not feasible. Trabecular metall patella may be indicate in the complex revision or even primary knee arthroplasty in which all that remains of the patella is a thin shell of anterior cortical. The short-term results of patellar resurfacing with trabecular metal have demonstrated favorable results.
The vast majority of total-joint-replacement components utilized are modular to some degree. Modularity increases the surgeon’s options in both primary and revision THA. Modular prostheses allow the surgeon intra-operative versatility, allowing adjustment of leg length, offset, neck length, and version. This is particularly helpful in CHD, posttraumatic arthritis and in hip revision. Modularity may be applied also to the neck, enlarging the range of choice for difficult cases. Howeverusing of a modular interface increases risk of fretting, wear debris, and dissociation and mismatching of components. A series of 87 revision THA performed between 1997 and 2003 using modular neck was reviewed. The pros-theses are AnCA-Fit with a cementless titanium anatomical stem and Profemur with a tapered revision titanium stem. Both provided with a modular neck inserted by morse taper and a hemispheric press-fitted cup. All the implants have a ceramic-ceramic coupling. Four cases were performed due to recurrent dislocation and 83 for implant loosening. Retrieved necks were studied searching for corrosion. No cases of disassembly or fracture of the neck were observed. Two cases of dislocation were treated with brace. Analysis of retrieved necks confirmed the absence of corrosion. Leg length discrepancy decreased from 57.7% to 22%. One post-operative infection was successfully treated with debridment. Modular neck system allows to correct intraoperatively leg length and offset, choosing between five interchangeable necks available in two lengths: straight, varus-valgus, ante-retroverted. Restoration of hip biomechanics prevents instability. Removal of the neck allows a better surgical exposure when femoral stem is retained. Moreover it allows to maintain ceramic-ceramic coupling. Modular prosthesis has some problems related to risk of corrosion, fretting, fracture or dislocation of components. We observed no cases of disassembly of components or fracture and comparative analysis between retrieved necks and those experimentally studied confirmed absence of corrosion.
The uncemented cup with iliac stem ensures immediate primary stability by fixation to the hipbone in acetabular loosening with severe bone defect. Homologous bone grafts contribute to restoring bone stock, which is a fundamental requirement for long lasting implant stability. From 2002 to 2004 we implanted 23 cups with iliac stems in 22 patients. In 7 cases there was also stem loosening, and so total hip arthroplasty was performed. In 2 patients the defect was grade 2b, in 5 grade 3a, and in 16 grade 3b according to Paprosky. A direct lateral approach was performed in the supine position. Morselized bone grafts were used in all cases by the “impaction grafting” technique, and in 4 cases modelled structural grafts were also employed. Mean follow-up has been 18 months (8–32). So far we have not had any cases of loosening. At follow-up x-rays showed remodelling of the grafts with integration. The cup with iliac stem enables primary stability on healthy bone tissue, and protects the grafts form mechanical stimulation, thus allowing them to integrate and restore bone-stock. It also restores the centre of rotation, and provides functional benefits and implant stability.
The authors studied the short-term results following patellar resurfacing using trabecular metal patella. Ten patients underwent primary (2 cases) or revision (8 cases) TKA with the use of a trabecular metal patella and were evaluated at a mean follow-up of 24 months. All patients had marked patellar bone deficiency or patellar absence precluding resurfacing with a standard cemented patellar button. The all polyethylene patella was cemented into the trabecular metal base and the remaining patella bone stock; additional fixation was provided by non-adsorbable sutures through the peripheral holes on the metal shell. No intraoperative complications occurred. There was no displacement of any trabecular metal patellar component and no patellar fractures. The fixation appeared excellent at three to six months radiographic evaluation with uniform bone contact in the peripheral regions in both lateral an Merchant radiographic views. The mean Knee Society scores improved in all patients.
The groups were thus divided: Group 1: lyophilised bone chips. Group 2: lyophilised bone chips + platelet gel Group 3: lyophilised bone chips + platelet gel + packed autologous medullary cells (Buffy coat). At six weeks X-rays, MRI and needle biopsies were carried out. The tissue underwent morphological and microstructural tests. Results confirmed that the use of platelet gel and packed medullary cells as adjuvant for the lyophilised bone aid bone repair and graft integration. Morphological and morphometric tests showed that at six week the newly formed bone of group 3 had better mechanical properties.
Modern metal-on-metal bearings produce less wear debris and osteolysis, but have the potential adverse effect of release of ions. Improved ceramic-on-ceramic bearings have the lowest wear of all, but the corrosion process has not been analysed. Our aim was to measure the serum ion release (ng/ml) in 23 patients having stable hip prostheses with a ceramic-on-ceramic coupling (group A) and to compare it with the release in 42 patients with a metal-on-metal bearing (group B) in the medium term. Reference values were obtained from a population of 47 healthy subjects (group C). The concentrations of chromium, cobalt, aluminium and titanium were measured. There was a significant increase of cobalt, chromium and aluminium levels (p <
0.05) in group B compared with groups A and C. Group A did not differ significantly from the control group. Despite the apparent advantage of a metal-on-metal coupling, especially in younger patients with a long life expectancy, a major concern arises regarding the extent and duration of ion exposure. For this reason, the low corrosion level in a ceramic-on-ceramic coupling could be advantageous.
The patients were divided into two groups according to the fracture site. Group 1 included 71 patients with medial fracture, and Group 2 contained 56 patients pertrochanteric or subtrochanteric fracture. All patients were assessed by the Merle d’Aubignè clinical evaluation method. Radiographically, the bone-implant interface was assessed by the presence of radiolucency lines according to the DeLee-Charnley method modified by Martell
MOD-B with antibiotic powder and PMMA Cylinders (A-MB-C) have been placed in saline solution and plasma for 4 weeks, compared with cylinders made with PMMA and antibiotic. The mechanical resistance of A-MB-C to compressive test has been performed subsequently. About biocompatibility, A-MB-C were implanted in sheep’s Ilium. After 3 moths an histologic evaluation has been performed.
The MOD-B + antibiotic + PMMA have released the higher quantity of antibiotic for all the 4 weeks. The A-MB-C resistance has been of 13.6 MPa, the same resistance of cancellous bone in the man’s femur. The histological result with a fluoroscopic microscope has been an osteogenesis in the full section of the cylinders.
Valgus knee is a complex deformity, characterised by varying degrees of flexion, external rotation and valgus deviation. Contracture of external ligamentous structures makes correction and soft tissue balance often difficult and may lead to persistent post-operative instability. Further problems include patellar tracking, bone defects, especially at the external femoral condyle, and the risk of external popliteal sciatic (EPS) nerve palsy after surgery. Krackow distinguished three types of valgus knee: type 1 with integral medial peripheral structures; type 2 with severe medial structure laxity and impossibility to correct passively; and type 3 which is the sequela of over-correction tibial osteotomy. From 1996 to 2003 we performed 64 fusions due to valgus knee in 41 females and 23 males, aged between 55 and 76 years (mean 67.5). Of these, 52 deformities were type 1, nine type 2, and three type 3. For type-1 lesions we always used prostheses with posterior stabilisation (PS), and balanced the capsulo-ligamentous structures. In type-2 lesions we used a vincolo condilare prosthesis with CCK in two cases and a cerniera prosthesis in two cases, whereas in the remaining five cases we used a PS prosthesis. In type-2 deformities we used a PS prosthesis with a modular tibial component with metal augments. Mean follow up was 45 months. Radiographically, valgus deformity fell from 22.4° (10° min – 35° max) to 5.4° (3° min – 9° max). Post-operative results, according to the HSS score, were excellent in 51 cases, fair in 11 cases, and poor in two cases, due to the need to perform revision in two stages in an infected prosthesis 6 months after surgery in one case, and aseptic loosening in another. Valgus knee due to arthritis can be successfully treated by total knee arthroplasty using various techniques, according to the clinical severity. EPS nerve palsy has been cited as a potential problem in total knee arthroplasty. We did not observe this complication in our series, probably because we maintain the knee in continuous slight flexion for the first 18–24 h.