Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Knee Prosthesis”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 739 records · Page 41Linked to original sources

Immunoscintigraphy of septic loosening of knee endoprosthesis: a retrospective evaluation of the antigranulocyte antibody BW 250/183.

Immunoscintigraphy with the use of the antigranulocyte antibody BW 250/183 is a reliable method for detecting infection, especially in septic loosening of hip prostheses, for which purpose quantitative interpretation of the time-activity course is employed. Therefore, we retrospectively studied whether similar results could be achieved in knee prostheses. We verified 28 scintigraphic examinations in 26 patients by histology. Scintigraphy was performed during an early (4-6 h post injection) and a late phase (23-25 h post injection). Infection was diagnosed when activity around the knee prosthesis increased by more than 10% compared with bone marrow. We found a sensitivity and a negative predictive value of 100%, a specificity of 80%, a positive predictive value of 81% and an accuracy of 89%. Specificity and accuracy are lower than in the evaluation of hip prostheses; however, in comparison to other scintigraphic modalities, scintigraphy with the antigranulocyte antibody BW 250/183 is superior in excluding infection and has better specificity and accuracy. Therefore, as in the case of hip prostheses, the described methodology appears to be the scintigraphic modality of choice for knee prostheses.

Aged↗

Failure of one design of surface replacement knee arthroplasty due to loosening deformation and wear of the plastic femoral component.

Twenty four knee prosthesis femoral and tibial components of the 'load angle inlay' design, removed for loosening and pain were examined in the scanning electron microscope, light microscope, and volume loss measured using a simple gauge. In all cases the deformation of the plastic (femoral) component was seen both by increase in the curvature of the inner surface and wear usually on the edge of the bearing surface. Two pairs were subluxed prior to removal from the patient and these not only produced gross deformation of the plastic components, but maximum volume loss of the components examined; the knees exhibited gross instability. The tibial (metal) components stood up remarkably well in all cases, both in wear and deformation which was minimal but sinking and rotation of the plateau did occur for the most part on the external side. Scratch patterns seen on the tibial components were clearly seen and gave an indication of the direction and amount of sliding between the components; in some cases these scratch lines were in more than one direction probably indicative of loosening and instability. Short deep scratches were usually indicative of bone and/or cement particles embedded in the plastic components, abrasive wear was seen on 92 per cent of the femoral components, and cracks were seen on two-thirds, usually parallel and close to the sides.

Adult↗

An analysis of the survival rate of total-condylar total knee prostheses with posterior stability.

Survival rate tables are an adequate and relatively new means of evaluating prostheses of the knee. These tables may be used to make a clear distinction between success and failure. In a study of 160 prostheses followed-up over a period of 9 years, a Total-Condylar knee prosthesis with posterior stability has a 90% probability of surviving for the entire period, based on mechanical and radiological failures, and a 96% probability based on failures that required its removal. The probability of mechanical or radiological failure is 1% per annum.

Adult↗

Arthroscopy after dysfunctional total knee arthroplasty: two cases with peg fracture of the polyethylene insert.

Arthroscopy may be indicated in patients with painful dysfunction of the knee joint following total joint replacement. Arthrofibrosis, impacted soft tissue, patellar malalignment, synovialitis, and intra-articular foreign bodies can be treated with the promise of a good outcome. Two cases of peg fracture of the polyethylene insert of a semiconstrained knee prosthesis are presented. In relation to fracture position, instability and locking-up of the joint were clinically manifest. When arthroscopy is used judiciously, its merits are found in ensuring the proper diagnosis and in the reliable planning of treatment. When the patient reports locking-up of the joint, the rare complication of a polyethylene peg fracture must be considered.

Arthroplasty, Replacement, Knee↗

Wear in carbon fiber-reinforced polyethylene (poly-two) knee prostheses.

The authors report a case of massive wear of carbon fiber-reinforced polyethylene used as an insert in a knee prosthesis. The finding, which was studied under a scanning electron microscope, in agreement with mechanical resistance and laboratory testing reported in the literature, confirms that this composite material (poly-two) is not more advantageous to use that ultra-high molecular weight polyethylene in terms of wear, despite favorable experimental premises.

Aged↗

[Endoprosthesis of the knee joint: current status and trends].

Knee joint endoprosthetics has proved to be at least as successful as hip joint endoprosthetics, although the total implantation rate has risen to only about 15%, which ignores its widespread unpopularity. There is a great variety of artificial knee joints, although according to ISO standards all models can be reduced to four basic ones. Deciding to use a stabilized, semi-constrained or unconstrained artificial knee prosthesis requires careful consideration especially if the possibility of its removal is taken into account. The main reason for unsatisfactory clinical results is still retropatellar pain. Intensive basic research is necessary in this area as well as in the development of new materials that might be used for new prosthetic designs. Designers as well as surgeons should aim at regaining the natural function level with no pain for the patient.

Humans↗

Tibial plateau-fibular head distance of normal Japanese knees measured in lateral view of roentgenogram.

In total knee arthroplasty, the top of fibular head sometimes has to be resected simultaneously during cutting tibial plateau. Therefore, tibial plateau-fibular head distance was measured in the 244 normal knees of 125 Japanese volunteers (80 men, 45 women), with average age of 27 years ranging from 21 to 40 years. Tibial plateau-fibular head distance was measured using lateral view of knee roentgenogram. The average distance was 6.1 +/- 2.5 mm in men (range, -0.5 to 12.5 mm), and 4.7 +/- 2.6 mm in women (range, -2.5 to 12.0 mm), which was thinner than that of tibial component of conventional knee prosthesis (6-8 mm or over). The relatively high level of fibular head in Japanese may disturb proper positioning of tibial component and transmit load to tibial component in weight bearing, resulting in gradual medial tilting of the tibial component. Resection of either a tip of the fibular head or a segment of the shaft may solve this problem.

Adult↗

Osseointegration in porous coated knee arthroplasty. The influence of component coating type in sheep.

Although cementless knee arthroplasty is a commonly performed procedure, to date very little was known about the process of osseointegration of knee arthroplasty components. Using a knee prosthesis that was specially designed for the sheep stifle joint, this process of osseointegration could be studied in vivo, together with its effects on clinical and functional performance, its influence on mechanical fixation, and its influence on component stability or migration over time. Additionally, the osseointegration capacity of a newly developed cast mesh porous coating could be examined. The rationale for this newly developed coating was to provide a surface texture with theoretically superior osseointegration capacity, by offering a larger and better controlled pore size, with higher ingrowth area compared to conventional bead type coatings. In summary, the conclusions that are drawn from this work are the following: 1. The degree of osseointegration of knee arthroplasty components is not correlated with clinical and functional performance. Knee arthroplasty components with fibrous integration can function as well as osseointegrated components at least during the first years after implantation. This explains the occasional reports in the literature of post mortem retrieved, well functioning knee arthroplasty components, with purely fibrous integration on histomorphometric analysis. 2. Fibrous integration of tibial knee arthroplasty components, however, leads to less mechanical fixation strength of these components. Osseointegrated components are much more strongly fixed to the underlying bone. This difference in mechanical fixation strength is detectable under physiologic loads. 3. Fibrous integration of tibial knee arthroplasty components leads to increased migration, becoming apparent after 1 year with radiostereometric analysis (RSA). Osseointegrated components are significantly more stable over time. 4. Fibrous integration is less desirable, since it leads to mechanically less rigidly fixed implants, and subsequently to migration over time. On the long-term, fibrous integration might therefore lead to loosening. 5. RSA is an effective tool to assess migration of knee arthroplasty components. The RSA migration of an uncemented component is also an indicator of its degree of osseointegration and its mechanical fixation strength, since RSA migration is correlated with these two parameters. RSA is therefore especially useful during the first postoperative years, since increased migration indicates fibrous integration and low mechanical fixation strength, suggesting an increased risk for subsequent loosening at a later stage. Patients with increased early component migration on RSA might therefore be advised to impose specific restrictions on their knee arthroplasty. 6. Osseointegration is not routinely achieved in conventional porous coated tibial knee arthroplasty components. The development of a theoretically superior cast mesh coating did not lead to a significantly higher degree of osseointegration. It is suggested that the lack of sufficiently small interface gaps and the lack of sufficiently small interface micromotion--two known prerequisites for reliable osseointegration to occur--are the main reasons inhibiting osseointegration, both in this animal model and in the human situation. 7. Significant osseointegration, however, does occur in the newly developed cast mesh coated components, when they are additionally coated with a vacuum plasma sprayed 50 microns hydroxyapatite layer. The newly developed cast mesh coating is ideally suited for such an additional hydroxyapatite coating. Remarkably high percentages of both bone ingrowth and ongrowth can be seen with these hydroxyapatite coated cast mesh coatings, higher than so far reported for current tibial knee arthroplasty components. These osseointegrated hydroxyapatite coated cast mesh components show significantly higher mechanical fixation strength and lower RSA migratio

Animals↗

Extensive osteolysis around an aseptic, stable, uncemented total knee replacement.

Extensive osteolysis occurred around an aseptic, well-fixed, stable, uncemented total knee prosthesis. At the time of revision, tibial polyethylene wear and minimal metal-on-metal contact were present. A hypertrophic synovium-like membrane abutted bone in regions of osteolysis. Examination of this membrane revealed polyethylene-wear debris and significant levels of chromium, cobalt, and titanium. Wear debris--polyethylene, metal, or a combination of both--may be responsible for the osteolytic process in this case.

Bone Cements↗

Reproducibility of intra-operative measurement of the mechanical axes of the lower limb during total knee replacement with a non-image-based navigation system.

OBJECTIVE: The restoration of a normal mechanical axis of the lower limb following total knee prosthesis (TKP) depends on the accuracy of the intra-operative measurement of the femoro-tibial angle. We have studied the reproducibility of intra-operative measurement of the coronal mechanical femoro-tibial axis with the OrthoPilot (Aesculap, Tuttlingen, Germany) non-image-based navigation system. MATERIAL AND METHODS: A consecutive series of 20 TKP (Aesculap SEARCH Evolution prosthesis) implanted by the same surgical team of two senior orthopedic surgeons was analyzed. They used a non-image-based navigation system that allows the mechanical axes of the femur and tibia to be defined with a kinematic analysis. The operating surgeon and assistant surgeon performed the kinematic analysis twice and once, respectively, and measured coronal mechanical femoro-tibial angles in maximal extension and at 90 degrees flexion without varus or valgus stress. RESULTS: The mean intra-observer variation in the measurement of the coronal mechanical femoro-tibial angle in maximal extension was 0.1 degrees (SD = 0.7 degrees). The mean intra-observer variation in the measurement of the coronal mechanical femoro-tibial angle at 90 degrees of knee flexion was 0.2 degrees (SD = 0.6 degrees). The mean inter-observer variation in the measurement of the coronal mechanical femoro-tibial angle in maximal extension was 0.1 degrees (SD = 0.7 degrees). The mean inter-observer variation in the measurement of the coronal mechanical femoro-tibial angle in maximal extension was 0.0 degrees (SD = 0.6 degrees). There were no significant differences and a high correlation between all paired intra- and inter-observer measurements. CONCLUSION: This system allows high reproducibility of the intra-operative measurement of the mechanical axes of the lower limb by a non-image-based kinematic registration of the hip, knee and ankle centers.

Arthroplasty, Replacement, Knee↗

Metallic debris arising from prosthetic abrasion: investigation of biodegradation of the materials and physiopathology of the bone.

The authors investigated the tissue around a failed knee prosthesis which had a metal-on-metal bearing made of chromium-cobalt-molybdenum alloy. Histological examination and the quantitative analysis of metallic particles found in the bone marrow (by fluorescent spectrometry and laser microsound) provided a detailed picture of the quantity, nature and distribution of the wear debris. The type and nature of the tissue response to the presence of the metal particles was determined by fluorescent microscopy and microradiography.

Aged↗

The treatment of osteoarthritis with unconstrained and constrained knee prostheses.

The first cases of knee prosthesis implantation at the orthopaedic department of the Freiburg university hospital are discussed. Surgery was indicated by advanced osteoarthritis which showed no improvement under conservative treatment. Indications concerning the choice of knee joint replacement with unconstrained or constrained prostheses are also discussed. Considerations of these indications as well as operative technique and consequent functional treatment usually produced good results. Follow up studies show equally good results for the GSB-total knee endoprosthesis (constrained) as for the surface type prosthesis (unconstrained).

Female↗

In vitro measurement of patellofemoral force after three types of knee replacement.

Using a new, non-invasive method, we measured the patellofemoral force (PFF) in cadaver knees mounted in a rig to simulate weight-bearing. The PFF was measured from 20 degrees to 120 degrees of flexion before and after implanting three designs of knee prosthesis. Medial unicompartmental arthroplasty with a meniscal-bearing prosthesis and with retention of both cruciate ligaments caused no significant change in the PFF. After arthroplasty with a posterior-cruciate-retaining prosthesis and division of the anterior cruciate ligament, the PFF decreased in extension and increased by 20% in flexion. Implantation of a posterior stabilised prosthesis and division of both cruciate ligaments produced a decrease in the PFF in extension but maintained normal load in flexion. There was a direct relationship between the PFF and the angle made with the patellar tendon and the long axis of the tibia. The abnormalities of the patellar tendon angle which resulted from implantation of the two total prostheses explain the observed changes in the PFF and show how the mechanics of the patellofemoral joint depend upon the kinematics of the tibiofemoral articulation.

Arthroplasty, Replacement, Knee↗

Systemic safety of high-dose antibiotic-loaded cement spacers after resection of an infected total knee arthroplasty.

The purpose of this study was to assess the systemic safety and potential adverse effects of using a high-dose antibiotic-impregnated cement spacer after resection arthroplasty of an infected total knee replacement. Between October 2000 and December 2002, 36 knees (34 patients) had a resection arthroplasty of an infected total knee prosthesis with placement of a high-dose antibiotic impregnated cement spacer. There were 24 men and 10 women with a mean age of 66.5 years (range, 48-84 years). All spacers placed contained an average of 3.4 batches of cement with an average total dose of 10.5 g of vancomycin (range, 3-16 g) and 12.5 g of gentamicin (range, 3.6-19.2 g). All patients were followed up post-operatively until reimplantation for evidence of renal failure. The preoperative creatinine ranged from 0.7 to 1.8 mg/dL. All patients were concomitantly treated with 6 weeks of intravenous organism-specific antibiotics. One patient with normal preoperative renal function (Cr 0.7 mg/dL) had a perioperative 1-day transient rise in serum creatinine (1.7 mg/dL) postoperatively that subsequently normalized. No patients showed any clinical evidence of acute renal insufficiency, failure, or other systemic side effects of the antibiotics. Treatment of patients with an infected total knee arthroplasty with high-dose vancomycin and gentamicin antibiotic spacers seems to be clinically safe.

Aged↗

Study of hardness and roughness modification in explanted joint components.

The significant wear of the UHMWPE bearings of explanted knee prostheses is produced mainly by micrometric debris ("third-body" wear) that diffuse toward the mobile metal-polymer interface. Here debris is crushed during the movement producing scratches in the metal and in the polymeric surfaces. Mechanical stress and the biological effects change the physical polymeric properties. In order to evaluate the area of UHMWE bearings submitted to high load stresses, in this work physical investigations are performed on the explanted knee prosthesis. Particularly, the roughness profile analysis (RPA) and the micro-hardness measurements (MHM) resulted suitable for the localisation of the mechanical and biological wear area. In the stressed zone, surface treatments could be applied in order to improve the mechanical resistance of the polymeric material. Particularly, the ion implantation with heavy ions is proposed to enhance the polymeric wear resistance. The Scanning Electron Microscopy (SEM), Energy Dispersive X-ray Spectrometry (EDX) and Infrared absorption spectroscopy (FTIR) techniques were also applied and results discussed.

Biocompatible Materials↗

Bone mineral density of the proximal tibia following uncemented arthroplasty.

Bone mineral density (BMD, g/cm2) was measured using dual-photon absorptiometry (DPA) in selected areas of the proximal tibia following uncemented PCA knee prosthesis. In nine patients with 14 alloplastic operations, measurements were taken at 3-6-month intervals for the first 3 1/2 years after operation. There was a significant increase in BMD of about 15% during the first 6 months after operation. The following year it remained increased, although not significantly, compared with the initial values, then gradually diminished. Increased bone density after arthroplasty may be explained mainly by stimulation of bone formation from weight bearing due to improved walking ability. Stress shielding of the proximal part of the supporting tibial bone did not seem to occur.

Adult↗

Blood loss after total knee replacement. Effects of tourniquet release and continuous passive motion.

We prospectively studied the cases of 121 patients who were being operated on for insertion of a unilateral total knee prosthesis with cement, and we placed them randomly in four groups. In Group I, the tourniquet was inflated throughout the operative procedure, and we released it postoperatively after a compressive dressing had been applied; a splint was used postoperatively for three days. In Group II, the tourniquet remained inflated throughout the operation, but no splint was applied postoperatively, and continuous passive motion was started immediately in the recovery room. In Group III, the tourniquet was released intraoperatively, and hemostasis was achieved by cauterization; postoperatively, a compressive dressing was applied, and a splint was used for three days. In Group IV, the tourniquet was released intraoperatively, hemostasis was established, and then the tourniquet was reinflated; a compressive dressing was applied, and continuous passive motion was started immediately in the recovery room. Hemoglobin and hematocrit values were monitored in all patients. Blood loss in suction drainage was recorded, and the total blood loss was calculated. The results show that total knee arthroplasty is associated with major loss of blood (mean, 1518 milliliters). The calculated blood loss for Groups I, II, and III averaged 1443 milliliters, while that for Group IV averaged 1793 milliliters. Loss in suction drainage correlated with total estimated blood loss and averaged 511 milliliters. The magnitude of blood loss after total knee arthroplasty should be appreciated, and special attention should be paid to the availability of adequate fluid and blood products, preferably blood donated by the patient preoperatively.

Adult↗

Metallic implant-associated lymphoma: a distinct subgroup of large B-cell lymphoma related to pyothorax-associated lymphoma?

Primary non-Hodgkin lymphoma arising at the site of metallic implant is very rare, and the possible carcinogenic effects of the metallic components and wear particles of the implant have not been answered despite many years of investigation. We report a case of large B-cell lymphoma occurring in a 78-year-old man who had a knee prosthesis implant for more than 30 years. The lymphoma was of microscopic size and found incidentally in the wear debris removed at surgical revision of the loosened prosthesis. The lymphoma expressed CD20, showed clonal rearrangements of immunoglobulin gene, and harbored Epstein-Barr virus (EBV). This case, together with previously reported cases, suggests that metallic implant-associated lymphoma is a distinctive subgroup of large B-cell lymphoma that shares many similarities with pyothorax-associated lymphoma and osteomyelitis-associated lymphoma, in that the lymphoma is an EBV-associated large B-cell lymphoma arising in a setting of chronic inflammation or irritation in a confined body space.

Arthritis, Infectious↗