To compare the effect of femoral bone tunnel configuration on tendon-bone healing in an anterior cruciate ligament (ACL) reconstruction animal model. Anterior cruciate ligament reconstruction using the plantaris tendon as graft material was performed on both knees of 24 rabbits (48 knees) to mimic ACL reconstruction by two different suspensory fixation devices for graft fixation. For the adjustable fixation device model (Socket group; group S), a 5 mm deep socket was created in the lateral femoral condyle (LFC) of the right knee. For the fixed-loop model (Tunnel group; group T), a femoral tunnel penetrating the LFC was created in the left knee. Animals were sacrificed at four and eight weeks after surgery for histological evaluation and biomechanical testing.Objectives
Methods
The purposes of this study were to clarify first, the incidence
of peroneal tendon dislocation in patients with a fracture of the
talus and second the factors associated with peroneal tendon dislocation. We retrospectively examined 30 patients (30 ankles) with a mean
age of 37.5 years, who had undergone internal fixation for a fracture
of the talus. Independent examiners assessed for peroneal tendon
dislocation using the pre-operative CT images. The medical records
were also reviewed for the presence of peroneal tendon dislocation.
The associations between the presence of dislocation with the patient
characteristics or radiological findings, including age, mechanism
of injury, severity of fracture, and fleck sign, were assessed using Fisher’s
exact tests.Aims
Patients and Methods
The aim of this study was to investigate the effect of granulocyte-colony stimulating factor (G-CSF) on mesenchymal stem cell (MSC) proliferation MSCs from rabbits were cultured in a control medium and medium with G-CSF (low-dose: 4 μg, high-dose: 40 μg). At one, three, and five days after culturing, cells were counted. Differential potential of cultured cells were examined by stimulating them with a osteogenic, adipogenic and chondrogenic medium. A total of 30 rabbits were divided into three groups. The low-dose group (n = 10) received 10 μg/kg of G-CSF daily, the high-dose group (n = 10) received 50 μg/kg daily by subcutaneous injection for three days prior to creating cartilage defects. The control group (n = 10) was administered saline for three days. At 48 hours after the first injection, a 5.2 mm diameter cylindrical osteochondral defect was created in the femoral trochlea. At four and 12 weeks post-operatively, repaired tissue was evaluated macroscopically and microscopically.Objectives
Methods
The extension and flexion gaps are affected by different factors in total knee arthroplasty (TKA). Flexion but not extension gap measurements are influenced by posterior cruciate ligament (PCL) preservation or resection and patella reduction or eversion and thigh weight. If the flexion gap is measured with the thigh placed on the tibia, the measurement results must include the thigh weight; nevertheless, there is no detailed report regarding the thigh weight influence on the flexion gap. In this study, we investigated how thigh weight affected flexion gap measurement. Four knees of whole-body fresh-frozen cadavers (Mongolian race) were investigated. The femur and tibia were dissected with a standard measured resection technique. After the femoral component was set, the flexion gap was measured with a knee balancer. The distraction force of 20, 30, and 40 pounds were loaded at the joint level. For each measurement, the influences of the patella reduced or everted (PR or PE) and the PCL preserved or resected (CR or PS) were estimated. The flexion gap was measured five times in four different categories (CR/PR, CR/PE, PS/PR, PS/PE) and the thigh weight was reduced by weights (0, 0.5, 1.0, 2.0, 3.0 kg) using a string and pulley system. During measurement, the femur was just placed on the tibia, and the knee flexion angle was maintained at 90 degrees with a goniometer. After all measurements, the lower limbs were resected, and the thighs were weighed with a scale. Steel-Dwasstest (non-parametric multiple comparison test) were performed for statistical analysis, and p < 0.05 was considered significant.INTRODUCTION
METHODS
In total knee arthroplalsties, there are risks of revision surgeries because of aseptic loosening, polyethylene wear, and metal component breakage. The data such as model, type, size, and manufacturing companies are required at the time of revision surgeries. However, it is sometimes difficult to acquire such data due to patient's change of address and the elimination and consolidation of hospitals in the long-term. Therefore, we try to use the Radio Frequency IDentification (RFID) in the total knee joint system. The FerVID family (Fujitsu Co. Ltd., Tokyo, Japan) was prepared as the RFID tag. It was radio-resistant below the dose of 50kGy, which allowed gamma sterilization. The RFID tags were embedded into the anterior side of GUR 1050 UHMWPE inserts and 0.3wt% vitamin E blended UHMWPE. The UHMWPE inserts were manufactured by thecompression molding method at the maximum temperature of 220°C and the maximum compressive force of 245kgf/cm2. The manufactured inserts were implanted in fresh cadaveric knees. The tibial base plate was made of Ti6Al4V. The femoral components were made of Co-Cr-Mo or Ti-6Al-4V. Communication Performance was measured with the interrogator (DOTR-920 MHz-band, Tohoku Systems Support Co. Ltd., Miyagi, Japan). The transmission output was up to 1W. Received Signal Strength Indicator (RSSI) was measured 500 times at 15 mm away from the surface of skin in the extension and 90° flexion of the knee (Fig1).Introduction
Materials and methods
The bioactive polyetheretherketone (PEEK) was fabricated by the combination of PEEK and CaO-SiO2 particles, which formed hydroxyapatite on its surfaces in simulated body fluid and showed good mechanical propeties. The study revealed osteoblast-like cell proliferation and gene expression on the bioactive PEEK. Peek and bioactive PEEK discs (24 mm in diameter and 2 mm in thickness) were prepared. Bioactive PEEk was produced by the combination of 80 vol% Peek powder and 20 vol% CaO-SiO2 particles (30CaO · 70SiO2). Discs were sterilized with ethylene oxide gas. The study was approved by the ethics committee in Chiba University. Human osteoblast-like cells were used in the study. The cells at passage 3–5 were used in the experiments. 2 × 105cells /disc were culture at 37°C in a humidified atmosphere with 5% CO2, and the media was replaced every 3 days. At days 3, 7, 21, the culture media, cells and discs were collected respectively. Cell attachment assay was performed. Cells were seeded at a density of 4 × 105 cells /well and incubated for 2 hours at 37 C in a humidified atmosphere with 5% CO2. The cells on the discs were evaluated by DNA content. The real-time PCR was performed with regard to type I collagen (COLI), osteocalcin (OC), osteonectin (ON), osteopontin (OPN), and GAPDH. The alkaline phosphatase activity (ALP) was measeured at 3, 7, and 21 days, which samples as used in the DNA-content assay. Alizalin Red Staining was performed at day 21 to quantify calcification deposits in discs. Results were analyzed using Student's The content of DNA showed similar increases on PEEK and bioactive PEEK in the course of day 3, 7, 21. The cell attachment of bioactive PEEK was two times larger than that of PEEK. Real-time PCR results of human osteoblast-like cells cultured on PEEK and bioactive PEEK discs were shown in Fig. 1. There were no significant differences between cells on PEEK and bioactive PEEK with respect to COL I and ON mRNA expression. However, human osteoblast-like cells on bioactive PEEK presented higher expression of OPN and OCN mRNA at day 21. No significant differences were found in ALP activity of both discs. Calcification deposits were observed only on bioactive PEEK at day 21Materials and Methods
Results
The aim of this study was to report a 3 year follow up of vitamin E add polyethylene in total knee arthroplasty. UHMWPE powder (GUR1050) was mixed with 0.3% of vitamin E before consolidation by direct compression molding. The vitamin E added UHMWPE was applied to the articular surface and patella in 65 patients (mean age, 69.6 years). Joint fluid concentrations of tocopherol and matrix metalloproteinase 9 were measured in vitamin E added UHMWPE cases one year after surgery, and were compared to those of conventional UHMWPE cases and osteoarthritis patients. Concentrations of α-tocopherol and γ-tocopherol were measured by using HPLC with ultraviolet-visible wavelength detection. Concentrations of matrix metalloproteinase 9 were detected by using enzyme immunoassay. The Average Knee Society score were 91.7(clinical) and 76.7(functional). There were three failures (1 supracondylar fracture, and 2 skin necrosis). The average concentrations of α-tocopherol were 281.8μg/dL (10 cases) in the vitamin E group, 371.8μg/dL (15 cases) in the conventional group, and 317.8μg/dL (46 cases) in the osteoarthritis group. There were no significant differences among three groups. The average concentrations of γ-tocopherol were 43.4μg/dL in the vitamin E group, 52.3μg/dL in the conventional group, and 49.8μg/dL in the osteoarthritis group. There were no significant differences among three groups. The average concentrations of matrix metalloproteinase 9 were 83.2 ng/mL in the vitamin E group, 78.4 ng/mL in the conventional group, and 17.4 ng/mL in the osteoarthritis group. There was no significant difference between the vitamin E group and the conventional group. However, The matrix metalloproteinase 9 concentrations of the osteoarthritis group were significantly lower than others. No cases exhibited measurable polyethylene wear or osteolysis and also no abnormal values relating to vitamin E on joint fluid examinations. At three year follow-up, vitamin E added polyethylene demonstrated the safe use for the human body.
The application of arthroscopic procedure for osteoarthritic knee is limited to rather initial stages of the disease. Here we report the results of new arthroscopic procedure, which was named arthroscopic posteromedial release, applied to relatively severe cases of medial type osteoarthrits (OA) Forty-eight knees of 46 patients of OA knees with flexion contracture were treated with arthroscopic posteromedial release. Thirty-two were female and 14 were male. All the patients had been treated conservatively beforehand. The mean age of the patients was 71.6 (range, 47 to 84 years), the average range of motion was 13 to 129 degrees. Only one case was classified stage II in Kellgren Lowrence x-ray classification, 13 and 34 cases were stage III and IV respectively. The average femoro-tibial angle was 183.4+-4.4 degrees. In surgery, we release the joint capsule along with the medial tibial condyle, arthroscopic debridement including medial meniscentomy was performed at the same time. If some cases, medial collateral ligament was cut transversely to obtain enough joint space. We use hyaluronan intra-articularly once a week for 5 weeks postoperatively. Patients were examined at 3,6,12,18 and 24 months after surgery and evaluated subjectively and objectively with the rating system of Japanese Orthopaedic Association knee score (JOA score). Clinical results were also classified excelletn, good, fair and poor by our criteria. Eighty-three per cent (40 knees) of patients were satisfied at their last follow up. Sixty-seven percent (32 knees) of the patients were excellent or good. Six knees were converted to TKA because of their persistent knee pain. Twenty-eight knees complained of night pain pre-operatively, but only four of them complained of it postoperatively Considering that most of the patients in this series were grade IV in x-rays and their joint surface of medial compartment showed large eburnation both femur and tibia, TKA is most preferable treatment conventionally. But our results showed this arthroscopic technique was one of the applicable choices for severe OA knees.
