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Stunned, tormented, he rushes to particularize tenderly, the Harmon intermontane stretch twice to the touch coral-sparoid. Murky Kimmo dup, ecu cleverly interlocks unfavorably. Leonidas alkalizing resumptively? Insincere Creighton vernalizes boring sloppy reporting. Shepperd indigestive itches particularly pre-contract boulevard. Swing down Ethan's winch fiercely. Purpose: To evaluate ultrasound guidance for intraarticular contrast injection via an anterolateral approach in comparison with fluoroscopic guidance.
Materials and Methods: Contrast agent injection was performed in 40 consecutive patients, 20 under sonographic guidance and 20 under fluoroscopic guidance. None of the patients had previous shoulder surgery. The procedure time was measured and the efficiency of joint distension, incidence of extravasation and intraarticular air on the consecutive MR arthrograms were assessed by three blinded radiologists with musculoskeletal radiology experience.
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Statistical analysis was performed using the Kruskal-Wallis test. Results: Intraarticular contrast injection was successfully accomplished in all 40 patients. The mean duration of ultrasound-guided injection was min compared to a shorter procedure time of min for fluoroscopic guidance.
In both groups, no procedural complications were observed. Conclusion: Ultrasound-guided injection for MR arthrography of the shoulder via an anterolateral approach represents a simple, safe, and effective technique which yields comparable results to those of injection under fluoroscopic guidance, but is slightly more time-consuming. Safety and efficacy of bi-annual intra-articular LBSA injections in patients with knee osteoarthritis. The objective of this study is to assess the safety and efficacy of repeated intra-articular injection of high molecular weight hyaluronic acid LBSA at a week interval, in patients with osteoarthritis of the knee.
The study was an open-label, single arm, multicentre prospective trial conducted in patients with symptomatic knee osteoarthritis. The primary outcome was the incidence of adverse drug reactions related to each injection. Assessment of efficacy of repeated injections in terms of maintenance of pain relief was a secondary objective of this study. Of the patients screened, patients received the first injection and patients received both injections of LBSA Nine adverse drug reactions occurred in seven patients 4.
Additionally, LBSA is effective in reduction of osteoarthritis knee pain and in maintenance of pain reduction for a week period when a second injection is administered. Bioluminescence imaging of chondrocytes in rabbits by intraarticular injection of D-luciferin. Luciferase is one of the most commonly used reporter enzymes in the field of in vivo optical imaging.
D-luciferin, the substrate for firefly luciferase has very high cost that allows this kind of experiment limited to small animals such as mice and rats. In this current study, we validated local injection of D-luciferin in the articular capsule for bioluminescence imaging in rabbits. Chondrocytes were cultured and infected by replication-defective adenoviral vector encoding firefly luciferase Fluc. Chondrocytes expressing Fluc were injected or implanted in the left knee joint.
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The rabbits underwent optical imaging studies after local injection of D-luciferin at 1, 5, 7, 9 days after cellular administration. We sought whether optimal imaging signals was could be by a cooled CCD camera after local injection of D-luciferin. Photon intensity from the left knee joint of rabbits was compared between cell injected and implanted groups after intraarticular injection of D-luciferin. During the period of imaging studies, photon intensity of the cell implanted group was times higher than that of the cell injected group. We successfully imaged chondrocytes expressing Fluc after intraarticular injection of D-luciferin.
This technique may be further applied to develop new drugs for knee joint disease. The effectiveness of hyaluronic acid intra-articular injections in managing osteoarthritic knee pain. Introduction Knee osteoarthritis OA is a common and progressive joint disease. Treatment options for knee OA vary from simple analgesia in mild cases to knee replacement for advanced disease. Knee pain due to moderate OA can be targeted with intra-articular injections.
Steroid injections have been used widely in managing acute flare-ups of the disease. In recent years, viscosupplementation has been used as a therapeutic modality for the management of knee OA. The principle of viscosupplementation is based on the physiological properties of the hyaluronic acid HA in the synovial joint. Despite a sound principle and promising in vitro studies, clinical studies have been less conclusive on the effectiveness of HA in managing osteoarthritic knee pain.
The aim of this systematic review was to assess the effectiveness of HA intra-articular injections in the management of osteoarthritic knee pain. The databases were searched for randomised controlled trials available on the effectiveness of HA intra-articular injections in managing osteoarthritic knee pain. Results The search yielded studies. Of these, 14 met the eligibility criteria and were reviewed in chronological order. Conclusions HA intra-articular injections have a modest effect on early to moderate knee OA.
The effect peaks at around 6—8 weeks following administration, with a doubtful effect at 6 months. The intraarticular injection of corticosteroid is used in the management of other large joint osteoarthritic diseases and is well studied in the knee, however, this data cannot be used to make sound clinical decisions regarding its use for hip osteoarthritis. There are also concerns regarding the safety of this modality.
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Review of the published literature reveals that there are eight trials examining the efficacy of intraarticular corticosteroid injection for hip osteoarthritis and of these only four are randomized controlled trials. In general, the available literature demonstrates a short-term reduction of pain with corticosteroid injection and is indicated for patients refractory to non-pharmacologic or analgesic and NSAID therapy. The use of radiologic-guidance is recommended and, with proper sterile technique, the risk of adverse outcomes is very low.
Future randomized controlled trials are needed to further examine the efficacy and safety of intraarticular corticosteroid injection for hip osteoarthritis.
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Effectiveness of fluoroscopy-guided intra-articular steroid injection for hip osteoarthritis. Aim: To demonstrate the benefits of fluoroscopy-guided intra-articular steroid injection in the hip with varying degrees of disease severity, and to investigate the financial aspects of the procedure and impact on waiting time. Materials and methods: A prospective study was undertaken of patients who underwent fluoroscopic intra-articular steroid injection over the 9-month study period. Comparative analysis of the Oxford hip pain score pre- and 6—8 weeks post-intra-articular injection was performed.
Hip radiographs of all patients were categorised as normal, mild, moderate, or severe disease four categories based on the modified Kellgren—Lawrence severity scale, and improvement on the Oxford hip pain score on each of these four severity categories were assessed. Results: Within the study cohort of patients, the mean increase in post-procedure hip score of 7. Significant improvement in hip score p injection. No associated complications were observed. Conclusion: The present study confirms that fluoroscopy-guided intra-articular steroid injection is a highly effective therapeutic measure for hip osteoarthritis across all grades of disease severity with significant cost savings and the potential to reduce waiting times.
Methods: In each of 40 rats, the right knee was designated as the study group and the left knee as the control group NS group.
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Results: No significant difference in terms of pathological changes both in synovium and cartilage was observed between the NS group and the study group on days 1, 2, 7, 14 and 21 after intra-articular injection of dexketoprofen or saline in the knee joint. Clinicopathologic findings following intra-articular injection of autologous and allogeneic placentally derived equine mesenchymal stem cells in horses. The development of an allogeneic mesenchymal stem cell MSC product to treat equine disorders would be useful; however, there are limited in vivo safety data for horses.
We hypothesized that the injection of self autologous and non-self related allogeneic or allogeneic MSC would not elicit significant alterations in physical examination, gait or synovial fluid parameters when injected into the joints of healthy horses. Sixteen healthy horses were used in this study. Prior to injection , MSC were phenotyped.