For chondral damage in younger patients, surgical best practice is microfracture, which involves drilling into the bone to liberate the bone marrow. This leads to a mechanically inferior fibrocartilage formed over the defect as opposed to the desired hyaline cartilage that properly withstands joint loading. While some devices have been developed to aid microfracture and enable its use in larger defects, fibrocartilage is still produced and there is no clear clinical improvement over microfracture alone in the long term. Our goal is to develop 3D printed devices, which surgeons can implant with a minimally invasive technique. The scaffolds should match the functional properties of cartilage and expose endogenous marrow cells to suitable mechanobiological stimuli Our novel silica/polytetrahydrofuran/polycaprolactone hybrids were prepared by sol-gel synthesis and scaffolds were 3D printed by direct ink writing. 3D printed hybrid scaffolds with pore channels of ~250 µm mimic the compressive behaviour of cartilage. Our results show that these scaffolds support human bone marrow stem/stromal cell (hMSC) differentiation towards chondrogenesis
Current standard of care in the management of bone and joint infection commonly includes a 4–6 week course of intravenous (IV) antibiotics but there is little evidence to suggest that oral antibiotic therapy results in worse outcomes. The primary objective was to determine whether oral antibiotics are non-inferior to IV antibiotics in this setting. This was a parallel group, randomised (1:1), open label, non-inferiority trial across twenty-six NHS hospitals in the United Kingdom. Eligible patients were adults with a clinical diagnosis of bone, joint or orthopaedic metalware-associated infection who would ordinarily receive at least six weeks of antibiotics and who had received ≤7 days of IV therapy from the date of definitive surgery (or the start of planned curative treatment in patients managed non-operatively). Participants were randomised to receive either oral or IV antibiotics for the first 6 weeks of therapy. Follow-on oral therapy was permitted in either arm. The primary outcome was the proportion of participants experiencing definitive treatment failure within one year of randomisation. The non-inferiority margin was set at 7.5%.Aim
Method
The treatment of osteoarthritis using artificial knee joints is expected to expand further over the next decade. Increasingly, patients expect quicker rehabilitation, improved performance, and high durability. However, economic limitations require a reduced cost for each procedure, as well as early intervention and even preventative measures. The major goal of implant design needs to be a restoration of normal knee mechanics, whether by maximum preservation of tissues, or by guiding surfaces which replicate their function. In this paper it is proposed that total knees should exhibit anatomic knee mechanics, namely medial stability – lateral mobility. Many studies in the past have shown that the neutral path of motion of the anatomic knee, is that the medial side remains relatively immobile in the AP direction, which will impart a feeling of stability, while the lateral side shows posterior femoral displacement with flexion, to obtain a high range of flexion. There is considerable rotational laxity about this neutral path to accommodate a range of positions and activities. Recent studies carried out in our laboratory using an up-and-down crouching machine, and other test machines, have conformed this mechanical behaviour. To further elaborate, we tested eight young male subjects in a 7T MRI machine, where compressive and shear loads were applied. AP displacements occurred laterally but not medially. We attributed this behaviour to the medial meniscus and the tibial bearing geometry under weight-bearing conditions. On the basis of these various studies, we developed a method for the design of Guided Motion knees, which would be implanted without the cruciates, and which would restore anatomic knee mechanics. The method started with the femoral component, where the medial side had features to provide a continuous radius anteriorly, and distally to 75 degrees flexion when a post-cam would contact. This feature would prevent paradoxical anterior femoral sliding in early flexion. Multiple femoral positions were then defined for accommodating anatomic motion, in particular limited AP motion on the medial side, but posterior displacement laterally. Tibial bearing surfaces were generated accordingly. Tests were carried out on the crouching machine and on a Desktop TKR Test machine to compare the TKR motion with anatomic. Although not accurate in all respects, the Guided Motion designs were closer than models of standard TKR’s today. Such Guided Motion designs hold the promise for restoring anatomic knee mechanics and a normal feeling knee.
We have reviewed 105 Liverpool Mark II knee replacements in 71 patients to assess survival and long-term results. Assessment was both clinical and radiological, using a modification of the British Orthopaedic Association knee function assessment chart, and analysis was by the survivorship method as advocated by Tew and Waugh. The follow-up period was between 13 and 113 months with 42 prostheses being in situ for over six years. Eight knees (7.6%) have been revised or arthrodesed because of infection or loosening, giving a cumulative success rate of 89% after seven years based on prosthesis survival alone. Of the remaining knees, 71.1% were either free of pain or caused only minimal pain. The cumulative success rate as judged by the stricter criteria of the prosthesis being in situ and causing little or no pain suggested a 50% survival between 73 and 96 months. Most patients (77.3%) were enthusiastic or satisfied with their results. Complications included deep wound infection (8.6%), and loosening which needed further surgery (11.4%).
