The acetabular component is a monobloc hemispherical cup manufactured from Ultra High Molecular Weight Polyethylene (UHMWPE), with a pure titanium particle coated surface. With heat and pressure, the particles are blasted into the polyethylene surface. The coating promote osseointegration. Stability of the cup is provided by 2 anchoring pegs on the weight bearing part on its outer surface. The inclination of pegs and holes diverge by 5 degrees providing a press-fit effect that increases the rigidity of the primary fixation and this is supplemented by screws inserted through the periphery of the cup. Tow cups designs are available, a full-profile and a bevelled cup. In all cases the bevelled cup was used. The purpose of this study was to assess the clinical performance with 15 years of this cup.
The diagnosis was osteoarthritis, rheumatic arthritis, femur neck fracture, developmental dysplasia of the hip (DDH). 1034 patients were contacted by telephone. Out of this patients group 539 patients (678 cups) were evaluated by clinical examination (HHS), radiographic investigation and social evaluation by the WOMAC and NHS score. 451 patients who had died unrelated to the operation. Lost of follow up were 65 patients (69 Cups) and 34 patients (48 cups) had to be revised.
Systemic factors are believed to be pivotal for the development of heterotopic ossification in severely-injured patients. In this study, cell cultures of putative target cells (human fibroblastic cells, osteoblastic cells (MG-63), and bone-marrow stromal cells (hBM)) were incubated with serum from ten consecutive polytraumatised patients taken from post-traumatic day 1 to day 21 and with serum from 12 healthy control subjects. The serum from the polytraumatised patients significantly stimulated the proliferation of fibroblasts, MG-63 and of hBM cells. The activity of alkaline phosphatase in MG-63 and hBM cells was significantly decreased when exposed to the serum of the severely-injured patient. After three weeks in 3D cell cultures, matrix production and osteogenic gene expression of hBM cells were equal in the patient and control groups. However, the serum from the polytraumatised patients significantly decreased apoptosis of hBM cells compared with the control serum (4.3% Increased proliferation of osteoblastic cells and reduced apoptosis of osteoprogenitors may be responsible for increased osteogenesis in severely-injured patients.