Patient selection is key to the success of medial unicondylar knee arthroplasty (UKA). Progression of arthritis is the most common indication for revision. Various methods of assessing the lateral compartment have been used including stress radiography, radioisotope bone scanning, MRI, and visualisation at the time of surgery. Arthroscopy is another means of assessing the integrity of the lateral compartment. We used per-operative arthroscopy as a means to confirm suitability for UKA in a consecutive series of 279 Oxford medial UKA. This study reports the long-term results of a previously published cohort of knees. Our series of UKA with per-operative arthroscopy (Group 1) was compared to all Oxford UKA (Group 2) and all UKA in the Australian Orthopaedic Association National Joint Replacement Registry (AOANJRR) (Group 3).Abstract
Introduction
Methods
Our aims were to design a novel scale marker which does not require such precise positioning, and to compare the accuracy of this new marker with a standard single ball marker.
The posterior marker consists of a 75x75cm square foam mat, incorporating multiple 25.4mm metal rods arranged in series down the centre. The anterior marker is made from five 25.4mm steel balls, linked in series at 20mm intervals. The mat is positioned just underneath the patient’s pelvis as they lie supine for their radiograph. The five balls are placed in the midline over the patient’s suprapubic region, and the x-ray is then taken. The radiographic dimensions of the ball and rod which are located between the hips are then measured. The magnification of the hips may then be calculated from these dimensions using a simple equation. To validate the new “double” marker, it was compared with a conventional single marker ball. 74 hip arthroplasty patients undergoing routine radiographic follow up were recruited. Both the new double marker and the single marker were applied at the time of x-ray, the magnification according to each was calculated, and these were compared to the true radiographic magnification as determined from the known dimensions of the prosthesis. All markers were positioned by independent radiographers trained in their use.