The Adora RSA (NRT, Denmark) is a new stereo X-ray system custom built for Radeostereometry. Images are acquired using CXDI50C digital detectors (Canon, Netherlands). Analysis software was written locally to detect both Tantalum markers and the spherical head of the hip implant, and for RSA reconstruction and kinematic analysis.

To assess geometric reproducibility, a planar grid phantom was constructed with 1400 2mm markers in a grid pattern over a 350 by 430 mm glass plate. Additionally 25 tantalum markers of each diameter 1.0, 0.8 and 0.5 mm were added within a 120mm square of the grid. The phantom was imaged repeatedly with translation and rotation over the detector. For small phantom movements of up to 10mm over the detector, very small measurement errors were observed of median 2 microns, maximum 6 microns. For larger movements, the errors increased to median 5 microns and maximum 50 microns. Errors also increased with decreasing exposure.

For RSA validation, an acetabular PE cup was cemented to a Sawbone pelvis. Tantalum markers were inserted into the pelvis (10), cement (4), and cup (10). A 28mm metal head was fixed to the cup. The phantom was imaged repeatedly without movement, then moved in translation (up to 100 mm) and rotation (all axes, up to 45 degrees), and with full X-ray repositioning. Precision errors were calculated on the assumption of no relative movement between components.

Results are given for repositioning movement categorised as none, small (less than 25mm or 15 degrees), medium (less than 50mm or 30 degrees), and large. For the head, the mean total point motion error was 4, 10, 14 and 24 micrometers. Mean error of segment fitting was less than 60 microns with no markers rejected from the composite segment of 24 markers. Cup migration total translation error was 10, 16, 24, and 35 micrometers with rotation errors less than 0.05 degrees.

Observed RSA errors were small, increasing with phantom movement. This is consistent with the geometric uniformity tests. X-ray exposure and tissue thickness were also identified as factors in precision. We conclude this system has excellent precision for Radiostereometry.

The reinfusion of perioperative cell salvage is one method employed to reduce exposure to donor blood. Data on the safety of this process, however, are scant. Notably, the effect of intraoperative, washed cell salvage reinfusion on prothrombotic markers has not been demonstrated. The risk of postoperative venous thromboembolism following major orthopaedic operations is not insignificant. The study objective was to assess the effect of cell salvage reinfusion on coagulation and platelet activation.

Twenty-one patients undergoing elective primary hip operations were recruited. Nine patients received washed cell salvage intraoperatively, and were compared with 12 patients undergoing similar surgery that did not. Two patients in the cell salvage group also received postoperative, unwashed cell salvage. Blood samples were collected pre-operatively, immediately post-operatively, and one day post-operatively for assays of platelet activation markers, P-selectin expression and fibrinogen binding by flow cytometry in diluted whole blood; coagulation activation marker, thrombin-antithrombin complex (TAT); D-dimer by ELISA, thrombin generation by chromogenic assay, and full blood count. Samples of cell salvage material were also analysed for prothrombotic markers.

There were no significant differences between the groups preoperatively. Postoperatively haemoglobin levels did not differ significantly between the cell salvage group and controls. Postoperative TAT and D-dimer were significantly higher in the cell salvage group compared with controls (p<0.05). One day postoperatively, there were significantly higher platelet P-selectin expression (p=0.006) and platelet fibrinogen binding (p=0.004) in the cell salvage group compared with controls. The white cell count (WCC) was also significantly higher (p=0.04). In the intraoperative washed cell salvage material, and in postoperative cell salvage, the platelet count was low, but significant proportions of platelets were activated, and levels of D-dimer were elevated compared with venous blood. The postoperative salvage material also contained high levels of TAT.

The results from this pilot study show the induction of a prothrombotic state following reinfusion of intraoperative, washed cell salvage in recipients undergoing primary elective hip operations. An inflammatory response to reinfusion is also indicated by the raised WCC. Further investigation into the safety of cell salvage is indicated.

Prosthesis migration and acetabular cup wear are useful short term measurement which may predict later implant outcome. However, the significance of the magnitude and pattern of the migration is very much dependent on the specific design studied. This study aimed to characterise patterns of migration by following four cemented femoral stem designs using Radiostereometry (RSA) within a prospective randomised longitudinal trial.

164 patients undergoing cemented femoral hip replacement for osteoarthritis were randomised to receive either an Exeter (Howmedica Stryker), Ultima Tapered Polished Stem (TPS) (Depuy), Ultima Straight Stem (USS) (Johnson and Johnson) or Elite Plus (Depuy) stem. Each subject received the OGEE PE cemented acetabular component (Depuy). RSA examinations were performed at 1 week and 6, 12, 18, 24 and 60 months post surgery. They were analysed using the UMRSA system (RSA Biomedical AB, Umea, Sweden), and our local geometric stem measurement software. 149 patients had RSA measurements available to 2 years, and 96 patients to 5 years. Differences were analysed using mixed linear modelling (SPSS).

Median linear proximal cup wear rate reduced to a minimum of 0.02-0.06mm/year in year two. Between 2 and 5 years the wear rate increased, being significantly higher for the Elite.

Cup migration was small but continuous. At 2 years it was median 0.3mm proximally, increasing to 0.5 mm at 5 years. Median rotations were less than 0.3 degrees.

Proximal migration was positive and increasing at all time points for all stems. For the tapered polished designs, while the overall magnitude was significantly higher, the rate of migration significantly decreased, whereas for the other stem designs it did not.

The TPS stem showed a tendency for posterior tilt which was significant compared to the other stems at 5 years.

All stems tended to retroversion, with the USS significantly less than the others and the Elite showing and relative increase at 5 years.

In summary migration patterns are characterised by the stem design, including where there were only small changes between designs. We are now testing measured migrations as predictors of outcome, and will continue to follow this group of patients to 10 years.