This study evaluated the biologic fixation of two different titanium porous coatings: a clinically successful sintered spherical bead coating [ The time-zero average peak push-out load (±S.D.) of the STIKTITE group (95±3 N) was found to be significantly greater (p <
0.02) than that of the spherical bead group (36±5 N). By six weeks in vivo, the average peak push-out load for the STIKTITE group was up to 1001±362 N, and that for the spherical bead group was up to 985±425 N, both representing a significant increase compared to their time-zero results (p <
0.0005). From six to twenty-six weeks in vivo, there was again a significant increase in the peak push-out load irrespective of group (p <
0.0005), with the average peak push-out loads up to 1620±406 N and 1444±446 N for the STIK-TITE and spherical bead groups, respectively. Histology revealed bone ingrowth in both groups that confirmed the findings of the mechanical push-out testing. While the STIKTITE group showed a trend toward greater biologic fixation, overall there was insufficient evidence to support differences between the two groups (p = 0.47) irrespective of the amount of time in vivo. The results of this study confirm the ability of the STIK-TITE coating to achieve superior initial stability. This improved initial stability reduces the reliance on adjunct fixation (such as screws) or large amounts of press-fit to prevent micromotion and create an environment suitable for long-term bone ingrowth. The results also suggest that the STIKTITE coating had a tendency to initiate and maintain bone ingrowth under load-bearing conditions to a level greater than that of a clinically successful sintered bead coating. Because loading of the implant can cause micromotion at the bone/implant interface, models like the one used in this study likely provide a more challenging and realistic representation of anticipated clinical conditions than models with minimal implant loading.
A prospective study of the relationship of first day straight leg raise (SLR) to end range of movement took place. The ability to do SLR was used to measure patients’ motivation. A standard medial parapatellar approach was used, all patients has osteoarthritis. Responses from 100 patients were analyzed (divided into 3 groups)
-Flexion on discharge (mean) was 74° -Flexion at end follow up (mean) was 104° Group II: 27% of patients SLR at day two postoperatively,
-Flexion on discharge (mean) was 66° -Flexion at end follow up (mean) was 97° Group III: 26% of patients SLR at day 3 or more postoperatively,
-Flexion on discharge (mean) was 66° -Flexion at end follow up (mean) was 95° Functional scores including WOMAC, SF-36 and pre-operative deformity did not vary even though Group I shows statistically significant increase in flexion at end follow up.