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PATELLA RESURFACING/NON-RESURFACING IN TOTAL KNEE ARTHROPLASTY – RESULTS OF A RANDOMISED CONTROLLED CLINICAL TRIAL AT A MINIMUM OF 10 YEARS



Abstract

Introduction and Aims: Problem: Patellar resurfacing in TKA remains controversial. Purpose: To evaluate the results of resurfacing/non-resurfacing of the patella in a randomised controlled clinical trial at a minimum of 10 years of follow-up.

Method: One hundred knees (90 patients) with osteoarthritis were enrolled in a prospective randomised controlled double-blinded trial using the same posterior cruciate retaining total knee replacement. Patients were randomised to resurfacing or non-resurfacing of the patella. Evaluations were performed pre-operatively and yearly to a minimum of 10 years (range 10.1–11.5 years) postoperatively. Disease-specific (Knee Society Clinical Rating System), functional (stair climbing, knee flexion/extension torques, patellar examination) outcomes were measured. Patient satisfaction, anterior knee pain, and patellofemoral questionnaires were completed. Intra-operative grading of the articular cartilage was performed.

Results: No patients were lost to follow-up; 46 knees remained alive. Nine revisions (9/90–10%) were performed – 7/48 (15%) in the non-resurfaced and 2/42 (5%) in the resurfaced group. Three knees in the non-resurfaced group were revised to a resurfaced patella for anterior knee pain. One resurfaced patella was complicated by AVN and fracture, requiring revision. No significant difference was found between the groups regarding revision rates, KSCR score, functional, satisfaction, anterior knee pain, patellofemoral, and radiographic outcomes. Intraoperative cartilage quality was not a predictor of outcome.

Conclusions: This study represents the longest follow-up to date of a randomised controlled clinical trial to examine patellar resurfacing in TKA. The results showed no significant difference between the groups for all outcome measures at a minimum of 10 years.

These abstracts were prepared by Editorial Secretary, George Sikorski. Correspondence should be addressed to Australian Orthopaedic Association, Ground Floor, The William Bland Centre, 229 Macquarie Street, Sydney, NSW 2000, Australia.

At least one of the authors is receiving or has received material benefits or support from a commercial source.