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FIVE-YEAR RESULTS OF THE INNEX™ UCOR TOTAL KNEE ARTHROPLASTY



Abstract

Introduction: Since the introduction of the Zimmer Innex UCOR (Ultra COgruent Rotating) mobile bearing total knee arthroplasty (TKA) system in 1999, there were close to 3000 primary TKAs performed at our institution utilizing this implant. We report on the first 396 5-year follow-up results and overall revisions in our total collective.

Methods: Between 1999 and 2006 there were 2734 primary Innex UCOR TKA performed (1748 female/987 male) at the Schulthess Clinic, Zurich. Primary diagnosis leading to TKA were OA (2462 – 90%), RA (144 – 5.3%), posttraumatic arthritis (65, 2.4%), necrosis (50, 1.8%) and misc causes (13 – 0.5%). The mean age of the females patients was 69y (33y – 92y), and 68y (31y – 93y) in the male population. To date 396 knees underwent clinical and radiological follow-up at 5 years (mean 5y 0m, range 4y 1m – 7y 2m), with 5% of the patients being lost to follow-up. Scoring was done, using the Knee Society Score (KSS). All patients had a full leg radiograph pre-operatively as well as at follow-up.

Results: Total KSS improved from 106.5 (6 – 184) pre-operatively to 179.5 (80 – 200) at follow-up, the knee score from 42.2 (2–93) to 92.1 (37 – 100), the function score from 64.3 (0–100) to 87.4 (10–100) respectively. The pain score increased from 17.7 (0–50) to 47.5 (20–50, 50 points maximum). ROM pre-operatively was 104.6° (0–145) and reached 117.2° at follow-up (55–145). Subjective evaluation by the patient at 5 years was excellent and good in 91%, fair in 8% and taxed poor by 1% of the patients. 95% of full leg radiographs showed a femorotibial angle of 182°–188°, 3% were < 182° (varus), 2% > 188° (valgus). Overall revision rate (95 of 2735) was 3.5%, 1.1% for infections and 1% for anterior knee pain and/or patella pathology. 0.6% were revised for instability, 0.3% for arthrofibrosis, and the remaining 0.5% for various problems.

Conclusion: These promising 5 year observations with the Innex UCOR mobile bearing TKA system suggest favorable overall midterm results. Further longer term follow-up evaluations are scheduled while 5 year follow-ups are ongoing, allowing for continuing reports on long-term performance.

Correspondence should be addressed to: EFORT Central Office, Technoparkstrasse 1, CH – 8005 Zürich, Switzerland. Email: office@efort.org