The Role of Polyethylene Design on Postoperative TKA Flexion: An Analysis of 1534 Cases

The range of motion after TKA depends on many patient, surgical technique, and implant factors. Recently, high-flexion designs have been introduced as a means of ensuring or gaining flexion after TKA. We therefore evaluated factors affecting postoperative flexion to determine whether implant design...

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Veröffentlicht in:Clinical orthopaedics and related research 2010-01, Vol.468 (1), p.108-114
Hauptverfasser: McCalden, Richard W., MacDonald, Steven J., Charron, Kory D. J., Bourne, Robert B., Naudie, Douglas D.
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Sprache:eng
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Zusammenfassung:The range of motion after TKA depends on many patient, surgical technique, and implant factors. Recently, high-flexion designs have been introduced as a means of ensuring or gaining flexion after TKA. We therefore evaluated factors affecting postoperative flexion to determine whether implant design influences longterm flexion. We prospectively collected data on patients receiving a primary Genesis II™ total knee replacement with a minimum of 1-year followup (mean, 5.4 years; range, 1–13 years). We recorded pre- and postoperative outcome measures, patient demographics, and implant design (cruciate retaining [CR, n = 160], posterior stabilized [PS, n = 1177], high-flex posterior stabilized [HF-PS, n = 197]). Backward stepwise linear regression modeling identified the following factors affecting postoperative flexion: preoperative flexion, gender, body mass index, and implant design. Independent of gender, body mass index, and preoperative flexion, patients who received a HF-PS and PS design implant had a mean of 8° and 5° more flexion, respectively, than those who received a CR implant. Patients with low flexion preoperatively ( 120°) were most likely to maintain or lose flexion postoperatively. Controlling for implant design, patients with high flexion preoperatively (> 120°) were more likely to gain flexion with the HF-PS design implant (HF-PS = 32.0%; PS = 15.1%; CR = 4.5%). Level of Evidence: Level II, prognostic study. See Guidelines for Authors for a complete description of levels of evidence.
ISSN:0009-921X
1528-1132
DOI:10.1007/s11999-009-1127-9