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Clinical results of Hi-tech Knee II total knee arthroplasty in patients with rheumatoid athritis: 5- to 12-year follow-up

DOI: 10.1186/1749-799x-7-9

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Abstract:

The present study was performed to evaluate the clinical results of primary TKA in RA using the cementless Hi-Tech Knee II CR-type prosthesis.We performed 32 consecutive primary TKAs using cementless Hi-Tech Knee II CR-type prosthesis in 31 RA patients. The average follow-up period was 8 years 3 months. Clinical evaluations were performed according to the American Knee Society (KS) system, knee score, function score, radiographic evaluation, and complications.The mean postoperative maximum flexion angle was 115.6°, and the KS knee score and function score improved to 88 and 70 after surgery, respectively. Complications, such as infection, occurred in 1 patient and revision surgery was performed. There were no cases of loosening in this cohort, and prosthesis survival rate was 96.9% at 12 years postoperatively.These results suggest that TKA using the cementless Hi-Tech Knee II CR-type prosthesis is a very effective form of treatment in RA patients at 5 to 12 years postoperatively. Further long-term follow-up studies are required to determine the ultimate utility of this type of prosthesis.The affected joints in patients with rheumatoid arthritis (RA) show chronic proliferative synovitis, which has been implicated in the destruction of articular cartilage and bone, resulting in joint disability [1]. Good clinical results of total knee arthroplasty (TKA) in patients with RA have been reported using several types of prosthesis [2-5]. The decisions regarding whether the posterior cruciate ligament (PCL) should be replaced or retained and whether the prosthesis should be fixed using cement or not are made at the surgeon's discretion. Long-term (≥ 10 years) follow-up studies of cruciate-retaining (CR) TKA without cement fixation of the prosthesis in patients with RA have indicated prosthesis survival rates of over 90% [6-8].Hi-Tech Knee II CR-type cementless TKA (Nakashima Medical, Okayama, Japan) was developed in 1994 at Chiba University and is currently in clinical use,

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