Poor short-term outcomes after computer-assisted rotating-platform total knee arthroplasty with a deep-trochlear-groove femoral component: Analysis of 19?patients
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Summary

Background

Congruent rotating tibial plateaus are designed to minimise wear after total knee arthroplasty (TKA). The Score? prosthesis has a congruent rotating tibial plateau, a deep trochlear groove, and uses a computer-assisted navigation system for ligament balancing. Although this prosthesis is widely utilized, no accurate data on outcomes are available.

Hypothesis

The innovative features of the Score? prosthesis, most notably patellar replacement with a highly constrained femoral component, do not jeopardize implant survival.

Patients and methods

In a pilot study, we retrospectively evaluated outcomes of 19?patients treated with Score? knee replacement between February and October?2006 (mean age, 66.8 years; range, 58-82 years). The evaluation criteria were the International Knee Society (IKS) scores and prosthesis survival rate estimated using Kaplan-Meier plots with failure defined as revision need to change the prosthesis.

Results

Mean follow-up was 35.3 months. The IKS knee score increased from 27.4 (5-60) preoperatively to 81.4 (45-99) at last follow-up (P < 0.0001). Mean mechanical axis was 181.2??180-186?? with 16 between 180??nd 183??Revision surgery was required in five cases (for patellar complications with combined motion-range limitation in flexion (< 90??and extension (5-20??in three cases, isolated motion-range limitation in one case, and recurvatum deformity with instability in one case). Prosthesis survival was 82 % (73-91 % ) after 24 months and 65 % (51-78 % ) after 44 months.

Discussion

The deep trochlear groove femoral component resulted in patellar complications, which were the most common reasons for revision surgery, together with motion-range limitation and instability possibly related to improper use of the navigation system. This small retrospective case-series study showed an unusually low prosthesis survival rate probably related to the implant design. We no longer use the Score? prosthesis, despite the availability of a dedicated navigation system, and we recommend careful monitoring of patients who have this prosthesis.

Level of evidence

Level IV, retrospective study.

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