Original Research

Minimum 5-Year Results With Duracon Press-Fit Metal-Backed Patellae

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References

The desired cut must be absolutely planar, and this should be checked by placing the edge of the blade across the interface. Repeated passes with the saw blade are needed if the cut is not 100% planar. Once the cut is made, the patella is sized with the patella sizers and drill guide. After the appropriate size is selected, the patella is drilled with a bit that is slightly undersized from the size of the pegs (1/32 inch smaller than the bit supplied by the manufacturer).

Once the patella is prepared, the rest of the knee arthroplasty is performed. The patella is press-fit as the last component to be inserted.

Radiologic Review

Radiographic analysis was performed by an independent reviewer according to the current Knee Society total knee arthroplasty roentgenographic evaluation and scoring system (Figure 2).16 The reviewer was an orthopedist specializing in hip and knee surgery. Radiographs the reviewer deemed questionable were shown to another independent hip and knee surgeon for validation. In all cases, the second reviewer confirmed the first reviewer’s initial recorded observations.

KSS (Knee Society Scale), WOMAC (Western Ontario and McMaster Universities Arthritis Index), and SF-36 (36-Item Short Form Health Survey) were also used to evaluate effectiveness in this protocol.

Survivorship Calculations

Kaplan-Meier survivorship was determined for all metal-backed patellae. For survival analysis, only knees with radiographic data were included (74 knees). Mean follow-up was 75.8 months (range, 60-105 months).

Seventy-four patients (88 knees) met the study criteria (Table). At minimum 5-year follow-up, complete data were acquired for 59 patients (72 knees). Of the total group, 14 knees did not have radiographic data. Those knees were categorized as lost to follow-up and were excluded from the survivorship analysis. The status of patients enrolled in the study at minimum 5-year follow-up is shown in the Table.

Mann-Whitney U test (nonparametric t test) was used to compare WOMAC and SF-36 scores between the “complete” and the “WOMAC and SF-36 only” data groups.

Statistical Analysis

Kaplan-Meier survivorship probabilities (asymmetric method) were calculated using SAS Version 9.2 (SAS Institute); 95% pointwise confidence limits were used.

The Mann-Whitney U test is a nonparametric analogue to the independent-samples t test. It was used here to compare WOMAC and SF-36 scores of patients with “complete” data with scores of patients with “WOMAC and SF-36 only” data. In either group, for patients who had primary bilateral knee arthroplasty, mean WOMAC and SF-36 scores were used.

Comparisons were made between the unilateral and bilateral knee arthroplasty groups. There were no differences in age, height, or weight (Mann-Whitney U test) or in sex, primary diagnosis, or number of patients lost to follow-up (Fisher exact test). Fisher exact test (vs χ2 test) was used for the contingency table analysis because of small cell sizes (eg, ≤10 females in ‘‘both knees” group), suggesting the unilateral and bilateral patients did not differ in demographics.

For all patient-reported questionnaires, bilateral patients were given the opportunity to note any differences between their knee arthroplasties, but none of these patients made any special notations. We interpreted this to mean that all survey responses from bilateral patients were applicable to both knee arthroplasties.

Results

Seventy-four patients (88 knees) were enrolled in the study: 31 women (41.2%) and 43 men (58.1%). At time of surgery, mean age was 59.7 years (range, 40-86 years), and mean body mass index was 30.6 (range, 19.1-39.6). Eighty-three knees were diagnosed with osteoarthritis, and 5 knees were diagnosed with posttraumatic arthritis. Mean time to follow-up was 74.8 months (range, 60-105 months). Fourteen knees (14 patients) were considered lost to follow-up. However, 8 patients (8 knees) were contacted by telephone about the status of their knee(s), and all 8 completed and returned the minimum 5-year follow-up WOMAC and SF-36 forms; they did not return for their minimum 5-year clinical or radiographic evaluations.

Asymmetric patellae were used in 24 knees, conversion patellae in 64 knees (88 knees total). Forty-nine months after surgery, 1 patella was revised for loosening at its interface with the bone. The 51-year-old active female patient’s asymmetric patella was revised to a conversion patella. The decision to implant another metal-backed device was based on its high density; proper intrusion of acrylic cement would have been questionable. Some early wear was observed on the tibial insert, which was replaced. Sixty-eight months after the revision, the patient was asymptomatic, with a KSS Pain score of 96 and a KSS Function score of 100 (Figure 3). Another revision, for tibial insert exchange only, was performed 48 months after surgery. During this revision, the patella was evaluated and found to be well fixed and functioning normally.

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