Participants
Ethical approval in accordance with the ethical standards in the 1964 Declaration of Helsinki was obtained prior to commencement of this study reporting function. The audit retrospectively identified all knee arthroplasty patients who had one UKA and one TKA on contralateral sides. Patients at least 6 months following the most recent surgery were identified from the surgical databases of three senior knee surgeons with a combined 70 year experience in both procedures which they do regularly. All three surgeons use a medial parapatellar approach and instrument the implants as guided by the company operational technique. The Oxford knee score questionnaire was collected for both knees rather than individually to prevent inducing conscious bias toward a particular limb. Pre-operative and post-operative radiographic analysis was undertaken to determine extent of OA disease and ensure satisfactory implant alignment, respectively (Fig. 1). Patient notes were examined to ensure no further surgery and range of motion at discharge.
Between 2000 and 2015 a total of 57 patients were identified by the clinical governance department who had undergone one of each procedure. After imaging review, 22 patients were automatically excluded due to other joint disease or arthroplasty procedures. This left 35 patients to be contacted by the research coordinator who removed 15 due to a safety exclusion protocol of our study ethics having had previous stroke (n = 2), unstable heart disease (n = 3), lung disease (n = 2), spine disease (n = 2), metastatic cancer (n = 3), and being uncontactable (n = 3). Twenty subjects agreed to take part, for which 2 never came for unknown reasons and 2 were unable to walk unaided during gait analysis due to balance difficulty. This left a total of 16 patients who consented to have their gait collected by a blinded assessor.
The arthroplasty subjects had a range of implant types and designs. A total of four different implants were used for the TKA and 2 for the UKA. There were 11 Smith Nephew (Memphis, Tennessee, USA) Genesis II cruciate retaining (all patella resurfaced), 3 MatOrtho (UK) Saiph medial pivot (all patella resurfaced), 1 DePuy (Warsaw, Indiana, USA) PFC Sigma posterior stabilised (patella resurfaced) and 1 Zimmer (Warsaw, Ind, USA) Nexgen cruciate retaining (patella resurfaced) TKA implants. There were 9 Smith Nephew (Memphis, Tennessee, USA) Accuris (two all poly tibia, remaining conventional metal-backed tibial component) and 7 Zimmer Biomet (Warsaw, Indiana, USA) Oxford (mobile bearing) UKA, all on the medial side.
Two further demographically similar groups of subjects with previous gait analysis were obtained from an established treadmill database for comparison. The healthy group of subjects consisted of members of the institution who had no history of joint disease or significant past medical history. The knee OA group consisted of ipsilateral knee OA patients with isolated medial compartmental disease awaiting surgery.
Gait instrumentation
A validated instrumented treadmill (Gaitway Kistler, Kistler Instrument Corporation, Amherst, NY) with a previously reported protocol, was used to collect patient gait data. It has been shown to be reliable and reproducible [10, 26]. The vertical component of the ground reaction forces (GRF) were collected on calibrated tandem Kistler force plates at a sample frequency of 100 Hz. All participants were weighed with the force plate prior to assessment, to allow normalisation for body weight as according Hof et al. [7] A standardised warmup and acclimatisation period of 6 min were completed before unaided gait collection. Gait collection only occurred after the patient felt a steady state had been achieved. The data collection period lasted 20 s for each condition with level walking tested first, followed by the uphill assessment.
Gait variables, processing and analysis
To avoid any perceived functional advantage of arthroplasty type, an analysis at a comfortable speed of 4.5 km/h was chosen based on a previously published work [26]. It found knee OA patients preferred walking speed being 4 km/h and controls being 5 km/h. A 5% incline at 4 km/h was also collected as it a common activity of daily living and has been shown to influence the condition to test gait [10]. Ground reaction force (GRF) was the focus of analysis as it reflects the load transmitted through the limb and thus will reveal any preference or limb dominance. Maximum force (Max Force), weight acceptance (WA), midstance (MS) and pushoff (PO) and the difference between weight acceptance and mid stance (WA–MS) were chosen based on previous studies showing an intra-class correlation coefficient of 0.93–0.99, signifying excellent reliability and repeatability [10].
A previously described and validated symmetry ratio (SR) [18] was also applied to the GRF to indicate the direction and percentage difference between limbs. Zero being complete symmetry with positive and negative percentage signifying more or less load to the numerator limb respectively. The limbs were divided into the arthroplasty group as UKA/TKA, the OA group as unaffected/OA affected, the control as right / left limb respectively.
$${\text{SR}} = ((X \cdot {\text{UKA}}/X \cdot {\text{TKA}}) - 1) \times 100\%$$
All trials were visually processed to ensure six consecutive strides were taken cleanly. Typically ten or more strides were collected so a Matlab (Mathworks, Mass, USA) script was written to extract the data from the Kistler software in a formatted manner for analysis. Statistical analysis was done with Matlab. Shapiro–Wilk test showed a normal distribution, therefore parametric tests were used. To determine difference between groups, a one-way analysis of variance (ANOVA) with Tukey post-hoc test was used, with significance set at p < 0.05 throughout. Paired T-tests were carried out to detect significant differences in GRF in the UKA and TKA limbs in the arthroplasty group and the knee OA limb compared to the unaffected limb in the knee OA group.
A minimum sample size of 9 was chosen based on a previous gait study with an analogous design comparing hip resurfacing and total hip arthroplasty, which showed a statistical and minimum clinical difference of 5% [1].