The Association of Gait Kinematics, Instability and Patient Reported Outcomes in Patients With Total Knee Replacement

The effect of TKR instability on gait is poorly understood. How does revision TKR surgery for instability alter gait and is there an associated change in patient satisfaction? Are there differences in gait between patients with an unstable TKR and a stable TKR? The objectives of this study are:

• To investigate the effect of a revision TKR operation on gait kinematics, in patients who have a primary TKR and instability.
• To investigate the association between changes in gait kinematics and patient satisfaction, before and after revision TKR surgery for patients with instability.
• To investigate differences in gait kinematics between dissatisfied patients with an unstable primary TKR, satisfied patients with a stable primary TKR and people who do not have a knee replacement.

The first part of the investigation will tackle the first two objectives and follow patients who are having a revision TKR due to an unstable knee before and after their operation. The second part will then compare these patients to those with a primary TKR and no instability and to a control group of participants who do not have knee replacements ('native knees') and do not have difficulty walking. This will determine the difference in kinematics between a native knee and a TKR with and without instability.

Age, height, weight, leg lengths, measurements of the TKR position on imaging (taken as part of routine clinical practice) and patient reported outcome scores will be documented.

The gait assessments will be carried out in the outpatient clinic or physiotherapy department. These patients will have their walking gait assessed using a treadmill-based portable 3D infrared camera system (Vicon Ltd, Oxford, UK). The raw data will be processed by Run3D (Run3D Ltd, Oxford, UK) and Visual3D (C-motion Inc, MD, USA) to calculate knee joint angles.

Analysis will focus on within subject (part 1) and between subject differences (part 2). The questions are novel and data will be largely exploratory. Measures, differences and correlations will be presented using descriptive statistics and, where appropriate, correlation and regression coefficients. Where possible, inferential statistics (such as t-tests) will formally test differences in knee kinematic measures and associations with PROMS. Statistical parametric mapping will be applied to analyse continuous quantities over the gait cycle. Published research indicates an effect size of 1.0 may be expected. This suggests sample sizes between 11 and 42 should be sufficient to determine statistically significant two-tailed differences (alpha=0.05, beta=0.2) within subjects or between groups, according to the comparison being assessed. A sample of 42 patients is targeted.

In the longer term, this study will enable a better understanding of the functional biomechanics of TKR instability and potentially develop an alternative quantitative measurement of outcome and instability.

Inclusion criteria

Patients awaiting revision TKR due to instability:

• Patients who have a primary total knee replacement.
• Patients who have an unstable knee replacement, as determined by the surgical team.
• Patients who are being listed for a revision total knee replacement.

Primary TKR without instability:

• Patients with a primary total knee replacement.
• Patients at least one year after their primary total knee replacement operation.

Exclusion criteria

Patients awaiting revision TKR due to instability:

• Patients who have suspected infection of the TKR.
• Patients who are awaiting a two-stage revision procedure.
• Patients who can walk less than one minute at a time.
• Patients who can walk for less than five minutes with rests.
• Patient who are not able to give informed consent.

Primary TKR without instability:

• Patients who have had a previous revision of the total knee replacement.
• Patients who have an unstable knee replacement, as determined by the surgical team.
• Patients who have aseptic loosening or wear, as determined by the surgical team.
• Patients who are not satisfied with their TKR (as determined by the study specific questionnaire).
• Patients who can walk for less than one minute at a time.
• Patients who can walk for less than five minutes with rests.
• Patient who are not able to give informed consent.