The FIRST knee prosthesis (Free Insert in Rotation Stabilized in Translation, Symbios SA) is a new ultra congruent, postero-stabilized total knee arthroplasty (TKA) with a mobile bearing expected to reduce significantly polyethylene wear, to improve the range of motion and the overall stability of the knee while ensuring a physiological ligament balance. We compared subjective and really objective results of this new TKA with two other widespread models of TKA. A clinical prospective monocentric cohort study of 100 consecutive patients (47–88 yrs) undergoing a FIRST TKA for primary osteoarthritis is currently being done. Pre- and post-operative follow-ups (6 weeks, 4,5 months and 1 year) are done with well-recognized subjective evaluations (EQ-5D and WOMAC scores) and semi-objective questionnaires (KSS score and radiography evaluation) as well as with a really objective evaluation using gait parameters from 6 walking trials, performed at different speeds with an ambulatory in field gait analysis system (Physilog®, BioAGM CH). The outcomes after one year of follow-up of 32 FIRST TKA are compared to 29 NexGen® postero-stabilized TKA (Zimmer Inc) with a fixed bearing and to 26 NexGen® TKA with a mobile bearing using the same methods. The gait cycle time of the FIRST TKA was statistically significantly shorter at normal speed of walk, as well as double-support periods, as compared to both standard models. The normal walking speed was significantly higher with faster swing speed and stride lengths for the new TKA. Significantly better coordination scores were observed at normal walking speed for the FIRST TKA as compared to the fixed-bearing TKAs. The FIRST TKA showed statistically significantly better really objective outcomes in terms of gait after one year of follow-up and similar subjective and semi-objective evaluations compared to two widespread TKA designs.
Two modules with 3 miniature capacitive gyroscopes and 3 miniature accelerometers were fixed by a patch on the dorsal side of the distal humerus, and one module with 3 gyroscopes and 3 accelerometers were fixed on the thorax. The subject wore the system during one day (8 hours), at home or wherever he/she went. We used a technique based on the 3D acceleration and the 3D angular velocities from the modules attached on the humerus.
Ten patients were studied using an ambulatory gait device (Physilog®). Each participant was asked to perform two walking trials of 30m long at 3 different speeds and to complete an EQ-5D questionnaire, a WOMAC and Knee Society Score. Lower limbs rotations were measured by four miniature angular rate sensors mounted respectively, on each shank and thigh. The outcomes of the eight patients undergoing total knee arthroplasty, recorded pre-operatively and post-operatively at 6 weeks, 3 months, 6 months and 1 year were compared to 2 age-matched healthy subjects.
This randomized controlled double-blind study included to date 14 patients: the gait signatures of four patients with mobile-bearing were compared to the gait signatures of nine patients with fixed-bearing pre-operatively and post-operatively at 6 weeks, 3 months and 6 months. Each participant was asked to perform two walking trials of 30m long at his/her preferred speed and to complete a EQ-5D questionnaire, a WOMAC and Knee Society Score (KSS). Lower limbs rotations were measured by four miniature angular rate sensors mounted respectively, on each shank and thigh. A new method for a portable system for gait analysis has been developed with very encouraging results regarding the objective outcome of total knee arthroplasty using mobile- and fixed-bearings.
The choice of the ideal outcome measure to assess total joint replacement remains a complex issue. However, gait analysis provides objective and quantifying evidences of treatment evaluation. Significant methodological advances are currently made in gait analysis laboratories and ambulatory gait devices are now available. The goal of this study was to provide gait parameters as a new objective method to assess total knee arthroplasty outcome between patients with fixed- and mobile-bearing, using an ambulatory device with minimal sensor configuration.
Obtaining consistently an optimal cup orientation in THA is vital to obtain adequate head coverage and maximum impingement free range of motion and thus reduce the incidence of polyethylene wear, cup loosening, and dislocation rates associated with a limited range of motion. It is clear that THA instability, the most frequent cause of early failure, is a complex problem related to a wide range of causes. However cup orientation is one of the surgeon dependant potentially modifiable variables that continue to have an important influence due to the lack of reliable means of assuring an adequate orientation of the components, particularly the cup anteversion. Standard mechanical guides like Muller’s have been shown to be inaccurate and imprecise. Not surprisingly, dislocation is the most frequent short term complication after a THA. Acetabular cup orientation is a key factor determining joint stability and one of the most important ones under the surgeons’ control. An in vitro study was used to determine the precision, reproducibility and ease of use of a new mechanical guide in comparison to a standard mechanical guide Müllers. The new guide (Gravity Assisted Navigation System) consists of a simple to use navigation tool. It uses the constant direction of the force of gravity identified by two bulls’ eye levels providing real time intraoperative augmented reality thus controlling the orientation of the pelvis. Visualisation of the guide from a single perspective is enough to determine in real time, the orientation of the cup in abduction and anteversion. By using anatomic repairs within the pelvis its flexion/extension is taken into consideration. As part of an invitro study, 310 press-fit acetabular cups were impacted into a plastic model of a pelvis by 5 surgeons (Power 90%, Type I error 5%), The orientation obtained was measured with respect to a fixed reference of 15° of anteversion and 45° of abduction. Results: an average of 10.4° anteversion ,(Range 3°to 21°, Standard of Deviation 5.0°) for Müller s guide and of 0.4° anteversion (Range 1° to 3°, Standard of Deviation 0.7°) for the new guide and an average of −4.7° abduction (Range 7° to −11°, Standard of Deviation 2.3°) for Müllers guide and 0.3° abduction (Range 0° to 3°, Standard of Deviation 0.5°) for the new guide. The average time required for the orientation of the cups was similar with both guides. (6 seconds for Mullers guide and 5 seconds for the new guide) The precision and reproducibility of the cup orientation obtained with the new guide were significantly better than those obtained with Müllers guide (p<
0.00001). The results obtained with with the new mechanical guide are encouraging. The in vitro results are encouraging, the high precision and accuracy are comparable to results obtained by computer assisted navigation systems in similar studies.