Introduction

Management of periprosthetic joint infection (PJI) after total knee arthroplasty (TKA) is a challenging task. Antibiotic management remains elusive due to differences in epidemiology and resistance between countries and reports. Increasing resistance of bacteria is a concern. The aim of this study was to investigate the development of antibiotic resistance of main causative bacteria in a single center.

Introduction

Differing levels of tendon retraction are found in full-thickness rotator cuff tears. The pathophysiology of tendon degeneration and retraction is unclear. Neoangiogenesis in tendon parenchyma indicates degeneration. Hypoxia inducible factor 1(HIF) and vascular endothelial growth factor (VEGF) are important inducers of neoangiogenesis. Rotator cuff tendons rupture leads to fatty muscle infiltration (FI) and muscle atrophy (MA). The aim of this study is to clarify the relationship between HIF and VEGF expression, neoangiogenesis, FI, and MA in tendon retraction found in full-thickness rotator cuff tears.

Aim: The assessment of shoulder mobility is essential for clinical follow-up of shoulder treatment. Only a few high sophisticated instruments for objective measurements of shoulder mobility are available. The interobserver dependency of conventional goniometer measurements is high. In the 1990s an isokinetic measuring system of BIODEX Inc. was introduced, which is a very complex but valid instrument. Since 2008 a new user-friendly system (DynaPort ShoulderTest-System) is available. Aim of this study is the validation of this measuring instrument with the BIODEX-System.

Methods: The DynaPort ShoulderTest-System is a small, light-weighted three-dimensional gyroscope that is fixed on the distal upper patient arm, recording abduction, fiexion and rotation. For direct comparison we fixed the DynaPort on the lever arm of the BIODEX-system. The accuracy of measurement was determined at different positions, angles and distances from the center of rotation as well as different motion speeds in the radius between 0° – 180° in steps of 20°. All measurements were repeated ten times and observed with a digital water level. As satisfactory accuracy we defined a difference between both systems below 5°. The statistical analysis was performed with a linear regression model.

Results: The evaluation showed very high accuracy of measurements. The maximum average deviation was 0,5°. Below 60° the DynaPort was underestimating comparing the BIODEX system, whereas in higher positions higher data was measured. At higher angles the differences between both got higher. The distance to the center of rotation as well as the position of the Dyna-Port on the lever arm and different motion speeds infiuenced the results. The highest significant matches were measured at highest distance from the center of rotation (1,8° vs. 3,1°, p < 0,05) and a highest motion speed (2,1° at 60°/s, vs. 3,1° at 30°/s, p < 0,05).

Conclusion: In summary the results showed a high correlation and good reproducibility of measurements. All deviations were inside the tolerance interval of 5 °. These laboratory trials are promising for the validation of this system in shoulder patients. The challenge for both systems will be the changing of the center of rotation in the shoulder joint at elevations higher than 90°.

Background: Increased contact stress with a femoral resurfacing prosthesis implanted in the medial femoral condyle and a non-functional meniscus is of concern for potential deleterious effects on tibiofemoral contact mechanics.

Methods: Peak contact pressures were determined in seven fresh frozen human cadaveric specimens using a pressure sensitive sensor placed in the medial compartment above the menisci. A knee simulator was used to test each knee in static stance positions (5°/15°/30°/45°) and through 10 dynamic knee-flexion cycles (5°–45°) with single body weight ground reaction force (GRF) which was adjusted to the living body weight of the cadaver donor. All specimens were tested in three different conditions: Untreated knee (A); Flush implantation of a 20mm resurfacing prosthesis (HemiCAP^®) in the weight bearing area of the medial femoral condyle (B); Complete radial tear at the posterior horn of the medial meniscus with the femoral resurfacing device in place (C).

Results: On average, flush device implantation resulted in no statistically significant differences when compared to the untreated normal knee. The meniscal tear resulted in a significant increase of the mean maximum peak contact pressures by 63%, 57%, and 57% (all P ≤ 0.05) at 15°, 30° and 45° static stance positions and 78% (P ≤ 0.05) through the dynamic knee flexion cycle. No significant different maximum peak contact pressures were observed at 5° stance position.

Conclusion: Possible effects of reduced meniscal tissue and biomechanical integrity of the meniscus must be considered in an in-vivo application of the resurfacing device.

Objectives: The aim of this study was to examine the influence of different prosthesis designs (Deep-Dish (DD) vs. posterior stabilized (PS)) on the patello-femoral pressure. The femoro-patellar pressure depends among other things on the AP stability of the knee joint. The use of DD has been described to be equally applicable with a resected or deficient PCL.

Methods: Fresh frozen human knee specimens (n = 8, 7 male, 1 female) underwent testing in a kinematic device simulating an isokinetic knee extension cycle from 120° of flexion to full extension. Knee motion was driven by a hydraulic cylinder applying sufficient force to the quadriceps tendon to produce an extension moment of 31 Nm. The amount of patellofemoral contact pressure and its distribution was measured by means of a pressure sensitive film (Tekscan^®, Inc., Boston, USA). Patellar contact pressure was examined first after implantation of a cruciate retaining TKA (Genesis II, Smith& Nephew, Memphis, USA). An 11 mm polyethylene (PE) DD insert was tested before and after resection of the PCL. Finally, the femoral component of the CR TKA was removed and replaced by a posterior stabilized (PS) model repeating measurements with an 11 mm PE inlay. The patella was not resurfaced throughout the whole procedure. A paired sampled t-test was applied for comparison of means and considered significant at p ≤ 0.05.

Results: There was no statistical significant difference of patello-femoral peak and mean contact pressures of the DD inlay before and after resection of the PCL. After implantation of the PS TKA peak pressure was significantly lower (Mean: 6.12 ± 2.37 MPa, Range: 10.68 – 3.30 MPa) in comparison with the DD type (7.12 ± 2.53 MPa, 11.94 – 3.55 MPa; p < 0.01) with a preserved PCL. Also the mean contact pressure turned out to be lower with the PS design (p < 0.006; PS: 3.58 ± 1.25 MPa, 5.91 – 2.08 MPa, DD: 4.27 ± 1.34 MPa, 6.66 – 2.18 MPa). The contact area was also significantly smaller with the PS design (p < 0.03, PS: 140.84 ± 40.04 mm2, 188.47 – 65.10 sq mm, DD: 175.97 ± 24.46 sq mm, 222.56 – 142.56 sq mm).

After resection of the PCL differences in contact pressures and contact area between DD and PS failed to reach statistical significance although there was an obvious tendency towards lower pressures with the PS-design.

Conclusions: The results of this study suggest that a posterior stabilized TKA design reduces the retropatellar peak and mean pressure as well as the contact area in comparison with a deep-dish design when the PCL is preserved. The better reproducible rollback with a PS model could serve as a possible explanation. However, this difference is less pronounced when a DD inlay is applied after resection of the PCL. Nevertheless, a PS rather than a DD design is recommended in the PCL deficient knee.

Objective: Decreased quadriceps strength may contribute to anterior knee pain after total knee arthroplasty (TKA). The quadriceps force necessary to establish full extension is strongly dependent on the position and the relative length of the lever arms over the knee joint. The purpose of this in vitro study was to investigate the amount of quadriceps force required to extend the knee isokinetically after TKA in dependence of different prosthesis designs and the state of the posterior cruciate ligament (PCL).

Methods: Eight fresh frozen human knee specimens were tested in a kinematic device that simulated an isokinetic knee extension cycle from 120° of flexion to full extension. Knee motion was driven by a hydraulic cylinder applying sufficient force to the quadriceps tendon to produce an extension moment of 31 Nm. The quadriceps force was measured using a load cell attached to the quadriceps tendon after implantation of a cruciate retaining (CR) TKA (Genesis II, Smith& Nephew, Memphis, Tn, USA) applying a conventional and a highly conforming polyethylene (PE) inlay before and after resection of the PCL. Finally, the femoral component of the CR TKA was replaced by a posterior stabilized (PS) design and measurements were redone.

Results: No significant differences in the average quadriceps force were detected between the different PCL retaining inlays (CR, highly conforming) as long as the PCL was intact. However, after resection of the PCL, the required quadriceps force increased significantly for both designs (CR: 4.7%, p < 0.01, Highly conforming: 3.5%, p < 0.03). After implantation of the PS femoral component quad force decreased to its initial levels with forces significantly lower compared to the PCL deficient knees provided with a CR (−6.0%, p < 0.01) or highly conforming (−5.1%, p < 0.01) inlay. With a PS design average quadriceps extension force was not significantly different from cruciate retaining TKA inlays at an intact PCL.

Conclusions: The data of this in vitro study suggest that the quadriceps extension force is significantly higher for knees after cruciate retaining TKA with PCL deficiency, independent of the use of a CR or DD inlay. Thus, the integrity of the PCL should be secured in clinical practice when using a cruciate preserving TKA design.

Introduction: Mobile bearing total knee arthroplasty (TKA) has been developed to theoretically provide a better, more physiological function of the knee and produce less polyethylene (PE) wear. The theoretical superiority of mobile bearing TKA’s over fixed bearing devices has not yet been proven in clinical studies.

The objective of the present study was to analyze in vivo the knee joint kinematics in the sagittal plane in a patient population that had received either a fixed or a mobile TKA in a prospective, randomized, patient- and observer-blinded, clinical study.

Methods: 31 patients were evaluated by means of fluoroscopy during unloaded flexion and extension against gravity, as well as during step-up and step-down with full weight bearing. In these 31 patients, 22 fixed bearing TKAs, 16 mobile-bearing TKAs and 19 natural knee joints were included.

All patients had been operated in a prospective, randomized, patient- and observer-blinded, clinical study, and had received either fixed or a mobile bearing, cruciate retaining Genesis II TKA for primary osteoarthritis.

Fluoroscopic radiographs were evaluated by measuring the „patella tendon angle” as a measure of antero-posterior translation as well as the “kinematic index” as a measure of reproducibility.

Results: During unloaded movement, fluoroscopic analysis did not show a significant difference between both types of prosthesis designs and the natural knee. In the weight-bearing movement, both types of TKA designs did not show the typically arched but a more linear patellar tendon angle curve, with a greater angle in extension and in flexion than the natural knees. This means that the femur glides anteriorly under load near extension and does not show the natural roll-back in flexion. In the mobile-bearing group, inter-individual deviations from the mean during weight-bearing movements were significantly less than in the fixed-bearing group.

Conclusions: In the present study, no functional advantage of mobile bearing TKA over fixed bearing devices could be found. Both TKA designs showed the typical kinematics of an anterior instability. Long-term follow-ups are necessary to elucidate the possible influence of lower PE wear on the incidence of aseptic loosenings.