Little guidance exists regarding the minimum screw length and number necessary to achieve fixation with reverse shoulder arthroplasty (rTSA). The goal of this study is to quantify the pre- and post-cyclic baseplate displacements associated with two baseplate designs of different sizes using multiple screw lengths and numbers in a low density polyurethane bone substitute model. The test was conducted according to ASTM F 2028–17. The baseplate displacements of standard and small reverse shoulder constructs (Equinoxe, Exactech, Inc.) were quantified in a 15pcf polyurethane block (Pacific Research, Inc.) before and after cyclic testing with an applied load of 750N for 10,000 cycles. Baseplates were constructed using 2 or 4 screws with 3 different poly-axial locking compression screw lengths: 4.5×18mm, 4.5×30mm, and 4.5×46mm. Five of each configuration were tested for a total of 30 specimens for each baseplate. A two-tailed, unpaired student's t-test (p<0.05) compared baseplate displacements before and after cyclic loading in both the superior-inferior (S/I) and anterior-posterior (A/P) directions. The standard and small results were then compared.Introduction
Methods
Since the early 2000s, highly cross-linked (HXL) UHMWPE's have become a popular option with multiple experimental and clinical studies showing that gamma or electron radiation doses between 50–100kGY reduce wear and potentially extend the bearing life of UHMWPE. However, the increased wear resistance came at a compromise to mechanical properties due to the cross-linking process. Vitamin E has been added to some HXL UHMWPE materials to offer a solution to the compromise by increasing oxidation resistance and maintaining sufficient fatigue strength. However, limited data is available on the effect of the fabrication process, especially the method of irradiation, on the properties of the Vitamin E blended HXL UHMWPE. The purpose of this study was to evaluate the effects of adding the antioxidant vitamin E to highly crosslinked UHMWPE on wear rates. Wear testing was performed on six highly crosslinked UHMWPE acetabular liners containing vitamin E (0.1% wt. alpha tocopherol) fabricated using the Cold Irradiation Mechanically Annealed (CIMA) process, initially cross-linked with approximately 100 kGy gamma irradiation, and terminally gamma sterilized. The liners were paired with three 40mm CoCr femoral heads and 40mm three ceramic femoral heads. Testing was completed per ASTM F1714 and ISO 14242 on an orbital hip joint wear simulator (Shore Western, California) and lubricated with 90% bovine calf serum, 20mM EDTA, 0.2% wt. NaN3 and DI water. A 1.1Hz Paul-type loading waveform with a peak of 2kN was used for a total of 5E6 wear cycles. Three loaded soak controls were used in parallel to adjust for fluid absorption. Samples were weighed every 5E5 wear cycles.INTRODUCTION
METHODS
Aseptic glenoid loosening is a common failure mode of reverse shoulder arthroplasty (rTSA). Achieving initial glenoid fixation can be a challenge for the orthopedic surgeon since rTSA is commonly used in elderly osteoporotic patients and is increasingly used in scapula with significant boney defects. Multiple rTSA baseplate designs are available in the marketplace, these prostheses offer between 2 and 6 screw options, with each screw hole accepting a locking and/or compression screw of varying lengths (between 15 to 50mm). Despite these multiple implant offerings, little guidance exists regarding the minimal screw length and/or minimum screw number necessary to achieve fixation. To this end, this study analyzes the effect of multiple screw lengths and multiple screw numbers on rTSA initial glenoid fixation when tested in a low density (15pcf) polyurethane bone substitute model. This rTSA glenoid loosening test was conducted according to ASTM F 2028–17; we quantified glenoid fixation of a 38mm reverse shoulder (Equinoxe, Exactech, Inc) in a 15 pcf low density polyurethane block (Pacific Research, Inc) before and after cyclic testing of 750N for 10k cycles. To evaluate the effect of both screw fixation and screw number, glenoid baseplates were constructed using 2 and 4, 4.5×18mm diameter poly-axial locking compression screws (both n = 5) and 2 and 4, 4.5×46mm diameter poly-axial locking compression screws (both n = 5). A two-tailed unpaired student's t-test (p < 0.05) compared prosthesis displacements to evaluate each screw length (18 vs 46mm) and each screw number (2 vs 4).Introduction
Methods
Achieving prosthesis fixation in patients with glenoid defects can be challenging, particularly when the bony defects are large. To that end, this study quantifies the impact of 2 different sizes of large anterior glenoid defects on reverse shoulder glenoid fixation in a composite scapula model using the recently approved ASTM F 2028–14 reverse shoulder glenoid loosening test method. This rTSA glenoid loosening test was conducted according to ASTM F 2028–14; we quantified glenoid fixation of a 38mm reverse shoulder (Equinoxe, Exactech, Inc) in composite/dual density scapulae (Pacific Research, Inc) before and after cyclic testing of 750N for 10k cycles. Anterior defects of 8.5mm (31% of glenoid width and 21% of glenoid height; n=7) and 12.5mm (46% of glenoid width and 30% of glenoid height; n=7) were milled into the composite scapula along the S/I glenoid axis with the aid of a custom jig. The baseplate fixation in scapula with anterior glenoid defects was compared to that of scapula without an anterior glenoid defect (n = 7). For the non-defect scapula, initial fixation of the glenoid baseplates were achieved using 4, 4.5×30mm diameter poly-axial locking compression screws. To simulate a worst case condition in each anterior defect scapulae, no 4.5×30mm compression screw were used anteriorly, instead fixation was achieved with only 3 screws (one superior, one inferior, and one posterior). A one-tailed unpaired student's t-test (p < 0.05) compared prosthesis displacements relative to each scapula (anterior defect vs no-anterior defect).Introduction
Methods
Reverse Total Shoulder Arthroplasty (rTSA) is currently advised against in patient populations with movement disorders, due to potential premature failure of the implants from the use of walking assistive devices. The objective of this study is to measure the amount of displacement induced by the simulated loading of axillary crutches on a rTSA assembly in a laboratory mimicking immediate postoperative conditions. 8 reverse shoulder baseplate/glenosphere assemblies (Equinoxe, Exactech, Inc) were fixated to 15 lb/ft3 density rigid polyurethane bone substitute blocks. Displacement of the assemblies in the A/P and S/I axes was measured using digital displacement indicators by applying a physiologically relevant 357N shear load parallel to the face of the glenosphere, and a nominal 50N compressive axial load perpendicular to the glenosphere. Westerhoff et al. reported Introduction
Methods
The General Social Survey estimates that 19 million Americans shoot firearms, with 10% of this population being over the age of 65. More reverse total shoulder arthroplasty (rTSA) are seeking to return to physical activity after surgery, but the effects of shooting a firearm on the fixation of a rTSA implant are unknown. This study will seek to examine the recoil effect of a firearm on a rTSA baseplate fixation, by recording the forces absorbed by a shooter and applying these forces to a rTSA implant assembly in laboratory conditions. A total of 5 shooters over a range of heights and bodyweights fired a single action 12 gauge shotgun with 3 ounce slugs 5 times each. An accelerometer was rigidly fixated to the barrel of the firearm to record impulse values upon firing. 8 reverse shoulder baseplate/glenosphere assemblies (Equinoxe, Exactech, Inc) were fixated to 15 lb/ft3 density rigid polyurethane bone substitute blocks for drop tower testing. Displacement was measured before and after testing using digital displacement indicators by applying a physiologically relevant 357N shear load parallel to the face of the glenosphere, and a nominal 50N compressive axial load perpendicular to the glenosphere as shown in Figure 1. Measurements were taken for the S/I axis, and the sample was rotated 90 degrees for the A/P axis. The glenosphere/baseplate assemblies were loaded in a drop tower apparatus at 0° of abduction and 90° flexion to replicate the orientation of the joint seen while shooting. The drop tower utilized a 1.079kg weight set at 8” with a rubber impulse specific materil between the weight and impactor to reproduce the highest average impulse seen in shooting. A total of 50 drops were performed, to simulate two rounds of trap shooting at 25 shots each. A Student's one-tailed, paired t-test was used to identify whether or not significant loosening occurred, where p<0.05 denoted a significant difference.Introduction
Methods
Cementless total knee arthroplasty (TKA) has several advantages compared to the cemented approach, including elimination of bone cement, a quicker and easier surgical technique, and potentially a stronger long-term fixation. However, to ensure the successful long-term biological fixation between the porous implant and the bone, initial press-fit stability is of great importance. Undesired motion at the bone-implant interface may inhibit osseointegration and cause failure of biological fixation. Initial stability of a cementless femoral implant is affected by implant geometry, bone press-fit dimension, and characteristics of the porous coating. The purpose of this study was to compare the initial fixation stability of two types of porous femoral implants by quantifying the pull-out force using a paired cadaveric study design. The two types of cementless TKA femoral implants evaluated in this study had identical implant geometry but different porous coatings (Figure 1). The first type had a conventional spherical-bead coating (Type A), while the second type had an innovative irregularly-shaped-powder coating (Type B). The porous coating thickness was equivalent for both types of implants, thus the dimensional press-fit with bone was also equivalent. Three pairs of cadaveric femurs were prepared using standard TKA surgical technique, with each pair of the femurs receiving one of each porous implant type. An Instron 3366 load frame (Norwood, MA, USA) was used to pull the femoral implant out from the distal femur bone (Figure 2). The testing fixture was designed to allow free rotation between the implant and the actuator. The pullout was performed under a displacement control scheme (5 mm/min). Peak pull-out force was recorded and compared between the two implant groups.Introduction
Methods
Implant stability immediately after implantation is vital for long term success and improvement in patient outcomes for total hip arthroplasty (THA). Of the many factors that influence stability and resistance to migration for press-fit metaphaseal-fixed stems, this work attempted to evaluate the effect of distal stem taper angle on initial stem axial stability. Two THA stem designs having a distal taper angle of 3.5° and 5° were evaluated with cadaveric specimens with a simulated walking gait while stem motion was measured with respect to the periprosthetic bone.Introduction
Methods
Ideally, a patient receiving a unicondylar knee replacement will have fully functional anterior and posterior cruciate ligaments. When at least one of the cruciate ligaments is not fully functional, femoral and tibial implant contact position can potentially increase along the anterior-posterior (AP) axis. Where unicondylar implant wear testing typically uses AP resistance assuming fully functional cruciate ligaments, the authors used reduced AP resistance intended to simulate deficient cruciate ligaments. Optetrak Logic® Uni (Exactech Inc, Gainesville, FL USA) unicondylar test specimens featuring an all-UHMWPE tibial component and a cobalt chromium femoral component were used in this study. The system has a semi-constrained articular geometry. Testing was conducted at an independent testing facility (EndoLab GMBH, Thansau, Rosenheim, Germany). A four-station knee simulator was used (EndoLab knee simulator) with two unicondylar knee implants per station, giving a total of eight test specimens. Two different tibial fixation designs (keeled and peg) with identical articulating surfaces were tested. Tibial test specimens were 6 mm in thickness. Unloaded soak controls were stored in distilled water at 37°C. The test was conducted according to ISO 14243–1: 2009 [1]. Test specimens were immersed in calf serum (PAA GmBH, Cölbe, LOT B00111-5126) with a protein content of 20 g/l. Custom polyurethane molds allowed for individual component measurement. Per the ISO 14243-1, a 7% medial offset was incorporated into the set-up. The unicondylar knee implants were set at neutral position in extension. Tibial rotational restraint was 0.36 Nm/° and zero when the test specimen was within ± 6° of the reference position. This test was conducted with an AP resistance of 9.3N/mm to maximize AP displacement and simulate deficient cruciate ligaments. Typical unicondylar knee wear testing is conducted with an AP resistance of 44N/mm, which assumes functional cruciate ligaments.Introduction
Methods
Initial fixation of noncemented implants is critical to achieve a stable bone/implant interface during the first few months after surgery to potentiate bone in-growth and avoid aseptic loosening. Numerous reverse shoulder glenoid implant designs have been conceived in an attempt to improve implant performance and decrease the rate of aseptic glenoid loosening, commonly reported to be 5%. Design variations include: baseplate profile, baseplate size, backside geometry, center of rotation, surface finish and coatings, fixation screw diameters, number of fixation screw options, and type of screw fixation. However, little comparative biomechanical data exist to substantiate one design consideration over another. To that end, this study quantified glenoid fixation before and after cyclic loading of simulated abduction of 6 different reverse shoulder glenoid designs when secured to a low density polyurethane bone substitute block. A displacement test quantified fixation of 6 different reverse shoulder designs: 38 mm Equinoxe standard offset (EQ), 38 mm Equinoxe lateral offset (EQL), 36 mm Depuy Delta III (DRS), 36 mm Zimmer, (ZRS), 32 mm neutral DJO RSP (DJO), and a 36 mm Tornier BIO-RSA (BIO), secured to a 0.24 g/cm3 polyurethane block as a shear (357 N) and compressive (50 N) load was applied before and after cyclic loading. (Figure 1) Glenoid displacement was measured relative to the block using dial indicators in the directions of the applied loads along the superior/inferior axis. A cyclic test rotated each glenosphere (n = 7 for each design) about a 55° arc of abduction at 0.5 Hz for 10k cycles as 750N was constantly applied. (Figure 2) Each implant was cycled using a 145° humeral liner of the appropriate diameter to ensure each device is subjected to the same shear load. A two-tailed unpaired student's t-test was used to compare pre- and post-cyclic mean displacements between designs; p < 0.05 denotes significance.Introduction
Methods
