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
A major challenge for total hip arthroplasty is to minimize wear and osteolysis in young, active patients. Alumina ceramic bearings have shown superior wear resistance and lubrication and do not carry the risk of ion release. In a prospective randomized study (ABC), 514 hips were implanted. All patients (average age, 53 years) received the same press-fit hydroxyapatite coated femoral stem; two thirds (345 hips) received alumina ceramic bearings, and one third (169 hips) received a cobalt-chrome-on-polyethylene bearing. A fourth arm (Trident) was included involving use of a metal-backed acetabular component implanted in 209 patients. At a mean follow-up of 35.2 months (range, 24–48 months), there was no significant difference in clinical performance between the patient cohorts. The cohort of patients included in the ABC, Trident, and extended access portion of the study represents a population of 2313 patients with no device related failures attributable to the ceramic on ceramic articulation used in these patients This new experience involves the use of improved ceramic materials and new design considerations that eliminate the risks and complications of past experiences with ceramic implants and provides a safe bearing option for young patients.