These authors report minimum two-year follow-up for all- polyethylene, biconvex augmented anatomic glenoid component for the management of shoulders with posterior glenoid erosion.
The authors emphasize several additional characteristics of this system: "This implant is available in four sizes, with 3 different amounts of augmentation. Also, given laterality-specific orientation of the pegs/augment it has right and left options. It also has two anchor options, a fluted peg design and a keeled option, with availability dependent on geographic regulatory clearance." and when this implant is used for a B3 or C (monoconcave) glenoid, removal of anterior bone is required to create the biconcavity to match the back of the component.
They conducted a retrospective review of patients having an anatomic total shoulder (aTSA) from 7 clinical sites using this biconvex posterior augmented glenoid (PAG).
86 of 110 consecutive patients during the study period (78% follow-up) met the inclusion criteria and were included in their analysis. Of the 86, 33 had a B1 glenoid, 43 had a B2 glenoid, 5 had a B3 glenoid, and 5 had a C glenoid.
Mean follow-up was 35 ± 10 months. There was one patient with both a prosthetic joint infection and radiographic glenoid loosening that required revision. 79/86 had a Lazarus score of 0 (no radiolucency seen about peg or keel) at final follow-up. The clinical results are shown below.
with a fluted peg: one thousand two hundred seventy individual patients from eleven centers.
The goal of Early Clinical and Radiographic Outcomes of Anatomic Total Shoulder Arthroplasty with a Bi-convex Posterior Augmented Glenoid for Patients with Posterior Glenoid Erosion: Minimum 2-Year Follow-Up was to present an experience with a more complex approach to managing arthritic shoulder with posterior glenoid bone loss using a glenoid component with a bi-convex backside and a sequence of specialized instrument as shown below and in this link
B3 glenoids, achieving >80% osseous integration into the central peg. These clinical and radiographic outcomes for type B2 and B3 glenoids were not inferior to those outcomes for other glenoid types.
This article does not present data on the increase in cost or surgical time for this implant in comparison to a standard polyethylene component, so the value of this technology (benefit to the patient / cost) cannot be evaluated at this point.
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