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Orthopaedic Proceedings
Vol. 100-B, Issue SUPP_3 | Pages 72 - 72
1 Apr 2018
Santos I Mahmoud M Thorwächter C Bourgeois A Müller P Pietschmann M Chevalier Y
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Background

While total shoulder arthroplasty (TSA) is a generally successful procedure, glenoid loosening remains a common complication. Though the occurrence of loosening was related to patient-specific factors, biomechanical factors related to implant features may also affect the fixation of the glenoid component, in particular increased glenohumeral mismatch that could result in eccentric loads and translations. In this study, a novel test setup was used to quantify glenohumeral pressures for different motion patterns after TSA.

Methods

Six cadaveric human shoulders were implanted with total shoulder replacements (Exactech, Inc., USA) and subjected to cyclic internal-external, flexion-extension and abduction-adduction rotations in a passive motion testing apparatus. The system was coupled to a pressure sensor system (Tekscan, Inc., USA) to acquire joint loads and to a Zebris system (Zebris Medical, GmbH, Germany) to measure joint kinematics. The specimens were subjected to a total of 2160 cycles and peak pressures were compared for each motion pattern.


Orthopaedic Proceedings
Vol. 100-B, Issue SUPP_3 | Pages 74 - 74
1 Apr 2018
Chevalier Y Chamseddine M Santos I Müller P Pietschmann M
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Introduction

Glenoid loosening, still a main complication for shoulder arthroplasty, was suggested to be related implant design, surgical aspects, and also bone quality. However, typical studies of fixation do not account for heterogeneity in bone morphology and density which were suggested to affect fixation failure. In this study, a combination of cyclic rocking horse tests on cadaver specimens and microCT-based finite element (microFE) analysis of specimens of a wide range of bone density were used to evaluate the effects of periprosthetic bone quality on the risks of loosening of anatomical keeled or pegged glenoid implants.

Methods

Six pairs of cadaveric scapulae, scanned with a quantitative computer tomography (QCT) scanner to calculate bone mineral density (BMD), were implanted with either cemented anatomical pegged or keeled glenoid components and tested under constant glenohumeral load while a humeral head component was moved cyclically in the inferior and superior directions. Edge displacements were measured after 1000, 4000 and 23000 test cycles, and tested for statistical differences with regards to changes or implant design. Relationships were established between edge displacements and QCT-based BMD below the implant. Four other specimens were scanned with high-resolution peripheral QCT (82µm) and implanted with the same 2 implants to generate virtual models. These were loaded with constant glenohumeral force, varying glenohumeral conformity and superior or inferior load shifts while internal stresses at the cement-bone and implant-cement interfaces were calculated and related to apparent bone density in the periprosthetic zone.


Orthopaedic Proceedings
Vol. 98-B, Issue SUPP_7 | Pages 75 - 75
1 May 2016
Chevalier Y Santos I Mueller P Pietschmann M
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Introduction

Glenoid loosening, still a main complication in shoulder arthroplasty, could be related to glenohumeral orientation and conformity, cementing techniques, fixation design and periprosthetic bone quality [1,2]. While past numerical analyses were conducted to understand the relative role of these factors, so far none used realistic representations of bone microstructure, which has an impact on structural bone properties [3]. This study aims at using refined microFE models including accurate cortical bone geometry and internal porosity, to evaluate the effects of fixation design, glenohumeral conformity, and bone quality on internal bone tissue and cement stresses under physiological and pathological loads.

Methods

Four cadaveric scapulae were scanned at 82µm resolution with a high resolution peripheral quantitative computer tomography (XtremeCT Scanco). Images were processed and virtually implantated with two anatomical glenoid replacements (UHMWPE Keeled and Pegged designs, Exactech). These images were converted to microFE models consisting of nearly 43 million elements, with detailed geometries of compact and trabecular bone, implant, and a thin layer of penetrating cement through the porous bone. Bone tissue, implant and cement layer were assigned material properties based on literature. These models were loaded with a central load at the glenohumeral surface, with the opposite bone surface fully constrained. Effects of glenohumeral conformity were simulated with increases of the applied load area from 5mm-radius to a fully conformed case with the entire glenoid surface loaded. The models were additionally subjected to a superiorly shifted load mimicking torn rotator cuff conditions. These models were solved and compared for internal stresses within the structures (Figure 1) with a parallel solver (parFE, ETH Zurich) on a computation cluster, and peak stresses in each region compared by design and related to apparent bone density.


The Journal of Bone & Joint Surgery British Volume
Vol. 85-B, Issue 8 | Pages 1190 - 1195
1 Nov 2003
Martos-Rodríguez A Santos-Alvarez I Campo-Ruíz V González S García-Ruiz JP Delgado-Baeza E

Our aim was to evaluate the expression of transcription factors CCAAT/enhancer-binding protein-beta (C/EBPβ) and C/EBP-homologous protein (CHOP) in the growth plate. Proximal tibial epiphyseal growth plates from ten 15-day-old Wistar rats were used. Additionally, anti-proliferating cell nuclear antigen (PCNA), anti-5-bromo-2’-deoxyuridine (BrdU) immunostaining, terminal transferase dUTP nick end-labelling (TUNEL) and nucleolar organiser region-associated proteins (AgNOR) techniques were peformed. The histological morphology of the growth plate from C/EBPβknock-out mice was also analysed.

The normal growth plate showed that C/EBPβ and CHOP factors are expressed both in the germinative/ upper proliferative and in the lower proliferative zones. Furthermore, BdrU+ and PCNA+ cells were present exclusively in the germinative and proliferative zones, while TUNEL+ and AgNOR+ cells were seen in all three zones of the growth plate. Acellular areas, hypocellularity, the increase in cell death and anomalies in the architecture of the cell columns were observed in the growth plates of C/EBPβ (−/ −) knockout mice.

We suggest that C/EBPβ and CHOP transcription factors may be key modulators participating in the chondrocyte differentiation process in the growth plate.