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1.
Osteoarthritis Cartilage ; 30(8): 1103-1115, 2022 08.
Article in English | MEDLINE | ID: mdl-35568111

ABSTRACT

OBJECTIVE: To determine changes of subchondral bone composition, micro-structure, bone marrow adiposity and micro-vascular perfusion in end-stage osteonecrosis of the femoral head (ONFH) compared to osteoarthritis (OA) using a combined in vivo and ex vivo approach. DESIGN: Male patients up to 70 years old referred for total hip replacement surgery for end-stage ONFH were included (n = 14). Fifteen patients with OA were controls. Pre-operative MRI was used to assess bone perfusion (dynamic contrast-enhanced (DCE) sequences) and marrow fat content (chemical shift imaging). Three distinct zones of femoral head subchondral bone - necrotic, sclerotic, distant - were compared between groups. After surgery, plugs were sampled in these zones and Raman spectroscopy was applied to characterize bone mineral and organic components (old and newly-formed), and contrast-enhanced micro-computed tomography (CE-µCT) to determine bone micro-structural parameters and volume of bone marrow adipocytes, using conventional 2D histology as a reference. RESULTS: In the necrotic zone of ONFH patients compared to OA patients: 1) the subchondral plate did not exhibit significant changes in composition nor structure; 2) the volume fraction of subchondral trabecular bone was significantly lower; 3) type-B carbonate substitution was less pronounced, 4) collagen maturity was more pronounced; and 5) bone marrow adipocytes were significantly depleted. The sclerotic zone from the ONFH group showed greater trabecular thickness, and higher DCE-MRI AUC and Ktrans. Volume fraction of subchondral bone, trabecular number, and Kep were significantly lower in the distant zone of the ONFH group. CONCLUSIONS: This study demonstrated alterations of subchondral bone microstructure, composition, perfusion and/or adipose content in all zones of the femoral head.


Subject(s)
Arthroplasty, Replacement, Hip , Femur Head Necrosis , Osteoarthritis , Femur/pathology , Femur Head/diagnostic imaging , Femur Head/pathology , Femur Head Necrosis/diagnostic imaging , Humans , Male , Osteoarthritis/pathology , X-Ray Microtomography/methods
2.
Eur J Dent Educ ; 21(4): e1-e6, 2017 Nov.
Article in English | MEDLINE | ID: mdl-27146633

ABSTRACT

INTRODUCTION: Endodontic therapy is often complicated and technically demanding. The aim of this study was to develop a reproducible biomimetic root canal model for pre-clinical and postgraduate endodontic training. MATERIAL AND METHODS: A specific ceramic shaping technique (3D printing and slip casting of a root canal mould) was developed to reproduce canal systems with the desired shape and complexity using a microporous hydroxyapatite (HAp)-based matrix. The microstructural morphology, pore size and porosity, as well as the Vickers microhardness of the ceramic simulators (CS) were assessed and were compared with natural dentin and commercial resin blocks. The reproducibility of the root canal shapes was assessed using the Dice-Sørensen similarity index. Endodontic treatments, from refitting the access cavity to obturation, were performed on the CS. Each step was controlled by radiography. RESULTS: Many properties of the CS were similar to those of natural dental roots, including the mineral component (HAp), porosity (20%, porous CS), pore size (3.4 ± 2.6 µm) and hardness (120.3 ± 18.4 HV). DISCUSSION: We showed that it is possible to reproduce the radio-opacity of a tooth and variations in root canal morphology. The endodontic treatments confirmed that the CS provided good tactile sensation during instrumentation and displayed suitable radiological behaviour. CONCLUSIONS: This novel anatomic root canal simulator is well suited for training undergraduate and postgraduate students in endodontic procedures.


Subject(s)
Dental Pulp Cavity/anatomy & histology , Endodontics/education , Models, Anatomic , Simulation Training , Ceramics , Printing, Three-Dimensional
3.
Acta Cardiol ; 35(5): 349-55, 1980.
Article in English | MEDLINE | ID: mdl-6970485

ABSTRACT

In a small preliminary clinical trial of guanabenz in 16 hypertensives also under treatment with diuretics (hydrochlorothiazide and amiloride), blood pressure was safely and completely controlled in 10 (64%), the criterion for "control" being a reduction to the strict level specified by the Society of Actuaries (130/85 m lambda Hg). The dosage of guanabenz was adjusted upward from 16 mg/day until blood pressure normalized or side effects intervened. The 16 patients accumulated 97 months of guanabenz treatment. The 6 unsuccessful cases included only 2 outright therapeutic failures; the other 4 patients discontinued treatment for various reasons: dry mouth and nausea (with good blood pressure reduction); aggravation of existing depression; or generalized urticaria. The fourth patient discontinued for reasons unknown.


Subject(s)
Guanabenz/administration & dosage , Guanidines/administration & dosage , Hypertension/drug therapy , Aged , Amiloride/administration & dosage , Blood Pressure/drug effects , Drug Evaluation , Drug Tolerance , Female , Guanabenz/adverse effects , Humans , Hydrochlorothiazide/administration & dosage , Male , Middle Aged
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