7 research outputs found

    The Effect of Optical Conditioning of Preparations with Scan Spray on Preparation Form

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    Svrha rada: Za primjenu sustava CAD/CAM u ordinacijama dentalne medicine potrebno je odabrati sprej za skeniranje. Njegovom primjenom mijenja se prekrivena preparacija, što može nepovoljno utjecati na rubno zatvaranje i interno prianjanje restauracije. Zadaća ovog istraživanja bila je odrediti utjecaj spreja na preparacijsku formu procjenom morfologije i debljine triju različitih sprejeva za skeniranje. Materijali i metode: Određivala se površinska morfologija prekrivanja triju (A, B, C) različitih sprejeva za skeniranje uz pomoć konfokalnoga laserskog mikroskopa. Debljina sprejem nanesenog premaza mjerila se na staklenoj pločici i u simuliranim kliničkim uvjetima profilometrom i uređajem za digitalizaciju površine. Podaci su analizirani jednosmjernim testom ANOVA (α = .05). Rezultati: Konfokalni laserski mikroskop prikazao je grubu i nepravilnu sprejem pokrivenu površinu nakon uporabe svih sprejeva, te se od spreja A preko spreja B do spreja C broj malih zrnaca povećavao. Srednja debljina prekrivanja na staklenoj pločici iznosila je za sprej A 25,3 Μm, za B 18,9 Μm i za C 19,2 Μm. Statistički značajne razlike bile su između sprejeva A i B (p=0,017). U simuliranim kliničkim uvjetima srednja debljina prekrivanja iznosila je za sprej A 15,5 Μm, za B 15,0 Μm i za C 13,3 Μm. Razlika je bila statistički značajna samo između sprejeva A i C (p=0,033). Zaključak: Premazi nakon korištenja različitih sprejeva imali su drugačije površinske morfologije i različite debljine. Posljedično tome primjena spreja za skeniranje utječe i na konačnu CAD/CAM restauraciju, premda se kliničkim korištenjem postigla prihvatljiva debljina prekrivanja.Objective: CAD/CAM systems require scan spray for chairside sampling of tooth surfaces. However, this leads to alterations of the sprayed preparation and may affect marginal and internal adaption of the restoration. The aim of this study was to define the effect of scan spray on preparation form by evaluating the morphologies and the thicknesses of three different scan sprays. Materials and Methods: The surface morphology of the coatings of different scan sprays (A, B, C) was evaluated by use of a confocal laser scanning microscope. The thicknesses of spray coatings were measured on a glass plate as well as under simulated clinical conditions using a profilometer and a surface digitalisation device. The data were analysed by a 1-way ANOVA (α = .05). Results: The confocal laser scanning microscopy showed rough and irregular formed coating surfaces of all sprays, whereas an increasing numbers of small spray particles were seen from spray A over spray B to spray C. Mean coating thicknesses on the glass plate were: spray A 25.3 Μm, spray B 18.9 Μm and spray C 19.2 Μm. Significant differences were detected between spray A and B (P = .017). Under simulated clinical conditions median coating thicknesses were: spray A 15.5 Μm, spray B 15.0 Μm and spray C 13.3 Μm. A statistically significant difference could be detected only between spray A and C (P = .033). Conclusions: The coatings of the used scan spray systems showed different surface morphologies and exhibited different thicknesses. Consequently, the application of scan sprays affects the precision of the final CAD/CAM restorations. However, the scan sprays under investigation showed acceptable coating thicknesses for clinical use

    Interradicular Root Canals in Mandibular First Molars: A Literature Review and Ex Vivo Study.

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    INTRODUCTION Successful endodontic treatment vastly depends to a high degree on an accurate knowledge of root canal system morphology. It is a prerequisite to be aware of all possible reservoirs where bacteria and/or toxins can persist, compromising the surrounding tissues; such knowledge results in endodontic success. METHODS The presence of interradicular canals and diverticula between the pulp chamber floor and the bifurcation area surface of 117 mandibular first molars was investigated. Access cavities were prepared, the teeth were embedded in plastic, and the pulp chambers were flooded with methylene blue and then centrifuged. An average of 4.2 (0.145 ± 0.03 mm thickness) slices per tooth were obtained by means of a diamond band saw. The presence of interradicular canals and diverticula was investigated using a light microscope (125×). RESULTS Interradicular canals were observed in 9 teeth. Seven teeth had 1 interradicular canal, and 2 teeth had 2 interradicular canals. Diverticula (blind interradicular canals) were observed in 11 teeth originating either on the pulp chamber floor or the bifurcation side. The number of diverticula per tooth varied between 1 and 5 and originated in 3 teeth in the pulp chamber floor and 8 teeth in the bifurcation area. Two teeth had both 1 interradicular canal and 3 diverticula. Of the 117 mandibular molars investigated, 18 had either 1 or 2 interradicular canals, 1 to 5 diverticula, or an interradicular canal and 3 diverticula. CONCLUSIONS Based on the results obtained with this ex vivo study and because of the difficulties involved in the clinical performance of mechanical cleaning of possibly existing interradicular canals, it is highly recommended to perform thorough chemical cleaning and disinfection of the pulp chamber floor area in order to enhance the sealing possibility of such structures and minimize treatment failure

    Retentive Strength of CAD/CAM-Fabricated All-Ceramic Crowns Luted on Titanium Implant Abutments Using Different Ceramic Materials and Luting Agents: An In Vitro Study

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    Objectives: This study aimed to determine the retentive strength of monolithic hybrid-all-ceramic crowns luted on titanium implant abutments. Material and Methods: In total, 450 crowns (75 each of Mark II, Empress CAD, e.max CAD, Suprinity, Enamic, Celtra Duo) were milled using a CAD/CAM system. The crowns were cemented onto sandblasted titanium implant abutments using five luting agents (Multilink Implant, Variolink II, RelyX Unicem, Fujicem, and Panavia 2.0). After thermocycling was performed (5000 cycles: 5–55 °C, 30-s dwell time), the crowns were removed using a universal testing machine. The location of luting-agent residue on the abutment and inner crown surfaces was evaluated. Analyses of variance (ANOVA) with the Bonferroni correction were performed to evaluate differences of retentive strength depending on the crown material and the kind of the luting agent. Results: The retentive strengths for the different ceramic materials were Vita Mark II: 652N-759N (SD:134N-146N), Empress CAD: 681N-822N (SD: 89N-146N), e.max CAD: 784N-1044N (SD: 109N-176N), Vita Enamic: 716N-1177N (SD: 132N-220N), Vita Suprinity: 867N-1488N (SD: 202N-278N), and Celtra Duo 772N-1335N (SD:151N-229N). After the removal trials, the visual documentation showed different adhesive residue location depending on the ceramic materials. Furthermore, the pull-off force was dependent on the choice of adhesives. No significant differences were found between different luting agents and the ceramic material Vita Mark II and Empress CAD. EmaxCAD showed significant differences with Unicem and FujiCem compared to Panavia, as did VitaSuprinity, VitaEnamic, and Celtra Duo (p < 0.001). Conclusions: The ceramic material used seems to influence the retentive strength and the use of certain luting agents results in a higher retentive strength for some ceramic materials

    Dental color matching: A comparison between visual and instrumental methods

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    Biomechanical Characterization of a New Acellular Dermal Matrix for Oral Soft Tissue Regeneration

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    Objectives Acellular dermal matrices (ADM) are a suitable alternative to autogenous soft tissue grafts (ASG). The aim of this study was to analyze the biomechanical properties and architectural features of ASG and ADM. Materials and methods ASG were harvested from the hard palate of fresh frozen body donors as connective tissue grafts and compared to ADM of porcine origin (NovoMatrix, NM; mucoderm, MD). Maximum load (ML, Newton [N]) and expansion (E, [mm]) were measured after rehydration in saline solution by tensile strength measurement. Light microscopy (LM) and scanning electron microscopy (SEM) were performed to analyze the architectural features of ASG and ADM in high resolution. Results ASG demonstrated a significantly decreased ML compared to NM and MD (p < 0.0001 and p = 0.019). NM showed a significantly increased ML compared to MD (p = 0.001). ASG demonstrated a non-significantly reduced E compared to NM (p = 0.13) and a significantly increased E compared to MD (p = 0.025). NM showed an increased E compared to MD (p < 0.0001). LM and SEM highlighted the surface characteristics and internal structures of ASG and ADM, such as the surface compact layer of MD and the densely packed, parallel running and ordered collagen fibers of NM and MD. Conclusions Significant differences concerning the biomechanical properties and architectural features of ASG, and ADM were found. Clinical relevance Information about the biomechanical properties and architectural features of ASG and ADM can contribute to a better understanding of the clinical performance and extend the application area

    The reproducibility of electronic color measurements of the marginal gingiva

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    Introduction!#!This study evaluated the reproducibility of electronic color determination system evaluations of the marginal gingiva, which could be important for adhesive cervical fillings or prosthetic restorations that imitate the gingiva.!##!Material and methods!#!In 50 subjects, the L*, a*, and b* color coordinates were evaluated five times at a point in the marginal area of a central incisor using different electronic color determination systems: (SP) Shadepilot, (ES) Easyshade, (CE) Crystaleye, and (SV) X-Rite. The mean color difference (ΔE) and its standard deviation between the five measurements from each participant were calculated separately for each device. Further ICC for interdevice reliability was determined.!##!Results!#!The L*, a*, and b* color coordinates and ΔE values differed significantly among the systems (p &amp;lt; 0.001). Within each patient and measurement system, ΔE ranged from 1.4 to 3.2 (SD 1.1-2.5), L* from 2.6 to 5.7 (SD 2.6-5.7), a* from 11.9 to 21.3 (SD 3.6-3.9), and b* from 15.1 to 28.9 (SD 1.7-4.3). Interdevice reliability ranged between 0.675 and 0.807.!##!Conclusions!#!Color determination of the marginal gingiva using the electronic tooth color determination systems tested herein showed limited reproducibility. The results obtained with the different measurement systems differed enormously.!##!Clinical relevance!#!These results show that the electronic color measurement devices tested allow no high reproducible determination of color coordinates of the marginal gingiva

    Marginal and Internal Precision of Zirconia Four-Unit Fixed Partial Denture Frameworks Produced Using Four Milling Systems

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    Background: CAD/CAM systems enable the production of fixed partial dentures with small and reproducible internal and marginal gaps. Purpose: The purpose of this study was to evaluate the reproducibility of the marginal and internal adaptations of four-unit fixed partial denture frameworks produced using four CAD/CAM systems. Materials and Methods: Prepared dies of a master model that simulated the loss of the first left molar were measured. Fifteen frameworks were manufactured using four CAD/CAM systems (A–D). The internal fit was determined by the replica technique, and the marginal gap was determined by microscopy. ANOVA was carried out to detect significant differences, and the Bonferroni adjustment was performed. The global level of significance was set at 5%. Results: The mean gap size ranged from 84 to 132 µm (SD 43–71 µm). The CAD/CAM systems showed significant variance (p &lt; 0.001), and system A (VHF) showed the smallest gaps. The smallest gaps for each system were in the molar part and in the marginal region of the frameworks (p &lt; 0.001). Conclusions: The CAD/CAM systems showed significantly different gap sizes, particularly between premolars and molars and among the marginal, axial and occlusal regions. All of the systems are suitable for clinical application
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