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Statement of problem When 3-dimensional printing casts, the operator can change the type of resin and the printing layer thickness, reducing the fabrication time. However, how these parameters affect the accuracy of 3-dimensionally printed casts is unknown. Purpose The purpose of this in vitro study was to evaluate the accuracy of 3-dimensionally printed casts by using a stereolithography (SLA) 3-dimensional printer (Forms2) with 3 different layer thickness (25, 50, and 100 μm) and 2 different resins (Gray and Cast) and by comparing the time to obtain each cast. Material and Methods One master cast was scanned, and a single file was printed several times. The printed casts were then scanned by using a laboratory scanner. The standard tessellation language (STL) files provided by the laboratory scanner were superimposed and compared by using a software program (Geomagic Control; 3D Systems). The 2-way ANOVA test was used for the trueness evaluation, followed by the Tukey test to identify differences among the groups (α=.05). Results No statistically significant differences in accuracy were found among the 3 different layers for either resin (P>.05). Printing time doubled as layer thickness decreased. Conclusions This study showed that when printing casts, the fastest printing settings can be used without losing accuracy and that the laboratory digital workflow can be accelerated with selection of the resin and cast layer, as the type of resin and layer thickness did not influence the quality of the casts.

Introduction A disharmonious smile results from excessive gingival exposure or gingival margin misalignment is a frequent finding in patients. The most common cause is altered passive eruption; however, in the case presented here, the esthetics of the smile is compromised also due to an inadequate implant placement and crown fabrication. Case presentation This case presented a combination of altered passive eruption and a buccally as well as deeply placed implant crown (#10) that led to disproportionate dimensions of an upper lateral incisor. Dual digitally guided crown lengthening surgical procedure for teeth #5 to #12 was performed aiming a better harmony of the smile. Treatment also included placement of tooth veneers and re-made of implant crown. A pleasant smile with appropriate colors and proportions was achieved. All esthetic and periodontal health parameters were maintained throughout the follow-up period (1 year). Conclusion The use of dual digitally guided crown lengthening help to accomplish precision and stability of esthetic outcome, as it guides for both, bone and soft tissue removal. Particularly, in challenging cases with high esthetic demand and complicated factors present, such as the case presented here, the digital approach provides tools to attain excellent treatment outcome.

Intraoral scanners (IOSs) have some inherent distortions caused by optical and/or software imperfections. However, how other factors such as operator experience, scan time, scanner type, and scan size influence scan accuracy is not clear.The purpose of this in vitro study was to evaluate the trueness and precision of scans performed by 3 professionals with different levels of experience by using 2 IOSs.Three operators with low, medium, and high levels of experience scanned a master model 10 times by using 2 IOSs (CEREC Omnicam; Dentsply Sirona and TRIOS 3; 3Shape), resulting in 10 standard tessellation language files for each group (N=60). Each standard tessellation language file was divided into 2 areas (prepared teeth and complete arch). Precision was evaluated by comparing the 10 scans from each examiner for each system. Trueness was evaluated by comparing each scan file with a reference scan obtained from a laboratory scanner (D2000; 3Shape). A 3D analysis software program (Geomagic Control; 3D Systems) was used to perform all the comparisons and superimpositions. The 3-way ANOVA test followed by the Tukey HSD test were used to assess precision and trueness. The 2-way ANOVA followed by the Tukey HSD test was used to assess scan time. The Pearson correlation test was performed between scan time and trueness for both scanners. An additional correlation was performed between scan time and number of images, as well as between number of images and trueness for the TRIOS 3.Statistically significant influences of operator (P.001), scanner (P.001), scan size (P.001), operator and scan size (P.001), and scanner and scan size (P.001) were observed. The TRIOS 3 group reported higher precision than the CEREC Omnicam group for complete-arch scans (P.001), although no difference was observed for scans of the prepared tooth. Medium- (P=.002) and low-experience operators (P.001) reported lower precision for complete-arch scans performed with CEREC Omnicam when compared with TRIOS 3. The low-experience operator reported significantly worse results for complete-arch scans in comparison with the medium- (P=.008 and P.001) and high-experience operators (P.001 and P=.001), by using TRIOS 3 and CEREC Omnicam, respectively. Medium- and high-experience operators reported similar results among themselves. The CEREC Omnicam scanner reported lower trueness for complete-arch scans when compared with the prepared tooth (P.001); for TRIOS 3, a difference was only observed for the low-experience operator when compared with the high-experience operator (P.001). The CEREC Omnicam reported lower trueness than the TRIOS 3, except for the medium-experience operator with the prepared tooth scan. Comparing the trueness between operators and considering the same scanner and scan size, all groups were similar. The low-experience operator had a longer scanning time than the medium- and high-experience operators. For TRIOS 3, the low-experience operator obtained the highest number of images during each scan.The accuracy of intraoral scans was influenced by operator experience, type of IOSs, and scan size. More experienced operators and smaller scan sizes made for more accurate scans. In addition, more experienced operators made faster scans, and the TRIOS 3 was more accurate than the CEREC Omnicam for complete-arch scans.

Objective Using a mouse osteoporotic model, this study aimed to determine the influence of hydrophilic titanium surfaces on gene expression and bone formation during the osseointegration process. Background Based on the previous evidence, it is plausible to assume that osteoporotic bone has a different potential of bone healing. Therefore, implant surface modification study that aims at enhancing bone formation to further improve short- and long-term clinical outcomes in osteoporosis is necessary. Material and methods Fifty female, 3-month-old mice were included in this study. Osteoporosis was induced by ovariectomy (OVX, test group) in 25 mice. The further 25 mice had ovaries exposed but not removed (SHAM, control group). Seven weeks following the ovariectomy procedures, one customized implant (0.7 × 8 mm) of each surface was placed in each femur for both groups. Implants had either a hydrophobic surface (SAE) or a hydrophilic treatment surface (SAE-HD). Calcium (Ca) and phosphorus (P) content was measured by energy-dispersive X-ray spectroscopy (EDS) after 7 days. The femurs were analyzed for bone-to-implant contact (BIC) and bone volume fraction (BV) by nano-computed tomography (nano-CT) after 14 and 28 days. Same specimens were further submitted to histological analysis. Additionally, after 3 and 7 days, implants were removed and cells were collected around the implant to access gene expression profile of key osteogenic (Runx2, Alp, Sp7, Bsp, Sost, Ocn) and inflammatory genes (IL-1β, IL-10, Tnf-α, and Nos2) by qRT-PCR assay. Statistical analysis was performed by ANOVA and paired t test with significance at P Results The amount of Ca and P deposited on the surface due to the mineralization process was higher for SAE-HD compared to SAE on the intra-group analysis. Nano-CT and histology revealed more BV and BIC for SAE-HD in SHAM and OVX groups compared to SAE. Analysis in OVX group showed that most genes (ie, ALP, Runx2) involved in the bone morphogenetic protein (BMP) signaling were significantly activated in the hydrophilic treatment. Conclusion Both surfaces were able to modulate bone responses toward osteoblast differentiation. SAE-HD presented a faster response in terms of bone formation and osteogenic gene expression compared to SAE. Hydrophilic surface in situations of osteoporosis seems to provide additional benefits in the early stages of osseointegration.

To evaluate and compare the accuracy of conventional and 3D-printed casts using five different 3D printers.In the control group (CG group, n = 5), five conventional impressions using light- and heavy-body polyvinyl siloxane were obtained from the master model, resulting in five stone models. In the test groups, five different scans were performed by a well-trained and experienced clinician using a TRIOS intraoral scanner. All data were exported as an STL file format, processed, and sent to five 3D printers. Five casts were manufactured in each group: SG (CARES P20, Straumann); FG (Form 2, Formlabs); WG (Duplicator 7, Wanhao); ZG (Zenith D, Zenith); and MG (Moonray S100, Moonray). Measurements of the accuracy (trueness and precision) of the casts obtained from conventional elastomeric impressions and 3D-printing methods were accomplished using a 3D analysis software (Geomagic Control).The FG group showed the lowest values for trueness (closer to real dimensions), which were similar to the SG group only (P.05). Groups MG, WG, and ZG presented higher values and were similar compared to each other. Data on precision demonstrated that all 3D-printed groups showed lower values for precision (smaller deviation) when compared to the control group.The trueness depends on the chosen 3D printer. All of the tested 3D printers were more precise than cast models obtained from conventional elastomeric impressions.

Objective: A single-blind randomized clinical trial was conducted to evaluate the effectiveness of desensitizing agents with different action mechanisms in reducing cervical dentin hyperse...

INTRODUCTIONS Intraoral scanner has been widely used for implant impression in partially edentulous cases; however, its accuracy in the impression of full-arch implant is still questionable. CLINICAL REPORT This clinical report presents a technique to check the accuracy of intraoral scanning for complete-arch implant restorations using an implant index cast (The Glossary of Prosthodontic Terms 9th Edition) and a three-dimensional printed cast. A clinical case of immediate loading on a maxillary edentulous patient illustrates the application of an implant index cast in implant fixed complete dentures (IFCDs). DISCUSSION The implant index cast was fabricated based on the immediate interim prosthesis and provides effective control of the fit of scanned files and printed models. Therefore, this approach allows a more predictable and accurate fit of the final prosthesis. CLINICAL SIGNIFICANCE In this article, we present a technique to check the accuracy of the final prosthesis without the need for a conventional impression and final cast in a digital workflow. This proposed approach is demonstrated through a case report of a maxillary edentulous patient restored with immediate loaded IFCDs.

Background: Different sizes of arch could influence in digital methods to obtaining dental impressions and 3D models. The purpose of this study was to evaluate and compare the accuracy of two intra-oral scanners and conventional impression methods for the fabrication of working casts. Methods: Conventional impressions of a reference cast were obtained. Digital impressions were obtained with two intra-oral scanners: Cerec Omnicam (CO) and 3Shape Trios (ST). The obtained digital stereolithographic casts were printed on Zenith D 3D printer. The reference cast and fabricated casts were scanned with a bench top scanner and saved in STL format. All STL records were analyzed in specific software: complete arch (CA), partial arch (PA) and prepared teeth area (PT). One-way and two-way analyses of variance were performed to compare the accuracy, followed by the Tukey test. Results: No significant intergroup differences in trueness and precision were observed for the two intra-oral scanners. 3D printed casts had the lowest trueness when complete arch was analyzed and differed statistically from the stone cast. For complete arch precision, stone cast presented better results, however statistically different only from the CO. Conclusions: The two intraoral scanner systems had similar accuracy. Stone casts had higher trueness than 3D printed casts for CA. For CA precision, 3D printed cast presented similar results to the stone cast.

The traditional protocol for guided surgery in a completely edentulous patient is time-consuming, requiring the fabrication of a radiographic guide and a dual cone beam computed tomography (CBCT) scan. Using intraoral scanners to scan the edentulous ridge and the existing denture has been advocated to simplify the process. This technique offers a versatile, precise, and predictable method for the digital planning workflow in edentulous patients for either a fixed or removable restoration. In addition, this approach can help improve the quality of the guide produced by reducing CBCT artifacts associated with the existing denture, as well as capture the soft-tissue contour to further improve the fit of the surgical guide.

Objective The aim of this split-mouth, triple-blind, randomized clinical trial was to evaluate the long-term clinical efficacy of experimental potassium oxalate concentration (10%) in relieving dentin hypersensitivity (DH), after a four-session application protocol. Methods Potassium oxalate gels with different concentrations (5 and 10%) were randomly assigned to half of the 31 patients from the sample in a split-mouth design. The desensitizers were applied following a four-session protocol, one session every 48 h. The primary outcome was the assessment of pain level with the visual analog scale (VAS, 0–10), at baseline, immediately after each desensitizing session, and also after the seventh day and along 1-,3-, 6-, 9- and 12-months follow-ups. Statistical analyses were performed using Friedman repeated measures and Wilcoxon signed rank tests (α = 0.05). Results For both groups, the minimum of three sessions were required for the achievement of lower DH levels. Regardless of the concentration, the desensitizing effect was maintained all the way to the end of the 6-month follow-up. The 10%-potassium oxalate group was more effective for both 9 and 12-months follow-up periods (p Conclusions When a four-session protocol is applied, both concentrations of potassium oxalate (5 and 10%) proved to be effective on DH reduction for up to six months. However, the higher concentration promoted better long-term results. Clinical Significance: The DH is an increasing condition in clinical practice, which affects the patient’s life quality. This study provides primary clinical evidence, suggesting that multiple application sessions and higher concentrations of potassium oxalate may result in maintenance of the desensitizing effect for more extended periods. Trial registered under number: ClinicalTrials.gov NCT03083496 .

Conselho Nacional de Desenvolvimento Científico e Tecnológico In order to test the stability of dentinal tubules occlusion promoted by tubular front sealing agents to corrosive / abrasive challenges, the aim of our study is to evaluate the occlusion and stability of tubule-occluded products for the treatment of dentin hypersensitivity. Fifty sound tooth were randomly assigned in five groups (n=10), CL: Self Adhesive Sealant (Clinpro XT), TM: Calcium phosphate (Teethmate Desensitizer), GL: Glutaraldehyde (5% Gluma Desensitizer), NP: nano calcium phosphate (Nano P), 5% potassium oxalate (Painless). They were prepared to expose dentinal tubules of the cervical region, just below the cement enamel junction, submitted to treatment and later the challenges with hydrochloric acid and brushing, to simulate oral cavity of patients with gastroesophageal reflux disease (GERD). The analyzes were performed by counting, area and perimeter of the tubules, surface roughness, volume variation, height and angle vertical step, using the laser confocal microscope to evaluate the power of tubule-occluding agents and durability after the acids challenges and brushing. All criteria evaluated were submitted to appropriate statistical analysis. The effectiveness of the tested agents was evidenced in relation to time periods, all groups showed statistical differences between the initial and after treatment stages however only the CL, TM, GL groups did not achieve statistical differences between treatment and post challenge stages, proving stronger. When compared between groups, the CL was the only group that promoted complete obliteration of all dentinal tubules, maintained this obliteration after the challenges, and presents statistics differences in relation to the other groups in all variables. The use of desensitizing agents is effective in dentinal tubule occlusion. The CL, TM, GL agents were more resistant against biocorrosive-erosive challenges; the CL group was group that promoted better tubule obliteration. The surface roughness was higher for the CL group after the challenges. O tratamento da hipersensibilidade dentinária é controverso, devido à falta de estudos que comprovam a efetividade e longa duração dos protocolos, assim como a sua estabilidade frente aos eventos de biocorrosão e abrasão que ocorrem na cavidade oral, principalmente em pacientes que sofrem de refluxo gastroesofágico. Esse tratamento é embasado nos princípios de vedamento do túbulo dentinário ou da dessensibilização das terminações nervosas periodontoblásticas dentro de cada túbulo. O objetivo do nosso trabalho foi avaliar o poder de obliteração e a durabilidade de produtos obliteradores para o tratamento da hipersensibilidade dentinária. Cinquenta (50) terceiros molares hígidos, foram preparados de modo a expor túbulos dentianários da região cervical, logo abaixo da junção cemento-esmalte e divididos aleatoriamente em cinco grupos CL: Selante autoadesivo (3M ESPE CLINPRO XT) (n=10), TM: Fosfato de cálcio (TEETHMATE DESENSITIZER KURARAY NORITAKE DENTAL INC.) (n=10), GL: Glutaraldeído 5% (GLUMA DESENSITIZER HERAEUS®) (n=10), NP: Fosfato de cálcio nano estruturado (NANO P FGM®) (n=10), PL: Oxalato de Potássio 5% (PAINLESS). Foram submetidos ao tratamento e posteriormente a desafios com ácido hidroclorídrico e escovação, para simular a cavidade oral, em pacientes portadores da doença do refluxo gastroesofágico. As análises foram realizadas por meio de contagem e perímetro dos túbulos, rugosidade de superfície e variação de volume, altura e degrau vertical utilizando microscópio confocal a laser, para avaliar a capacidade de obliteração dos produtos e a estabilidade após os desafios ácidos e de escovação. Os dados foram submetidos aos testes estatísticos apropriados (α=0,05). A eficácia dos agentes testados foi evidenciada em relação a períodos de tempo. Todos os grupos apresentaram diferença estatística entre os estágios iniciais e pós o tratamento (p

The objective of this clinical study was to determine the effect of adding desensitizing agents in homemade experimental whitening gel Carbamide peroxide 16%. 60 young patients were selected (between 18-28 years), who used randomly (by lottery) the whitening gel DA (with desensitizing agent) or whitening gel CO (without desensitizing agent) characterized as control of a double-blind study, ie the patient and the evaluator did not know the product that was being used. Teeth 15, 14, 13, 12, 11, 21, 22, 23, 24 and 25 were bleached. The guidelines of how to apply the bleaching agents were performed by an experienced and calibrated team, and the application accompanied by examiners in several phases. To measure the color we used a Visual Range Vita Classical through visual inspection by the evaluators and patient information. A comparative test regarding each individual stimulation caused by mechanical attrition and thermal probe with clinical test was done (air syringe) in order to verify the presence of sensitivity in three phases: before treatment, after 7 and 14 days. Data were collected using Visual Analogue Scale (VAS) adapted to four criteria: no pain, mild pain, moderate pain and severe pain. The correlation of the data x teeth sensitivity were obtained separately, and tabulated for further comparative analysis. The results showed that there was no difference between the groups in terms of bleaching effect. In the post-operative sensitivity test, the subjects who used the product without desensitizing showed higher levels of sensitivity in different types of teeth, regardless of sex or age. It was concluded that the addition of desensitizing agent in the carbamide peroxide 16% whitening gel produced less post-bleaching sensitivity index. We emphasize that from the teeth evaluated, the premolars showed higher sensitivity index, followed by the canines and incisors. There was no difference in the bleaching capacity of the products used, demonstrating that the addition of desensitizing did not affect the efficacy of the treatment.