Ten-year clinical performance of zirconia posterior fixed partial dentures.

BACKGROUND: With the constantly increasing demand for metal-free solutions in dental therapy, numerous ceramic restorations have found their way into everyday clinical practice, but long-term clinical data are limited. OBJECTIVE: The aim of this prospective clinical study was to evaluate three- and four-unit fixed partial dentures in the posterior region made of zirconium dioxide frameworks veneered with feldspathic porcelain after 10 years in clinical use. METHODS: Based on the two studies published in 2009 and 2012, in which the all-ceramic FDPs were evaluated after 3 and 5 years of function, a clinical evaluation of a total of 17 restorations after 10 years with regard to their condition and long-term stability was carried out in the course of this study. The restorations were fabricated using feldspathic ceramic-veneered, yttria-stabilised, tetragonal zirconium dioxide as the framework material. The data collection was based on modified CDA criteria and included, for example, the shape, shade, surface condition and the success and survival rates of the restorations. RESULTS: The all-ceramic prostheses embodied excellent biocompatibility and colour reproduction. As a result of an increased incidence of chipping fractures, the success rate was 60%. The survival rate, however, was 88.2%, as 2 of the 17 restorations were lost. CONCLUSION: All-ceramic concepts for FDP constructions in the posterior region achieved satisfactory results in terms of durability after 10 years. The main problem was chipping, as has been generally recognised. Nevertheless, the materials were characterised by excellent aesthetics and biocompatibility, which ultimately makes them a good alternative to conventional restorative options. TRIAL REGISTRATION: This study is registered in DRKS-German Clinical Trials Register with the register number DRKS00021743.

Investigation of the palatal soft tissue volume: a 3D virtual analysis for digital workflows and presurgical planning.

BACKGROUND: In mucogingival and implant surgery, an autologous soft tissue graft from the palate is the gold standard for reconstructing missing keratinised soft tissue and volume. Previously, presurgical measurements of the graft harvesting site were described with two-dimensional (2D) linear measurements. The present observational clinical study aimed to evaluate a three-dimensional (3D) measurement method for determining the present palatal soft tissue volume for each patient individually. METHODS: Pre-existing cone beam computed tomography (CBCT) scans of 20 patients were converted into 3D Standard Tessellation Language models of the bone surface. Intraoral impressions of the maxilla were taken and digitised to visualise the gingival surface. The resulting virtual models of bone (reference value) and gingival (actual value) surfaces were merged, with tooth surfaces used for registration. The region between the central incisors and the hard palate was subdivided into 5 regions of interest (ROIs). The distance between palatal bone and gingival surface was analysed both volumetrically and linearly, and the results were statistically evaluated for the ROIs. RESULTS: The average gingival surface area on the palate was 19.1 cm2, and the mean volume was 58.2 cm3 (± 16.89). Among the ROIs, the mean linear value was highest in the most distal region, from the second molar to the hard palate (4.0 ± 1.09 mm) and lowest in the canine region (1.9 ± 0.63 mm). For mean distance, significant differences were found for the anterior palate and the most posterior palate in comparison with all other ROIs (p < 0.01). The volume measurements also declined significantly and steadily between the posterior (1.9 ± 1.0 cm3) and anterior palates (0.4 ± 0.2 cm3). CONCLUSIONS: By merging digital data, palatal soft tissue could be quantified virtually. The results were reliable and comparable to previous findings with linear measurement methods. This 3D soft tissue volume analysis method fully exploited the diagnostic potential of data that are frequently collected for presurgical planning in oral surgery (i.e., CBCT + surface scans). This evaluation method might be useful for volumetric and linear measurements in other applications in anatomy and for determining palatal soft tissue dimensions in the planning stage before surgical interventions. TRIAL REGISTRATION: This observational clinical trial was retrospectively registered in the German Clinical Trials Register, reference number: DRKS00023918.

Wear of feldspathic-ceramic-veneered zirconia posterior FPDs after 10 years.

BACKGROUND: The abrasion behavior of various ceramics is rarely investigated, though it is relevant for the clinical success of such restorations. The aim of this in vivo study was to evaluate the wear of feldspathic-ceramic-veneered zirconium oxide frameworks over a period of at least 10 years. METHODS: The abrasion behavior of 15 bridge constructions from 15 different participants was examined after a period of 3, 5, and 10 years using plaster models, which were then subjected to a scanning process on the Atos II industrial scanner and digitized for three-dimensional evaluation of the abrasion by the corresponding software (ATOS Professional 7.6). The individual post-examination models were compared to the baseline model and deviations calculated in the sense of the largest, punctual loss of material in millimeters ("minimal distance"), the average abrasion in millimeters ("mean distance"), and the volume decrease in cubic millimeters ("integrated distance"). Statistical analyses were performed using the Wilcoxon sign rank test or mixed regression models. Multiple testing was considered by Benjamini-Hochberg correction. The significance level was set at 0.05. RESULTS: We found steadily increasing wear of the ceramic. The average volume decrease was significant (P < 0.001) at 3 years and 10 years (- 3.25 mm3 and - 8.11 mm3, respectively). CONCLUSIONS: The results of this study indicate that the rate of volume loss in feldspathic-ceramic-veneered zirconia frameworks in the posterior region increases significantly over time. An increasing frequency of parameters was observed, particularly in the second half of the study period. However, the use of this class of materials can be considered clinically acceptable. Trial registration This study is registered in DRKS - German Clinical Trials Register with the register number DRKS00021743. https://www.drks.de/drks_web/navigate.do?navigationId=trial.HTML&TRIAL_ID=DRKS00021743.

Effect of Luting Materials on the Accuracy of Fit of Zirconia Copings: A Non-Destructive Digital Analysis Method.

The marginal accuracy of fit between prosthetic restorations and abutment teeth represents an essential aspect with regard to long-term clinical success. Since the final gap is also influenced by the luting techniques and materials applied, this study analyzed the accuracy of the fit of single-tooth zirconia copings before and after cementation using different luting materials. Forty plaster dies with a corresponding zirconia coping were manufactured based on a single tooth chamfer preparation. The copings were luted on the plaster dies (n = 10 per luting material) with a zinc phosphate (A), glass-ionomer (B), self-adhesive resin (C), or resin-modified glass-ionomer cement (D). The accuracy of fit for each coping was assessed using a non-destructive digital method. Intragroup statistical analysis was conducted using Wilcoxon signed rank tests and intergroup analysis by Kruskal-Wallis and Mann-Whitney U tests (α = 0.05). Accuracy of fit was significantly different before/after cementation within A (0.033/0.110 µm) and B (0.035/0.118 µm; p = 0.002). A had a significantly increased marginal gap compared to C and D, and B compared to C and D (p ≤ 0.001). Significantly increased vertical discrepancies between A and B versus C and D (p < 0.001) were assessed. Of the materials under investigation, the zinc phosphate cement led to increased vertical marginal discrepancies, whereas the self-adhesive resin cement did not influence the restoration fit.

Stress Distribution within the Peri-Implant Bone for Different Implant Materials Obtained by Digital Image Correlation.

Stress distribution and its magnitude during loading heavily influence the osseointegration of dental implants. Currently, no high-resolution, three-dimensional method of directly measuring these biomechanical processes in the peri-implant bone is available. The aim of this study was to measure the influence of different implant materials on stress distribution in the peri-implant bone. Using the three-dimensional ARAMIS camera system, surface strain in the peri-implant bone area was compared under simulated masticatory forces of 300 N in axial and non-axial directions for titanium implants and zirconia implants. The investigated titanium implants led to a more homogeneous stress distribution than the investigated zirconia implants. Non-axial forces led to greater surface strain on the peri-implant bone than axial forces. Thus, the implant material, implant system, and direction of force could have a significant influence on biomechanical processes and osseointegration within the peri-implant bone.

Impact of Scanbody Geometry and CAD Software on Determining 3D Implant Position.

The implementation of CAD software in the digital production of implant prosthetics stands as a pivotal aspect of clinical dentistry, necessitating high precision in the alignment of implant scanbodies. This study investigates the influence of scanbody geometry and the method of superimposing in CAD software when determining 3D implant position. A standardized titanium model with three bone-level implants was digitized to create reference STL files, and 10 intraoral scans were performed on Medentika and NT-Trading scanbodies. To determine implant position, the generated STL files were imported into the Exocad CAD software and superimposed-automatically and manually-with the scanbody geometries stored within the software's shape library. Position accuracy was determined by a comparison of the 3D-defined scanbody points from the STL matching files with those from the reference STL files. The R statistical software was used for the evaluation of the data. In addition, mixed linear models and a significance level of 0.05 were applied to calculate the p-values. The manual overlay method was significantly more accurate than the automatic overlays for both scanbody types. The Medentika scanbodies showed slightly superior precision compared to the NT-Trading scanbodies. Both scanbody geometry and the type of alignment in the CAD software significantly affect digital workflow accuracy. Manual verification and adjustment of the automatic alignment process are essential for precise implant positioning.

Comparison of digital and visual tooth shade selection.

OBJECTIVE: In dental restorations, color determination is very important for achieving esthetic results. The aim of this study was to compare visual shade selection using digital methods and to assess the repeatability of the utilized intraoral scanners. MATERIALS AND METHODS: In 31 probands, tooth color was determined on teeth 11, 13, and 16. Shade selection was performed visually by a dentist and digitally using Trios 3 and Cerec Omnicam. Three measurements were performed to determine the repeatability of intraoral scanners. Fleiss' κ was used for statistical evaluation of the repeatability and Cohen's κ was used for comparison of methods. RESULTS: The visual method showed only slight agreement with Trios 3 (Cohen's κ: 0.198) and Cerec Omnicam (Cohen's κ: 0.115). Moderate agreement was found between Trios 3 and Cerec Omnicam (Cohen's κ: 0.452). In terms of repeatability, Trios 3 scored higher overall than Cerec Omnicam (Fleiss' κ: 0.612 vs. 0.474). CONCLUSION: Intraoral scanners can facilitate the workflow in clinical practice. They are a good supplement for color determination, but should additionally be confirmed by the visual method. Clinical significance: The use of digital instruments is increasingly being preferred over conventional treatments. Therefore, it is essential to continuously improve the accuracy of intraoral scanners for color selection in order to offer an alternative to visual methods.

Comparison of Digital and Conventional Impressions Based on the 3D Fit of Crowns.

PURPOSE: To evaluate intraoral scanners, scannable impression materials, and conventional methods for impression-taking with regard to precision and accuracy. MATERIALS AND METHODS: Ten impressions per technique were initially taken from a cobalt-chromium (Co-Cr) master model (chamfer preparation for the maxillary right first molar) for fabricating Co-Cr crown copings. The test specimens, their respective metal master model, and the plaster casts from the conventional impressions were then digitized with the light-optical Atos Triple Scanner. The fit of the dental crown copings was measured in two and three dimensions using computer-aided design software. Global differences between the methods were determined using Kruskal-Wallis test, and pairwise comparisons were performed with Mann-Whitney U test. The significance level was set at .05. RESULTS: The 2D analysis showed that the average absolute marginal distance of the crown copings was 0.026 mm when fabricated with the digital impression method and 0.038 mm when fabricated with the conventional method (P = .028). However, the 3D analysis revealed that the conventional group had a smaller marginal gap (0.028 mm) compared to the digital group (0.06 mm; P = .015). CONCLUSION: This study showed that, in the field of single-crown prosthetics, digital impressions and the use of scannable impression material could serve as alternatives to conventional methods in the future.

Trueness of full-arch dental models obtained by digital and conventional impression techniques: an in vivo study.

The aim of this study was to compare the trueness of complete- and partial-arch impressions obtained using conventional impression materials and intraoral scanners in vivo. Full-arch impressions were taken using polyether and polyvinylsiloxane. Gypsum casts were digitized using a laboratory scanner (IM, AF). Casts obtained from polyether impressions were also scanned using an industrial blue light scanner to construct 3D reference models. Intraoral scanning was performed using CEREC Omnicam (CO) and Trios 3 (TR). Surface matching software (Atos Professional) enabled to determine the mean deviations (mean distances) from the reference casts. Statistically significant discrepancies were calculated using the Wilcoxon signed-rank test. The mean distance for trueness ranged from 0.005 mm (TR) to 0.023 mm (IM) for the full arch, from 0.001 mm (CO) to 0.068 mm (IM) for the anterior segment, and from 0.019 mm (AF) to 0.042 mm (IM) for the posterior segment. Comparing the anterior vs. the posterior segment, significantly less deviations were observed for anterior with CO (p < 0.001) and TR (p < 0.001). Full-arch comparisons revealed significant differences between AF vs. IM (p = 0.014), IM vs. CO (p = 0.002), and IM vs. TR (p = 0.001). Full-arch trueness was comparable when using Affinis and the two intraoral scanners CEREC Omnicam and Trios 3. The digital impression devices yielded higher local deviations within the complete arch. Digital impressions of the complete arch are a suitable and reliable alternative to conventional impressions. However, they should be used with caution in the posterior region.Trial registration: Registration number at the German Clinical Trial Register (04.02.2022): DRKS00027988 ( https://trialsearch.who.int/ ).