The purpose of this study was to investigate the influence of cervical preflaring on determination of the initial apical file in maxillary lateral incisors. Forty human lateral incisors with complete root formation were used. After standard access cavities, a size 06 K-file was inserted into each canal until the apical foramen was reached. The WL (WL) was set 1 mm short of the apical foramen. Four groups (n=10) were formed at random, according to the type of cervical preflaring performed. Group 1 received the initial apical instrument without previous preflaring of the cervical and middle root canal thirds. Group 2 had the cervical and middle root canal thirds enlarged with nickel-titanium Orifice Opener instruments. Group 3 had the cervical and middle root canal thirds enlarged with Gates-Glidden drills. Titanium-nitrite treated, stainless steel LA Axxess burs were used for preflaring the cervical and middle root canal thirds of group 4. Each canal was sized using manual K-files, starting with size 08 files with passive movements until the WL was reached. File sizes were increased until a binding sensation was felt at the WL, and the instrument size was recorded for each tooth. The apical region was then observed under a stereoscopic magnifier, images were recorded digitally and the differences between root canal and maximum file diameters were recorded (in mm) for each sample. Significant differences were found between the groups regarding the anatomical diameter at the WL and the first file to bind the canal (p = 0.01). The major discrepancy was found when no preflaring was performed (0.1882 mm average). Canals preflared with Orifice Opener instruments (0.0485 mm average) and Gates-Glidden drills (0.1074 mm average) also showed great discrepancy. The LA Axxess burs produced the smallest differences between anatomical diameter and first file to bind (0.0119 mm average). Instrument binding technique for determining anatomical diameter at WL was not accurate. Preflaring of the cervical and middle thirds of the root canal improved anatomical diameter determination; the instrument used for preflaring played a major role on determination of the anatomical diameter at the WL. Canals preflared with LA Axxess burs created a more accurate relationship between file size and anatomical diameter.
Resonance frequency analysis (RFA) has become the main tool used to assess the osseointegration of dental implants. The objective of this study was to verify the relationship between the ISQ values with different prosthetic abutments and with the implant platform. The hypothesis was that ISQ values changes according to the abutment height. Twelve patients were included, whose contribution to the study was 31 dental implants (external hexagon connection implants, 4.1x10 mm). The temporary implant-supported crown and prosthetic components were removed and the following smartpegs were inserted, one at a time: type 1, in the implant platform (G1); type A3, in the microunit component with 1mm transmucosal height (G2) and type A3, in the microunit component with 5mm transmucosal height (G3). In all the smartpegs, RFA measurements were taken on mesial, distal, buccal and lingual surfaces. All evaluations were performed by a single calibrated examiner (ICC = 0.989). Data were analyzed by Friedman and Spearman correlation tests and log-linear marginal regression (p<0.05). The mean age of participants was 52.83 (± 3.77) years. There was statistically significant difference (p<0.001) among the mean ISQ of G1 (88.27 ±5.70); G2 (72.75 ±4.73) and G3 (66.33 ±3.67). There was statistically significant negative correlation between the ISQ and the measurement distance (rs:-0.852; p<0.001; R2:0.553). Measurement distance was significantly associated (p<0.001) with ISQ value in the log-linear regression. The abutment height has a significant impact on resonance frequency analysis measurements. The higher the transmucosal abutment height, the lower the implant stability quotient value. Clinically, the ISQ measured on the abutment cannot be compared with values measured on the implant platform.
Clinical comparison of short and conventional implants placed in the posterior region of the mandible. A pilot study ResumoObjetivo: Avaliar e correlacionar os valores de densidade óssea radiográfica, altura óssea peri-implantar e de frequência de ressonância nos implantes curtos e convencionais instalados na região posterior da mandíbula após a instalação da prótese provisória. Material e método: Esse estudo piloto clínico prospectivo contou com a participação de 11 pacientes que foram divididos previamente em dois grupos: implantes curtos (n=18) (5,0 x 5,5 mm e 5,0 x 7,0 mm) e implantes convencionais (n=23) (4,0 x 10 mm e 4,0 x 11,5 mm). Foram executadas análise da frequência de ressonância, altura óssea e densidade óssea peri-implantar. Os implantes foram avaliados nos períodos T0 (imediatamente após a instalação do provisório), T1 (após 90 dias) e T2 (após 180 dias). Resultado: Não houve diferenças estatisticamente significativas entre os grupos com relação a densidade óssea radiográfica (152,50 ± 15,39 vs. 157,60 ± 28,46, para implantes convencionais e curtos respectivamente no período T2), estabilidade dos implantes (Implantes convencionais: 66,76 ± 10,39 no período T0 e 61,85 ± 8,38 no período T2 vs. Implantes curtos: 57,50 ± 12,17 no período T0 e 61,53 ± 7,39 no período T2) e quanto a perda óssea periimplantar (0,03 mm vs. -0,17 mm, em implantes convencionais e curtos no período T2, respectivamente). Adicionalmente a isso, não foram detectados correlação significativa entre densidade radiográfica com altura óssea peri-implantar e nem com a frequência de ressonância. Conclusão: Verificou-se que os implantes curtos apresentaram um comportamento semelhante aos implantes de comprimento convencionais com relação à frequência de ressonância, a densidade radiográfica peri-implantar e a manutenção dos níveis ósseos periimplantares.Descritores: Reabsorção óssea; densidade óssea; próteses e implantes. AbstractObjective: To evaluate and correlate the values of radiographic bone density, peri-implant bone height and resonance frequency analysis (RFA) of short or conventional implants placed in the posterior region of the mandible after installing a prosthesis. Material and method: Eleven patients were selected for this prospective parallel pilot study. The prostheses were supported by two types of implants: short implants (n = 18) (5.0 x 5.5 mm and 5.0 x 7.0 mm) and conventional implants (n = 23) (4.0 x10 mm and 4.0 x 11.5 mm). The implants were evaluated by RFA, by measuring the bone height, and peri-implant bone density. The implants were evaluated at the periods T0 (immediately after installation of the prosthesis), T1 (after 90 days), and T2 (after 180 days). Result: There were no statistically significant differences between groups with respect to radiographic bone density (152.50 ± 15.39 vs. 157.60 ± 28.46, for conventional and short implants, respectively at T2), stability of the implants (Conventional implants: 66.76 ± 10.39 at T0, and 61.85 ± 8.38 at T2 vs. Short implants: 57.50 ± 12.17 at T0, and 61.53 ± ...
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