The aim of this study was to quantitatively evaluate the amount of apically extruded debris by single-file reciprocating instruments with different working lengths and apical preparation sizes. Eighty human single-rooted mandibular incisors were used and conventional access cavities were prepared. Then, the specimens were divided into four groups (n=20), according to root canal instrumentation: Reciproc size 25, .08 taper and Reciproc size 40, .06 taper instruments were used at the foramen; Reciproc size 25, .08 taper and Reciproc size 40, .06 taper instruments were used 1 mm short of the foramen. Distilled water was used as an irrigant and the apically extruded debris were collected in pre-weighted glass vials and dried afterwards. The mean weight of debris was weighed with a microbalance and statistically analyzed using one-way analysis of variance and the post hoc Tukey multiple comparison test (p<0.05). The results showed that all experimental groups were associated with debris extrusion. No significant difference was found in the amount of apically extruded debris among all experimental groups (p>0.05). The present study demonstrated that the working length and the apical preparation size did not have a significant effect on debris extrusion when performing single-file reciprocating instrumentation.
The electronic method has been studied and improved aiming to add precision, speed and reliability of the measurement technique to determine the exact location of the working length. Currently, the root canal preparation recommends prior to determine the tooth length and consequent perform instrumentation of the apical portion, a previous preflaring of the cervical and middle thirds in various techniques. This procedure may provide a reduction in system impedance, leading to read errors by the apex locators. Objective: Investigate the influence of preflaring of the cervical and middle thirds on the accuracy of measuring the working length by apex locators. Material and methods: Twenty-five mesial roots of molars were used and had their crowns cut at the cemento-enamel junction. The actual measure of each root canal was performed and then the samples were embedded into a mixture of alginate, used as a conducting medium, where electronic measurements were taken with apex locator before and after preflaring of the canals with Gates-Glidden drills in descending order (#4, #3, #2). Measurements obtained by electronic method were then compared with the actual measurement of the root canal. The results were tabulated and submitted to the Student t test Results: The results show that there was no statistical significance (p<0.05) between the readings before and after preflaring. Readings closer to the foraminal ending occurred in the group after preflaring with Gates Glidden. Conclusion: It was concluded that preflaring with Gates Glidden drills were not able to influence significantly the accuracy of apex locator in determining the exact working length.
During endodontic treatment, the maintennance of the aseptic chain is mandatory. Therefore, all substances, instruments, and medications inserted into root canals must be free of microorganisms. Objective: To evaluate in vitro and microbiologically the contamination of absorbent paper points. Material and methods:Absorbent paper points of different brands and under different conditions were evaluated and subdivided into the following groups: esterilized by the manufacturer (G1 to G5), not esterilized by the manufacturer (G6), esterilized in autoclave by the operator (G7), and intentionally contaminated (G8). The two last groups were the positive and negative controls, respectively. All paper points were unpacked and immersed into tubes with culture medium for 48 hours and then analyzed according to culture broth turbidity. Results: Only the samples esterilized by the manufacturers Dentsply® (G1), Endopoints®(G2), and Meta® (G3), and the samples esterilized in autoclave by the operator (G7) did not evidence microbial growth after 48 hours. G7) did not evidence microbial growth after 48 hours. ) did not evidence microbial growth after 48 hours. Although sterilized by the manufacturer, both the brands Tanari®(G4) and Roeko® (G5) showed bacterial contamination; Dentsply®(G6) non-sterile paper points also showed bacterial contamination. non-sterile paper points also showed bacterial contamination.Conclusion: Paper point esterilization before clinical use should be Paper point esterilization before clinical use should berecommended regardless of the commercial brand.
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