Postoperative Endodontic Pain after Treatment Using XP-endo Finisher: A Randomized Clinical Trial.

Introduction: This randomized clinical trial aimed to determine whether the XP-endo finisher combined with or without foraminal enlargement has any significant effect on the incidence and intensity of postoperative pain in necrotic pulps. Materials and Methods: Clinical pain levels were measured after 6, 12, 24, 48, and 72 hours and at 7 postoperative days. All treatments were performed by an endodontist in a single visit. One hundred and twenty patients were included. All patients had a single tooth treated. The patients were divided into four groups: No FE (None Foraminal Enlargement) (n=30), FE (Foraminal Enlargement) (n=30), No FE+XPF (None Foraminal Enlargement+XP-endo Finisher) (n=30) and XPF+FE (XP-endo Finisher and Foraminal Enlargement) (n=30). The canals were irrigated with sodium hypochlorite, shaped using WaveOne Gold Medium file, and then filled by using a matching single cone and AH-Plus sealer. The cavity was filled using glass ionomer cement. Pain intensity was assessed using the visual analog scale. The data were analyzed with the ANOVA and Games-Howell test. The significance level was 5%. Results: The XPF+FE group experienced a higher level of pain, being classified on the visual analog scale as moderate for 48 postoperative hours and mild for 7 postoperative days (P<0.05). In the other groups, the pain was mild, only with different time intervals (P>0.05). Conclusions: Foraminal enlargement associated with XP-endo Finisher may cause moderate postoperative pain.

Regenerative Endodontic Treatment of a Traumatized Immature Necrotic Permanent Incisor: A Case Report.

The current case report documents the clinical approach adopted for a traumatized immature necrotic permanent upper left central incisor after a bike accident. The treatment involved regenerative endodontic procedures (REPs) using "High Plasticity Mineral Trioxide Aggregate" (MTA Repair HP) as a cervical barrier over blood clot. The preservation included three years of follow-up appointments of clinical evaluations and periapical digital radiographs. Cone beam computer tomography (CBCT) was taken at six and thirty-six months for the evaluation of root development.

Accuracy of Different Imaging CBCT Systems for the Detection of Natural External Radicular Resorption Cavities: An Ex Vivo Study.

OBJECTIVE: The aim of this study was to compare the sensitivity and specificity of 3 different systems of cone-beam computed tomography (CBCT) in the detection of natural external root resorption (ERR) cavities using microtomography as the gold standard. METHOD: A sample of 126 ex vivo teeth were submitted to a microtomography examination to verify the presence/absence of ERR cavities. Then, they were divided into the control group: 85 teeth that did not present with an ERR cavity; and experimental group: 41 teeth that presented with 1 or more ERR cavities. The size of the natural ERR cavities varied from 2.46 mm3 to 3.11 mm3, which corresponded to cavities of 1.67 mm and 1.81 mm in diameter, respectively. The teeth were placed on a dry human mandible for scanning in each of the 3 protocols with different voxel sizes: 0.25 mm, 0.20 mm, and 0.166 mm. RESULTS: The accuracy of the 3 protocols evaluated in this study are listed in decreasing order: 60.3% for a voxel size of 0.20 mm, 56.7% for a voxel size of 0.166 mm, and 46.7% for a voxel size of 0.25 mm; these are smaller values than previous studies have obtained using artificial ERR cavities. Statistically significant results were not found among the 3 CBCT protocols that were used (P > .05), and the receiver operating characteristic curve shows the small differences found between the protocols. CONCLUSION: The results indicate that CBCT presents, for natural ERR, lower sensitivity and specificity values than those detected in previous studies of artificial cavities. The results demonstrate that natural ERR is neither easily observed nor accurately located by CBCT, as previous studies using artificial ERR indicated.

Management of Multiple Dental Trauma: Case Report with Eight-Year Follow-up.

This case report documents the clinical approach adopted for two maxillary incisors with intrusion and horizontal root fracture in the middle third after trauma. The proposed procedures involved maintaining pulp vitality and periodontal stability of the fractured teeth with 8 years of follow-up.

Biocompatibility of Acetazolamide and Its Association with Calcium Hydroxide in Rat Subcutaneous Tissue.

Introduction: The aim of this study was to evaluate the biocompatibility of acetazolamide and its association with the calcium hydroxide in rat subcutaneous tissues as an intracanal medication for an avulsed tooth. Methods and Materials: Three medications with acetazolamide base were evaluated: group 1 liquid acetazolamide associated with calcium hydroxide powder (LACH); group 2 liquid acetazolamide (LA); and group 3 acetazolamide powder associated with physiological saline (PAPS). The calcium hydroxide associated to physiological saline represented the control group. The medications were implanted in subcutaneous tissues of thirty-nine male rats for 7, 15 and 45 days; after surgery the animals were sacrificed and the sections were stained with hematoxylin and eosin to be evaluated qualitatively or semi-quantitatively with an optical microscope. The inflammation intensity and type of inflammatory cells and the repair process, were assessed. The obtained data were statistically compared through the Kruskal-Wallis test conducted at the 5% level of significance. Results: On the seventh day, there was statistically significant difference between PAPS and LA, in relation to the number of neutrophils (P=0.0016). There was a statistically significant difference in the total number of inflammatory cells in PAPS compared to LACH (P=0.0038) on the fifth day. The total number of inflammatory cells from PAPS was significantly higher in relation to LACH (P=0.0038), as well as LA from LACH (P=0.0038) on forty fifth day. A statistically significant reduction in the value of lymphocytes was also observed in LACH (P=0.0072) and LA (P=0.0010) groups in the same period. Conclusion: The results of this animal study suggest that the association of the liquid acetazolamide with the calcium hydroxide promoted an inflammation reduction and a faster repair process than in the LA and PAPS groups evaluated in 15 and 45 days.

Evaluation of intracanal acetazolamide in late reimplanted rat teeth.

OBJECTIVE: The aim of this study was to evaluate the use of acetazolamide combined with different agents as intracanal medication in late reimplanted rat teeth. MATERIALS AND METHODS: In 100 Wistar rats, divided into 5 groups of 20, one of the following medications was used: Acetazolamide liquid (AL); AL with calcium hydroxide powder (ALHC); acetazolamide powder with AL; acetazolamide powder with physiological solution; and calcium hydroxide with physiological solution (control). At 30 and 60 days after reimplantation, the animals were sacrificed, tissues were processed, and cuts were stained with hematoxylin and eosin. An optical microscope was used to determine the following: percentage of inflammatory root resorption (RRI); percentage of substitute root resorption (RRS); and presence of ankylosis. The data obtained was submitted for statistical analysis. RESULTS: Group ALHC had a significantly higher RRS than the control group at 60 days (P = 0.01). Group AL showed significantly less ankylosis than the other groups, including the control, at 30 days. AL showed results similar to those of the control group with respect to RRS. CONCLUSION: Acetazolamide has the potential to be an effective intracanal medication.