Marsupialization is an effective and conservative treatment option for OKC. Nevertheless, future studies should conduct even longer follow-up periods to evaluate any recurrence of lesions.

The aim of this study was to evaluate the effects of exposing dental implants to the maxillary sinus cavity. This is a retrospective study. Thirteen patients with 18 implants that had radiographic evidence of implant exposure to the maxillary sinuses participated in this study. We evaluated the patient's radiographs immediately after implant insertion and 12 months after operation with the patient's clinical signs and symptoms due to sinusitis. Thirteen patients with 18 implants in the maxillary sinus had no signs and symptoms of sinusitis. Radiography showed thickening of the sinus membranes in 2 patients. All penetrated implants were successfully integrated, and there were no radiographic signs of bone loss or other complications.The exposure of implants to the maxillary sinuses caused no problems in the maxillary sinuses, and bone formation occurred in THE maxillary floor when penetration of maxillary sinuses occurred without tearing of the membrane.

The aim of this study was to evaluate the recovery complications following the use of 2 anesthetic protocols in orthognathic surgery, namely, propofol with remifentanil and isoflurane with remifentanil. Sixty-two patients with American Society of Anesthesiologists physical status I were selected. All underwent bimaxillary orthognathic surgery. Propofol with remifentanil was used as an anesthesia in group 1 (n = 32), and isoflurane with remifentanil was used in the patients in group 2 (n = 30). Early recovery complications consisting of pain, postoperative nausea and vomiting (PONV), shivering, and agitation were evaluated and documented. The length of the operation and duration of recovery were documented for all patients. Analysis of the data demonstrated no relationship between age and recovery time (P > 0.05). Analysis of data with χ(2) and independent t-tests did not show any difference between the 2 groups with regard to pain, agitation, PONV, and shivering (P > 0.05). Logistic regression was used to evaluate the effect of the operation time on recovery complications. The analysis showed that pain and PONV were significantly higher in those who experienced a longer operation time. With increasing operation time longer than 165 minutes, 64% of patients experienced pain, and 89% of them had PONV. General anesthesia can be provided via intravenously administered medications and/or inhaled volatile anesthetics. No significant difference in early recovery time was found in patients when either isoflurane or propofol was used to maintain the anesthesia. However, the length of the operation played a major role in increasing early recovery complications.

A prospective study was done to compare rigid intermaxillary fixation and guiding elastic for treatment of condylar fractures in pediatric patients. Sixty-one children younger than 12 years with condylar fractures were studied in 2 groups. Group 1 consisted of 31 patients who were treated with arch bar and intermaxillary fixation for 7 to 12 days, and group 2 consisted of 30 patients who were treated with arch bar and elastics without rigid intermaxillary fixation. Patients had minimal function during treatment time, which lasted 7 to 12 days. Evaluation of deviation on opening between both groups (groups 1 and 2) with a χ test did not show any relationship between them. Incidence of temporomandibular dysfunction signs was 25.8% in group 1 patients and 23.3% in group 2 patients. Comparison of temporomandibular dysfunction signs in both treatment groups did not show a statistically significant relationship. Our study showed the same results using guiding elastics as using rigid intermaxillary fixation in pediatric condylar fractures. Guiding elastic is more tolerable, and children have function during treatment.

The aim of our study was to evaluate the biodegradable plates (PG910/PDO) for reconstruction of various sizes of the orbital floor defects in the blow-out fractures. We included patients who had an impure blow-out fracture. All patients had a recent trauma and also the surgical intervention was done between 1 and 10 days after trauma. The amount of the orbital floor defect was measured in each case through computed tomography scan. In the surgical intervention, a biodegradable plate was used for the reconstruction of the orbital floor defect along with titanium miniplates used for bone fixation in orbital rim. Due to aesthetic reasons, all patients underwent secondary surgery including removal of titanium miniplates after 18 months. The orbital floor was reevaluated during the removal of the miniplates. The clinical evaluation of remnant defects and biodegradable plates (presence of complete or partial resorption) were documented for each patient. In our study a total of 15 patients (10 males and 5 females) underwent the orbital floor reconstruction using biodegradable miniplates. The size of the orbital floor defects was meanly 3.51 ± 1.29 cm(2). Results demonstrated that 4 out of 15 patients had a remnant defect after resorption of the biodegradable plate. In 10 out of 15 patients, the biodegradable plates completely replaced with fibrous tissues after 18 months. Remaining five patients had partial resorption of plates. There was not any relationship between the defect size and the remnant defects (p > 0.05). A significant relationship was seen between the defect size and the plates' resorption rate (p < 0.001). There is a significant relationship between the resorption rate and the remnant defect. The risk to have remnant defects have been increased as the plates had incomplete resorption. The use of biodegradable plates is an appropriate option for reconstruction of the orbital floor defects. The defect size does not have any effect on the stability of the plate. However, incomplete plate resorption increases the risk of remnant defects in the orbital floor. The larger defects lead to slow degradation of biodegradable plates.