The aim of this comparative retrospective clinical study was to assess the effect of age on immediate loaded full-arch mandibular rehabilitation in younger vs. elderly patients. Patients with an age between 45 and 60 years (younger group, YG) or with an age more or equal to 75 years (older group, OG), requiring a mandibular full-arch rehabilitation were scheduled for the present study.
View Article and Find Full Text PDFThe aim of this study was to assess and compare the marginal bone loss between two different categories of implants (Winsix, Biosafin, Ancona, Italy) having the same diameter and belonging to the Torque Type (TT) line, in the internal hexagon version (TTi, Group A) and in the external hexagon configuration (TTx, Group B). Patients with one or more straight implants (insertion parallel to the occlusal plane) in the molar and premolar regions in association with tooth extraction at least 4 months prior to implant insertion, who have a fixture diameter of 3.8 mm, who followed up for at least 6 years, and whose radiographic records were available were enrolled in this study.
View Article and Find Full Text PDFThe aim of this retrospective clinical study was to evaluate and compare implant survival, marginal bone loss, and clinical and prosthetic complications in healthy patients and patients with type I diabetes undergoing full arch implant-prosthetic rehabilitation. A total of 47 patients needing total fixed rehabilitation of one or both arches were enrolled for this study. Based on the absence of any systemic diseases (Group A) or the presence of type I diabetes (Group B), the sample was divided into two groups.
View Article and Find Full Text PDFThe aim of the present study was to evaluate the efficacy of an air purifier device (professional XXl inn-561 innoliving) with HEPA 14 filter in reducing the number of suspended particles generated during dental procedures as a vector of COVID-19 transmission. The survey was conducted on 80 individuals who underwent Oral Surgery with dental Hygiene Procedures, divided into two groups based on the operational risk classification related to dental procedures: a Test Group (with application of filtering device) and a Control Group (without filtering device). All procedures were monitored throughout the clinical controls, utilising professional tools such as molecular particle counters (Lasair III 350 L 9.
View Article and Find Full Text PDFPurpose: The aim of this case-control study was to investigate the occurrence of bleeding events related to maxillary sinus elevation with a lateral window in patients under direct oral anticogulant therapy.
Materials And Methods: Seventyseven consecutive patients were scheduled for unilateral maxillary sinus floor elevation using a lateral window approach. Participants were divided into two groups: group A, formed by 37 patients who were under novel oral anticoagulation therapy (rivaroxaban/apixaban), and a control group, composed of 40 healthy subjects.