This study investigated the effect of initial nonsurgical treatment in patients with peri-implantitis with or without prescription of an antibiotic regimen consisting of amoxicillin and metronidazole. For this purpose, patients with peri-implantitis were randomized into a group of initial treatment with antibiotics and a group without antibiotics. They were re-evaluated 12 weeks after treatment. Analyses were performed at the patient level at 1 peri-implant pocket per patient. Both groups showed significant peri-implant pocket depth reductions after initial treatment. Treatment with antibiotics resulted in a higher mean reduction in peri-implant pocket depth than when no antibiotics were used, but this difference did not reach statistical significance. Only 2 implants, 1 in each group, showed a successful outcome of a peri-implant pocket depth ofunder ≤ 5 mm and with an absence of bleeding and pus after probing. Initial treatment with or without antibiotics is ultimately not sufficient to fully treat peri-implantitis; additional surgical procedures will often be required.
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http://dx.doi.org/10.5177/ntvt.2023.04.23004 | DOI Listing |
J Adv Periodontol Implant Dent
July 2024
Department of Periodontics, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Background: The purpose of this study was to review the literature on the efficacy of different surgical regenerative methods for peri-implantitis treatment.
Methods: A preliminary search was conducted in seven electronic databases. The studies included in the analysis implemented surgical regenerative treatment in at least one study group.
Clin Oral Implants Res
December 2024
Head of Department of Prosthodontics, Dental School, Sigmund Freud Medical University of Vienna, Vienna, Austria.
Purpose: To evaluate the performance and clinical outcome of vertical and horizontal bone augmentation (VHBA) in posterior maxillary regions combining lateral window sinus floor elevation (LWSFE) with a horizontal bone shell technique applying the maxillary facial sinus wall as a bone plate.
Materials And Methods: In 18 patients, LWSFE was combined with a horizontal bone shield augmentation procedure utilizing the maxillary facial sinus bone wall as a lateral bone plate. Both the sinus cavity and the lateral bone box created were grafted with a mixture of autogenous bone/venous blood and bovine bone mineral.
Int J Oral Maxillofac Surg
December 2024
Department of Periodontology, Faculty of Dentistry, Kutahya Health Sciences University, Kutahya, Turkey. Electronic address:
The aim of this randomized clinical trial was to compare a non-grafted socket shield technique (SST) with simultaneous guided bone regeneration (GBR) in immediate implant placement in terms of clinical, aesthetic, and radiographic parameters. Patients with an unrestorable tooth in the maxillary aesthetic region were included. The patients were randomized to SST and GBR groups.
View Article and Find Full Text PDFEvid Based Dent
December 2024
Lancashire Oral Surgery Clinic, Blackpool, England.
Data Sources: Randomised control trials were identified via searches of PubMed, Embase, Web of Science and The Cochrane Library.
Study Selection: Only randomised control trials involving adults with at least a single dental implant which had experienced peri-implant mucositis or peri-implantitis were considered. Within studies, one cohort must have been treated with a combination of mechanical debridement (MD) and non-surgical strategies, and the other solely by mechanical debridement.
Int Dent J
November 2024
Hamdan Bin Mohammed College of Dental Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai Health, Dubai, United Arab Emirates; Honorary Senior Lecturer, the Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, UK. Electronic address:
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