Aouini Walid, Lambert France, Vrielinck Luc, Vandenberghe Bart
Department of Periodontology and Oral Surgery, CHU of Liege, Faculty of Medicine, University of Liege, 4000 Liège, Belgium.
Department of Oral and Maxillofacial Surgery, St John's Hospital, 3600 Genk, Belgium.
J Clin Med. 2019 May 7;8(5):616. doi: 10.3390/jcm8050616.
The aim of the study was to evaluate the proportion of patients recommended for full-arch mandibular restoration that would be eligible for treatment with a recently developed premanufactured full-arch prosthesis (Trefoil™, Nobel Biocare) based on the morphology of their lower jaw. Anonymized cone beam computed tomography (CBCT) data from 100 partially and fully edentulous patients referred for full-arch mandibular restoration were retrospectively collected from an imaging center database. Using custom-built software, CBCTs of mandibles were registered to a reference CBCT of a patient treated previously with a premanufactured full-arch prosthesis to determine if patients had adequate horizontal width and vertical height for implant placement. Bone height and thickness around simulated implants and distances to the incisive canal were evaluated. Mandibular arch width and semi-automated volume calculations were also performed. Using the system-specific 5.0 mm diameter implants with lengths of 13 and 11.5 mm, 85% and 86% of patients, respectively, were eligible for treatment with the standardized prosthesis. Eligibility was higher for men than women (odds ratio = 3.9, = 0.045) due to increased bone volume. Based on mandibular morphology, our results suggest that the standardized treatment concept could serve a large percentage of patients with edentulous mandibles or failing dentition in the mandible.
本研究的目的是根据下颌形态,评估推荐进行全牙弓下颌修复的患者中,有资格使用最近开发的预制成型全牙弓假体(Trefoil™,诺贝尔生物保健公司)进行治疗的比例。从一家影像中心数据库中回顾性收集了100例因全牙弓下颌修复而转诊的部分缺牙和全口无牙患者的匿名锥形束计算机断层扫描(CBCT)数据。使用定制软件,将下颌的CBCT与先前使用预制成型全牙弓假体治疗的患者的参考CBCT进行配准,以确定患者是否有足够的水平宽度和垂直高度来植入种植体。评估了模拟种植体周围的骨高度和厚度以及到切牙管的距离。还进行了下颌弓宽度和半自动体积计算。使用特定系统的直径5.0 mm、长度分别为13和11.5 mm的种植体,分别有85%和86%的患者有资格使用标准化假体进行治疗。由于骨量增加,男性的符合资格率高于女性(优势比=3.9,P=0.045)。基于下颌形态,我们的结果表明,标准化治疗方案可为很大比例的下颌无牙或下颌牙列缺失患者提供治疗。