首页> 美国卫生研究院文献>International Journal of Environmental Research and Public Health >A Novel Full-Digital Protocol (SCAN-PLAN-MAKE-DONE®) for the Design and Fabrication of Implant-Supported Monolithic Translucent Zirconia Crowns Cemented on Customized Hybrid Abutments: A Retrospective Clinical Study on 25 Patients
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A Novel Full-Digital Protocol (SCAN-PLAN-MAKE-DONE®) for the Design and Fabrication of Implant-Supported Monolithic Translucent Zirconia Crowns Cemented on Customized Hybrid Abutments: A Retrospective Clinical Study on 25 Patients

机译:一种新颖的全数字协议(SCAN-PLAN-MAKE-DONE®)用于设计和制造结合在定制混合基台上的植入物支撑的整体式半透明氧化锆冠:25位患者的回顾性临床研究

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摘要

Purpose: To present a novel, full-digital protocol for the design and fabrication of implant-supported monolithic translucent zirconia crowns cemented on customized hybrid abutments. Methods: The present retrospective clinical study was based on data from patients who had been treated with single Morse-taper connection implants (Exacone®, Leone Implants, Florence, Italy) and were prosthetically restored with monolithic translucent zirconia crowns, cemented on customized hybrid abutments. The full-digital protocol (SCAN-PLAN-MAKE-DONE®) consisted of 8 phases: (1) intraoral scan of the implant position with scanbody; (2) computer-assisted design (CAD) of the individual abutment (saved as “supplementary abutment design” in external folder) and temporary crown; (3) milling of the individual zirconia abutment and of the temporary polymethyl-methacrylate (PMMA) crown, with extraoral cementation of the zirconia abutment on the relative titanium bonding base, to generate an individual hybrid abutment; (4) clinical application of the individual hybrid abutment and cementation of the temporary PMMA crown; (5) two months later, intraoral scan of the individual hybrid abutment in position; (6) CAD of the final crown with margin line design on the previously saved “supplementary abutment design”, superimposed on the second scan of the abutment in position; (7) milling of the final crown in monolithic translucent zirconia, sintering, and characterization; and (8) clinical application of the final crown. All patients were followed for a period of 1 year. The primary outcomes of this study were the marginal adaptation of the final crown (checked clinically and radiographically), the quality of occlusal and interproximal contact points at delivery, and the aesthetic integration; the secondary outcomes were the 1-year survival and success of the implant-supported restoration. An implant-supported restoration was considered successful in the absence of any biological or prosthetic complication, during the entire follow-up period. Results: In total, 25 patients (12 males, 13 females; 26–74 years of age; mean age 51.1 ± 13.3 years) who had been restored with 40 implant-supported monolithic translucent zirconia crowns were included in this study. At delivery, the marginal adaptation was perfect for all crowns. However, there were occlusal issues (2/40 crowns: 5%), interproximal issues (1/40 crowns: 2.5%), and aesthetic issues (1/40 crowns: 2.5%). The overall incidence of issues at delivery was therefore 10% (4/40 crowns). At 1 year, one implant failed; thus the survival of the restorations was 97.5% (39/40 crowns in function). Among the surviving implant-supported restorations, three experienced complications (one loss of connection between the hybrid abutment and the implant, one decementation of the zirconia abutment, and one decementation of the zirconia crown). The success of restorations amounted to 92.4%. Conclusions: The restoration of single Morse-taper connection implants with monolithic translucent zirconia crowns cemented on customized hybrid abutments via the novel SCAN-PLAN-MAKE-DONE® full-digital protocol seems to represent a reliable treatment option. However, further studies on a larger number of patients and dealing with different prosthetic restorations (such as implant-supported fixed partial prostheses) are needed to confirm the validity of this protocol.
机译:目的:提出一种新颖的全数字协议,用于设计和制造粘结在定制混合基台上的植入物支撑的单块半透明氧化锆冠。方法:本回顾性临床研究基于以下患者的数据:使用单摩尔斯锥连接植入物(Exacone ®,Leone植入物,佛罗伦萨,意大利)进行治疗的患者,并用整体半透明氧化锆修复牙冠,固定在定制的混合基台上。全数字协议(SCAN-PLAN-MAKE-DONE ®)分为8个阶段:(1)用扫描体对植入物位置进行口腔内扫描; (2)单个基台的计算机辅助设计(CAD)(在外部文件夹中另存为“辅助基台设计”)和临时牙冠; (3)研磨单个的氧化锆基台和临时的聚甲基丙烯酸甲酯(PMMA)牙冠,并在相对的钛键合基体上进行氧化锆基台的口腔外固结,以产生单个的混合基台; (4)PMMA临时牙冠的单个混合基台和胶结的临床应用; (5)两个月后,对单个混合基台进行口腔内扫描; (6)在先前保存的“辅助基台设计”上以边缘线设计制作最终牙冠的CAD,并叠加在基台的第二次扫描上; (7)在整体式半透明氧化锆中研磨最终的冠状物,进行烧结和表征; (八)最终牙冠的临床应用。所有患者均接受了为期一年的随访。这项研究的主要结果是最终冠的边缘适应性(临床和影像学检查),分娩时咬合和近端接触点的质量以及美学融合。次要结果是植入物支持的修复物的1年生存率和成功率。在整个随访期间,在没有任何生物或修复并发症的情况下,植入物支持的修复被认为是成功的。结果:本研究共纳入了25例患者,其中40例植入物支持的整体式半透明氧化锆冠修复了患者(男性12例,女性13例;年龄26-74岁;平均年龄51.1±13.3岁)。交付时,边缘调整适用于所有表冠。但是,存在咬合问题(2/40牙冠:5%),近牙间问题(1/40牙冠:2.5%)和美学问题(1/40牙冠:2.5%)。因此,发货时问题的总发生率为10%(4/40冠)。一年后,一枚植入物失败;因此,修复体的存活率为97.5%(功能为39/40冠)。在幸存的种植体支持的修复体中,有3种经历了并发症(一种是混合基台与种植体之间的连接断开,一种氧化锆基台的脱落,另一种是氧化锆牙冠的脱落)。修复成功率为92.4%。结论:通过新颖的SCAN-PLAN-MAKE-DONE ®全数字化方案,用固定在定制混合基台上的整体式半透明氧化锆冠修复单个莫氏锥度连接植入物似乎代表了一种可靠的治疗选择。但是,需要对大量患者进行进一步研究,并应对不同的修复体(例如植入物支持的固定部分修复体),以确认该方案的有效性。

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