Department of Prevention and Communal Dentistry, Sechenov First Moscow State Medical University, 119992 Moscow, Russia.
Int J Environ Res Public Health. 2019 Jan 24;16(3):317. doi: 10.3390/ijerph16030317.
To present a novel, full-digital protocol for the design and fabrication of implant-supported monolithic translucent zirconia crowns cemented on customized hybrid abutments.
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.
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%.
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.
介绍一种新型的全数字化方案,用于设计和制作通过定制混合基台粘接的种植体支持的整体式半透明氧化锆冠。
本回顾性临床研究基于接受莫氏锥度连接种植体(Exacone,Leone Implants,佛罗伦萨,意大利)治疗并通过定制混合基台粘接的整体式半透明氧化锆冠修复的患者数据。全数字化方案(SCAN-PLAN-MAKE-DONE)包括 8 个阶段:(1)使用扫描体对内种植体位置进行口腔内扫描;(2)进行个性化基台(保存为“补充基台设计”在外部文件夹中)和临时冠的计算机辅助设计(CAD);(3)个体化氧化锆基台和临时聚甲基丙烯酸甲酯(PMMA)冠的铣削,将氧化锆基台外粘接在相对的钛粘接基底上,以生成个体化混合基台;(4)个体化混合基台的临床应用和临时 PMMA 冠的粘接;(5)两个月后,对在位的个体化混合基台进行口腔内扫描;(6)在之前保存的“补充基台设计”上进行带有边缘线设计的最终冠的 CAD,叠加在在位基台的第二次扫描上;(7)整体式半透明氧化锆最终冠的铣削、烧结和特性;(8)最终冠的临床应用。所有患者均随访 1 年。本研究的主要结局为最终冠的边缘适应性(临床和放射学检查)、交付时的咬合和邻面接触点的质量以及美学整合;次要结局为种植体支持修复的 1 年存活率和成功率。在整个随访期间,没有任何生物学或修复体并发症的情况下,种植体支持修复被认为是成功的。
共有 25 名患者(12 名男性,13 名女性;26-74 岁;平均年龄 51.1±13.3 岁)接受了 40 个种植体支持的整体式半透明氧化锆冠修复,纳入本研究。在交付时,所有冠的边缘适应性均完美。然而,存在咬合问题(2/40 冠:5%)、邻面问题(1/40 冠:2.5%)和美学问题(1/40 冠:2.5%)。因此,交付时的总体问题发生率为 10%(4/40 冠)。1 年后,1 颗种植体失败;因此,修复体的存活率为 97.5%(在位的 40 个种植体支持修复体中的 39 个)。在存活的种植体支持修复体中,有 3 个发生并发症(1 个混合基台与种植体之间的连接丧失,1 个氧化锆基台脱粘,1 个氧化锆冠脱粘)。修复体的成功率为 92.4%。
通过新型 SCAN-PLAN-MAKE-DONE 全数字化方案,用定制混合基台粘接的整体式半透明氧化锆冠修复单莫氏锥度连接种植体似乎是一种可靠的治疗选择。然而,需要进一步对更多患者进行研究,并涉及不同的修复体(如种植体支持的固定局部义齿),以确认该方案的有效性。