在基台水平进行种植体稳定性测量的可靠性。回顾性临床试验及体外研究。

José Joaquim da Rocha Ferreira, Luís Filipe Meira Machado, Marco Paulo Lages Parente, João Carlos Tomás Ramos
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引用次数: 0

摘要

目的-一次使用一个基台的概念包括间接测量种植体的稳定性,而无需移除先前放置的基台。本研究旨在验证在基台水平测量种植体稳定商是否与在种植体水平获得的值相同。材料和方法:回顾性临床研究和体外研究。对于每项研究,在种植体水平测量的种植体稳定商定义了对照组。试验组分为3个子组,分别对应3种不同的多单元基台:直基台(MUAS)和17°角基台(MUA17),均为2.5 mm环;30°角基台(MUA30),均为3.5 mm环。数据比较采用Wilcoxon符号秩检验和Kruskal-Wallis检验。结果-临床结果:对照组(种植体59枚;79.14 [SD=3.39])的测量值显著高于对照组(73.22 [SD=8.54]);ClinicalMUA17亚组(16个基台;66.38 [SD=1.20])和ClinicalMUA30(16个基台;69.19 [SD=0.96])的测量值低于对照组。ClinicalMUAS(27个基台;79.67 [SD=1.48])亚组与对照组比较(相关系数为0.68)。体外结果:对照组测量(36个植入物;68例,02例[SD=1.81])显著高于试验组(62.57例[SD=2.87])。对照组测量值也高于各测试亚组(各12个基牙):MUAS (65.44 [SD=0.73]);Mua17 (60 [sd =0.43]);Mua30 (62.29 [sd = 0.35])。结论:根据本研究的结果,在基台水平测定种植体稳定商的结果低于在种植体水平测量的结果,并且可能不能准确反映种植体的实际稳定性。未来的研究将需要探索种植体水平和基台水平测量的种植体稳定商之间是否存在相关性,以及在何种情况下存在相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reliability of the Implant Stability Measurement Performed at the Abutment Level. A Retrospective Clinical Trial and an In Vitro Research.

Purpose - The use of the one abutment one time concept involves the indirect measurement of the implant stability without removing the previously placed abutment. This study aims to verify whether measuring the implant stability quotient at the abutment level is identical to the value obtained at the implant level. Material And Methods - A retrospective clinical study and an in vitro study were performed. For each study, the implant stability quotient measured at the implant level defined the control groups. The values obtained after the abutment seating composed the test groups, which were divided into three test sub-groups, corresponding to three different multi-unit abutments: straight (MUAS) and 17° angled (MUA17), both with 2.5 mm collar, and 30° angled (MUA30) with 3.5 mm collar. Data was compared by the Wilcoxon signed rank test and Kruskal-Wallis test. Results - Clinical results: the control group (59 implants; 79.14 [SD=3.39]) showed significantly higher measurements than the test group (73.22 [SD=8.54]); the sub-groups ClinicalMUA17 (16 abutments; 66.38 [SD=1.20]) and ClinicalMUA30 (16 abutments; 69.19 [SD=0.96]) measurements were lower than the control group. No differences were found for the ClinicalMUAS (27 abutments; 79.67 [SD=1.48]) sub-group when compared with the control group (correlation of 0.68). In vitro results: the control group measurements (36 implants; 68,02 [SD=1.81]) were significantly higher than the test group (62.57 [SD=2.87]). The control group measurements were also higher than each test sub-group (12 abutments each): MUAS (65.44 [SD=0.73]); MUA17 (60 [SD=0.43]); MUA30 (62.29 [SD = 0.35]). Conclusions: Based on the results of this study, determining the implant stability quotient at abutment level results in lower values than measurements at implant level, and may not accurately reflect the actual implant stability. Future research will need to explore whether, and under what circumstances a correlation exists between the implant stability quotient measured at the implant level and at the abutment level.

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