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一项为期三年的随机临床试验,旨在评估纳米复合树脂与混合复合树脂的临床性能和磨损情况。

Three-year randomized clinical trial to evaluate the clinical performance and wear of a nanocomposite versus a hybrid composite.

作者信息

Palaniappan Senthamaraiselvi, Bharadwaj Dimple, Mattar Daniela Lima, Peumans Marleen, Van Meerbeek Bart, Lambrechts Paul

机构信息

Leuven BIOMAT Research Cluster, Catholic University of Leuven, Leuven, Belgium.

出版信息

Dent Mater. 2009 Nov;25(11):1302-14. doi: 10.1016/j.dental.2009.06.001. Epub 2009 Jul 3.

Abstract

OBJECTIVES

Compare the 3-year clinical performance (wear as an additional parameter) of a nanocomposite and a microhybrid composite, versus ADA guidelines (2001) using direct (clinical/USPHS) and indirect (quantitative/3D laser scan and qualitative/SEM) methods, in parallel.

MATERIALS AND METHODS

18 Filtek Supreme and 17 Z100 restorations were placed in molars (split mouth model) and bonded with Single bond Adhesive. Restorations were evaluated at baseline and 6-, 12-, 24-, 36-months of clinical service according to modified USPHS criteria. The gypsum replicas at each recall were used for 3D-Pro-laser scanning to quantify wear and the epoxy resin replicas were observed under SEM to study the qualitative wear patterns. Repaired restorations were considered functionally present and not failed. Restorations were judged as failed, whenever completely replaced or when scored Delta due to material related factors impairing clinical function.

RESULTS

Filtek Supreme appeared better polishable than Z100 (p=0.0078; McNemar test). However, there were no significant differences between groups for other criteria including wear (p>0.05; Mann-Whitney U test). Qualitatively, fatigue wear at heavy occlusal contact areas (OCA), pitting at light OCA and scratches/striations along the food escape pathways were evident in almost all worn surfaces under SEM.

CONCLUSIONS

At 3 years, nanocomposite and microhybrid composite meet ADA Acceptance Guidelines (2001) for tooth-colored restorative materials for posterior teeth.

摘要

目的

采用直接(临床/美国公共卫生服务部)和间接(定量/三维激光扫描和定性/扫描电子显微镜)方法,并行比较纳米复合树脂和微混合复合树脂与美国牙科协会(ADA)2001年指南相比的3年临床性能(磨损作为附加参数)。

材料与方法

将18个Filtek Supreme修复体和17个Z100修复体置于磨牙(对侧半口模型)中,并用单键粘合剂粘结。根据改良的美国公共卫生服务部标准,在基线以及临床使用6个月、12个月、24个月和36个月时对修复体进行评估。每次复诊时的石膏模型用于三维激光扫描以量化磨损,环氧树脂模型在扫描电子显微镜下观察以研究定性磨损模式。修复后的修复体视为功能正常,未失败。当修复体完全替换或因材料相关因素影响临床功能而评分为Delta时,判定为失败。

结果

Filtek Supreme的可抛光性似乎优于Z100(p = 0.0078;McNemar检验)。然而,在包括磨损在内的其他标准方面,两组之间没有显著差异(p>0.05;Mann-Whitney U检验)。定性地说,在扫描电子显微镜下,几乎所有磨损表面在重度咬合接触区域(OCA)的疲劳磨损、轻度OCA的点蚀以及沿食物排出路径的划痕/条纹都很明显。

结论

3年后,纳米复合树脂和微混合复合树脂符合美国牙科协会2001年关于后牙牙齿颜色修复材料的验收指南。

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