A CLINICAL EVALUATION OF DIRECT VENEERS MADE WITH TWO TYPES OF COMPOSITES

Laura Irgang, R. M. Vieira, M. Erhardt, F. Coelho-de-Souza, F. Demarco
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引用次数: 1

Abstract

Objectives: the aim of this study was to provide a retrospective clinical evaluation of direct composite veneers performed with microfilled or universal composites, through two evaluation criteria (FDI and USPHS). Materials and methods: patients should be in compliance with the inclusion criteria: having a composite veneer in anterior teeth made either with microfilled or universal using composites (microhybrid/nanohybrid), conventional dentin-bonding agents and for a minimum of 6 months period in service. A calibrated blind examiner assessed the veneers using the FDI and USPHS criteria and the results were subjected to statistical analysis by the Mann-Whitney test (p<0.05). Results: Twenty-eight patients (mean age 42.9 year-old) and seventy-four composite veneers were examined. The mean period of time in service was three years, with periods varying from six months up to ten years. Three cases of total failure (veneers lost, universal composites group) occurred in the surveyed patients, out of 17 failures in total. In general, the veneers showed a clinical satisfactory outcome (77% survival rate). Concerning the two composite types, better clinical performance was observed for microfilled in relation to surface luster, surface staining, colour match and marginal adaptation. Conclusion: In this interim evaluation, direct composite veneers demonstrated an acceptable clinical behavior. Microfilled composite veneers showed a better performance compared to universal composites. The two criteria (USPHS and FDI) were similar in the clinical evaluation process. Clinical relevance: direct composite veneers have a good clinical performance, microfilled composites are interesting options regarding esthetic properties.
两种复合材料直接贴面的临床评价
目的:本研究的目的是通过两个评估标准(FDI和USPHS)对微填充或通用复合材料直接复合贴面进行回顾性临床评估。材料和方法:患者应符合纳入标准:在前牙中使用微填充或通用复合材料(微混合/纳米混合),常规牙本质粘接剂制成的复合贴面,并至少使用6个月。经过校准的盲检者使用FDI和USPHS标准对贴面进行评估,结果通过Mann-Whitney检验进行统计分析(p<0.05)。结果:共检查28例患者(平均年龄42.9岁)和74例复合贴面。平均服务时间为三年,期间从六个月到十年不等。在总共17例失败的患者中,发生了3例完全失败(贴面丢失,通用复合材料组)。总的来说,贴面显示了临床满意的结果(77%的存活率)。在两种复合类型中,微填充在表面光泽、表面染色、颜色匹配和边缘适应方面的临床表现更好。结论:在这个中期评估中,直接复合贴面表现出可接受的临床行为。与通用复合材料相比,微填充复合材料表现出更好的性能。两种标准(USPHS和FDI)在临床评价过程中相似。临床相关性:直接复合贴面具有良好的临床性能,微填充复合材料在美学性能方面是有趣的选择。
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