...
首页> 外文期刊>Medical principles and practice: international journal of the Kuwait University, Health Science Centre >Clinical Evaluation of Resin-Based Composites in Posterior Restorations: A 3-Year Study
【24h】

Clinical Evaluation of Resin-Based Composites in Posterior Restorations: A 3-Year Study

机译:树脂基复合材料在后路修复中的临床评估:3年研究

获取原文

摘要

Objectives: The aim of this study was to evaluate the clinical performance of a nanohybrid and a microhybrid composite in class I and II restorations after 3 years. Subjects and Methods: A total of 82 class I and class II restorations were performed in 31 patients (10 males and 21 females) using Grandio and QuiXfil with self-etch adhesives (Futurabond and Xeno III). The restorations were clinically evaluated by 2 operators 1 week after placement (baseline) and at 6 months and 1, 2, and 3 years using modified United States Public Health Service (USPHS) criteria. At the 3-year follow-up, 62 class I and class II cavities were reevaluated in 23 patients (7 males and 16 females). Statistical analysis was performed using Pearson's χ2 and Fisher's exact tests (p < 0.05). Results: At the 6-month follow-up, all restorations received Alfa scores with respect to each evaluation criterion. At the 1-year follow-up, 2 QuiXfil restorations had to be replaced and Grandio restorations started to deteriorate in terms of marginal adaptation. At the end of 2 years, 9 Grandio restorations showed significant deterioration of the surface properties, demonstrating Bravo scores. At the end of 3 years, no significant differences were observed regarding color match, marginal adaptation, secondary caries, marginal discoloration, and anatomic form loss between the evaluated materials in 25 class I and 37 class II restorations. At the 3-year follow-up, Grandio restorations had 21% Bravo scores and showed significant deterioration of the surface properties, which were still clinically acceptable according to USPHS criteria. Three QuiXfil and 1 Grandio restorations were replaced because of secondary caries and loss of retention. Conclusions: Both the nanohybrid (Grandio) and the microhybrid (QuiXfil) composites were clinically functional after 3 years.
机译:目的:本研究的目的是评估3年后纳米混合和微混合复合材料在I类和II类修复物中的临床表现。研究对象和方法:使用Grandio和QuiXfil以及自蚀刻胶(Futurabond和Xeno III)对31例患者(10例男性和21例女性)进行了82例I级和II级修复。使用修改后的美国公共卫生服务(USPHS)标准,由两名操作人员在放置后1周(基线),分别在6个月,1、2和3年对修复体进行临床评估。在3年的随访中,对23例患者(男性7例,女性16例)中的62个I级和II级腔进行了重新评估。使用Pearson的χ 2 和Fisher的精确检验进行统计学分析(p <0.05)。结果:在6个月的随访中,所有修复体均获得了针对每个评估标准的Alfa评分。在为期1年的随访中,必须更换2个QuiXfil修复体,而Grandio修复体的边缘适应性开始恶化。在2年结束时,有9个Grandio修复体显示了表面性能的显着下降,显示了Bravo得分。在3年末,在25种I类和37种II类修复物中,在颜色匹配,边缘适应性,继发龋齿,边缘变色和解剖形态损失方面没有观察到显着差异。在为期3年的随访中,Grandio修复体的Bravo评分为21%,并且表面性能明显下降,根据USPHS标准,临床上仍可接受。由于继发龋齿和固位力丧失,更换了3个QuiXfil和1个Grandio修复体。结论:3年后,纳米混合(Grandio)和微混合(QuiXfil)复合材料均具有临床功能。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号