Department of Preventive and Restorative Sciences, School of Dental Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
J Esthet Restor Dent. 2022 Dec;34(8):1213-1220. doi: 10.1111/jerd.12948. Epub 2022 Aug 7.
To evaluate and compare the clinical performance of two nano-hybrid giomer restorative composite materials after 5 years.
Forty-four pairs of restorations (total n = 88) of a flowable giomer (Beautifil Flow Plus F00; Shofu Inc., Kyoto, Japan) and a conventional nano-hybrid giomer restorative material (Beautifil II; Shofu Inc.) were placed in Class I cavities after the application of a dentin adhesive (FL-Bond II; Shofu Inc.) and a flowable liner (Beautifil Flow Plus F03; Shofu Inc). After 5 years, 32 pairs of restorations were assessed using the modified United States Public Health Service criteria. Both tested materials were compared using Fisher's exact test and each tested clinical criterion for each material was analyzed separately with respect to different follow-up periods using Friedman's test (a = 0.05).
None of the restorations showed complete retention loss, post-operative sensitivity, secondary caries or color change. There were no significant changes to any of the clinical criteria for each material during the 5-year evaluation period (p > 0.05) and no significant differences between the two materials in all clinical parameters after 5 years (p > 0.05).
Five-year clinical performance of both two nano-hybrid giomer restorative materials was comparably acceptable and not significantly different for any of the parameters evaluated.
Nano-hybrid giomer-based materials are clinically acceptable for the restoration of occlusal cavities as they demonstrate excellent performance after 5 years.
评价和比较两种纳米混合玻璃离子修复复合材料在 5 年后的临床性能。
44 对修复体(共 88 个),分别为一种流动型玻璃离子(Beautifil Flow Plus F00;Shofu Inc.,京都,日本)和一种传统纳米混合玻璃离子修复材料(Beautifil II;Shofu Inc.),在应用牙本质粘结剂(FL-Bond II;Shofu Inc.)和流动型衬垫(Beautifil Flow Plus F03;Shofu Inc.)后,放置在 I 类窝洞内。5 年后,使用改良美国公共卫生服务标准评估 32 对修复体。使用 Fisher 确切检验比较两种测试材料,并用 Friedman 检验分别分析每种材料的每个测试临床标准,针对不同的随访时间(α=0.05)。
没有任何修复体出现完全保留损失、术后敏感、继发龋或颜色变化。在 5 年评估期间,每种材料的所有临床标准均未发生显著变化(p>0.05),5 年后两种材料的所有临床参数均无显著差异(p>0.05)。
两种纳米混合玻璃离子修复材料在 5 年的临床性能均可接受,且在评估的任何参数上均无显著差异。
基于纳米混合玻璃离子的材料在 5 年后表现出优异的性能,可用于修复牙合面窝洞,临床效果可接受。