Oper Dent. 2020 Jan/Feb;45(1):E32-E42. doi: 10.2341/19-078-C. Epub 2019 Nov 18.
The aim of this clinical study was to evaluate the clinical performance of Class II restorations of a high-viscosity glass ionomer material, of a bulk-fill composite resin, and of a microhybrid composite resin.
One hundred nine Class II restorations were performed in 54 patients using three different restorative materials: Charisma Smart Composite (CSC; a conventional composite resin), Filtek Bulk Fill Posterior Restorative (FBF; a high-viscosity bulk-fill composite), and Equia Forte Fil (EF; a high-viscosity glass ionomer). Single Bond Universal adhesive (3M ESPE, Neuss, Germany) was used for both conventional and bulk-fill composite resin restorations. The restorations were evaluated using modified US Public Health Service criteria in terms of retention, color match, marginal discoloration, anatomic form, contact point, marginal adaptation, secondary caries, postoperative sensitivity, and surface texture. The data were analyzed using the chi-square, Fisher, and McNemar tests.
Eighty-four restorations were evaluated at two-year recalls. There were clinically acceptable changes in composite resin restorations (FBF and CSC). In addition, no statistically significant difference was observed between the clinical performances of these materials in terms of all criteria (0.05). However, there was a statistically significant difference between the EF group and the FBF and CSC groups in all parameters except for marginal discoloration, secondary caries, and postoperative sensitivity (0.05).
The tested bulk-fill and conventional composite resins showed acceptable clinical performance in Class II cavities. However, if EF is to be used for Class II restoration, its use should be carefully considered.
本临床研究旨在评估一种高粘度玻璃离子体材料、一种块状填充型复合树脂和一种微混合复合树脂的 II 类修复体的临床性能。
在 54 名患者中使用三种不同的修复材料进行了 109 个 II 类修复:魅力智能复合材料(CSC;常规复合树脂)、Filtek Bulk Fill Posterior Restorative(FBF;高粘度块状填充型复合树脂)和 Equia Forte Fil(EF;高粘度玻璃离子体)。单键通用粘结剂(3M ESPE,德国 Neuss)用于常规和块状填充型复合树脂修复。根据改良的美国公共卫生服务标准,使用保留、颜色匹配、边缘变色、解剖形态、接触点、边缘适应性、继发龋、术后敏感和表面质地来评估修复体。使用卡方、Fisher 和 McNemar 检验对数据进行分析。
84 个修复体在两年的随访中进行了评估。复合树脂修复体(FBF 和 CSC)有临床可接受的变化。此外,在所有标准方面,这些材料的临床性能之间没有观察到统计学上的显著差异(0.05)。然而,EF 组与 FBF 和 CSC 组在所有参数上均存在统计学差异,除了边缘变色、继发龋和术后敏感(0.05)。
测试的块状填充型和常规复合树脂在 II 类窝洞中显示出可接受的临床性能。然而,如果要将 EF 用于 II 类修复,则应谨慎考虑其使用。