Ozer F, Irmak O, Yakymiv O, Mohammed A, Pande R, Saleh N, Blatz M
Oper Dent. 2021 Jan 1;46(1):E60-E67. doi: 10.2341/17-353-C.
The clinical performance of both conventional and flowable giomer restorative materials was particularly good in Class I restorations after three years of service.
This study evaluated and compared the clinical performance of a flowable and a conventional giomer restorative material after three years. Forty-four pairs of restorations (total n=88) were placed in Class I cavities with either a flowable giomer (Beautifil Flow Plus F00; Shofu Inc, Kyoto, Japan) or a conventional giomer restorative material (Beautifil II; Shofu Inc) after the application of a dentin adhesive (FL-Bond II; Shofu Inc) and a flowable liner (Beautifil Flow Plus F03; Shofu Inc). After 3 years, 39 pairs of restorations were evaluated with the modified United States Public Health Service criteria, and digital color photographs of restorations were taken at each patient visit. The evaluation parameters were as follows: color match, marginal integrity, marginal discoloration, retention, secondary caries formation, anatomic form, surface texture, and postoperative sensitivity. Evaluations were recorded as a clinically ideal situation (Alpha), a clinically acceptable situation (Bravo), or a clinically unacceptable situation (Charlie). Data were analyzed with Fisher's exact and McNemar tests (α=0.05).None of the restorations showed retention loss, postoperative sensitivity, secondary caries, or color change. The performance of Beautifil II in terms of marginal integrity, marginal discoloration, and surface anatomic form was significantly lower at the 36-month follow-up than at baseline (p=0.007). There were no significant differences between the baseline and 36-month follow-up scores for the other criteria for Beautifil II (p>0.05). No differences were found between the baseline and the 36-month follow-up scores for any of the criteria for Beautifil Flow Plus F00 (p>0.05). No statistically significant difference in overall clinical performance was found between the 2 materials after 36 months (p>0.05).The three-year clinical performance of both restorative materials (Beautifil Flow Plus F00 and Beautifil II) was very good and not significantly different for any of the parameters evaluated.
在使用三年后,传统型和可流动型聚硅氧烷修复材料在I类修复中的临床性能都特别好。
本研究评估并比较了可流动型和传统型聚硅氧烷修复材料在三年后的临床性能。在应用牙本质粘结剂(FL-Bond II;日本京都松风株式会社)和可流动衬层(Beautifil Flow Plus F03;日本京都松风株式会社)后,将44对修复体(共88个)置于I类窝洞中,分别使用可流动型聚硅氧烷(Beautifil Flow Plus F00;日本京都松风株式会社)或传统型聚硅氧烷修复材料(Beautifil II;日本京都松风株式会社)。三年后,根据修改后的美国公共卫生服务标准对39对修复体进行评估,并在每次患者就诊时拍摄修复体的数码彩色照片。评估参数如下:颜色匹配、边缘完整性、边缘变色、固位、继发龋形成、解剖形态、表面质地和术后敏感性。评估记录为临床理想情况(Alpha)、临床可接受情况(Bravo)或临床不可接受情况(Charlie)。数据采用Fisher精确检验和McNemar检验进行分析(α=0.05)。所有修复体均未出现固位丧失、术后敏感、继发龋或颜色变化。在36个月随访时,Beautifil II在边缘完整性、边缘变色和表面解剖形态方面的性能显著低于基线水平(p=0.007)。Beautifil II其他标准在基线和36个月随访评分之间无显著差异(p>0.05)。Beautifil Flow Plus F00任何标准在基线和36个月随访评分之间均未发现差异(p>0.05)。36个月后,两种材料在总体临床性能上无统计学显著差异(p>0.05)。两种修复材料(Beautifil Flow Plus F00和Beautifil II)三年的临床性能都非常好,在评估的任何参数上均无显著差异。