Oter B, Deniz K, Cehreli S B
Department of Pediatric Dentistry, Başkent University İstanbul Research and Training Hospital, İstanbul, Turkey.
Department of Oral and Maxillofacial Surgery, Başkent University İstanbul Research and Training Hospital, İstanbul, Turkey.
Niger J Clin Pract. 2018 Nov;21(11):1484-1491. doi: 10.4103/njcp.njcp_151_18.
In pediatric clinic practice, bulk fill composite is gaining importance for shortened clinical time with a limited shrinkage.
The present study evaluated the 1 year clinical performance of bulk fill composite and conventional composite material in occlusal caries of primary molars.
The study was designed as randomized single blind clinical trial and a total of 160 restorations were placed in the cavities of the 80 patients.
Each patient received two restorations: one with Filtek Z250 (3M ESPE, St Paul, MN 55144, USA); the other restored with Filtek Bulk-Fill Restorative (FBF) (3M ESPE, St Paul, MN, USA). All restorations were clinically evaluated after baseline, 6 months, and 1 year in terms of retention, color matching, marginal discoloration, marginal adaptation, secondary caries, surface texture, anatomic form, and postoperative sensitivity.
Besides the descriptive statistical methods, the Friedman test and the Wilcoxon Signed Ranks were used.
Bulk fill was found to be worse compared to control with regard to postoperative sensitivity at baseline without statistical significance (P > 0.05). All of the evaluated restorations were retained and were still in function after 1 year (P > 0.05). With respect to marginal discoloration and marginal integrity, there were no significant differences between bulk fill and composite restorations at all intervals (P > 0.05).
Based on this short term data, restoration of Class I cavities with both bulk fill and conventional composite restorations can be performed successfully. Postoperative sensitivity can be an issue with the restorations completed with Bulk fill restorative.
在儿科临床实践中,大块充填复合树脂因能缩短临床操作时间且收缩率有限而愈发重要。
本研究评估了大块充填复合树脂和传统复合树脂材料用于乳牙咬合面龋的1年临床性能。
本研究设计为随机单盲临床试验,共80例患者的龋洞置入了160颗修复体。
每位患者接受两种修复:一种用Filtek Z250(美国明尼苏达州圣保罗市3M ESPE公司,邮编55144);另一种用Filtek大块充填修复材料(FBF)(美国明尼苏达州圣保罗市3M ESPE公司)。所有修复体在基线、6个月和1年后进行临床评估,评估内容包括固位、颜色匹配、边缘变色、边缘适应性、继发龋、表面质地、解剖形态和术后敏感情况。
除描述性统计方法外,还使用了Friedman检验和Wilcoxon符号秩检验。
在基线时,大块充填修复体在术后敏感方面比对照组差,但无统计学意义(P>0.05)。所有评估的修复体均得以保留,1年后仍在发挥功能(P>0.05)。在所有时间点,大块充填修复体与复合树脂修复体在边缘变色和边缘完整性方面均无显著差异(P>0.05)。
基于这些短期数据,I类洞用大块充填复合树脂修复体和传统复合树脂修复体均可成功修复。大块充填修复体完成的修复可能存在术后敏感问题。