*Leyla Kerimova Köse, DDS, Baskent University Faculty of Dentistry, Department of Restorative Dentistry, Ankara, Turkey.
Burcu Oglakci, DDS, Bezmialem Vakif University Faculty of Dentistry, Department of Restorative Dentistry, Istanbul, Turkey.
Oper Dent. 2024 Sep 1;49(5):551-563. doi: 10.2341/23-128-L.
This study aimed to analyze the presence of defects within the adhesive interface formed with five bioactive dental materials and caries-affected dentin concerning the timing of radiotherapy (before or after the restorative procedures) by micro-CT.
A total of 96 carious human molars were randomly allocated into the following groups based on the timing of the radiotherapy sequence: radiotherapy followed by restoration (RT1) or restoration followed by radiotherapy (RT2). Then, six subgroups were established within these groups based on the type of materials used (n=8). Following cavity preparation and caries removal, a universal adhesive (G-Premio Bond) was administered in self-etch mode or accompanied by applying suitable cavity conditioners according to the manufacturers' guidelines. Subsequently, restorations were performed using five bioactive restorative materials (resin-modified glass-ionomer [Fuji II LC], high-viscosity glass-ionomer hybrid [EQUIA Forte HT], giomer [Beautifil II], alkasite [Cention N], and dual-cure bulk-fill composite [Activa Bioactive Restorative]) and a conventional microhybrid resin composite (Filtek Z250). The radiotherapy regimen encompassed 60 Grays (Gy) administered at a rate of 2 Gy/day over 6 weeks, 5 days a week. Micro-CT analysis was employed to assess adhesive defects at the interface between caries-affected dentin and the restorations. The data were analyzed using Kruskal-Wallis, Mann-Whitney U, and Dunn tests (α=0.05).
RT2 caused significantly higher adhesive defects than RT1 for the Filtek Z250 and Activa Bioactive Restorative subgroups (p<0.05). For RT1, no significant differences were found in adhesive defects among all tested subgroups (p>0.05). By contrast, for RT2, adhesive defects were significantly higher for the Activa Bioactive Restorative and Cention N subgroups than for the EQUIA Forte HT and Beautifil II subgroups (p<0.05).
When using most bioactive restorative materials, the timing of radiotherapy had no significant influence on the adhesive interface. Regarding restoration following a radiotherapy protocol, a favorable impact was identified with high-viscosity glass ionomer hybrid cement and giomer bioactive restorations compared with dual-cure bioactive bulk-fill composite and alkasite restorations.
本研究旨在通过微 CT 分析在放疗(修复前或修复后)时机不同的情况下,五种生物活性牙科材料与龋损牙本质之间的黏附界面是否存在缺陷。
共 96 颗人磨牙随机分为两组,根据放疗顺序的时间:放疗后修复(RT1)或修复后放疗(RT2)。然后,在这些组内根据材料类型(n=8)进一步分为六个亚组。在牙体预备和去龋后,根据制造商的指南,以自酸蚀模式或同时使用合适的牙本质处理剂,涂覆通用黏结剂(G-Premio Bond)。随后,使用五种生物活性修复材料(树脂改良型玻璃离子体[Fuji II LC]、高粘度玻璃离子体混合体[EQUIA Forte HT]、玻璃离子体[Beautifil II]、alkasite [Cention N]和双重固化块状填充复合材料[Activa Bioactive Restorative])和传统的微混合树脂复合材料(Filtek Z250)进行修复。放疗方案为 60 格雷(Gy),分 6 周,每周 5 天,每天 2 Gy。采用微 CT 分析评估龋损牙本质与修复体之间的黏附缺陷。采用 Kruskal-Wallis、Mann-Whitney U 和 Dunn 检验(α=0.05)对数据进行分析。
对于 Filtek Z250 和 Activa Bioactive Restorative 亚组,RT2 引起的黏附缺陷显著高于 RT1(p<0.05)。对于 RT1,所有测试亚组之间的黏附缺陷无显著差异(p>0.05)。相反,对于 RT2,Activa Bioactive Restorative 和 Cention N 亚组的黏附缺陷显著高于 EQUIA Forte HT 和 Beautifil II 亚组(p<0.05)。
当使用大多数生物活性修复材料时,放疗时机对黏附界面没有显著影响。对于放疗方案后的修复,与双重固化生物活性块状填充复合材料和 alkasite 修复体相比,高粘度玻璃离子混合水泥和 giomer 生物活性修复体具有更好的影响。