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Seven-year clinical performance of resin composite versus resin-modified glass ionomer restorations in noncarious cervical lesions

机译:树脂复合材料与树脂修饰的玻璃离子聚合物修复物在非龋性宫颈病变中的七年临床表现

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Purpose: The purpose of this study was to comparatively assess the seven-year clinical performance of a one-bottle etch-and-rinse adhesive with resin composite (RC) and resin-modified glass ionomer (RMGI) restorations in noncarious cervical lesions. Methods and Materials: One operator placed 70 restorations (35 restorations in each group) in 30 patients under rubber dam isolation without mechanical preparation. The restorations were directly assessed by two independent examiners, using modified US Public Health Service criteria at baseline and 6, 12, 24, 60, and 84 months. The obtained data were tabulated and statistically analyzed using the Fisher and McNemar tests. A difference was significant if p<0.05. Results: Twenty patients were available for recall after seven years (66.6%), and 25 RC and 26 RMGI restorations out of 70 restorations were evaluated. Excellent agreement was registered for all criteria between examiners (κ≥0.85). Alfa and bravo scores were classified as clinically acceptable. The McNemar test detected significant differences within RC restorations between baseline and seven-year evaluations for anatomic form, marginal integrity, and retention (p<0.05). For RMGI restorations, a significant difference was identified for marginal integrity (p<0.05). As to material comparison, the Fisher exact showed a better retention performance for RMGI restorations than for RC restorations (p<0.05). Twelve composite restorations were dislodged (52.0% retention) and three ionomer restorations were lost (88.5% retention). The cumulative success rate for RC and RMGI was 30% and 58.1%, respectively. Conclusions: After seven years of service, the clinical performance of RMGI restorations was superior to that of the adhesive system/resin composite restorations in this study.
机译:目的:本研究的目的是比较评估一瓶非树脂宫颈病变中含树脂复合物(RC)和树脂改性玻璃离子交联剂(RMGI)的单瓶蚀刻和冲洗粘合剂的七年临床表现。方法和材料:一名操作员在没有机械准备的情况下将30例患者的70个修复体(每组35个修复体)置于橡胶坝隔离下。由两名独立的检查员在基线以及第6、12、24、60和84个月使用修改后的美国公共卫生服务标准直接评估修复体。使用Fisher和McNemar检验将获得的数据制成表格并进行统计分析。如果p <0.05,则差异显着。结果:七年后有20例患者可供召回(66.6%),并且在70个修复物中评估了25个RC和26个RMGI修复。检验员之间所有标准均达成了极好的协议(κ≥0.85)。 Alfa和bravo得分被归类为临床可接受。 McNemar测试在基线和7年评估的解剖形态,边缘完整性和保留之间评估了RC修复体之间的显着差异(p <0.05)。对于RMGI修复体,其边缘完整性存在显着差异(p <0.05)。在材料比较方面,Fisher精确度显示RMGI修复体比RC修复体具有更好的保留性能(p <0.05)。移出十二个复合修复体(保留52.0%),丢失三个离聚物修复体(保留88.5%)。 RC和RMGI的累计成功率分别为30%和58.1%。结论:经过7年的服务,RMGI修复体的临床性能优于本研究中的粘合系统/树脂复合修复体。

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