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一种新型通用简化粘合剂:18个月临床评估

A new universal simplified adhesive: 18-month clinical evaluation.

作者信息

Perdigão J, Kose C, Mena-Serrano A P, De Paula E A, Tay L Y, Reis A, Loguercio A D

出版信息

Oper Dent. 2014 Mar-Apr;39(2):113-27. doi: 10.2341/13-045-C. Epub 2013 Jun 26.

Abstract

PURPOSE

To evaluate the 18-month clinical performance of a multimode adhesive (Scotchbond Universal Adhesive, SU, 3M ESPE, St Paul, MN, USA) in noncarious cervical lesions (NCCLs) using two evaluation criteria.

MATERIALS AND METHODS

Thirty-nine patients participated in this study. Two-hundred restorations were assigned to four groups: ERm, etch-and-rinse + moist dentin; ERd, etch-and-rinse + dry dentin; Set, selective enamel etching; and SE, self-etch. The composite resin, Filtek Supreme Ultra (3M ESPE), was placed incrementally. The restorations were evaluated at baseline, and at 18 months, using both the World Dental Federation (FDI) and the United States Public Health Service (USPHS) criteria. Statistical analyses were performed using Friedman repeated-measures analysis of variance by rank and McNemar test for significance in each pair (α=0.05).

RESULTS

Five restorations (SE: 3; Set: 1; and ERm: 1) were lost after 18 months (p>0.05 for either criteria). Marginal staining occurred in four and 10% of the restorations evaluated (p>0.05), respectively, for USPHS and FDI criteria. Nine restorations were scored as bravo for marginal adaptation using the USPHS criteria and 38%, 40%, 36%, and 44% for groups ERm, ERd, Set, and SE, respectively, when the FDI criteria were applied (p>0.05). However, when semiquantitative scores (or SQUACE) for marginal adaptation were used, SE resulted in a significantly greater number of restorations, with more than 30% of the total length of the interface showing marginal discrepancy (28%) in comparison with the other groups (8%, 6%, and 8%, respectively, for ERm, ERd, and Set).

CONCLUSIONS

The clinical retention of the multimode adhesive at 18 months does not depend on the bonding strategy. The only differences between strategies were found for the parameter marginal adaptation, for which the FDI criteria were more sensitive than the USPHS criteria.

摘要

目的

使用两种评估标准评估一种多模式粘合剂(3M ESPE公司生产的Scotchbond通用粘合剂,SU,美国明尼苏达州圣保罗)在非龋性颈部病变(NCCLs)中的18个月临床性能。

材料与方法

39名患者参与了本研究。200个修复体被分为四组:ERm,酸蚀冲洗+湿润牙本质;ERd,酸蚀冲洗+干燥牙本质;Set,选择性釉质酸蚀;以及SE,自酸蚀。使用Filtek Supreme Ultra复合树脂(3M ESPE)分层放置。在基线时以及18个月时,使用世界牙科联盟(FDI)和美国公共卫生服务(USPHS)标准对修复体进行评估。使用Friedman秩次重复测量方差分析和McNemar检验进行统计学分析,以确定每对数据的显著性(α=0.05)。

结果

18个月后有5个修复体(SE组:3个;Set组:1个;ERm组:1个)脱落(两种标准下p>0.05)。对于USPHS和FDI标准,分别有4%和10%的评估修复体出现边缘染色(p>0.05)。使用USPHS标准时,9个修复体边缘适应性被评为优秀;应用FDI标准时,ERm、ERd、Set和SE组的修复体边缘适应性分别为38%、40%、36%和44%(p>0.05)。然而,当使用边缘适应性的半定量评分(或SQUACE)时,与其他组(ERm、ERd和Set组分别为8%、6%和8%)相比,SE组有显著更多修复体的界面总长度超过30%出现边缘差异(28%)。

结论

多模式粘合剂在18个月时的临床保留率不取决于粘结策略。在边缘适应性参数方面发现了不同策略之间的唯一差异,对于该参数,FDI标准比USPHS标准更敏感。

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