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树脂基直接后牙修复体与玻璃离子修复体的临床疗效——临床结局参数的最新荟萃分析

Clinical efficacy of resin-based direct posterior restorations and glass-ionomer restorations - An updated meta-analysis of clinical outcome parameters.

作者信息

Heintze Siegward D, Loguercio Alessandro D, Hanzen Taíse A, Reis Alessandra, Rousson Valentin

机构信息

R&D, Ivoclar Vivadent AG, Schaan, Liechtenstein.

Department of Restorative Dentistry, State University of Ponta Grossa, Brazil.

出版信息

Dent Mater. 2022 May;38(5):e109-e135. doi: 10.1016/j.dental.2021.10.018. Epub 2022 Feb 24.

Abstract

OBJECTIVE

The present review is an update of a systematic review that has been published in 2012. Meanwhile, many new clinical trials on resin composites had been published. New materials such as bulk fill resin composites and new glass-ionomer (GIC) based materials had been introduced. The focus of this review was to evaluate the longevity in relation to the material class and adhesive class, while adjusting for a possible study bias effect.

MATERIAL AND METHODS

The database PUBMED/SCOPUS were searched for clinical trials on posterior resin composites. The inclusion criteria were: (1) studies published between 2000 and 2019, (2) prospective clinical trial with at least 2 years of observation; (2) minimal number of restorations at last recall = 20; (3) report on drop-out rate; (4) report of operative technique and used materials; (5) utilisation of Ryge, modified Ryge or FDI evaluation criteria. The bias of each study was assessed by two independent reviewers using Cochrane Collaboration's tool for assessing risk of bias in randomised trials. For the statistical analysis, linear mixed models fitted on the individual data recorded along time have been used with random effects to account for study, patients and experiment effects. P-values smaller than 0.05 were considered significant.

RESULTS

Of the 423 clinical trials, 62 studies (including 110 experiments) met the inclusion criteria. Material class was divided according to the composite filler in microhybrid (39 experiments/2807 restorations), nanohybrid (24 experiments/1254 restorations), and hybrid (22 experiments/1255 restorations). So-called bulk fill materials were treated as a separate category (9 experiments/506 restorations) as were the GIC (11 experiments/2121 restorations) and the compomer materials (5 experiments/238 restorations). Only one study (1.6%) had low risk of bias, 42 (67.7%) were assessed to have unclear risk of bias and 19 (30.6%) had a high risk of bias. In 52.3% of the studies Class II and Class I restorations had been placed. After 10 years, the survival rate for resin composite restorations dropped to about 85-90% with no significant difference between hybrid, microhybrid and nao-hybrid resin materials. The main reasons for restoration replacement were bulk fractures and wear, which accounted for a about 70% of replacements. Caries at the restorative margins accounted for about 20% of the replacements, and retention loss, inacceptable colour match or marginal integrity, endodontic treatment or cusp fracture for about 10% of the replacements of the resin composite restorations. For compomer and GIC restorations the mean overall survival rate was about 80% after 6 years. For GIC, the main reasons for failure were substantial loss of anatomical contour along with loss of proximal contacts and retention loss. Mainly fractures reduced the longevity of compomers restorations. Also, there was no statistically significant difference between hybrid, micro-hybrid, nano-hybrid and bulk fill resin composites with regard to colour match, surface texture, material fractures, and anatomical form.

CONCLUSIONS

Posterior resin composite restorations that were placed with the enamel etch technique showed the best overall performance; the longevity was not significantly influenced by the filler type or viscosity of resin composite material. With regard to colour match, surface texture and anatomical form, nanohybrid resins were not significantly superior to hybrid or microhybrid resin composites. Compomer and GIC restorations demonstrated considerable shortcomings and had a significant shorter longevity.

摘要

目的

本综述是对2012年发表的一篇系统综述的更新。与此同时,许多关于树脂复合材料的新临床试验已经发表。诸如大块充填树脂复合材料和新型玻璃离子(GIC)基材料等新材料也已被引入。本综述的重点是评估与材料类别和粘结剂类别相关的使用寿命,同时调整可能的研究偏倚效应。

材料与方法

在数据库PUBMED/SCOPUS中检索关于后牙树脂复合材料的临床试验。纳入标准为:(1)2000年至2019年发表的研究;(2)至少观察2年的前瞻性临床试验;(2)最后一次回访时修复体的最小数量=20;(3)报告脱落率;(4)报告手术技术和使用的材料;(5)采用Ryge、改良Ryge或FDI评估标准。由两名独立的评审员使用Cochrane协作网用于评估随机试验偏倚风险的工具对每项研究的偏倚进行评估。对于统计分析,使用对随时间记录的个体数据拟合的线性混合模型,并采用随机效应来考虑研究、患者和实验效应。P值小于0.05被认为具有统计学意义。

结果

在423项临床试验中,62项研究(包括110项实验)符合纳入标准。材料类别根据复合填料分为微混合(39项实验/2807个修复体)、纳米混合(24项实验/1254个修复体)和混合(22项实验/1255个修复体)。所谓的大块充填材料被视为一个单独的类别(9项实验/506个修复体),玻璃离子(GIC)材料(11项实验/2121个修复体)和复合体材料(5项实验/238个修复体)也是如此。只有一项研究(1.6%)偏倚风险低,42项(67.7%)被评估为偏倚风险不明确,19项(30.6%)偏倚风险高。在52.3%的研究中放置了II类和I类修复体。10年后,树脂复合材料修复体的生存率降至约85 - 90%,混合、微混合和纳米混合树脂材料之间无显著差异。修复体替换的主要原因是大块折断和磨损,约占替换的70%。修复边缘的龋坏约占替换的20%,固位丧失、颜色匹配或边缘完整性不可接受、根管治疗或牙尖折断约占树脂复合材料修复体替换的10%。对于复合体和GIC修复体,6年后的平均总体生存率约为80%。对于GIC,失败的主要原因是解剖外形的大量丧失以及邻面接触丧失和固位丧失。主要是折断降低了复合体修复体的使用寿命。此外,在颜色匹配、表面质地、材料折断和解剖外形方面,混合、微混合、纳米混合和大块充填树脂复合材料之间无统计学显著差异。

结论

采用釉质酸蚀技术放置的后牙树脂复合材料修复体总体性能最佳;使用寿命不受树脂复合材料的填料类型或粘度的显著影响。在颜色匹配、表面质地和解剖外形方面,纳米混合树脂并不显著优于混合或微混合树脂复合材料。复合体和GIC修复体存在相当多的缺点,使用寿命明显较短。

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