Clinical effectiveness of restorative materials for the restoration of carious primary teeth without pulp therapy: a systematic review.

S Amend, C Boutsiouki, K Bekes, D Kloukos, N N Lygidakis, R Frankenberger, N Krämer
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引用次数: 5

Abstract

Purpose: To systematically search the available evidence and evaluate the clinical effectiveness of restorative materials for restoration of carious primary teeth. The findings aimed to support the European Academy of Paediatric Dentistry (EAPD) guidelines development.

Methods: Literature search was performed by searching 4 electronic databases for eligible randomised controlled clinical trials (RCTs) comparing restorative materials for the restoration of carious primary teeth up to December 28th, 2020. Quality assessment was performed with the revised Cochrane risk-of-bias tool for randomized trials (RoB 2).

Results: Of 1685 identified articles 29 RCTs were finally deemed as eligible for inclusion. Annual failure rates were: Amalgam 1-28%; atraumatic restorative treatment 1.2-37.1%; glass-ionomer cement (GIC) 7.6-16.6%, metal-reinforced GIC 29.9%, resin-modified GIC 1.9-16.9%, high-viscosity GIC 2.9-25.6%; glass carbomer ≤ 46.2%; compomer 0-14.7%; composite resin (CR) 0-19.5%, bulk-fill CR 0-16.9%; zirconia crowns 3.3%, composite strip crowns 15%, and preformed metal crowns (Hall-Technique) 3.1%. Secondary caries, poor marginal adaptation, loss of retention, and fracture of restoration were reported as reasons for failure. Four studies were evaluated at unclear and 25 at high risk of bias. Clinical and methodological heterogeneity, and the diversity of tested materials across included studies did not allow for meta-analyses.

Conclusions: Within the limitations of this systematic review, namely, the heterogeneity and the overall high risk of bias among included studies, clear recommendations based on solid evidence for the best restorative approach in primary teeth cannot be drawn. There is a need for future thoroughly implemented RCTs evaluating restorations in primary teeth to close this knowledge gap.

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修复材料在无牙髓治疗的情况下修复龋性乳牙的临床疗效:一项系统综述。
目的:系统地检索现有证据,评价各种修复材料在乳牙龋病修复中的临床效果。研究结果旨在支持欧洲儿科牙科学会(EAPD)指南的制定。方法:检索截至2020年12月28日符合条件的rct (randomised controlled clinical trials,随机对照临床试验)文献,比较修复材料对乳牙龋病的修复效果。使用改进的Cochrane随机试验风险偏倚工具进行质量评估(RoB 2)。结果:在1685篇确定的文章中,29篇随机对照试验最终被认为符合纳入条件。年失败率为:汞合金1-28%;非创伤性修复治疗1.2-37.1%;玻璃离子水泥(GIC) 7.6-16.6%,金属增强GIC 29.9%,树脂改性GIC 1.9-16.9%,高粘度GIC 2.9-25.6%;玻璃炭≤46.2%;compomer 0 - 14.7%;复合树脂(CR) 0-19.5%,块状填充CR 0-16.9%;氧化锆冠3.3%,复合条冠15%,预成型金属冠(Hall-Technique) 3.1%。继发性龋齿、边缘适应不良、固位丧失和修复体骨折是失败的原因。4项研究评价为不明确,25项评价为高偏倚风险。临床和方法学的异质性以及纳入研究的测试材料的多样性不允许进行荟萃分析。结论:在本系统综述的局限性内,即纳入研究的异质性和总体偏倚风险较高,无法基于确凿证据提出关于乳牙最佳修复方法的明确建议。未来需要全面实施评估乳牙修复体的随机对照试验,以缩小这一知识差距。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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