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Clinical performance of bulk-fill and conventional resin composite restorations in posterior teeth: a systematic review and meta-analysis

机译:散粒填充和常规树脂复合修复后的临床表现:系统评价和荟萃分析

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ObjectivesThe purpose of this systematic review was to compare the clinical performance of bulk-fill resin composites with conventional resin composites used for direct restorations of posterior teeth.MethodsThis review followed the PRISMA statement. This review was registered at PROSPERO (registration number CRD42016053436). A search of the scientific literature was performed by two independent reviewers using the PubMed/MEDLINE, Embase, The Cochrane Library, and Web of Science databases from commencement until January 2018. The research question was Do bulk-fill resin composites have a clinical performance comparable to conventional resin composites in posterior restorations? Only studies evaluating class I and II direct restorations in permanent teeth with a follow-up period of at least 1year were included. The RevMan 5 program was used for meta-analysis, calculating the relative risk (RR) and 95% confidence interval (CI) of the dichotomous outcome (restoration failure or success).ResultsTen articles were selected, comprising 941 analyzed restorations. The mean follow-up period was 33.6months (12-72 months). No statistically significant differences in the failure rate were observed between conventional and base/flowable bulk-fill resin composites (p=0.31; RR 1.49; 95% CI 0.69-3.25) or full-body/sculptable bulk-fill resin composites (p=0.12; RR 1.89; 95% CI 0.84-4.24).ConclusionsThe present systematic review and meta-analysis indicate similar clinical performances of bulk-fill and conventional resin composites over a follow-up period of 12 to 72months.Clinical significanceBased on the results of this study, the bulk-fill resin composites could be an alternative for direct restorations in posterior teeth. However, clinical trials of longer duration are required.
机译:该系统审查的客观目的是比较散装 - 填充树脂复合材料的临床性能,其具有用于直接修复后牙的常规树脂复合材料。方法审查遵循PRISMA陈述。该评论在Prospero注册(注册号码CRD42016053436)。在2018年1月之前,两个独立审查员的搜索是由两个独立的审查员进行的两个独立审查员和科学数据库网络。研究问题是批量填充树脂复合材料的临床表现可比较在后修复后的常规树脂复合材料?仅包括评估I级和II型恒牙直接修复的研究,其中包含至少1年的后续时间。 Revman 5程序用于Meta分析,计算二分辨率结果(恢复失败或成功)的相对风险(RR)和95%置信区间(CI)。选择了物品,包括941分析的修复物。平均随访时间为33.6个月(12-72个月)。在常规和碱/可流体填充树脂复合材料之间观察到失败率的统计学显着差异(P = 0.31; RR 1.49; 95%CI 0.69-3.25)或全体/尺寸散装树脂复合材料(P = 0.12; rr 1.89; 95%ci 0.84-4.24)。本发明的控制性综合性和荟萃分析表明,在12至72个月的随访期间,散装填充和常规树脂复合材料的类似临床表演。临床表现为结果本研究,块状填充树脂复合材料可以是后牙直接修复的替代方案。但是,需要更长的持续时间的临床试验。

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