Sharif Mohammad O, Catleugh Melanie, Merry Alison, Tickle Martin, Dunne Stephen M, Brunton Paul, Aggarwal Vishal R, Chong Lee Yee
School of Dentistry, The University of Manchester, Coupland III Building, Oxford Road, Manchester, UK, M13 9PL.
Cochrane Database Syst Rev. 2014 Feb 8;2014(2):CD005971. doi: 10.1002/14651858.CD005971.pub3.
Composite filling materials have been increasingly used for the restoration of posterior teeth in recent years as a tooth-coloured alternative to amalgam. As with any filling material composites have a finite life-span. Traditionally, replacement was the ideal approach to treat defective composite restorations, however, repairing composites offers an alternative more conservative approach to the tooth structure where restorations are partly still serviceable. Repairing the restoration has the potential of taking less time and may sometimes be performed without the use of local anaesthesia hence it may be less distressing for a patient when compared with replacement.
To evaluate the effects of replacing (with resin composite) versus repair (with resin composite) in the management of defective resin composite dental restorations in permanent molar and premolar teeth.
For the identification of studies relevant to this review we searched the Cochrane Oral Health Group's Trials Register (to 24 July 2013); the Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library 2013, Issue 6); MEDLINE via OVID (1946 to 24 July 2013); EMBASE via OVID (1980 to 24 July 2013); BIOSIS via Web of Knowledge (1969 to 24 July 2013); Web of Science (1945 to 24 July 2013); and OpenGrey (to 24 July 2013). Researchers, experts and organisations known to be involved in this field were contacted in order to trace unpublished or ongoing studies. No restrictions were placed on the language or date of publication when searching the electronic databases.
Trials were selected if they met the following criteria: randomised controlled trial (including split-mouth studies), involving replacement and repair of resin composite restorations in adults with a defective molar restoration in a permanent molar or premolar teeth.
Two review authors independently assessed titles and abstracts for each article identified by the searches in order to decide whether the article was likely to be relevant. Full papers were obtained for relevant articles and both review authors studied these. The Cochrane Collaboration statistical guidelines were to be followed for data synthesis.
The search strategy retrieved 298 potentially eligible studies, after de-duplication. After examination of the titles and abstracts, full texts of potentially relevant studies were retrieved but none of the retrieved studies met the inclusion criteria of the review.
AUTHORS' CONCLUSIONS: There are no published randomised controlled trials relevant to this review question. There is therefore a need for methodologically sound randomised controlled trials that are reported according to the Consolidated Standards of Reporting Trials (CONSORT) statement (www.consort-statement.org/). Further research also needs to explore qualitatively the views of patients on repairing versus replacement and investigate themes around pain, anxiety and distress, time and costs.
近年来,复合填充材料作为汞合金的牙齿颜色替代材料,越来越多地用于后牙修复。与任何填充材料一样,复合材料的使用寿命有限。传统上,替换是治疗有缺陷的复合修复体的理想方法,然而,修复复合材料为牙齿结构提供了一种更保守的替代方法,因为修复体部分仍可使用。修复修复体有可能花费更少的时间,有时可以在不使用局部麻醉的情况下进行,因此与替换相比,对患者来说可能痛苦更小。
评估在恒牙磨牙和前磨牙中,用树脂复合材料替换(与用树脂复合材料修复)有缺陷的树脂复合材料牙齿修复体的效果。
为了识别与本综述相关的研究,我们检索了Cochrane口腔健康组试验注册库(至2013年7月24日);Cochrane对照试验中心注册库(CENTRAL)(Cochrane图书馆2013年第6期);通过OVID检索MEDLINE(1946年至2013年7月24日);通过OVID检索EMBASE(1980年至2013年7月24日);通过Web of Knowledge检索BIOSIS(1969年至2013年7月24日);Web of Science(1945年至2013年7月24日);以及OpenGrey(至2013年7月24日)。联系了已知参与该领域的研究人员、专家和组织,以追踪未发表或正在进行的研究。在搜索电子数据库时,对语言或出版日期没有限制。
如果试验符合以下标准,则选择该试验:随机对照试验(包括双侧对照研究),涉及在恒牙磨牙或前磨牙中有缺陷的磨牙修复体的成人中替换和修复树脂复合材料修复体。
两位综述作者独立评估通过搜索识别出的每篇文章的标题和摘要,以确定该文章是否可能相关。获取相关文章的全文,两位综述作者都对这些文章进行了研究。数据合成应遵循Cochrane协作组织的统计指南。
检索策略在去重后检索到298项潜在符合条件的研究。在检查标题和摘要后,检索了潜在相关研究的全文,但检索到的研究均未符合综述的纳入标准。
没有与本综述问题相关的已发表随机对照试验。因此,需要根据《试验报告统一标准》(CONSORT)声明(www.consort-statement.org/)报告的方法学上合理的随机对照试验。进一步的研究还需要定性地探索患者对修复与替换的看法,并调查围绕疼痛、焦虑和痛苦、时间和成本的主题。