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Correlation of clinical performance with 'in vitro tests' of restorative dental materials that use polymer-based matrices

机译:使用基于聚合物的基质的修复性牙科材料的临床表现与“体外测试”的相关性

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摘要

Objective. Review correlations of in vivo clinical performance with in vitro laboratory tests of restorative dental materials involving polymer-based matrices. Identify those factors interfering with the process. Materials and methods. An evidence-based dentistry approach was used to identify clinical trials, critical reviews, and meta-analyses involving correlations. Factors impacting meaningful correlations were reviewed. The limited bona fide correlations were reviewed. Results. In vitro tests include physical, chemical, mechanical, and biological properties. Clinical research measurements routinely include 10-15 categories of clinical observations of performance such as color match, caries resistance, marginal integrity, surface texture, and others, but do not correspond well with laboratory properties. Clinical trials of restorative dental materials represent a small fraction of the total research in this arena (typically <10% of dental materials research over many years). Trials are generally short-term (2-5 years) and are designed primarily to test product "safety and efficacy." A large number of risk factors (operator, design, material, intraoral location, patient) affect clinical outcomes and are not simulated well in laboratories. Little long-term information exists for clinical performance other than on composite wear. Very few meaningful correlations of laboratory tests and clinical results are demonstrated. Conclusions/recommendations. New studies should be focused on recovering restorations from service and characterizing them with the same tests as normally conducted in the laboratory. Many more long-term clinical trials that involve 10-20 years of observations are needed. Those trials should include planned restoration recovery to assess changes in laboratory properties of interest.
机译:目的。审查涉及基于聚合物的基质的修复性牙科材料的体内临床表现与体外实验室测试的相关性。确定那些干扰过程的因素。材料和方法。基于证据的牙科方法被用于识别临床试验,重要评价以及涉及相关性的荟萃分析。审查了影响有意义的相关性的因素。审查了有限的善意关联。结果。体外测试包括物理,化学,机械和生物学特性。临床研究测量通常包括10-15个类别的临床表现观察值,例如颜色匹配,抗龋齿,边缘完整性,表面纹理等,但与实验室特性不太吻合。修复性牙科材料的临床试验仅占该领域总研究的一小部分(多年来,通常少于牙科材料研究的10%)。试用通常是短期的(2-5年),主要用于测试产品的“安全性和有效性”。大量风险因素(操作者,设计,材料,口腔内位置,患者)会影响临床结果,并且在实验室中无法很好地模拟。除了复合材料磨损以外,几乎没有关于临床表现的长期信息。实验室测试与临床结果之间几乎没有有意义的关联。结论/建议。新的研究应侧重于从服务中恢复修复体,并使用与实验室中正常进行的相同测试对它们进行表征。需要更多的涉及10-20年观察的长期临床试验。这些试验应包括计划的修复恢复,以评估目标实验室特性的变化。

著录项

  • 来源
    《Dental materials》 |2012年第1期|p.52-71|共20页
  • 作者

    Stephen C. Bayne;

  • 作者单位

    Cariology, Restorative Sciences, and Endodontics, School of Dentistry, University of Michigan, 1011 North University Avenue, Ann Arbor, MI 48109-1078, United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    laboratory properties; clinical properties; clinical trials; correlation;

    机译:实验室性质;临床特性;临床试验;相关性;

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