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How to qualify and validate wear simulation devices and methods

机译:如何鉴定和验证磨损模拟设备和方法

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The clinical significance of increased wear can mainly be attributed to impaired aesthetic appearance and/or functional restrictions. Little is known about the systemic effects of swallowed or inhaled worn particles that derive from restorations. As wear measurements in vivo are complicated and time-consuming, wear simulation devices and methods had been developed without, however, systematically looking at the factors that influence important wear parameters. Wear simulation devices shall simulate processes that occur in the oral cavity during mastication, namely force, force profile, contact time, sliding movement, clearance of worn material, etc. Different devices that use different force actuator principles are available. Those with the highest citation frequency in the literature are - in descending order - the Alabama, ACTA, OHSU, Zurich and MTS wear simulators. When following the FDA guidelines on good laboratory practice (GLP) only the expensive MTS wear simulator is a qualified machine to test wear in vitro; the force exerted by the hydraulic actuator is controlled and regulated during all movements of the stylus. All the other simulators lack control and regulation of force development during dynamic loading of the flat specimens. This may be an explanation for the high coefficient of variation of the results in some wear simulators (28-40%) and the poor reproducibility of wear results if dental databases are searched for wear results of specific dental materials (difference of 22-72% for the same material). As most of the machines are not qualifiable, wear methods applying the machine may have a sound concept but cannot be validated. Only with the MTS method have wear parameters and influencing factors been documented and verified. A good compromise with regard to costs, practicability and robustness is the Willytec chewing simulator, which uses weights as force actuator and step motors for vertical and lateral movements. The Ivoclar wear method run on the Willytec machine shows a mean coefficient of variation in vertical wear of 12%. Force measurements have revealed that in the beginning of the stylus/specimen contact phase the force impulse is 3-4 times higher during dynamic loading than during static loading. When correlating material properties to the wear results of 23 composite resins subjected to the Ivoclar method, some parameters could be identified and incorporated into a wear formula to predict wear with the Ivoclar method. A round robin test evaluating the wear of ten dental materials with five wear simulation methods showed that the results were not comparable, as all methods follow different wear testing concepts. All wear methods lack the evidence of their clinical relevance because prospective studies correlating in vitro with long-term in vivo results with identical materials are not available. For direct restorative materials, amalgam seems to be a realistic reference material. For indirect, namely crown and bridge materials, low strength ceramic is appropriate.
机译:增加磨损的临床意义主要可归因于美学外观和/或功能限制受损。对于从修复体中吞咽或吸入的磨损颗粒的全身作用了解甚少。由于体内的磨损测量既复杂又费时,因此已经开发了磨损模拟设备和方法,但是没有系统地研究影响重要磨损参数的因素。磨损模拟设备应模拟咀嚼过程中在口腔中发生的过程,即力,力分布,接触时间,滑动运动,磨损材料的间隙等。可以使用采用不同力致动器原理的不同设备。文献中被引用频率最高的是-降序排列的阿拉巴马州,ACTA,OHSU,苏黎世和MTS磨损模拟器。当遵循FDA关于良好实验室规范(GLP)的指南时,只有昂贵的MTS磨损模拟器才是合格的体外测试设备;在触控笔的所有运动过程中,液压致动器施加的力均受到控制和调节。所有其他模拟器在动态加载扁平样本期间都缺乏对力发展的控制和调节。这可能是由于某些磨损模拟器中结果的变异系数较高(28-40%)以及如果在牙科数据库中搜索特定牙科材料的磨损结果而导致的磨损结果可重复性较差的原因(差异为22-72%对于相同的材料)。由于大多数机器都不合格,因此使用机器的磨损方法可能有合理的概念,但无法验证。只有使用MTS方法,才可以记录和验证磨损参数和影响因素。 Willytec咀嚼模拟器是在成本,实用性和耐用性方面的一个很好的折衷方案,它使用砝码作为力致动器和步进马达进行垂直和横向运动。在Willytec机器上运行的Ivoclar磨损方法显示出垂直磨损的平均变化系数为12%。力的测量表明,在测针/试样接触阶段开始时,动态加载期间的力脉冲是静态加载期间的3-4倍。当将材料特性与接受Ivoclar方法的23种复合树脂的磨损结果进行关联时,可以识别一些参数并将其合并到磨损公式中,以使用Ivoclar方法预测磨损。循环测试使用五种磨损模拟方法评估了十种牙科材料的磨损,结果并不具有可比性,因为所有方法均遵循不同的磨损测试概念。所有的佩戴方法都缺乏其临床相关性的证据,因为尚无前瞻性研究将具有相同材料的体外与长期体内结果相关联。对于直接修复材料,汞合金似乎是现实的参考材料。对于间接材料,即冠和桥材料,低强度陶瓷是合适的。

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