牙种植体制造过程中危险因素的表征与控制

Researc H Article, Amirhossein Emamian, H. Ramezanpour, H. Yousefi, J. S. Care
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引用次数: 0

摘要

减法生产在种植体生产中非常流行。为了提高种植体的成活率,在产品的技术文档中进行了全面的风险分析。目的研究牙种植体在制造过程、应用、长期使用和所谓的成活率中最常见的风险因素,包括种植体相关风险、外科相关风险、患者相关风险和维护相关风险。方法对直接或间接影响产品质量的潜在危险因素进行重要性评价。在评价阶段,根据影响因素的严重程度和发生概率对影响因素进行排序,纳入风险判据表。使用了称为缓解的适当度量来将风险标准化到可接受的标准。标准化可以通过降低风险的严重程度或通过降低其发生的概率,甚至两者兼而有之。从危险情况中前进是任何风险因素的预期目标。结果比较了缓解前阶段和缓解后阶段的等效风险评估因子。主要目的是观察这些因素的风险水平是否降低到可接受或有条件可接受的范围。落入有条件可接受的区域,使产品的应用受到足够的警告,这就要求用户或操作人员采取足够的预防措施。对于大多数风险因素,人们担心测量只能在发生的频率上改善它们,然而,结果表明也有改善严重性的解决方案。通过全面的研究,完成了风险分析文件,但在未来,这个行业的风险分析文件可以更加完整。在进一步的研究中,将严重性或概率的步骤离散为更精细的步骤,并最终将其转化为连续形式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterizing and Controlling the Risk Factors in Manufacturing Dental Implants
Background Subtractive manufacturing have been popular in dental implant production. In order to increase the survival rate of the dental implants, a comprehensive risk analysis has been performed in the technical documentation of the products. Purpose In this paper the most common risk factors categorized as implant-related, surgeon-related, patient-related, and maintenance-related risks in the manufacturing process, application, the long term usage and the so-called survival rate of dental implants are studied. Methods The importance of any of the potential risk factors which is directly or indirectly related to the product quality is assessed. In the evaluation stage, the factors are sorted based on their severity and probability of occurrence, brought to the risk criterion table. Proper measurement called as mitigations were used to standardize the risks to the acceptable criteria. The standardization could be through reducing the severity of the risk or through reducing the probability of its occurrence, or even both of them. Advancing from the hazardous situations was an expected aim for any of the risk factors. Results The equivalent risk assessment factors are compared in pre-mitigation and post-mitigation stages. The main aim was to see whether the risk level of the factors reduces to the acceptable or conditionally acceptable region. Falling in to the conditionally acceptable region makes the application of the product to be under sufficient warnings, which orders to take enough pre-cautions for the user or operator. For most of the risk factors, there was a concern that the measurements are able to only improve them in the frequency of occurrence, however, the results show that there are solutions to improve the severity as well. Conclusion Through this comprehensive study, the risk analysis file is completed however it can be even more complete, in the future, at this industry. In the further studies, discretizing the steps of severity or probability to finer steps, and ultimately converting them to a continuous form would be aimed.
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