一种确定危险因素的混合方法

Esra Dinler, K. D. Atalay, Ezgi Güler
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引用次数: 0

摘要

在风险分析中,风险的量化、已识别风险的建模以及如何进行决策都是要考虑的问题。公司在生产医疗器械时必须遵守和执行的最低水平的风险分析活动。制造商应考虑设备可能包含的所有风险,以表明医疗设备是安全的。制造商还必须证明该设备应该生产,因为该设备的好处大于风险。本研究提出了一种测量医疗器械对患者危险因素的方法。据此,建立了数学模型,并将该模型应用于某公司生产的设备,得到了计算结果。本研究开发的聚合方法,基于田口损失函数和使用犹豫模糊的排序偏好技术,通过相似于理想溶液(HF-TOPSIS)方法,确保患者可能发生的风险最小化,并确定需要考虑的风险类型。此外,将本文方法得到的风险类型的重要性排序与TOPSIS方法进行了比较。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A new hybrid method to determine the hazardous risk factors
Abstract In risk analysis, the quantification of risk, the modeling of identified risk, and how to make decisions are all topics considered. Risk analysis activity that companies must comply with and perform at a minimum level to produce medical devices. Manufacturers should consider all risks that the device may contain to indicate that the medical device is safe. Manufacturers must also justify that this device should be manufactured because the benefit of the device is greater than the risk. This study proposes a method to measure the risk factors of the medical devices on the patient. Accordingly, a mathematical model is developed, the model is applied to a device manufactured in a company, and the results are obtained. The aggregated method developed in this study, based on the Taguchi loss function and using the hesitant fuzzy the technique for order preference by similarity to ideal solution (HF-TOPSIS) method, ensures that the risks that may occur for the patient are minimized and the risk types to be taken into account are determined. In addition, the order of importance of the risk types obtained with the proposed method in the study is compared with the TOPSIS method.
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