Advancement of post-market surveillance of medical devices leveraging artificial intelligence: ECG devices case study.

IF 1.4 4区 医学 Q4 ENGINEERING, BIOMEDICAL
Madžida Hundur, Lemana Spahić, Faruk Bećirović, Lejla Gurbeta Pokvić, Almir Badnjević
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引用次数: 0

Abstract

Background: After 25 years of implementing the Medical Devices Directive (MDD), in 2017, the new Medical Devices Regulation (MDR) came into force, establishing stricter requirements for post-market surveillance of the safety and performance of medical devices (MD). For electrocardiogram (ECG) devices, which are crucial for monitoring cardiac activities, these requirements are essential to ensure the reliability and accuracy of diagnosing cardiac conditions and timely treatment.

Objective: This study aims to enhance post-market surveillance of ECG devices by leveraging Machine Learning (ML) algorithms to predict the operational status of these devices. Specifically, the research focuses on classifying the success or failure of ECG device operations based on performance and safety parameters. The ultimate goal is to improve the management strategies of ECG devices in healthcare institutions, ensuring optimal functionality and increasing the reliability of diagnostic procedures.

Method: During the inspection process of ECG devices conducted by an accredited laboratory in accordance with ISO 17020 standard in numerous healthcare institutions in Bosnia and Herzegovina, a total of 5577 samples were collected. Various machine learning algorithms, including Decision Tree (DT), Logistic Regression (LR), Random Forest (RF), Gaussian Naive Bayes (NB), and Support Vector Machine (SVM), were employed for result comparison and selection of the most accurate algorithm.

Results: All algorithms demonstrated good performance, but the Random Forest (RF) algorithm stood out, achieving 100% accuracy in predicting the success/unsuccess status of the device. While the results of this research are specific to the collected data from EKG devices, the developed algorithms can be applied to other similar datasets, offering opportunities for broader use in the medical environment.

Conclusion: Implementing machine learning algorithms for automated systems in healthcare institutions can significantly enhance the quality of patient diagnosis and treatment. Additionally, these systems can optimize costs associated with managing medical devices. Improved post-market surveillance using ML can address challenges related to ensuring device reliability and safety.

利用人工智能的医疗器械上市后监测的进展:心电设备案例研究。
背景:在实施医疗器械指令(MDD) 25年后,2017年,新的医疗器械法规(MDR)生效,为医疗器械(MD)的安全性和性能的上市后监管建立了更严格的要求。对于监测心脏活动至关重要的心电图(ECG)设备来说,这些要求对于确保诊断心脏疾病的可靠性和准确性以及及时治疗至关重要。目的:本研究旨在通过利用机器学习(ML)算法来预测这些设备的运行状态,从而加强心电设备的上市后监测。具体而言,研究重点是基于性能和安全参数对心电设备操作的成功或失败进行分类。最终目标是改善医疗机构中ECG设备的管理策略,确保最佳功能并提高诊断程序的可靠性。方法:在波黑多家医疗机构的心电设备检测过程中,由认可的实验室按照ISO 17020标准进行检测,共采集样品5577份。采用决策树(DT)、逻辑回归(LR)、随机森林(RF)、高斯朴素贝叶斯(NB)和支持向量机(SVM)等多种机器学习算法进行结果比较,选择最准确的算法。结果:所有算法都表现出良好的性能,但随机森林(RF)算法脱颖而出,在预测设备成功/不成功状态方面达到100%的准确率。虽然这项研究的结果是特定于从心电图设备收集的数据,但开发的算法可以应用于其他类似的数据集,为在医疗环境中更广泛的应用提供了机会。结论:在医疗机构的自动化系统中实施机器学习算法可以显著提高患者的诊断和治疗质量。此外,这些系统可以优化与管理医疗设备相关的成本。使用ML改进上市后监控可以解决与确保设备可靠性和安全性相关的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Technology and Health Care
Technology and Health Care HEALTH CARE SCIENCES & SERVICES-ENGINEERING, BIOMEDICAL
CiteScore
2.10
自引率
6.20%
发文量
282
审稿时长
>12 weeks
期刊介绍: Technology and Health Care is intended to serve as a forum for the presentation of original articles and technical notes, observing rigorous scientific standards. Furthermore, upon invitation, reviews, tutorials, discussion papers and minisymposia are featured. The main focus of THC is related to the overlapping areas of engineering and medicine. The following types of contributions are considered: 1.Original articles: New concepts, procedures and devices associated with the use of technology in medical research and clinical practice are presented to a readership with a widespread background in engineering and/or medicine. In particular, the clinical benefit deriving from the application of engineering methods and devices in clinical medicine should be demonstrated. Typically, full length original contributions have a length of 4000 words, thereby taking duly into account figures and tables. 2.Technical Notes and Short Communications: Technical Notes relate to novel technical developments with relevance for clinical medicine. In Short Communications, clinical applications are shortly described. 3.Both Technical Notes and Short Communications typically have a length of 1500 words. Reviews and Tutorials (upon invitation only): Tutorial and educational articles for persons with a primarily medical background on principles of engineering with particular significance for biomedical applications and vice versa are presented. The Editorial Board is responsible for the selection of topics. 4.Minisymposia (upon invitation only): Under the leadership of a Special Editor, controversial or important issues relating to health care are highlighted and discussed by various authors. 5.Letters to the Editors: Discussions or short statements (not indexed).
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