CPAP Hardware/Simulation and Control Design for Respiratory Disorders: A Review

Athraa Sabeeh Mikha, Hadeel K. Aljobouri
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引用次数: 1

Abstract

Continuous Positive Airway Pressure (CPAP) ventilation remains a mainstay treatment for different respiratory disorders. Good pressure stability and pressure reduction during exhalation are of major importance condition to ensure the clinical efficacy and comfort of CPAP therapy.  Obstructive Sleep Apnea (OSA) and today coronavirus (COVID-19) are the main two diseases mitigated by the CPAP. This paper introduced a systematic review of the CPAP design in terms of the hardware design, Simulation-based CPAP system, control algorithm, and the measured performance. The accuracy is used as measurement of performance and calculated from the pressure value. The accuracy was compared to the predefined U.S. Food and Drug Administration (FDA)-based threshold value in which it considers this value as a reference. The results related to the modern CPAP devices introduced in this study to explain the accuracy of experimental CPAP. These were compared with a commercial CPAP devices. Also, it was revealed how the results coincide with the error ratio defined by the FDA as an evaluation measurement. The FDA error ratio determines the performance of the optimized CPAP device. This work is the first review that presented the knowledge about engineering design of the CPAP system, so it will be the first in the literature.
呼吸系统疾病的CPAP硬件/仿真和控制设计综述
持续气道正压通气(CPAP)仍然是治疗各种呼吸系统疾病的主要方法。良好的压力稳定性和呼气时的减压是保证CPAP治疗临床疗效和舒适性的重要条件。阻塞性睡眠呼吸暂停(OSA)和冠状病毒(COVID-19)是CPAP缓解的两种主要疾病。本文从硬件设计、基于仿真的CPAP系统、控制算法和测量性能等方面对CPAP设计进行了系统的综述。精度作为性能的度量,由压力值计算得到。将准确度与预定义的美国食品和药物管理局(FDA)的阈值进行比较,FDA将此值视为参考值。本研究介绍了与现代CPAP设备相关的结果,以解释实验CPAP的准确性。将这些与商用CPAP设备进行比较。此外,还揭示了结果如何与FDA定义的误差率相吻合,误差率是一种评估测量方法。FDA错误率决定了优化后的CPAP设备的性能。这是第一个介绍CPAP系统工程设计知识的综述,因此它将是文献中的第一个。
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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