Nonclinical Bench Performance Testing of a Very Low-Cost Nonelectric Bubble Continuous Positive Airway Pressure (bCPAP) and Blenders Device Designed for Newborn Respiratory Support.

IF 1.3 Q4 ENGINEERING, BIOMEDICAL Medical Devices-Evidence and Research Pub Date : 2022-06-27 eCollection Date: 2022-01-01 DOI:10.2147/MDER.S318218
Patricia S Coffey, Alec Wollen
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Abstract

Purpose: Bubble continuous positive airway pressure (bCPAP) is often used to treat respiratory distress experienced by some 15 million preterm infants born globally every year. In low- and middle-income countries, improvised bCPAP devices are used, often without a blender that protects the infant from the sequelae of excessive oxygen exposure.

Materials and methods: The aim of this bench testing was to assess the mechanical safety and performance of the PATH bCPAP and blenders device, which provides a stable and reliable source of pressurized blended gas without the requirement for a source of compressed medical air or electricity. The device includes two fixed ratio blenders: a "low" blend that provides 37% oxygen and a "high" blend that provides 60% oxygen. We performed bench testing to characterize the performance of the bCPAP and blenders, including respiratory circuit verification, blender verification, conditioned humidity testing, and sound measurement.

Results: Test results for all performance variables met the acceptance criteria of our product requirement specification. The device provides a fixed ratio of air and oxygen that is consistent over the entire range of clinically relevant pressures (4 to 8 cmH2O) and remains consistent despite changes in flow (2 to 7 liters per minute). The blend is stable within ± 5% of the blenders' nominal blend ratio when used with a 100% oxygen source, irrespective of the flow and pressure from the oxygen source or the flow and pressure of the blended gas delivered to the neonate. Sound and humidity test results were within specifications.

Conclusion: This very low-cost nonelectric bCPAP and blenders device is optimally designed to deliver a stable and reliable source of pressurized blended gas.

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对专为新生儿呼吸支持设计的超低成本无电气泡持续气道正压(bCPAP)和混合器设备进行非临床台架性能测试。
目的:气泡持续气道正压(bCPAP)通常用于治疗全球每年约 1500 万早产儿的呼吸窘迫。在中低收入国家,使用的是简易的 bCPAP 设备,通常没有搅拌器来保护婴儿免受过量氧气暴露的后遗症:该装置可提供稳定可靠的加压混合气体源,无需压缩医用空气源或电力。该装置包括两个固定比例的混合器:提供 37% 氧气的 "低 "混合器和提供 60% 氧气的 "高 "混合器。我们对 bCPAP 和混合器的性能进行了台架测试,包括呼吸回路验证、混合器验证、条件湿度测试和声音测量:结果:所有性能变量的测试结果均符合我们的产品要求规范的验收标准。设备提供的固定空气和氧气比例在整个临床相关压力范围(4 至 8 cmH2O)内保持一致,并且在流量变化(每分钟 2 至 7 升)时也保持一致。在与 100% 氧气源一起使用时,无论氧气源的流量和压力如何,也无论输送给新生儿的混合气体的流量和压力如何,混合气体都能稳定在混合器标称混合比率的 ± 5% 范围内。声音和湿度测试结果均符合规范:这款成本极低的非电动 bCPAP 和混合器设备经过优化设计,可提供稳定可靠的加压混合气体源。
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来源期刊
Medical Devices-Evidence and Research
Medical Devices-Evidence and Research ENGINEERING, BIOMEDICAL-
CiteScore
2.80
自引率
0.00%
发文量
41
审稿时长
16 weeks
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