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内部过滤效率评估经汽化过氧化氢消毒的过滤式防护口罩(FFR)。

In-House Filtration Efficiency Assessment of Vapor Hydrogen Peroxide Decontaminated Filtering Facepiece Respirators (FFRs).

机构信息

Radiation Biology Section, Biomedical Physics Department, King Faisal Specialist Hospital and Research Centre (KFSH&RC), Riyadh 11211, Saudi Arabia.

Emerging Technology Unit, Biomedical Physics Department, King Faisal Specialist Hospital and Research Centre (KFSH&RC), Riyadh 11211, Saudi Arabia.

出版信息

Int J Environ Res Public Health. 2021 Jul 4;18(13):7169. doi: 10.3390/ijerph18137169.

DOI:10.3390/ijerph18137169
PMID:34281105
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8297238/
Abstract

To cope with the shortage of filtering facepiece respirators (FFRs) caused by the coronavirus disease (COVID-19), healthcare institutions have been forced to reuse FFRs using different decontamination methods, including vapor hydrogen peroxide (VHP). However, most healthcare institutions still struggle with evaluating the effect of VHP on filtration efficiency (FE) of the decontaminated FFRs. We developed a low-cost in-house FE assessment using a novel 3D-printed air duct. Furthermore, we assessed the FE of seven types of FFRs. Following 10 VHP cycles, we evaluated the FE of KN95 and 3M-N95 masks. The 3M-N95 and Benehal-N95 masks showed significant lower FE (80.4-91.8%) at fine particle sizes (0.3-1 µm) compared to other FFRs (FE ≥ 98.1%, < 0.05). Following 10 VHP cycles, the FE of KN95 masks was almost stable (FE stability > 99.1%) for all particle sizes, while 3M-N95 masks were stable only at 2 and 5 µm (FE stability > 98.0%). Statistically, FE stability of 3M-N95 masks at 0.3, 0.5, and 0.7 µm was significantly lower ( ≤ 0.006) than 2 and 5 µm. The in-house FE assessment may be used as an emergency procedure to validate the decontaminated FFRs, as well as a screening option for production control of FFRs. Following VHP cycles, both masks showed high stability at 5 µm, the size of the most suspected droplets implicated in COVID-19 transmission.

摘要

为应对新型冠状病毒病(COVID-19)导致的过滤式口罩(FFR)短缺,医疗机构被迫使用不同的消毒方法(包括汽化过氧化氢)重复使用 FFR。然而,大多数医疗机构仍在努力评估 VHP 对消毒 FFR 过滤效率(FE)的影响。我们使用新型 3D 打印空气管道开发了一种低成本的内部 FE 评估方法。此外,我们评估了七种 FFR 的 FE。经过 10 个 VHP 循环后,我们评估了 KN95 和 3M-N95 口罩的 FE。与其他 FFR(FE≥98.1%,<0.05)相比,3M-N95 和 Benehal-N95 口罩在细颗粒(0.3-1 µm)下的 FE 明显较低(80.4-91.8%)。经过 10 个 VHP 循环后,KN95 口罩在所有颗粒尺寸下的 FE 几乎保持稳定(FE 稳定性>99.1%),而 3M-N95 口罩仅在 2 和 5 µm 时保持稳定(FE 稳定性>98.0%)。统计学上,3M-N95 口罩在 0.3、0.5 和 0.7 µm 处的 FE 稳定性明显较低(≤0.006)。内部 FE 评估可作为验证消毒 FFR 的紧急程序,也可作为 FFR 生产控制的筛选选项。经过 VHP 循环后,两种口罩在 5 µm 时均表现出高稳定性,5 µm 是 COVID-19 传播中最可疑飞沫的大小。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5a6/8297238/69acdbf62d9c/ijerph-18-07169-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5a6/8297238/75838906279b/ijerph-18-07169-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5a6/8297238/29bd9578b056/ijerph-18-07169-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5a6/8297238/69acdbf62d9c/ijerph-18-07169-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5a6/8297238/75838906279b/ijerph-18-07169-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5a6/8297238/29bd9578b056/ijerph-18-07169-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5a6/8297238/69acdbf62d9c/ijerph-18-07169-g003.jpg

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Ultraviolet-C as a Viable Reprocessing Method for Disposable Masks and Filtering Facepiece Respirators.
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紫外线-C作为一次性口罩和过滤式面罩呼吸器的可行再处理方法
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