Multicycle Autoclave Decontamination of N95 Filtering Facepiece Respirators.

IF 0.5 Q4 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Nathen E Bopp, Donald H Bouyer, Christopher M Gibbs, Joan E Nichols, Corrie A Ntiforo, Miguel A Grimaldo
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引用次数: 27

Abstract

Introduction: During pandemic situations like the one caused by the emergent coronavirus SARS-CoV-2, healthcare systems face the challenge of limited personal protective equipment and impaired supply chains. This problem poses a threat to healthcare workers, first responders, and the public, which demands solutions that can span the gap between institutional shortages and resupplies.

Objectives: To examine the efficacy of autoclave-based decontamination for the reuse of single-use surgical masks and N95 filtering facepiece respirators (FFRs). This method is the most readily available form of decontamination in the hospital and laboratory settings.

Methods: Three models of N95 FFRs and two procedural masks were evaluated in this study. A moist heat autoclave using four different autoclave cycles: 115°C for one hour, 121.1°C for 30 minutes, 130°C for two minutes, and 130°C for four minutes was used. After the autoclave process, the FFRs were NIOSH fit tested and particle counting was performed for both coarse particles of 5 micrometers (µM) and fine particles from 0.1µM to 1.0µM.

Results: We observed negligible alterations in the functionality and integrity of 3M 1805 and 3M 1870/1870+ N95 FFRs after three autoclave cycles. Surgical masks also showed minimal changes in functionality and integrity. The 3M 1860 FFR failed fit test after a single autoclave decontamination cycle.

Discussion and conclusion: The study finds that specific surgical masks and N95 FFR models can withstand autoclave decontamination for up to three cycles. Additionally, the autoclave cycles tested were those that could be readily achieved by both clinical and research institutions.

Abstract Image

Abstract Image

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N95过滤式口罩的多循环高压灭菌净化。
在SARS-CoV-2等突发冠状病毒引起的大流行情况下,卫生保健系统面临着个人防护装备有限和供应链受损的挑战。这一问题对卫生保健工作者、急救人员和公众构成威胁,因此需要能够弥补机构短缺和再补给之间差距的解决方案。目的:探讨高压灭菌对一次性医用口罩和N95过滤式口罩(FFRs)重复使用的消毒效果。这种方法是医院和实验室环境中最容易获得的净化形式。方法:对3种N95型ffr和2种程序性口罩进行评价。使用四种不同循环的湿热高压灭菌器:115°C 1小时,121.1°C 30分钟,130°C 2分钟,130°C 4分钟。经过高压灭菌处理后,对ffr进行NIOSH贴合测试,并对5微米(µM)的粗颗粒和0.1µM至1.0µM的细颗粒进行颗粒计数。结果:经过三次高压灭菌循环后,我们观察到3M 1805和3M 1870/1870+ N95 ffr的功能和完整性发生了可忽略不计的变化。医用口罩在功能和完整性方面也显示出很小的变化。3M 1860 FFR在一次高压灭菌器净化循环后未能通过配合测试。讨论和结论:研究发现,特定的外科口罩和N95 FFR型号可以承受高达三个周期的高压灭菌消毒。此外,测试的高压灭菌器循环是那些可以很容易地实现临床和研究机构。
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
Applied Biosafety
Applied Biosafety Environmental Science-Management, Monitoring, Policy and Law
CiteScore
2.50
自引率
13.30%
发文量
27
期刊介绍: Applied Biosafety (APB), sponsored by ABSA International, is a peer-reviewed, scientific journal committed to promoting global biosafety awareness and best practices to prevent occupational exposures and adverse environmental impacts related to biohazardous releases. APB provides a forum for exchanging sound biosafety and biosecurity initiatives by publishing original articles, review articles, letters to the editors, commentaries, and brief reviews. APB informs scientists, safety professionals, policymakers, engineers, architects, and governmental organizations. The journal is committed to publishing on topics significant in well-resourced countries as well as information relevant to underserved regions, engaging and cultivating the development of biosafety professionals globally.
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