Christie-Holmes Natasha, Tyli Rachel, Budylowski Patrick, Guvenc Furkan, Weiner Amit, Poon Betty, Speck Mary, Naugler Stephenie, Rainville Allen, Ghalami Ayoob, McCaw Shannon, Hayes Steven, Mubareka Samira, Gray-Owen Scott D, Rotstein Ori D, Kandel Rita A, Scott James A
Combined Containment Level 3 Unit, Temerty Faculty of Medicine, University of Toronto, Toronto, ON Canada M5S 1A8.
Dalla Lana School of Public Health, University of Toronto, 223 College Street, Toronto, ON, Canada, M5T 1R4.
Am J Infect Control. 2021 Oct;49(10):1227-1231. doi: 10.1016/j.ajic.2021.07.012. Epub 2021 Jul 25.
The COVID-19 pandemic highlighted the need for evidence-based approaches to decontamination and reuse of N95 filtering facepiece respirators (FFRs). We sought to determine whether vapourized hydrogen peroxide (VHP) reduced SARS-CoV-2 bioburden on FFRs without compromising filtration efficiency. We also investigated coronavirus HCoV-229E as a surrogate for decontamination validation testing.
N95 FFRs were laced with SARS-CoV-2 or HCoV-229E and treated with VHP in a hospital reprocessing facility. After sterilization, viral burden was determined using viral outgrowth in a titration assay, and filtration efficiency of FFRs was tested against ATSM F2299 and NIOSH TEB-STP-APR-0059.
Viable SARS-CoV-2 virus was not detected after VHP treatment. One replicate of the HCoV-229E laced FFRs yielded virus after processing. Unexpired N95 FFRs retained full filtration efficiency after VHP processing. Expired FFRs failed to meet design-specified filtration efficiency and therefore are unsuitable for reprocessing.
In-hospital VHP is an effective decontaminant for SARS-CoV-2 on FFRs. Further, filtration efficiency of unexpired respirators is not affected by this decontamination process.
VHP is effective in inactivating SARS-CoV-2 on FFRs without compromising filtration efficiency. HCoV-229E is a suitable surrogate for SARS-CoV-2 for disinfection studies.
2019冠状病毒病大流行凸显了对N95过滤式面罩呼吸器(FFR)进行基于证据的去污和再利用方法的需求。我们试图确定汽化过氧化氢(VHP)是否能降低FFR上的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)生物负荷,同时又不影响过滤效率。我们还研究了冠状病毒HCoV-229E作为去污验证测试的替代物。
在医院的再处理设施中,将SARS-CoV-2或HCoV-229E接种到N95 FFR上,并用VHP进行处理。灭菌后,通过滴定试验中的病毒生长来确定病毒负荷,并根据美国材料与试验协会(ASTM)F2299和美国国家职业安全与健康研究所(NIOSH)TEB-STP-APR-0059对FFR的过滤效率进行测试。
VHP处理后未检测到活的SARS-CoV-2病毒。一组接种HCoV-229E的FFR在处理后产生了病毒。未过期的N95 FFR在VHP处理后保持了完全的过滤效率。过期的FFR未能达到设计规定的过滤效率,因此不适合再处理。
医院内的VHP是FFR上SARS-CoV-2的有效去污剂。此外,未过期呼吸器的过滤效率不受此去污过程的影响。
VHP能有效灭活FFR上的SARS-CoV-2,且不影响过滤效率。HCoV-229E是SARS-CoV-2消毒研究的合适替代物。