Flammability of Respirators and other Head and Facial Personal Protective Equipment.

Samy Rengasamy, George Niezgoda, Ron Shaffer
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Abstract

Background: Personal protective equipment (PPE) is worn by workers in surgical settings to protect them and patients. Food and Drug Administration (FDA) clears some PPE (e.g., surgical masks (SM)) as class II medical devices, and regulates some (e.g. surgical head cover) as class I exempt devices. For respiratory protection, National Institute for Occupational Safety and Health (NIOSH)-approved N95 filtering facepiece respirators (FFRs), and powered air-purifying respirators (PAPRs) are used. One type of PPE, "surgical N95 respirators", is a NIOSH-approved FFR that is also cleared by the FDA for use in medical settings. The surgical environment poses unique risks such as the potential for surgical fires. As part of its substantial equivalence determination process, FDA requests testing of flammability and other parameters for SM and surgical N95 respirators. A lack of data regarding flammability of PPE used in healthcare exists. We hypothesize that commonly used PPE, regardless of whether regulated and/or cleared by FDA or not, will pass an industry standard such as the 16 CFR 1610 flammability test.

Methods: Eleven N95 FFR models, eight surgical N95 respirator models, seven SM models, five surgical head cover models, and five PAPR hood models were evaluated for flammability with a 45 degree flammability tester using the 16 CFR 1610 method. Three common fabrics were included for comparison.

Results: All of the PPE samples regulated/and or cleared by FDA or not, passed the flammability test at class 1 (normal flammability), meaning they are less likely to burn. Only one of the three common fabrics, a cotton fabric at the lowest basis weight, was class 3 (high flammability).

Conclusions: The results obtained in the study suggest that NIOSH-approved N95 FFRs would likely pass the 16 CFR 1610 flammability standard. Moreover, results suggest that NIOSH is capable of undertaking flammability testing using the 16 CFR 1610 standard as the flammability results NIOSH obtained for N95 FFRs were comparable to the results obtained by a third party independent laboratory.

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呼吸器和其他头部和面部个人防护设备的易燃性。
背景:手术环境中的工作人员佩戴个人防护装备(PPE)以保护他们和患者。美国食品和药物管理局(FDA)将一些个人防护装备(例如外科口罩(SM))清除为II类医疗器械,并将一些(例如外科头罩)规定为I类豁免器械。对于呼吸防护,使用国家职业安全与健康研究所(NIOSH)批准的N95过滤式面罩呼吸器(ffr)和动力空气净化呼吸器(papr)。一种类型的个人防护装备,“外科N95呼吸器”,是niosh批准的FFR,也被FDA批准用于医疗环境。手术环境带来了独特的风险,如潜在的手术火灾。作为其实质等效性确定过程的一部分,FDA要求测试SM和外科N95呼吸器的可燃性和其他参数。缺乏关于卫生保健中使用的个人防护用品易燃性的数据。我们假设常用的PPE,无论是否受到FDA的监管和/或批准,都将通过行业标准,如16 CFR 1610可燃性测试。方法:采用45度可燃性测试仪,采用16 CFR 1610法对11个N95 FFR模型、8个N95医用口罩模型、7个SM模型、5个医用头罩模型和5个PAPR罩模型进行可燃性评价。包括三种常见的织物进行比较。结果:所有的PPE样品都通过了1级(正常可燃性)的可燃性测试,这意味着它们不太可能燃烧。在三种常见织物中,只有一种是最低基重的棉织物,属于3级(高可燃性)。结论:研究结果表明,niosh批准的N95 ffr很可能通过16 CFR 1610可燃性标准。此外,结果表明NIOSH能够使用16 CFR 1610标准进行可燃性测试,因为NIOSH获得的N95 ffr可燃性结果与第三方独立实验室获得的结果相当。
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