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A respirator fit test checks whether a respirator properly fits the face of someone who wears it. The fitting characteristic of a respirator is the ability of the mask to separate a worker's respiratory system from ambient air.
This is achieved by tightly pressing the mask flush against the face (without gaps) to ensure an efficient seal on the mask perimeter. Because wearers cannot be protected if there are gaps, it is necessary to test the fit before entering into contaminated air. Multiple forms of the test exist.
Scientific studies have shown that if the mask size and shape is correctly fitted to the employees’ face, they will be better protected in hazardous workplaces. [1]
Facial hair such as a beard can interfere with proper fit. [2]
The effectiveness of various types of respirators was measured in laboratories and in the workplace. [3] These measurements showed that in practice, the effectiveness of negative pressure tight fitting respiratory protective devices (RPD) depends on leakage between mask and face, rather than the filters/canisters. [4] This decrease in efficiency due to leakage manifested on a large scale during World War I, when gas masks were used to protect against chemical weapons. Poor fit or poorly situated masks could be fatal. The Russian army began to use short-term exposure to chlorine at low concentrations to solve this problem in 1917. [5] [6] Such testing helped convince the soldiers that their gas masks were reliable - because respirators were a novelty. [7] Later, industrial workers were trained in gas chambers in the USSR (in preparation for the Second World War), [8] [9] [10] and late [11] '. German firefighters used a similar test between the First and Second World Wars. [12] Diluted chloropicrin was used to test industrial gas masks. [13] The Soviet Army used chloropicrin in tents with a floor space of 16 square meters. [14]
Respirator selection and use are regulated by national legislation in many countries. [15] [16] [17] These requirements include a test of negative pressure mask for each individual wearer.
Qualitative and quantitative fit test methods (QLFT & QNFT) exist. Detailed descriptions are given in the US standard, developed by Occupational Safety and Health Administration OSHA. [15] This standard regulates respirator selection and organization (Appendix A describes fit testing). Compliance with this standard is mandatory for US employers.
These methods use the reaction of workers to the taste or smell of a special material (if it leaks into mask) - gas, vapors or aerosols. Such reactions are subjective, making this test dependent on the subject reporting results honestly. A qualitative fit test starts with an unfiltered/non-respirator sampling of the substance of choice to verify that the subject can detect it accurately. Substances include:
Equipment can determine the concentrations of a control substance (challenge agent) inside and outside the mask or to determine the flow rate of air flowing under the mask. Quantitative methods are more accurate and reliable than qualitative methods because they do not rely on subjective sensing of the challenge agent. Perhaps the most important consideration is the fact that unlike qualitative methods, the quantitative methods provide a data-based, defensible metric.
An aerosol test is carried out by measuring the internal and external aerosol concentrations. The aerosol can be artificially created (to check the mask), or a natural atmospheric component. The ratio of external concentration to the concentration under the mask is called a fit factor (FF). [19] U.S. law requires employers to offer employees a mask with large enough fit factor. For half face-piece masks (used when the concentration of harmful substances is not more than 10 PEL), the fit factor should not be less than 100; and for full face masks (not more than 50 PEL), the fit factor should not be less than 500. The safety factor of 10 compensates for the difference between testing and workplace conditions. To use an atmospheric aerosol one needs a PortaCount or AccuFIT device. These devices increase the size of the smallest particles through a process of vapor condensation (Condensation Particle Counting or CPC), and then determines their concentration (by count). Aerosols may be: sodium chloride, calcium carbonate, and others. This method has been used as gold standard for determining whether or not a given respirator fits a healthcare worker in healthcare settings and research laboratories. [20] [21] [22] [23]
Recently OSHA approved a Fast Fit Protocol which enables the AAC/CPC (Ambient Aerosol Concentration/Condensation Particle Counting) method to be performed in less than three minutes. The major advantage of the AAC/CPC method is that the test subject is moving and breathing while the fit factor is being measured. This dynamic measurement is more representative of the actual conditions under which the respirator is used in the workplace.
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These methods appeared later than aerosol. When a worker inhales, a portion of the aerosol is deposited in their respiratory organs, and the concentration measured during the exhalation becomes lower than during inhalation. During inhalation leaked unfiltered air trickles under the mask, not actually mixing with air under the mask. If such a stream collides with the sampling probe, the measured concentration becomes higher than the actual value. But if the trickle does not come into contact with a probe the concentration becomes lower.
Control Negative Pressure (CNP) directly measures facepiece leakage. This measurement tells you how much air has leaked into the respirator, and this is converted into a fit factor. Using a challenge pressure of 53.8 – 93.1 L/min, the CNP devices stress the mask as an employee would while breathing heavily under extreme physical conditions. The manufacturer of the CNP device claims that the use of air as a standard (non-varying) gaseous challenge agent provides a more rigorous test of mask fit than an aerosol agent. If air leaks into a respirator, there is a chance that the particles, vapors, or gas contaminants also may leak in. Recently-approved Redon protocols allow a fit test to be performed in under 3 minutes.[ citation needed ] The CNP Method of fit testing is OSHA, NFPA and ISO certified (among others).
Dichot method differs from CNP in that common filters are installed on the mask and the air is pumped out from the mask at high speed. In this case, a vacuum exists under the mask. The degree of negative pressure depends on the resistance of the filters and on the amount of leaking air. The resistance of the filter is measured with a sealed attachment of the mask to a dummy. This allows the operator to determine the amount of air leaking through the gaps.
U.S. law began to require employers to assign and test a mask for each employee prior to assignment to a position requiring the use of a respirator and thereafter every 12 months, and optionally, in case of circumstances that could affect fit (injury, tooth loss, etc.). [18] Other developed countries have similar requirements. [17] [24] A U.S. study showed that this requirement was fulfilled by almost all large enterprises. In small enterprises, with fewer than 10 workers, it was broken by about half of employers in 2001. [25] The main reason for such violations may be the cost of specialized equipment for quantitative fit tests, insufficient accuracy of qualitative fit tests and the fact that small organizations have fewer rigorous compliance processes.
The main advantage of qualitative fit test methods is the low cost of equipment, while their main drawback is their modest precision, and that they cannot be used to test tight-fitting respirators that are intended for use in atmospheres that exceed 10 PEL (due to the low sensitivity). To reduce the risk of choosing a respirator with poor fit, the mask needs to have a sufficiently high fitting characteristic. Multiple masks must be examined to find the "most reliable", although poor test protocols may give incorrect results. Re-checks require time and increase costs. In 2001, the most commonly used QLFT was irritant smoke and saccharin, but in 2004, NIOSH advised against using irritant smoke.
CNP is a relatively inexpensive and fast method among quantitative methods. [26] However, it is not possible to fit test the disposable filtering face-piece mask (such as the N95, N99, and N100 masks) with CNP. Fit tests with an atmospheric aerosol may be used on any respirator, but the cost of earlier devices (PortaCount) and the duration of the test was slightly greater than CNP. However the newer OSHA Fast Fit Protocols for CNC methods, and introduction of newer instruments, have made all quantitative fit test devices equivalent in price and time required for testing. The CNP method has at present about 15% of the fit test market in industry. [25] The Current CNC instruments are the PortaCount 8040 and the AccuFIT 9000.
Fit test method | Respirator types | Devices for testing | ||
---|---|---|---|---|
Filtering half facepiece | Elastomeric half facepiece respirators and elastomeric full facepiece mask, used in workplaces with concentrations of contaminants up to 10 PEL | Elastomeric full facepiece mask, used in workplaces with concentrations of contaminants up to 50 PEL | ||
Qualititative fit test methods | ||||
Isoamyl acetate | Unlikely to pass [lower-alpha 1] | Yes | No | Allegro-0202 et al. |
Saccharin | Yes | Yes | No | 3М FT-10 et al. |
Bitrex | Yes | Yes | No | 3М FT-30 et al. |
Irritant smoke [lower-alpha 2] | Class-100 filters only [28] | Yes | No | Allegro-2050, VeriFit, RAE 10-123-01 et al. |
Quantitative fit test methods | ||||
Control Negative Pressure (CNP) [lower-alpha 3] | Impossible to pass [lower-alpha 4] | Yes | Yes | FitTester 3000 (DNI Nevada/OHD), Quantifit (OHD) |
Ambient Aerosol method (CPC) | Yes | Yes | Yes | PortaCount, Accufit 9000 |
Generated Aerosol method (Aerosol Photometer) | Oil-resistant filters only [lower-alpha 5] | Yes | Yes | TDA-99M, TSI 8587A |
A gas mask is an item of personal protective equipment used to protect the wearer from inhaling airborne pollutants and toxic gases. The mask forms a sealed cover over the nose and mouth, but may also cover the eyes and other vulnerable soft tissues of the face. Most gas masks are also respirators, though the word gas mask is often used to refer to military equipment, the scope used in this article. Gas masks only protect the user from ingesting or inhaling chemical agents, as well as preventing contact with the user's eyes. Most combined gas mask filters will last around 8 hours in a biological or chemical situation. Filters against specific chemical agents can last up to 20 hours.
Personal protective equipment (PPE) is protective clothing, helmets, goggles, or other garments or equipment designed to protect the wearer's body from injury or infection. The hazards addressed by protective equipment include physical, electrical, heat, chemical, biohazards, and airborne particulate matter. Protective equipment may be worn for job-related occupational safety and health purposes, as well as for sports and other recreational activities. Protective clothing is applied to traditional categories of clothing, and protective gear applies to items such as pads, guards, shields, or masks, and others. PPE suits can be similar in appearance to a cleanroom suit.
A surgical mask, also known by other names such as a medical face mask or procedure mask, is a personal protective equipment used by healthcare professionals that serves as a mechanical barrier that interferes with direct airflow in and out of respiratory orifices. This helps reduce airborne transmission of pathogens and other aerosolized contaminants between the wearer and nearby people via respiratory droplets ejected when sneezing, coughing, forceful expiration or unintentionally spitting when talking, etc. Surgical masks may be labeled as surgical, isolation, dental or medical procedure masks.
A respirator is a device designed to protect the wearer from inhaling hazardous atmospheres including lead fumes, vapours, gases and particulate matter such as dusts and airborne pathogens such as viruses. There are two main categories of respirators: the air-purifying respirator, in which respirable air is obtained by filtering a contaminated atmosphere, and the air-supplied respirator, in which an alternate supply of breathable air is delivered. Within each category, different techniques are employed to reduce or eliminate noxious airborne contaminants.
The term immediately dangerous to life or health (IDLH) is defined by the US National Institute for Occupational Safety and Health (NIOSH) as exposure to airborne contaminants that is "likely to cause death or immediate or delayed permanent adverse health effects or prevent escape from such an environment." Examples include smoke or other poisonous gases at sufficiently high concentrations. It is calculated using the LD50 or LC50. The Occupational Safety and Health Administration (OSHA) regulation defines the term as "an atmosphere that poses an immediate threat to life, would cause irreversible adverse health effects, or would impair an individual's ability to escape from a dangerous atmosphere."
A respirator cartridge or canister is a type of filter that removes gases, volatile organic compounds (VOCs), and other vapors from air through adsorption, absorption, or chemisorption. It is one of two basic types of filters used by air-purifying respirators. The other is a mechanical filter, which removes only particulates. Hybrid filters combine the two.
The National Personal Protective Technology Laboratory (NPPTL) is a research center within the National Institute for Occupational Safety and Health located in Pittsburgh, Pennsylvania, devoted to research on personal protective equipment (PPE). The NPPTL was created in 2001 at the request of the U.S. Congress, in response to a recognized need for improved research in PPE and technologies. It focuses on experimentation and recommendations for respirator masks, by ensuring a level of standard filter efficiency, and develops criteria for testing and developing PPE.
The NIOSH air filtration rating is the U.S. National Institute for Occupational Safety and Health (NIOSH)'s classification of filtering respirators. The ratings describe the ability of the device to protect the wearer from solid and liquid particulates in the air. The certification and approval process for respiratory protective devices is governed by Part 84 of Title 42 of the Code of Federal Regulations. Respiratory protective devices so classified include air-purifying respirators (APR) such as filtering facepiece respirators and chemical protective cartridges that have incorporated particulate filter elements.
A powered air-purifying respirator (PAPR) is a type of respirator used to safeguard workers against contaminated air. PAPRs consist of a headgear-and-fan assembly that takes ambient air contaminated with one or more type of pollutant or pathogen, actively removes (filters) a sufficient proportion of these hazards, and then delivers the clean air to the user's face or mouth and nose. They have a higher assigned protection factor than filtering facepiece respirators such as N95 masks. PAPRs are sometimes called positive-pressure masks, blower units, or just blowers.
The respiratory protective devices (RPD) can protect workers only if their protective properties are adequate to the conditions in the workplace. Therefore, specialists have developed criteria for the selection of proper, adequate respirators, including the Assigned Protection Factors (APF) - the decrease of the concentration of harmful substances in the inhaled air, which to be provided with timely and proper use of a certified respirator of certain types (design) by taught and trained workers, when the employer performs an effective respiratory protective device programme.
Respirators, also known as respiratory protective equipment (RPE) or respiratory protective devices (RPD), are used in some workplaces to protect workers from air contaminants. Initially, respirator effectiveness was tested in laboratories, but in the late 1960s it was found that these tests gave misleading results regarding the level of protection provided. In the 1970s, workplace-based respirator testing became routine in industrialized countries, leading to a dramatic reduction in the claimed efficacy of many respirator types and new guidelines on how to select the appropriate respirator for a given environment.
An N95 respirator is a disposable filtering facepiece respirator or reusable elastomeric respirator filter that meets the U.S. National Institute for Occupational Safety and Health (NIOSH) N95 standard of air filtration, filtering at least 95% of airborne particles that have a mass median aerodynamic diameter of 0.3 micrometers under 42 CFR 84, effective July 10, 1995. A surgical N95 is also rated against fluids, and is regulated by the US Food and Drug Administration under 21 CFR 878.4040, in addition to NIOSH 42 CFR 84. 42 CFR 84, the federal standard which the N95 is part of, was created to address shortcomings in the prior United States Bureau of Mines respirator testing standards, as well as tuberculosis outbreaks, caused by the HIV/AIDS epidemic in the United States. Since then, N95 respirator has continued to be solidified as a source control measure in various pandemics that have been experienced in the United States and Canada, including the 2009 swine flu and the COVID-19 pandemic.
Hazard controls for COVID-19 in workplaces are the application of occupational safety and health methodologies for hazard controls to the prevention of COVID-19. Multiple layers of controls are recommended, including measures such as remote work and flextime, personal protective equipment (PPE) and face coverings, social distancing, and enhanced cleaning programs. Recently, engineering controls have been emphasized, particularly stressing the importance of HVAC systems meeting a minimum of 5 air changes per hour with ventilation or MERV-13 filters, as well as the installation of UVGI systems in public areas.
Mechanical filters, a part of particulate respirators, are a class of filter for air-purifying respirators that mechanically stops particulates from reaching the wearer's nose and mouth. They come in multiple physical forms.
During the COVID-19 pandemic, face masks or coverings, including N95, FFP2, surgical, and cloth masks, have been employed as public and personal health control measures against the spread of SARS-CoV-2, the virus that causes COVID-19.
In epidemiology, a non-pharmaceutical intervention (NPI) is any method used to reduce the spread of an epidemic disease without requiring pharmaceutical drug treatments. Examples of non-pharmaceutical interventions that reduce the spread of infectious diseases include wearing a face mask and staying away from sick people.
Source control is a strategy for reducing disease transmission by blocking respiratory secretions produced through breathing, speaking, coughing, sneezing or singing. Multiple source control techniques can be used in hospitals, but for the general public wearing personal protective equipment during epidemics or pandemics, respirators provide the greatest source control, followed by surgical masks, with cloth face masks recommended for use by the public only when there are shortages of both respirators and surgical masks.
Elastomeric respirators, also called reusable air-purifying respirators, seal to the face with elastomeric material, which may be a natural or synthetic rubber. They are generally reusable. Full-face versions of elastomeric respirators seal better and protect the eyes.
The European respirator standards refer to the filtering half mask classification by EN 149, EN 14683, and EN 143, all European standards of testing and marking requirements for respirators. FFP standard masks cover the nose, mouth and chin and may have inhalation and/or exhalation valves.
A supplied-air respirator (SAR) or air-line respirator is a breathing apparatus used in places where the ambient air may not be safe to breathe. It uses an air hose to supply air from outside the danger zone. It is similar to a self-contained breathing apparatus (SCBA), except that SCBA users carry their air with them in high pressure cylinders, while SAR users get it from a remote stationary air supply connected to them by a hose. They may be equipped with a backup air tank in case the air-line gets cut.