Performance data for fabric filters using either woven or felt bags can be better understood when fault processes such as pinhole bypass and seepage are considered. Penetration straight through the dust cake and fabric may not be important by comparison. Observed trends of increased penetration with increased filtration velocity, constant or slightly increased penetration with increasing particle diameter, and constant penetration with additional dust loading can be explained by fault processes. The pulse-jet experimental work described here, done over many filtration and cleaning cycles, shows that penetration increases substantially with increasing filtration velocity and that this increase is due entirely to seepage.
A commercial computer-aided design tool used by the lighting industry was modified to predict fluence rates for upper-room ultraviolet germicidal irradiation. Experimental validation based on more than 1600 measurements and 3 types of commercial ultraviolet fixtures, which was done in an experimental chamber and in a homeless shelter having fixtures in continuous use for over 7 years, showed differences in measured and predicted average upper-room fluence rates of less than 10%. The computer-aided design tool, however, was not very successful at predicting fluence rates at specific room locations, a capability that is needed for mating computational fluid dynamics with ultraviolet germicidal irradiation. Although not an objective of this study, it was also found that the three types of fixtures used in this study have surprisingly significant differences in efficiency based on fixture ultraviolet power output and electrical input. One fixture type had an efficiency that was more than five times that of another. For comparison purposes, a standard method for measuring and reporting fixture efficiency is needed.
RATIONALE:Drug-resistant tuberculosis transmission in hospitals threatens staff and patient health. Surgical face masks used by patients with tuberculosis (TB) are believed to reduce transmission but have not been rigorously tested.OBJECTIVES:We sought to quantify the efficacy of surgical face masks when worn by patients with multidrug-resistant TB (MDR-TB).METHODS:Over 3 months, 17 patients with pulmonary MDR-TB occupied an MDR-TB ward in South Africa and wore face masks on alternate days. Ward air was exhausted to two identical chambers, each housing 90 pathogen-free guinea pigs that breathed ward air either when patients wore surgical face masks (intervention group) or when patients did not wear masks (control group). Efficacy was based on differences in guinea pig infections in each chamber.MEASUREMENTS AND MAIN RESULTS:Sixty-nine of 90 control guinea pigs (76.6%; 95% confidence interval [CI], 68-85%) became infected, compared with 36 of 90 intervention guinea pigs (40%; 95% CI, 31-51%), representing a 56% (95% CI, 33-70.5%) decreased risk of TB transmission when patients used masks.CONCLUSIONS:Surgical face masks on patients with MDR-TB significantly reduced transmission and offer an adjunct measure for reducing TB transmission from infectious patients.
A natural TB infection model using guinea pigs may provide useful information for investigating differences in transmission efficiency and establishment of active disease by clinical TB strains in a highly susceptible host under controlled environmental conditions. We sought to examine the capacity of naturally transmitted multidrug-resistant Mycobacterium tuberculosis to establish infection and produce active disease in guinea pigs. Guinea pigs were continuously exposed for 4 months to the exhaust air of a 6-bed multidrug-resistant tuberculosis inpatient hospital ward in South Africa. Serial tuberculin skin test reactions were measured to determine infection. All animals were subsequently evaluated for histologic disease progression at necropsy. Although 75% of the 362 exposed guinea pigs had positive skin test reactions [>= 6 mm], only 12% had histopathologic evidence of active disease. Reversions (>= 6 mm change) in skin test reactivity were seen in 22% of animals, exclusively among those with reactions of 6 -13 mm. Only two of 86 guinea pigs with reversion had histological evidence of disease compared to 47% (31/66) of guinea pigs with large, non-reverting reactions. Immunosuppression of half the guinea pigs across all skin test categories did not significantly accelerate disease progression. In guinea pigs that reverted a skin test, a second positive reaction in 27 (33%) of them strongly suggested re-infection due to ongoing exposure. These results show that a large majority of guinea pigs naturally exposed to human-source strains of multidrug-resistant tuberculosis became infected, but that many resolved their infection and a large majority failed to progress to detectable disease. (C) 2011 Elsevier Ltd. All rights reserved.
ABSTRACT Influenza virus has been found to persist in the environment for hours to days, allowing for secondary transmission of influenza via inanimate objects known as fomites. We evaluated the efficacy of heat and moisture for the decontamination of surfaces for the purpose of preventing of the spread of influenza. Aqueous suspensions of influenza A virus were deposited onto stainless steel coupons, allowed to dry under ambient conditions, and exposed to temperatures of 55°C, 60°C, or 65°C and relative humidity (RH) of 25%, 50%, or 75% for up to 1 h. Quantitative virus assays were performed on the solution used to wash the viruses from these coupons, and results were compared with the solution used to wash coupons treated similarly but left under ambient conditions. Inactivation of influenza virus on surfaces increased with increasing temperature, RH, and exposure time. Reductions of greater than 5 logs of influenza virus on surfaces were achieved at temperatures of 60 and 65°C, exposure times of 30 and 60 min, and RH of 50 and 75%. Our data also suggest that absolute humidity is a better predictor of surface inactivation than RH and allows the prediction of survival using two parameters rather than three. Modest amounts of heat and adequate moisture can provide effective disinfection of surfaces while not harming surfaces, electrical systems, or mechanical components, leaving no harmful residues behind after treatment and requiring a relatively short amount of time.
BACKGROUND:Surfaces in congregate settings, such as vehicles used for mass transportation, can become contaminated with infectious microorganisms and facilitate disease transmission. We disinfected surfaces contaminated with H1N1 influenza viruses using hydrogen peroxide (HP) vapor at concentrations below 100 ppm and triethylene glycol (TEG)-saturated air containing 2 ppm of TEG at 25 degrees C.METHODS:Influenza viruses in aqueous suspensions were deposited on stainless-steel coupons, allowed to dry at ambient conditions, and then exposed for up to 15 minutes to 10 to 90 ppm of HP vapor or TEG-saturated air. Virus assays were done on the solution used to wash the viruses from these coupons and from coupons treated similarly but without exposure to HP or TEG vapor.RESULTS:After 2.5 minutes, exposure to 10-ppm HP vapor resulted in 99% inactivation. For air saturated with TEG at 25 to 29 degrees C, the disinfection rate was about 1.3 log(10) reductions per hour, about 16 times faster than the measured natural inactivation rate under ambient conditions.CONCLUSIONS:Vapor concentrations of 10 ppm HP or 2 ppm TEG can provide effective surface disinfection. At these low concentrations, the potential for damage to even the avionics of an airplane would be expected to be minimal. At a TEG vapor concentration of 2 ppm, there are essentially no health risks to people.
This paper reports results from a field study designed to demonstrate a method for evaluating a building's in-duct ultraviolet germicidal irradiation (UVGI) system using naturally occurring airborne microorganisms and to evaluate its potential effectiveness against selected airborne microorganisms. Forty-eight 64 in. (1.63 m) long ultraviolet germicidal lamps were installed perpendicular to airflow and upstream of the cooling coils in a heating, ventilating, and air-conditioning (HVAC) system for a retail space in a large New York City office building. A portable in-duct UVGI apparatus was used to benchmark ultraviolet susceptibility of naturally occurring airborne microorganisms. Benchmarking was accomplished by measuring the portable apparatus's efficiency for inactivating UVGI-resistant microorganisms in the laboratory at various operating conditions. Inactivation efficiency for both the in-duct UVGI-equipped HVAC system and portable in-duct UVGI apparatus were then measured simultaneously using naturally occurring microorganisms. If the UVGI-equipped HVAC system had higher inactivation efficiency than the portable in-duct UVGI apparatus, then the UVGI-equipped HVAC system's efficiency for inactivating the UVGI-resistant microorganisms used in the laboratory would be expected to be higher than the efficiency of the portable in-duct UVGI apparatus. Based on the results for the tested UVGI-equipped HVAC system, the expected efficiency was at least 88% for Bacillus subtilis var. niger spores, a common surrogate for Bacillus anthracis spores.
In the event of a smallpox outbreak due to bioterrorism, delays in vaccination programs may lead to significant secondary transmission. In the early phases of such an outbreak, transmission of smallpox will take place especially in locations where infected persons may congregate, such as hospital emergency rooms. Air disinfection using upper-room 254 nm (UVC) light can lower the airborne concentrations of infective viruses in the lower part of the room, and thereby control the spread of airborne infections among room occupants without exposing occupants to a significant amount of UVC. Using vaccinia virus aerosols as a surrogate for smallpox we report on the effectiveness of air disinfection, via upper-room UVC light, under simulated real world conditions including the effects of convection, mechanical mixing, temperature and relative humidity. In decay experiments, upper-room UVC fixtures used with mixing by a conventional ceiling fan produced decreases in airborne virus concentrations that would require additional ventilation of more than 87 air changes per hour. Under steady state conditions the effective air changes per hour associated with upper-room UVC ranged from 18 to 1000. The surprisingly high end of the observed range resulted from the extreme susceptibility of vaccinia virus to UVC at low relative humidity and use of 4 UVC fixtures in a small room with efficient air mixing. Increasing the number of UVC fixtures or mechanical ventilation rates resulted in greater fractional reduction in virus aerosol and UVC effectiveness was higher in winter compared to summer for each scenario tested. These data demonstrate that upper-room UVC has the potential to greatly reduce exposure to susceptible viral aerosols. The greater survival at baseline and greater UVC susceptibility of vaccinia under winter conditions suggest that while risk from an aerosol attack with smallpox would be greatest in winter, protective measures using UVC may also be most efficient at this time. These data may also be relevant to influenza, which also has improved aerosol survival at low RH and somewhat similar sensitivity to UVC.
ABSTRACTInterest in airborne smallpox transmission has been renewed because of concerns regarding the potential use of smallpox virus as a biothreat agent. Air disinfection via upper-room 254-nm germicidal UV (UVC) light in public buildings may reduce the impact of primary agent releases, prevent secondary airborne transmission, and be effective prior to the time when public health authorities are aware of a smallpox outbreak. We characterized the susceptibility of vaccinia virus aerosols, as a surrogate for smallpox, to UVC light by using a benchtop, one-pass aerosol chamber. We evaluated virus susceptibility to UVC doses ranging from 0.1 to 3.2 J/m2, three relative humidity (RH) levels (20%, 60%, and 80%), and suspensions of virus in either water or synthetic respiratory fluid. Dose-response plots show that vaccinia virus susceptibility increased with decreasing RH. These plots also show a significant nonlinear component and a poor fit when using a first-order decay model but show a reasonable fit when we assume that virus susceptibility follows a log-normal distribution. The overall effects of RH (P< 0.0001) and the suspending medium (P= 0.014) were statistically significant. When controlling for the suspending medium, the RH remained a significant factor (P< 0.0001) and the effect of the suspending medium was significant overall (P< 0.0001) after controlling for RH. Virus susceptibility did not appear to be a function of virus particle size. This work provides an essential scientific basis for the design of effective upper-room UVC installations for the prevention of airborne infection transmission of smallpox virus by characterizing the susceptibility of an important orthopoxvirus to UVC exposure.
The objective of this research was to study the factors that relate to the effectiveness of upper-room ultraviolet germicidal irradiation for inactivating airborne microorganisms. The work was conducted in a room-sized chamber designed and furnished for investigations of this nature. Nebulized Serratia marcescens, Bacillus subtilis spores, and vaccinia virus were used as test aerosols. Most data were collected from steady-state experiments comparing the number of viable organisms in the chamber air remaining with UV lamps turned on to the number with UV lamps turned off, but some decay experiments were conducted to compare the two methods. UV power level had a strong influence but was fully effective only in the presence of air mixing that produced vigorous vertical air currents. A conclusion of the study is that an upper-room ultraviolet installation is a complex system that requires careful integration of UV luminaires, UV power, and room ventilation arrangements.
Seven years of experience operating upper-room ultraviolet irradiation systems (UVGI) in 14 homeless shelters in six cities has taught the Tuberculosis Utraviolet Shelter Study (TUSS) many valuable lessons about maintaining uninterrupted UV services and acceptable intervals between UV lamp changes and cleaning activities. One year (9,000 hours) of continuous illumination resulted in a reduction in UVC output of the two types of low pressure mercury Lamps by 17 percent for the quartz, instant start tubular lamp and 25 percent for the preheat compact lamps. The reduction over time was due to metal accumulations on the inside of the glass plus increasing opaqueness (solarization) due to UV irradiation. Cleaning frequency was found to be highly site-specific. Lamp failure was infrequent and within the manufacturers' stated life period.
After decades of neglect, the resurgence of tuberculosis in the United States between 1985 and 1992 renewed interest in the use of upper room ultraviolet germicidal irradiation to interrupt the transmission of airborne infections. More recently the bioterrorism threat and the appearance of new pathogens with the potential for airborne spread, such as severe acute respiratory syndrome (SARS), have stimulated installations of upper-room irradiation systems. The objective is to flood the entire volume of a room above 6.5 ft with high intensity ultraviolet germicidal irradiation, while minimizing unintentional irradiance below 6.5 ft to avoid eye and skin irritation. Air exchanges between the upper and lower room result in air disinfection of the occupied space. Designers of these systems have adopted the practice of limiting the maximum lower room irradiance at every point to less than the continuous 8-hour time-weighted average threshold limit value, severely limiting the irradiation intensity in the upper room and thereby reducing one of the two major factors determining germicidal effectiveness, the other being room air mixing. The hypothesis of this study is that eye and skin exposure will be well below the recommended safe dose even when maximum eye-level irradiance levels in the room exceed the 8-hour continuous exposure threshold limit. The method employed was to have subjects wear a small photometer that recorded total ultraviolet dose over the period of exposure while subjects went about their normal routine, and comparing this value with a hypothetical dose calculated from the highest measured eye-level irradiance. The results of the study, based on a limited number of observations, confirmed the hypothesis. Observed doses were one-third to a factor of a hundred or more lower than the doses calculated from maximum eye-level irradiances measurements in the occupants' spaces.
ABSTRACT Experimental systems have been built in laboratories worldwide to investigate the influence of various environmental parameters on the efficacy of UV germicidal irradiation (UVGI) for deactivating airborne microorganisms. It is generally recognized that data from different laboratories might vary significantly due to differences in systems and experimental conditions. In this study we looked at the effect of the composition of the suspending medium on the size and UVGI susceptibility of Serratia marcescens in an experimental system built in our laboratory. S. marcescens was suspended in (i) distilled water, (ii) phosphate buffer, (iii) 10% fetal calf serum, (iv) phosphate-buffered saline (saline, 0.8% sodium chloride), and (v) synthetic saliva (phosphate-buffered saline with 10% fetal calf serum). At low humidity (36%), S. marcescens suspended in water-only medium was the most susceptible to UVGI, followed by those in serum-only medium. The count median diameters (CMDs) for culturable particles from water-only and serum-only media were 0.88 and 0.95 μm, respectively, with the measurements based on their aerodynamic behavior. The bacteria suspended in phosphate buffer, synthetic saliva, and phosphate-buffered saline had similar UVGI susceptibility and CMD at 1.0, 1.4, and 1.5 μm, respectively. At high humidity (68%) the CMD of the particles increased by 6 to 16%, and at the same time UVGI susceptibility decreased, with the magnitude of decrease related to the type of suspending medium. In conclusion, the choice of suspending medium influenced both size and UVGI susceptibility of S. marcescens . These data are valuable for making comparisons and deciding on the use of an appropriate medium for various applications.
Bioterrorism is an area of increasing public health concern. The intent of this article is to review the air cleansing technologies available to protect building occupants from the intentional release of bioterror agents into congregate spaces (such as offices, schools, auditoriums, and transportation centers), as well as through outside air intakes and by way of recirculation air ducts. Current available technologies include increased ventilation, filtration, and ultraviolet germicidal irradiation (UVGI) UVGI is a common tool in laboratories and health care facilities, but is not familiar to the public, or to some heating, ventilation, and air conditioning engineers. Interest in UVGI is increasing as concern about a possible malicious release of bioterror agents mounts. Recent applications of UVGI have focused on control of tuberculosis transmission, but a wide range of airborne respiratory pathogens are susceptible to deactivation by UVGI. In this article, the authors provide an overview of air disinfection technologies, and an in-depth analysis of UVGI-its history, applications, and effectiveness.
A historical review of laboratory fume hoods leads to a consideration of the current status of structural design, operating characteristics (with special reference to face velocity), safety (relative to standardized test results), energy conservation, and certification methods. Noteworthy are (1) the increasing complexity of instrumentation designed to assure full safety function plus airflow modulation to minimize energy consumption; (2) the extreme plasticity of accepted and recommended face velocity values; (3) the insensitivity of standardized hood test protocols to variations in face velocity; and (4) a serious lack of correlation between operator risk, face velocity, and standard hood test results. Safety considerations lead to the selection of laboratory fume hoods having the highest demonstrated containment capability. This is in spite of the fact that most hood operations have a low hazard rating. Energy savings could be realized if the face velocity of each hood could be modulated to match the risk associated with the work being conducted.
In this study, we explored the efficacy of upper-room ultraviolet germicidal irradiation (UVGI) in reducing the concentration of Serratia marcescens and Mycobacterium bovis bacille Calmette-Guérin (BCG) aerosols in enclosed places. We constructed a facility (4.5 m x 3 m x 2.9 m) in which both ceiling- and wall-mounted UV fixtures (UV output: 10W and 5W respectively) were installed. The use of ceiling- and wall-mounted UV fixtures (total UV output: 15W) without mixing fan reduced the concentration of S. marcescens aerosols by 46% (range: 22-80%) at 2 air changes per hour (ACH) and 53% (range: 40-68%) at 6 ACH. The use of ceiling- and wall-mounted UV fixtures with mixing fan increased the UV effectiveness in inactivating S. marcescens aerosols to 62% (range: 50-78%) at 2 ACH and to 86% (81-89%) at 6 ACH. For BCG aerosols, UV effectiveness in inactivating BCG aerosols at 6 ACH were 52% (range: 11-69%) by ceiling-mounted UV fixture only (total UV output: 10W) and 64% (51-83%) by both ceiling- and wall-mounted UV fixtures (total UV output: 15W). Our results indicated that the equivalent ventilation rate attributable to upper-room UVGI for BCG aerosols ranged from 1 ACH to 22 ACH for ceiling-mounted UV fixtures and from 6.4 ACH to 28.5 ACH for ceiling- and wall-mounted UV fixtures. Both generalized linear and generalized additive models were fitted to all our data. The regression results indicated that the number of UV fixtures, use of mixing fan, and air exchange rate significantly affected UV effectiveness (p < 0.01, 0.01, 0.01 respectively). However, the strain difference (S. marcescens vs. BCG) appeared less important in UV effectiveness (p = 0.26). Our results also indicated that UV effectiveness increased at higher temperature ((italic)p(/italic) < 0.01), lower dry-bulb temperature ((italic)p(/italic) = 0.21), and colder air from a supply grill located near the ceiling (p = 0.22).
Ultraviolet germicidal irradiation (UVGI) is one method currently used to reduce transmission of airborne infectious diseases such as tuberculosis. UVGI is defined as optical radiation in the shortwave UV-C spectrum capable of killing microorganisms and has been demonstrated to be effective against certain airborne bacteria. Because prolonged direct exposure to low intensity UVGI can cause skin and eye irritation, fixtures appropriate for upper room air disinfection are installed above eye level and designed to limit the vertical emission spread to prevent excessive exposure to occupants, Accurate UVGI fixture emission profiles, in combination with appropriate room ventilation measurements, are needed to calculate the dose to airborne microorganisms and estimate the effectiveness of these air disinfection devices in preventing disease transmission in susceptible populations. Manufacturers of fixtures usually provide nominal wattage and horizontal centerplane intensity levels, but to quantify the dose to exposed airborne microorganisms adequately in realistic room applications it is necessary to measure the three-dimensional emission profile for various fixture designs. This article evaluates several UVGI fixtures available for upper room installations and illustrates practical methods for evaluating effective radiation output. Typical emission diagrams are included.
Mycobacterium tuberculosis (MTB) is transmitted through the air, and can be captured on ventilation air filters. People handling these filters may be exposed to infectious material. We studied the survival of strains of Mycobacterium on high efficiency particulate air (HEPA) filter material. We used a model ventilation system to evaluate survival over time of Mycobacterium chelonae and H37Ra (an avirulent stain of MTB) aerosolized and then captured on HEPA filter material. Survival curves for M. chelonae incubated at 55% and 75% RH under static conditions were not different with less than 4% survival at 24 hours. H37Ra was subjected to continuous airflow at the design airflow for the filter material following deposition on the HEPA filter material, and less than 0.1% of cells survived to 48 hours (RH not controlled). H37Ra was resistant to immobilized biocide (trimethoxysilylpropyl dimethyloctadecyl ammonium chloride) on HEPA filter material as well as the same biocide in solution. Finally, survival of H37Ra and virulent MTB strain (H37Rv) were not different following deposition onto HEPA filter material from liquid suspension and incubation under static conditions.