Search

Mobile whole‐room UVGI devices are used in healthcare settings to control surface‐borne pathogens. Unfortunately, no standard method comparing the efficacy of these devices is available. We accessed the effect of shadows on UVC 254 nm inactivation. The evaluation of a mobile whole‐room UVGI device used spores of Bacillus atrophaeus as a surrogate for Clostridium difficile and Staphylococcus aureus as a surrogate for MSRA. Inactivation after 10 min of exposure varied significantly depending on whether the spores received direct UV exposure (4.3 log reduction), both direct and reflected UV exposure (3.0–4.0 log reduction) or reflected UV exposure alone (<1.0 log reduction). The susceptibility (z‐value) for inactivation of B. atrophaeus spores on a glass surface was estimated to be 0.00312 m2 J−1. Staphylococcus aureus microbial log reductions were approximately 5.5 for direct UV exposure, 3.6–5.2 for both direct and reflected UV exposure and approximately 2.75 for only reflected UV exposure. Our measurement of reflected dose ranged from 0.46% to 1.47%. Based on our findings, B. atrophaeus spores should be considered as a model organism for testing the impact of shadows on mobile whole‐room UVGI device inactivation. Optimizing the reflected component of whole‐room UVGI is important, especially for UVC‐resistant organisms. [ABSTRACT FROM AUTHOR]

Mobile whole‐room UVGI devices are used in healthcare settings to control surface‐borne pathogens. Unfortunately, no standard method comparing the efficacy of these devices is available. We accessed the effect of shadows on UVC 254 nm inactivation. The evaluation of a mobile whole‐room UVGI device used spores of Bacillus atrophaeus as a surrogate for Clostridium difficile and Staphylococcus aureus as a surrogate for MSRA. Inactivation after 10 min of exposure varied significantly depending on whether the spores received direct UV exposure (4.3 log reduction), both direct and reflected UV exposure (3.0–4.0 log reduction) or reflected UV exposure alone (<1.0 log reduction). The susceptibility (z‐value) for inactivation of B. atrophaeus spores on a glass surface was estimated to be 0.00312 m2 J−1. Staphylococcus aureus microbial log reductions were approximately 5.5 for direct UV exposure, 3.6–5.2 for both direct and reflected UV exposure and approximately 2.75 for only reflected UV exposure. Our measurement of reflected dose ranged from 0.46% to 1.47%. Based on our findings, B. atrophaeus spores should be considered as a model organism for testing the impact of shadows on mobile whole‐room UVGI device inactivation. Optimizing the reflected component of whole‐room UVGI is important, especially for UVC‐resistant organisms. [ABSTRACT FROM AUTHOR]

Abstract Background A previous observational study detected a strong positive relationship between sick leave absences and carbon dioxide (CO2) concentrations in office buildings in the Boston area. The authors speculated that the observed association was due to a causal effect associated with low dilution ventilation, perhaps increased airborne transmission of respiratory infections. This study was undertaken to explore this association. Methods We conducted an intervention study of indoor CO2 levels and sick leave among hourly office workers employed by a large corporation. Outdoor air supply rates were adjusted periodically to increase the range of CO2 concentrations. We recorded indoor CO2 concentrations every 10 minutes and calculated a CO2 concentration differential as a measure of outdoor air supply per person by subtracting the 1–3 a.m. average CO2 concentration from the same-day 9 a.m. – 5 a.m. average concentration. The metric of CO2 differential was used as a surrogate for the concentration of exhaled breath and for potential exposure to human source airborne respiratory pathogens. Results The weekly mean, workday, CO2 concentration differential ranged from 37 to 250 ppm with a peak CO2 concentration above background of 312 ppm as compared with the American Society of Heating, Refrigeration and Air-conditioning Engineers (ASHRAE) recommended maximum differential of 700 ppm. We determined the frequency of sick leave among 294 hourly workers scheduled to work approximately 49,804.2 days in the study areas using company records. We found no association between sick leave and CO2 differential Conclusions The CO2 differential was in the range of very low values, as compared with the ASHRAE recommended maximum differential of 700 ppm. Although no effect was found, this study was unable to test whether higher CO2 differentials may be associated with increased sick leave.

The characterization of the susceptibility of an important orthopoxvirus to upper-room 254-nm germicidal UV (UVC) exposure is presented. It provides an essential scientific basis for the design of effective upper-room UVC installations for the prevention of airborne infection transmission of smallpox virus.

The primary objective of the present work was to develop and validate a simple method for measuring the ultraviolet (UV) emission rate of louvered UV fixtures designed for upper-room ultraviolet germicidal irradiation (UVGI). A secondary objective was to compare the emission rates and energy usage of a few commercially available fixtures and explain the reasons for the differences observed. The ultraviolet emission rate of fixtures designed for upper-room UVGI is clearly an important metric for specifying the UV dosing requirements for a particular application—that is, determining how many UV fixtures should be installed in a given room. UV emission rate is also important for evaluating how efficiently the fixture utilizes the required electrical power input. The ratio of the UV emission rate to the electrical input is a useful parameter for ranking or improving fixtures. In this article, we describe “UV sensor traverse” and its validation. UV sensor traverse is a simple method for measuring UV emission rate by traversing the louvered face of a fixture with a UV sensor. Using this method, we show that a commercially available fixture with a cylindrical parabolic reflector with a tubular lamp has about 84% of the UV radiation exiting the fixture emitted from the back of the lamp, compared to only 21% for a fixture with a flat reflector and compact lamps. The energy-use efficiency of the former fixture is about five times greater than that of the latter fixture. In the fixture with the parabolic reflector, UV rays are redirected by the reflector so that they tend to be parallel to the louvers, allowing significantly more of the UV radiation emitted from the back of the lamp to exit the fixture than a fixture with a flat reflector, which simply alters the direction of the UV rays. To conserve energy and minimize the number of louvered UV fixtures required, well-designed parabolic reflectors are essential. [ABSTRACT FROM AUTHOR]

Room air filters, which usually closely resemble high-efficiency particulate air (HEPA) filters, should be designed to maximize the clean air delivery rate (CADR) rather than operate at the very high collection efficiencies and relatively high pressure drops associated with HEPA filters. That is, for fixed electrical energy consumption, filters should remove the most particles possible. This can be accomplished by designing room filters that operate at lower collection efficiencies and higher airflow rates than HEPA filters. Based on filtration theory, the CADR of a fibrous filter is maximized with respect to filter thickness and air velocity at fixed energy consumption and filtration area. For very small particles for which diffusional deposition is the predominant collection mechanism, it is shown that a filter thickness resulting in a collection efficiency of 82% is optimal. For somewhat larger particles having diameters close to the filter's most penetrating size, direct interception is included in the analysis. The importance of inertial impaction and electrostatic deposition is also considered. This article supports the belief that room air filters used for enhancing indoor air quality can be improved significantly and suggests a methodology to accomplish this improvement. [ABSTRACT FROM AUTHOR]

Background: Eggcrate upper-room ultraviolet germicidal irradiation (UVGI), an engineering control method for reducing the airborne transmission of infectious diseases, was recently developed as an alternative to conventional upper-room UVGI using conventional louvered fixtures. A UV screen, which is composed of open-cell eggcrate panels supported in a frame designed for a conventional suspended ceiling, was used to minimize UV radiation in the lower room. A ceiling fan, which was blowing upward directly above the microbiological source, provided vertical air exchange between the upper and lower room. This system has been shown to be significantly more effective than conventional upper-room UVGI. Study Design In the present study, the microbiological source location and the airflow direction due to the ceiling fan were varied in order to evaluate their impact on germicidal efficacy. Results: The test results clearly showed that placing an aerosol source directly underneath an upward blowing ceiling fan produces the maximum efficacy. Conclusions: The likely explanation for this outcome is that the fan sucks the microorganisms emitted by the source into the UV beam before being mixed with the air in the room. This is somewhat analogous to local exhaust ventilation in which the contaminant is removed prior to being mixed with the air in the room. Thus, when possible, the ceiling fan should be blowing upward and directly above the source. However, for experimental testing, the source location should be varied in order to access the range of germicidal efficacies that can be expected.

Background: Rhinovirus, the most common cause of upper respiratory tract infections, has been implicated in asthma exacerbations and possibly asthma deaths. Although the method of transmission of rhinoviruses is disputed, several studies have demonstrated that aerosol transmission is a likely method of transmission among adults. As a first step in studies of possible airborne rhinovirus transmission, we developed methods to detect aerosolized rhinovirus by extending existing technology for detecting infectious agents in nasal specimens. Methods: We aerosolized rhinovirus in a small aerosol chamber. Experiments were conducted with decreasing concentrations of rhinovirus. To determine the effect of UV irradiation on detection of rhinoviral aerosols, we also conducted experiments in which we exposed aerosols to a UV dose of 684 mJ/m2. Aerosols were collected on Teflon filters and rhinovirus recovered in Qiagen AVL buffer using the Qiagen QIAamp Viral RNA Kit (Qiagen Corp., Valencia, California) followed by semi-nested RT-PCR and detection by gel electrophoresis. Results: We obtained positive results from filter samples that had collected at least 1.3 TCID50 of aerosolized rhinovirus. Ultraviolet irradiation of airborne virus at doses much greater than those used in upper-room UV germicidal irradiation applications did not inhibit subsequent detection with the RT-PCR assay. Conclusion: The air sampling and extraction methodology developed in this study should be applicable to the detection of rhinovirus and other airborne viruses in the indoor air of offices and schools. This method, however, cannot distinguish UV inactivated virus from infectious viral particles.