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Humans commonly exhale aerosols comprised of small droplets of airway-lining fluid during normal breathing. These ''exhaled bioaerosols'' may carry airborne pathogens and thereby magnify the spread of certain infectious diseases, such as influenza, tuberculosis, and severe acute respiratory syndrome. We hypothesize that, by altering lung airway surface properties through an inhaled nontoxic aerosol, we might substantially diminish the number of exhaled bioaerosol droplets and thereby provide a simple means to potentially mitigate the spread of airborne infectious disease independently of the identity of the airborne pathogen or the nature of any specific therapy. We find that some normal human subjects expire many more bioaerosol particles than other individuals during quiet breathing and therefore bear the burden of production of exhaled bioaerosols. Administering nebulized isotonic saline to these ''high-producer'' individuals diminishes the number of exhaled bioaerosol particles expired by 72.10 ؎ 8.19% for up to 6 h. In vitro and in vivo experiments with saline and surfactants suggest that the mechanism of action of the nebulized saline relates to modification of the physical properties of the airway-lining fluid, notably surface tension.drug delivery ͉ lung ͉ infectious disease ͉ influenza I t has long been understood that exhaled bioaerosol particles provide an important vector for the spread of certain infectious diseases (1, 2). Viruses known to spread from humans and͞or animals through breathing, sneezing, and coughing include measles, influenza virus (3, 4), adenovirus (5), African swine fever virus (6), foot and mouth disease virus (7), varicellazoster virus (chicken pox) (8), infectious bronchitis virus (9), and smallpox, among others (10). Airborne bacteria include anthrax, Escherichia coli (11), Klebsiella pneumoniae (12), Francisella tularensis (13), and tuberculosis (14). Normal mouth breathing (more than coughing, nose breathing, or talking) has been observed to produce the largest number of airborne droplets (15,16). These droplets are primarily Ͻ1 m in size, because larger droplets tend to be filtered out of the expired air by the lungs (16). Given the variable dimensions of common viral and bacterial pathogens (Ϸ25 nm to 5 m), the ability of exhaled bioaerosol droplets of a given size to carry pathogen obviously varies with pathogen type. Bioaerosols seem to form by the passage of air, during inhalation and exhalation, over the mucus layer lining the lungs (17) or possibly through the reopening of closed small airways, destabilizing the mucus surface through an interplay of surface tension and viscous forces to form small airborne droplets, as has been simulated in vitro via ''cough machine '' experiments (18). In this study, we aimed to explore the ability to transiently diminish the number of exhaled bioaerosol droplets in normal human subjects by delivery of a simple, safe, liquid aerosol. We also aimed to understand the mechanism of the effect of the inhaled aerosol through in vitro cough...

Of 67 office workers 27 (40%) had documented tuberculin skin test conversions after an estimated 4-wk exposure to a coworker with cavitary tuberculosis. Worker complaints for more than 2 yr before the tuberculosis exposure prompted investigations of air quality in the building before and after the tuberculosis exposure. Carbon dioxide concentrations in many parts of the building were found to be above recommended levels, indicating suboptimal ventilation with outdoor air. We applied a mathematical model of airborne transmission to the data to assess the role of building ventilation and other transmission factors. We estimated that ventilation with outside air averaged about 15 feet 3/min (cfm) per occupant, the low end of acceptable ventilation, corresponding to CO2 levels of about 1,000 ppm. The model predicted that at 25 cfm per person 18 workers would have been infected (a 33% reduction) and at 35 cfm, a level considered optimal for comfort, that 13 workers would have been infected (an additional 19% reduction). Further increases in outdoor air ventilation would be impractical and would have resulted in progressively smaller increments in protection. According to the model, the index case added approximately 13 infectious doses (quanta) per hour (qph) to the office air during the exposure period, 10 times the average infectiousness reported in a large series of tuberculosis cases. Further modeling predicted that as infectiousness rises, ventilation would offer progressively less protection. We conclude that outdoor air ventilation that is inadequate for comfort may contribute to airborne infection but that the protection afforded to building occupants by ventilation above comfort levels may be inherently limited, especially when the level of exposure to infection is high.

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.Keywords: infection control; multidrug-resistant tuberculosis; transmission; surgical maskOf an estimated 9 million new cases of tuberculosis (TB) in 2008 globally (1), 440,000 were multidrug-resistant TB (MDR-TB) (2), and more than half of those are believed to have occurred in previously untreated patients, the result of transmission of already drug-resistant strains (2). Recent reports of infection with highly drug-resistant strains of Mycobacterium tuberculosis among patients and health care workers illustrate the dire consequences of nosocomial transmission, especially in areas where HIV is endemic (3, 4). Although once believed to arise primarily from unsupervised or erratic treatment of drug-susceptible TB, MDR-TB and extensively drug-resistant TB (XDR-TB) are now known to be transmissible and have emerged as important threats to patients who enter hospitals for drug-susceptible TB (reinfection) or other illnesses, to the clinical staff caring for them, and to occupants of other congregate settings, such as correctional facilities and shelters. One study in Russia found that hospitalization, rather than treatment nonadherence, conferred a sixfold greater relative risk for the acquisition of MDR-TB by patients (5), whereas another study in Latvia revealed that previous hospitalization was a highly significant risk factor for MDR-TB (odds ratio, 18.33; P , 0.002) (6). In addition, health care workers in diverse settings have been shown to be disproportionately exposed to and infected with drugsusceptible and drug-resistant TB (4, 7). TB among health care workers erodes the already limited supply of hospital personnel in many resource-constrained settings, both directly through illness and indirectly through fear of working in such high-risk envi...

To halt the global tuberculosis epidemic, transmission must be stopped to prevent new infections and new cases. Identification of individuals with tuberculosis and prompt initiation of effective treatment to rapidly render them non-infectious is crucial to this task. However, in settings of high tuberculosis burden, active case-finding is often not implemented, resulting in long delays in diagnosis and treatment. A range of strategies to find cases and ensure prompt and correct treatment have been shown to be effective in high tuberculosis-burden settings. The population-level effect of targeted active case-finding on reducing tuberculosis incidence has been shown by studies and projected by mathematical modelling. The inclusion of targeted active case-finding in a comprehensive epidemic-control strategy for tuberculosis should contribute substantially to a decrease in tuberculosis incidence.

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The opportunities for human immunodeficiency virus (HIV) care and treatment created by new treatment initiatives promoting universal access are also creating unprecedented opportunities for persons with HIV-associated immunosuppression to be exposed to patients with infectious tuberculosis (TB) within health care facilities, with the attendant risks of acquiring TB infection and developing TB disease. Infection control measures can reduce the risk of Mycobacterium tuberculosis transmission even in settings with limited resources, on the basis of a 3-level hierarchy of controls, including administrative or work practice, environmental controls, and respiratory protection. Further research is needed to define the most efficient interventions. The importance of preventing transmission of M. tuberculosis in the era of expanding HIV care and treatment in resource-limited settings must be recognized and addressed.

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.