Development of a methodology for the quantification of reaerosolization of a biological contaminate surrogate particle from a military uniform fabric.

In a mass casualty medical evacuation after a bioaerosol (BA) dispersal event, a decontamination (DC) method is needed that can both decontaminate and prevent biological particle (BP) re-aerosolization (RA) of contaminated clothes. However, neither the efficacy of current DC methods nor the risk of...

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Publicado en:Journal of Occupational & Environmental Hygiene Vol. 20; no. 12; pp. 574 - 586
Autores principales: Cooksey, George, Slagley, Jeremy, Cooper, Casey, Lewis, Douglas, Helm, Alisha
Formato: pictorial research tables/charts Journal Article
Publicado: Taylor & Francis Ltd Dec2023
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Dec2023
      vid: 20
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      pub: Taylor & Francis Ltd
      place: Philadelphia, Pennsylvania
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        10.1080/15459624.2023.2248209
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        atl: Development of a methodology for the quantification of reaerosolization of a biological contaminate surrogate particle from a military uniform fabric.
      aug:
        au:
          Cooksey, George
          Slagley, Jeremy
          Cooper, Casey
          Lewis, Douglas
          Helm, Alisha
        affil: Department of Systems Engineering and Management, Air Force Institute of Technology, Dayton, Ohio, USA
      sug:
        subj:
          Aerosols Adverse Effects
          Particulate Matter Adverse Effects
          Military Health
          Uniforms
          Decontamination, Hazardous Materials Methods
          Human
          Experimental Studies
          Microscopy Methods
          Ultraviolet Rays
          Confidence Intervals
          Data Analysis Software
          Military Personnel
          Emergency Medical Services
          Funding Source
      ab: In a mass casualty medical evacuation after a bioaerosol (BA) dispersal event, a decontamination (DC) method is needed that can both decontaminate and prevent biological particle (BP) re-aerosolization (RA) of contaminated clothes. However, neither the efficacy of current DC methods nor the risk of BP RA is greatly explored in the existing literature. The goals of this study were to develop a repeatable method to quantify the RA of a biological contaminant off military uniform fabric swatches and to test the efficacy of one DC protocol (high-volume, low-pressure water) using 1 µm polystyrene latex (PSL) spheres as a surrogate. A four-step methodology was developed: contamination using a Collison Nebulizer; RA using a laboratory mixer and aerosol collection using an inhalable air sampler with a polyvinyl chloride filter; DC using a gravity-fed water shower; and quantification using ultraviolet microscopy via both visual and computer techniques. All results for uncontaminated control samples showed little to no presence of PSL sphere-like particles, while the contaminated experimental trials showed that RA was much lower after DC with water at the 99% confidence level (p-value = 0.0081). The water DC showed an average ∼73% reduction in particle RA, along with a change in air sampler filter deposition patterns from aerosol-like (before DC) to droplet-like (after DC). The fluorescent sphere contamination method for testing the DC residual risk of RA was repeatable and successful.
      pubtype: Academic Journal
      doctype:
        pictorial
        research
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      ougenre: Unknown
    language: English
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