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Original Articles

Military Deployment Human Exposure Assessment: Urine Total and Isotopic Uranium Sampling Results

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Pages 697-714 | Accepted 01 Dec 2003, Published online: 12 Aug 2010
 

Abstract

Currently the Department of Defense (DoD) does not use exposure biomarkers to measure service members’ exposure to environmental chemicals. Blood and urine exposure biomarkers for volatile organic compounds (VOC), selected heavy metals, depleted uranium (DU), and chemical warfare agents are currently available but have not been field tested or validated by the DoD in military deployments as a tool to document exposures. The Military Deployment Human Exposure Assessment Study, a prospective cohort of 46 soldiers deployed to Bosnia, was designed to field test blood and urine exposure biomarkers as a mechanism to document exposures to these chemicals during military deployments. Blood and urine were collected before, during, and after deployment. Standard questionnaire, environmental, and occupational monitoring data collection methods were conducted for comparison to the exposure biomarker results. This article compares and reports the pre-, during, and postdeployment urine total and isotopic uranium measurements and compares them to perceived exposures captured on questionnaire, to environmental data collected by the United Nations Environmental Program in Bosnia, and to standard U.S. urine uranium reference levels (CDC, 2003). Additionally, the questionnaire and environmental and occupational measurements are reported. The results of the study indicate that exposure biomarkers may be a valuable tool to the DoD in exposure and risk assessment with regard to environmental and occupational exposures to uranium.

This research was funded with grants from the Uniformed Services University of the Health Sciences (Protocol T87OY), U.S. Army Center for Health Promotion and Preventive Medicine Deployment Environmental Surveillance Program (Project 47-MA-7678-02), U.S. Centers for Disease Control and Prevention, and Armed Forces Institute of Pathology. This work was completed in partial fulfillment of requirements for the DrPH degree at USUHS. The authors acknowledge the following for their contributions: Dr. Coleen Weese; John Resta; LTC Michael Roy, MC, USA; Col Gary Gackstetter, USAF, BSC; Cara Olsen, MS.

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