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Authors
- Karen K. Wong, U.S. Centers for Disease Control and Prevention, AtlantaFollow
- Richard T. Davey, National Institutes of Health, Bethesda, Maryland
- Angela L. Hewlett, University of Nebraska Medical Center
- Colleen S. Kraft, Emory University, Atlanta
- Aneesh K. Mehta, Emory University, Atlanta
- Mark J. Mulligan, Emory University, Atlanta
- Allison Beck, Emory University, Atlanta
- William Dorman, US Army Medical Research Institute of Infectious Diseases, Frederick, Maryland
- Christopher J. Kratochvil, University of Nebraska Medical Center, Omaha
- Lilin Lai, Emory University, Atlanta
- Tara N. Palmore, National Institutes of Health, Bethesda, Maryland
- Susan Rogers, Emory University, Atlanta, Georgia
- Philip W. Smith, University of Nebraska Medical Center, OmahaFollow
- Anthony F. Suffredini, Critical Care Medicine Department, Clinical Center, National Institutes of Health
- Mark Wolcott, US Army Medical Research Institute of Infectious Diseases, Frederick
- Ute Ströher, U.S. Centers for Disease Control and Prevention, Atlanta
- Timothy M. Uyeki, U.S. Centers for Disease Control and Prevention, AtlantaFollow
Date of this Version
2016
Citation
Clinical Infectious Diseases (2016) doi: 10.1093/cid/ciw256.
Abstract
From September 2014–April 2015, six persons who had occupational exposures to Zaire ebolavirus in West Africa received investigational agents rVSV-ZEBOV or TKM-100802 for post-exposure prophylaxis and were monitored in the U.S. All patients experienced self-limited symptoms after PEP; none developed Ebola virus disease.
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Comments
US government work