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Prospective Surveillance for Cardiac Adverse Events in Healthy Adults Receiving Modified Vaccinia Ankara Vaccines: A Systematic Review

Overview of attention for article published in PLOS ONE, January 2013
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Title
Prospective Surveillance for Cardiac Adverse Events in Healthy Adults Receiving Modified Vaccinia Ankara Vaccines: A Systematic Review
Published in
PLOS ONE, January 2013
DOI 10.1371/journal.pone.0054407
Pubmed ID
Authors

Marnie L. Elizaga, Sandhya Vasan, Mary A. Marovich, Alicia H. Sato, Dale N. Lawrence, Bernard R. Chaitman, Sharon E. Frey, Michael C. Keefer

Abstract

Vaccinia-associated myo/pericarditis was observed during the US smallpox vaccination (DryVax) campaign initiated in 2002. A highly-attenuated vaccinia strain, modified vaccinia Ankara (MVA) has been evaluated in clinical trials as a safer alternative to DryVax and as a vector for recombinant vaccines. Due to the lack of prospectively collected cardiac safety data, the US Food and Drug Administration required cardiac screening and surveillance in all clinical trials of MVA since 2004. Here, we report cardiac safety surveillance from 6 phase I trials of MVA vaccines.

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Mendeley readers

The data shown below were compiled from readership statistics for 41 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United Kingdom 1 2%
United States 1 2%
Unknown 39 95%

Demographic breakdown

Readers by professional status Count As %
Researcher 7 17%
Student > Ph. D. Student 5 12%
Student > Bachelor 4 10%
Student > Master 4 10%
Student > Doctoral Student 2 5%
Other 6 15%
Unknown 13 32%
Readers by discipline Count As %
Medicine and Dentistry 17 41%
Nursing and Health Professions 3 7%
Immunology and Microbiology 3 7%
Agricultural and Biological Sciences 2 5%
Arts and Humanities 1 2%
Other 2 5%
Unknown 13 32%