| Literature DB >> 34245636 |
Sara W Heinert1, Jonathan McCoy1, Robert Eisenstein1, Jessica Rowley2.
Abstract
In February 2021, the U.S. Food and Drug Administration (FDA) provided Emergency Use Authorization for the Janssen vaccine- the first one-dose COVID-19 vaccine to become available in the U.S. The one-dose regimen expanded opportunity to vaccinate in settings that can reach vulnerable communities for which returning to a site for a second vaccine dose may prove difficult. With 139 million visits annually in the U.S.1 and a tendency to serve in a safety net capacity for underserved patients2 , the emergency department (ED) is one such setting. This article is protected by copyright. All rights reserved.Entities:
Year: 2021 PMID: 34245636 DOI: 10.1111/acem.14334
Source DB: PubMed Journal: Acad Emerg Med ISSN: 1069-6563 Impact factor: 3.451