Freeman, Patricia R.
McAninch, Jana
Dasgupta, Nabarun
Oyler, Douglas R.
Slavov, Krassimir
Collins, Candice
Hargrove, Sarah
Freeman, Edward
Miracle, Dustin
Slavova, Svetla
Funding for this research was provided by:
U.S. Food and Drug Administration (HHSF223201810183C)
U.S. Food and Drug Administration (HHSF223201810183C)
U.S. Food and Drug Administration (HHSF223201810183C)
U.S. Food and Drug Administration (HHSF223201810183C)
U.S. Food and Drug Administration (HHSF223201810183C)
U.S. Food and Drug Administration (HHSF223201810183C)
Article History
Received: 27 June 2023
Accepted: 21 August 2023
First Online: 1 September 2023
Declarations
:
: ND is on the Scientific Advisory Board for the non-profit RADARS System of Denver Health and Hospitals Authority, Denver, Colorado.
: The University of Kentucky Institutional Review Board approved the study (Protocol # 47384) and granted a waiver of the informed consent process as the study uses retrospectively obtained secondary data of decedents, only aggregated numbers are reported, with frequencies ≤ 5 and rates based on ≤ 10 events suppressed according to state vital statistics data reporting policy.
: Not applicable.