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Authors
Li, Yong
Barve, Kanchan
Cockrell, Meghan
Agarwal, Amal
Casebeer, Adrianne
Dixon, Suzanne W.
Poonawalla, Insiya
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Article History
Received: 12 September 2023
Accepted: 3 December 2023
First Online: 15 December 2023
Declarations
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: The Humana Healthcare Research Human Subject Protection Office (HHR HSPO) used the US Department of Health and Human Services regulations 45 CFR 46 and the Office of Human Research Protections Guidance on Coded Private Information or Specimens Use in Research, Guidance (2008) to grant an informed consent waiver because it was determined this study did not constitute human subjects research and did not require institutional review board oversight. The decision was based on the determination that the investigation involved only analysis of coded information, and the investigators could not readily identify the individuals from which the information was derived.
: Not applicable.
: All authors are employees of Humana Inc. and/or Humana Healthcare Research or were employed by Humana Inc. at the time of the work.
