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Empowering Hospitalized Patients with Diabetes: Implementation of a Hospital-Wide CGM Policy with EHR-Integrated Validation for Dosing Insulin

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posted on 2024-08-14, 14:16 authored by Ming Yeh Lee, Susan M. Seav, Loice Ongwela, Julie J. Lee, Rachel Aubyrn, Fang Y. Cao, Anna Kalinsky, Olivia Aparicio Ramos, Yunzi Gu, Kailee Kingston, Maja Ivanovic, Bruce A. Buckingham, Dimpi Desai, Rayhan A. Lal, Marilyn Tan, Marina Basina, Michael S. Hughes

Objective: We aimed to assess the feasibility, clinical accuracy, and acceptance of a hospital-wide continuous glucose monitor (CGM) policy with electronic health record (EHR)-integrated validation for insulin dosing.

Research Design and Methods: A hospital policy was developed and implemented at Stanford Health Care for using personal CGMs in lieu of fingerstick blood glucose (FSBG) monitoring. It included requirements specific to each CGM, accuracy monitoring protocols, and EHR integration. User experience surveys were conducted among a subset of patients and nurses.

Results: From November 2022 to August 2023, 135 patients used the CGM protocol in 185 inpatient encounters. This included 26% non-English speakers, 27% with type 1 diabetes, and 23% with automated insulin delivery systems. Most used CGMs were Dexcom G6 (44%) and Libre 2 (42%). Of 1506 CGM validation attempts, 87.8% met the /20 criteria for CGM-based insulin dosing and 99.3% fell within Clarke Zones A or B. User experience surveys were completed by 27 nurses and 46 patients. Most nurses found glucose management under the protocol effective (74%), easy to use (67%), and efficient (63%); 80% of nurses preferred inpatient CGM to FSBG. Most patients liked the CGM protocol (63%), reported positive CGM interactions with nursing staff (63%), and felt no significant interruptions to their diabetes management (63%).

Conclusions: Implementation of a hospital-wide inpatient CGM policy supporting multiple CGM types with real-time accuracy monitoring and integration into the EHR is feasible. Initial feedback from nurses and patients was favorable, and further investigation toward broader use and sustainability is needed.

Funding

M.Y.L. is the Elizabeth and Russell Siegelman Postdoctoral Fellow of the Stanford Maternal and Child Health Research Institute and is supported by the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) of the National Institutes of Health (NIH) under grant T32DK007217. R.A.L. receives support from the NIDDK (grant 1K23DK122017 and P30DK116074) and from Juvenile Diabetes Research Foundation. M.S.H. received support from the NIDDK (grant 5K12DK122550, 1K23DK138267, and P30DK116074).

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