Introduction and Objective: Steroid-induced hyperglycemia poses a significant management challenge in hospitalized patients with diabetes, with limited data to inform best practices. We compared automated insulin delivery (AID) with multiple daily injections plus continuous glucose monitoring (MDI+CGM) to assess inpatient glycemic outcomes. Methods: In this inpatient randomized controlled trial, adults with type 1 or type 2 diabetes receiving corticosteroids (≥10mg prednisone) were assigned to AID or to continue MDI. Both groups received real-time CGM. The primary endpoint was time in range (70-180 mg/dl). Key secondary endpoints: mean glucose, time above range, and time below 70 mg/dl. Results: Thirty-nine hospitalized participants receiving corticosteroids (prednisone-equivalent dose range: 10-1,250 mg) were assigned to AID (n=19; 62± 13 years; A1c 7.6%) or MDI+CGM (n=20, 60±11 years, A1c 8.1%). The mean percentage of time participants were in the target glucose range of 70 to 180 mg/dL was 69±14% in the AID group vs 44±21% in the control group (adj difference, 27%, 95% CI, 21 to 34, p0.001), Figure. Mean glucose was lower with AID compared to control (161± 21 vs 199 ± 34 mg/dL, p0.001). Patients on AID spent 14% less time 250 (95% CI, -18 to -9%). There was no difference in time below 70 or 54 mg/dL. Conclusion: AID was associated with higher time in range than MDI+CGM in patients with diabetes exposed to corticosteroids in the hospital. Disclosure S. Brown: Research Support; Current; Insulet Corporation, Tandem Diabetes Care, Inc., Dexcom, Inc. Research Support; Ended; Roche Diabetes Care, Tolerion, Inc. R. Lal: Consultant; Current; Abbott Diabetes, Adaptyx Biosciences. Consultant; Ended; Biolinq, Capillary Biomedical, Deep Valley Labs. Consultant; Current; Gluroo, Portal Diabetes, Tidepool. Advisory Panel; Ended; ProventionBio, Lilly, Sanofi, Rezolute. M.S. Hughes: Consultant; Current; Dexcom, Inc., Sanofi, Sequel Med Tech, LLC. T. Akcan: None. M. Basina: None. J. Kirby: Stock/Shareholder; Current; PS Fertility. R. Parab: None. J.M. Feeley: Research Support; Current; Dexcom, Inc. M. Stumpf: None. K. Miller: None. J.C. Costin: None. N. Reyes: None. M.C. Sanchez Valenzuela: None. Z. Wen: None. C. Alix: None. L. Chadalawada: None. M. Weber: None. T. Idrees: Research Support; Current; AbbVie Inc. R.S. Kingman: None. B. Suh: None. M. Morgan: None. Y. Liu: None. M. Lee: None. M. Tan: Advisory Panel; Ended; Vertex Pharmaceuticals Incorporated. Consultant; Current; Novo Nordisk, Amylyx. K. Kingston: None. L. Peng: None. R.W. Beck: Research Support; Current; MannKind Corporation, Abbott Diabetes, Dexcom, Inc., Tandem Diabetes Care, Inc., Sequel Med Tech, DreaMed Diabetes, Ltd. Consultant; Ended; Novo Nordisk, Eli Lilly and Company. Consultant; Current; Zucara Therapeutics. G. Davis: Research Support; Current; Insulet Corporation, Sequel Med Tech. F.J. Pasquel: Research Support; Current; Dexcom, Inc., Insulet Corporation, Ideal Medical Technologies. Research Support; Ended; Novo Nordisk, Tandem Diabetes Care, Inc. Consultant; Ended; Insulet Corporation. Funding The National Institute of Diabetes and Digestive and Kidney Diseases (R01DK138366), with device support from Insulet and Dexcom, Inc.
BROWN et al. (Fri,) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: