4.4 Article

Utility and Safety of Backup Insulin Regimens Generated by the Bionic Pancreas: A Randomized Study

Journal

DIABETES TECHNOLOGY & THERAPEUTICS
Volume 25, Issue 6, Pages 437-441

Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/dia.2022.0461

Keywords

Artificial pancreas; Bionic pancreas; Type 1 diabetes; Automated insulin delivery

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This article describes how the bionic pancreas (BP) autonomously doses insulin without carbohydrate counting, using qualitative meal announcements. In case of device malfunction, the BP generates backup insulin doses for injection or pump users, including long-acting insulin dose, a four-period basal insulin profile, short-acting meal doses, and a glucose correction factor. In a 13-week trial, participants using the BP had similar glycemic outcomes compared to those using their prestudy insulin regimen, with both groups having higher mean glucose and lower time-in-range than while using the BP. In conclusion, a backup insulin regimen automatically generated by the BP can be safely implemented if needed.
The bionic pancreas (BP) is initialized with body weight only and doses insulin autonomously without carbohydrate counting, instead using qualitative meal announcements. In case of device malfunction, the BP generates and continuously updates backup insulin doses for injection or pump users, including long-acting insulin dose, a four-period basal insulin profile, short-acting meal doses, and a glucose correction factor. Following a 13-week trial in type 1 diabetes, participants using the BP (6-83 years) completed 2-4 days, in which they were randomly assigned to their prestudy insulin regimen (N = 147) or to follow BP-provided guidance (N = 148). Glycemic outcomes with BP guidance were similar to those reinstituting their prestudy insulin regimen, with both groups having higher mean glucose and lower time-in-range than while using the BP during the 13-week trial. In conclusion, a backup insulin regimen automatically generated by the BP can be safely implemented if need arises to discontinue use of the BP. Clinical Trial Registry: clinicaltrials.gov; NCT04200313.

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