This study evaluated 6-month effectiveness and safety of automated insulin delivery (AID) in comparison with multiple daily injections (MDI) in pediatric and adult type 1 diabetes (T1D).
International guidelines endorse automated insulin delivery (AID) as the standard of care for adults and children with type 1 diabetes (T1D), with evidence from systematic reviews showing superior glycemic outcomes compared with MDI or CSII, including improved HbA1c and time in range without increased hypoglycemia. The Medtronic MiniMed™ 670G, the first approved AID system, and its successor, the Bluetooth‑enabled 770G, use the same adaptive algorithm to automate basal insulin delivery; prior trials have shown their safety and efficacy versus CSII. Building on this evidence, the present study reports results from a parallel randomized controlled trial comparing MM670G/770G AID with MDI, with or without CGM, in pediatric and adult T1D populations.
Researchers
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Margaret Lawson
Senior Scientist, CHEO Research Institute
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Caroline Zuijdwijk
Investigator, CHEO Research Institute

