הכינוס השנתי הדיגיטלי של החברה הישראלית לפדיאטריה קלינית - חיפ"ק 2021

Hybrid closed loop system with automated insulin corection boluses for treatment of adolesents and young adults with type 1 diabetes

רויטל נימרי 1 Benyamin Grosman 2 Anirban Roy 2 Judith Nir 1 Naama Fisch Shvalb 1 Natali Kurtz 2 Neta Loewenthal 3,5 Michal Gillon-Keren 1 Ido Muller 4 Eran Atlas 4 Moshe Phillip 1,6
1The Jesse Z and Sara Lea Shafer Institute for Endocrinology and Diabetes, National Center for Childhood Diabetes, Schneider Children’s Medical Center of Israel, Petah Tikvah, Israel
2Medtronic Diabetes, Medtronic, Northridge, California, USA
3Pediatric, Soroka Medical Center, Beer-Sheva, Israel
4Diabetes, DreaMed Diabetes Ltd, Israel
5Medicine, Ben-Gurion University of the Negev, Beer-Sheva, Israel
6Medicine, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel

Background: The Medtronic MiniMed™ 670G system adjusts basal insulin delivery in response to continuous glucose monitoring levels and is already in use in clinical practice. We tested the home-based feasibility of the new MiniMed™ advanced hybrid closed-loop (AHCL) system, which includes several algorithm enhancements and an optional auto-correction bolus mode. Methods: Twelve adolescents and young adults (eight females) with type 1 diabetes [median (interquartile range)] aged 16.6 (15.9, 18.2) years and diabetes duration of 7.1 (4.7, 8.8) years] participated in this single-arm study. The first stage was a 6-day open-loop run-in period, with the predictive low-glucose suspend feature on. This was followed by 6 days/5 nights in a supervised hotel setting, using the AHCL system including closed-loop challenges (missed meal bolus, late meal bolus, and physical activity); and lastly, 3 weeks with unrestricted home use. Glycemic parameters were compared between the open-loop and closed-loop periods. Results: Participants spent 93.3% (4.7) of the time in SmartGuard™ Auto Mode. HbA1c levels decreased from median (interquartile range) 7.1% (6.7,7.9) at baseline to 6.8% (6.6,7.4) at study end, after 4 weeks (P=0.0027). Time in range (70-180 mg/dl) was 68.4% (10.6) and time below 70 mg/dl was 4% (3.5) during open-loop; and 74% (6.1) and 2.6% (1.9), respectively, during the closed-loop at home phase (P=0.05, P=0.22). Time in range increased during the nighttime, from 64.6% (17.4) to 80.7% (7.8), P=0.008, without change in time below 70 mg/dl (P=0.18). No serious adverse events occurred. Conclusions: The new AHCL system demonstrated safety and effectiveness in controlling day and night glucose levels.