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Trial of Hybrid Closed-Loop Control in Young Children with Type 1 Diabetes
R Paul Wadwa1, Zachariah W Reed1, Bruce A Buckingham1
1From the Barbara Davis Center for Diabetes, University of Colorado, Anschutz Medical Campus, Aurora (R.P.W., G.P.F.); the Jaeb Center for Health Research, Tampa, FL (Z.W.R., J.L., C.K., R.W.B.); the Department of Pediatrics, Division of Pediatric Endocrinology and Diabetes, Stanford University School of Medicine, Stanford (B.A.B.), and the Division of Pediatric Endocrinology, University of California, San Francisco, San Francisco (L.E.) - both in California; and the University of Virginia Center for Diabetes Technology, Charlottesville (M.D.D., M.S., M.D.B.).
Insights
Closed-loop insulin delivery systems improve glycemic control in young children with type 1 diabetes. Virtual initiation of these systems is safe and effective, increasing time in target glucose range.
Area of Science:
- Pediatrics
- Endocrinology
- Biomedical Engineering
Background:
- Type 1 diabetes management in young children presents unique challenges.
- Closed-loop insulin delivery systems offer potential for improved glycemic control.
- The safety and efficacy of virtually initiating these systems in very young children remain under investigation.
Purpose of the Study:
- To evaluate the efficacy and safety of initiating a closed-loop insulin delivery system virtually in children younger than 6 years with type 1 diabetes.
- To compare glycemic outcomes between a closed-loop system and standard diabetes care in this age group.
Main Methods:
- A 13-week, multicenter, randomized trial comparing closed-loop insulin delivery with standard care (insulin pump or multiple daily injections with continuous glucose monitoring).
- Participants were children aged 2 to <6 years with type 1 diabetes.
- The primary outcome was the percentage of time glucose levels were within the 70 to 180 mg/dL target range.
Main Results:
- The closed-loop group spent significantly more time in the target glucose range (mean adjusted difference of 12.4 percentage points) compared to standard care.
- Similar improvements were observed for time above 250 mg/dL, mean glucose levels, and HbA1c.
- No significant difference in time below 70 mg/dL was noted; severe hypoglycemia and diabetic ketoacidosis occurred rarely in both groups.
Conclusions:
- Virtual initiation of closed-loop insulin delivery systems is effective in improving glycemic control in young children with type 1 diabetes.
- Closed-loop systems demonstrate a favorable safety profile in this population.
- These findings support the use of closed-loop systems for managing type 1 diabetes in very young children.
Background:
Closed-loop control systems of insulin delivery may improve glycemic outcomes in young children with type 1 diabetes. The efficacy and safety of initiating a closed-loop system virtually are unclear.
Methods:
In this 13-week, multicenter trial, we randomly assigned, in a 2:1 ratio, children who were at least 2 years of age but younger than 6 years of age who had type 1 diabetes to receive treatment with a closed-loop system of insulin delivery or standard care that included either an insulin pump or multiple daily injections of insulin plus a continuous glucose monitor. The primary outcome was the percentage of time that the glucose level was in the target range of 70 to 180 mg per deciliter, as measured by continuous glucose monitoring. Secondary outcomes included the percentage of time that the glucose level was above 250 mg per deciliter or below 70 mg per deciliter, the mean glucose level, the glycated hemoglobin level, and safety outcomes.
Results:
A total of 102 children underwent randomization (68 to the closed-loop group and 34 to the standard-care group); the glycated hemoglobin levels at baseline ranged from 5.2 to 11.5%. Initiation of the closed-loop system was virtual in 55 patients (81%). The mean (±SD) percentage of time that the glucose level was within the target range increased from 56.7±18.0% at baseline to 69.3±11.1% during the 13-week follow-up period in the closed-loop group and from 54.9±14.7% to 55.9±12.6% in the standard-care group (mean adjusted difference, 12.4 percentage points [equivalent to approximately 3 hours per day]; 95% confidence interval, 9.5 to 15.3; P<0.001). We observed similar treatment effects (favoring the closed-loop system) on the percentage of time that the glucose level was above 250 mg per deciliter, on the mean glucose level, and on the glycated hemoglobin level, with no significant between-group difference in the percentage of time that the glucose level was below 70 mg per deciliter. There were two cases of severe hypoglycemia in the closed-loop group and one case in the standard-care group. One case of diabetic ketoacidosis occurred in the closed-loop group.
Conclusions:
In this trial involving young children with type 1 diabetes, the glucose level was in the target range for a greater percentage of time with a closed-loop system than with standard care. (Funded by the National Institute of Diabetes and Digestive and Kidney Diseases; PEDAP ClinicalTrials.gov number, NCT04796779.).
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