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.
Abstract

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