Abstract

IntroductionThe purpose of this study was to assess the effectiveness of advanced- (a-HCL) vs. standard-hybrid closed-loop (s-HCL) systems use up to 6 months of treatment in a real-world setting of children and adolescents with T1DM.MethodsWe retrospectively evaluated all T1DM pediatric users of MiniMed™ 670G system (s-HCL) and 780G system (a-HCL). HbA1c and BMI were collected at baseline and three and six months after HCL start. Data on glycemic control were extracted from reports generated with CareLink™ Personal Software in Manual Mode, at HCL start, after one, three, and six months after HCL beginning.ResultsThe study included 44 individuals with a median age of 13.3 years (range 2- 21 years), 20 on s-HCL, and 24 on a-HCL. a-HCL users had a significantly lower HbA1c compared to s-HCL after six months of HCL use (7.1 vs. 7.7%). Significant differences in HbA1c between a-HCL and s-HCL users were found in children aged 7-14 years (7.1 vs. 7.7% after six months) and in those with a worse (HbA1c >8%) glycemic control at the beginning (7.1 vs. 8.1% after six months). No significant changes in HbA1c were found in a-HCL users that previously used a s-HCL system. Nevertheless, only the use of a-HCL significantly predicted a lower HbA1c after six months. All sensor-specific measures of glycemic control improved from Manual to Auto mode, in both s-HCL and a-HCL, without increasing time spent in hypoglycemia. However, the percentage of individuals with TIR>70% increased significantly in a-HCL users, who attained this target earlier and more stably: younger age, a higher rate of auto-correction, and a lower amount of CHO inserted predicted a TIR>70%. BMI SDS did not significantly change throughout the study period.ConclusionThis real-world study suggests that effectiveness might be greater in a-HCL than in s-HCL, with significant changes in HbA1c, and reaching earlier and more stably the target of TIR >70%, without increasing hypoglycemia or BMI. At the same time, previous users of s-HCL systems did not show any further improvement with a-HCL. Children under the age of 14 years of age, not represented in previous studies, seem to benefit the most from a-HCL pumps as well as individuals with the worst glycemic control.

Highlights

  • The purpose of this study was to assess the effectiveness of advanced- vs. standard-hybrid closed-loop (s-HCL) systems use up to 6 months of treatment in a real-world setting of children and adolescents with type 1 diabetes mellitus (T1DM)

  • We retrospectively evaluated all individuals with T1DM followed at the Diabetes Pediatric Unit of the Institute for Maternal and Child Health “Burlo Garofolo” who started using an HCL system (s-HCL Medtronic MiniMedTM 670G from February 1st, 2019 until September 29th, 2020 or advanced hybrid closed-loop (a-HCL) Medtronic MiniMedTM 780G from October 26th, 2020 until April 1st, 2021) and had at least six months offollow-up

  • No significant changes in HbA1c were found in a-HCL users that previously used a s-HCL system (Table 2)

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Summary

Introduction

The purpose of this study was to assess the effectiveness of advanced- (aHCL) vs. standard-hybrid closed-loop (s-HCL) systems use up to 6 months of treatment in a real-world setting of children and adolescents with T1DM. Three fundamental components constitute hybrid closed-loop (HCL) systems: a sensor for continuous glucose monitoring (CGM), pumps necessary for continuous subcutaneous insulin infusion (CSII), and an algorithm for automated insulin delivery, increasing or suspending basal insulin infusion based on glucose values wirelessly transmitted by the sensor [5, 6]. These systems are called “hybrid” since pre-prandial boluses are not fully automatized: boluses must be delivered by the users before the meal, calculating insulin units on pre-prandial blood glucose level and the grams of carbohydrates to be consumed

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