Publication: Non-adjunctive flash glucose monitoring system use during summer-camp in children with type 1 diabetes: the free-summer study
Program
KU-Authors
KU Authors
Co-Authors
Piona, Claudia
Dovc, Klemen
Mutlu, Gul Y.
Grad, Klara
Gregorc, Petra
Battelino, Tadej
Bratina, Natasa
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Embargo Status
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Abstract
Background: A factory-calibrated sensor for intermittently scanned continuous glucose monitoring (isCGM) is accurate and safe in children with type 1 diabetes (T1D). Data on isCGM effectiveness as a replacement for self-monitoring of blood glucose (SMBG) in this population is scarce. Objective: The aim of this study was to evaluate the non-adjunctive use of isCGM in children with T1D during 2 weeks in a challenging summer-camp setting. Methods: In this two-arm, parallel, randomized, outpatient clinical trial we enrolled 46 children (25 females, meanSD: age 11.12.6years, glycated hemoglobin (HbA1c) 7.4%0.7%): 26 in the isCGM group were blinded for the SMBG and insulin dosing was isCGM-based, whereas 20 in the control group were blinded for isCGM and performed SMBG-based insulin dosing. The primary outcome of intention-to-treat analysis was between-group difference in the proportion of time within range 3.9 to 10 mmol/L (TIR). Results: There was no significant difference in TIR (3.9-10 mmol/L) between the two groups. In participants with suboptimal metabolic control (HbA1c>7%) we observed a significant reduction in time spent above 10 mmol/L (P<0.05) and an improvement in TIR (P = 0.05) in the isCGM group. No severe hypoglycemic events or serious adverse events occurred. Overall mean absolute relative difference (MARD) between isCGM and SMBG was 18.3%, with median absolute relative difference (ARD) of 8%. Consensus error grid analysis demonstrated 82.2% and 95.2% of results in zone A, and zone A+B, respectively. Conclusion: The non-adjunctive use of isCGM was as safe and effective as SMBG, and reduced time spent in hyperglycemia in a sub-population of children with T1D with suboptimal glycemic control.
Source
Publisher
Wiley
Subject
Endocrinology, Metabolism, Pediatrics
Citation
Has Part
Source
Pediatric Diabetes
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Edition
DOI
10.1111/pedi.12729