Glycemic variability and hypoglycemic excursions with continuous glucose monitoring compared to intermittently scanned continuous glucose monitoring in adults With highest risk type 1 diabetes
File(s)Avari et al -I Hart GV.docx (1.1 MB)
Accepted version
Author(s)
Avari, Parizad
Moscardo, Vanessa
Jugnee, Narvada
Oliver, Nick
Reddy, Monika
Type
Journal Article
Abstract
BACKGROUND: The I-HART CGM study has shown that real-time continuous glucose monitoring (rtCGM) has greater beneficial impact on hypoglycemia than intermittently scanned continuous glucose monitoring (iscCGM) in adults with type 1 diabetes at high risk (Gold score ≥4 or recent severe hypoglycemia using insulin injections). In this subanalysis, we present the impact of rtCGM and iscCGM on glycemic variability (GV). METHODS: Forty participants were recruited to this parallel group study. Following two weeks of blinded rtCGM (DexcomG4), participants were randomized to rtCGM (Dexcom G5; n = 20) or iscCGM (Freestyle Libre; n = 20) for eight weeks. An open-extension phase enabled participants on rtCGM to continue for a further eight weeks and those on iscCGM to switch to rtCGM over this period. Glycemic variability measures at baseline, 8- and 16-week endpoints were compared between groups. RESULTS: At the eight-week endpoint, between-group differences demonstrated significant reduction in several GV measures with rtCGM compared to iscCGM (GRADE%hypoglycemia, index of glycemic control [IGC], and average daily risk range [ADRR]; P < .05). Intermittently scanned continuous glucose monitoring reduced mean average glucose and glycemic variability percentage and GRADE%hyperglycemia compared with rtCGM (P < .05). At 16 weeks, the iscCGM group switching to rtCGM showed significant improvement in GRADE%hypoglycemia, personal glycemic status, IGC, and ADRR. CONCLUSION: Our data suggest most, but not all, GV measures improve with rtCGM compared with iscCGM, particularly those measures associated with the risk of hypoglycemia. Selecting appropriate glucose monitoring technology to address GV in this high-risk cohort is important to minimize the risk of glucose extremes and severe hypoglycemia. CLINICAL TRIAL REGISTRATION: ClinicalTrials.gov NCT03028220.
Date Issued
2019-08-02
Date Acceptance
2019-08-01
Citation
Journal of Diabetes Science and Technology, 2019, 14 (3), pp.567-574
ISSN
1932-2968
Publisher
SAGE Publications
Start Page
567
End Page
574
Journal / Book Title
Journal of Diabetes Science and Technology
Volume
14
Issue
3
Copyright Statement
© 2019 Diabetes Technology Society. The final, definitive version of this paper has been published in Journal of Diabetes Science and Technology by Sage Publications Ltd. All rights reserved. It is available at: https://journals.sagepub.com/doi/10.1177/1932296819867688
Sponsor
DexCom Inc.
Identifier
https://www.ncbi.nlm.nih.gov/pubmed/31375042
Grant Number
Iperial IIS-2015-014
Subjects
continuous glucose monitoring
glycemic variability
hypoglycemia episodes
intermittently scanned continuous glucose monitoring
type 1 diabetes
Publication Status
Published
Coverage Spatial
United States
Date Publish Online
2019-08-02