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Suboptimal glycemic control in adolescents and young adults with type 1 diabetes from 2011 to 2020 across Australia and New Zealand: Data from the Australasian Diabetes Data Network (ADDN) Registry
Journal article   Open access   Peer reviewed

Suboptimal glycemic control in adolescents and young adults with type 1 diabetes from 2011 to 2020 across Australia and New Zealand: Data from the Australasian Diabetes Data Network (ADDN) Registry

Steven James, Allison L Perry, J Lower, M Harris and Maria E Craig
Pediatric Diabetes, Vol.23(6), pp.736-741
2022
PMID: 35561056
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Suboptimal glycaemic control in adolescents and young adults with type 1 diabetes from 2011 to 2020 across Australia and New Zealand1.03 MBDownloadView
Accepted Version Open Access
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https://doi.org/10.1111/pedi.13364View
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Abstract

Adolescents Glycaemic control HbA1c Type 1 diabetes Young adults UniSC Diversity Area - Life Stages
Background: Competing challenges in adolescence and young adulthood can distract from optimal type 1 diabetes (T1D) self-management, and increase risks of premature morbidity and mortality. There are limited data mapping the glycaemic control of people with T1D in this age group, across Australasia. Methods: Clinical data were extracted from the Australasian Diabetes Data Network, a prospective clinical diabetes registry. Inclusion criteria were individuals with T1D aged 16-25 years at their last recorded T1D healthcare visit (from 1st January 2011 to 31st December 2020), with T1D duration of at least one year. Data were stratified by two last recorded T1D healthcare visit ranges, while Generalised Estimated Equation (GEE) modelling was used to examine factors associated with HbA1c across visits during the ten year period. Results: Data from 6329 young people (52.6% male) attending 24 diabetes centers across Australasia were included. At the last visit within the most recent five years, mean+SD age was 18.5+2.3 years, T1D duration was 8.8+4.7 years and HbA1c was 8.8±1.8% (72.2±19.9mmol/mol); only 12.3% had an HbA1c below the international target of <7.0% (53mmol/mol). Across all T1D healthcare visits, in GEE modelling, higher HbA1c was associated with female sex (B=0.20; 95% CI 0.12 to 0.29, p<0.001), longer T1D duration (B=0.04, 0.03 to 0.05, p<0.001). Lower HbA1c was associated with attendance at a paediatric T1D healthcare setting (B=-0.33, -0.45 to -0.21, p<0.001) and use of CSII vs. BD/MDI therapy (B=-0.49, -0.59 to 0.40, p<001). Conclusions: This Australasian study demonstrates widespread and persistent sub-optimal glycaemic control in young people with T1D, highlighting the urgent need to better understand how healthcare services can support improved glycaemic control in this population. This article is protected by copyright. All rights reserved.

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Endocrinology & Metabolism
Pediatrics

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