Affordable Access

Severe hypoglycemia and ketoacidosis over one year in Italian pediatric population with type 1 diabetes mellitus: A multicenter retrospective observational study

Authors
Journal
Nutrition Metabolism and Cardiovascular Diseases
0939-4753
Publisher
Elsevier
Volume
24
Issue
5
Identifiers
DOI: 10.1016/j.numecd.2013.11.004
Keywords
  • Type 1 Diabetes
  • Severe Hypoglycemia
  • Diabetes Ketoacidosis
  • Children And Adolescents
Disciplines
  • Medicine

Abstract

Abstract Background and aims Evaluation of incidence and correlates of severe hypoglycemia (SH) and diabetes ketoacidosis (DKA) in children and adolescents with T1DM. Methods and results Retrospective study conducted in 29 diabetes centers from November 2011 to April 2012. The incidence of SH and DKA episodes and their correlates were assessed through a questionnaire administered to parents of patients aged 0–18 years. Incidence rates and incident rate ratios (IRRs) were estimated through multivariate Poisson regression analysis and multilevel analysis. Overall, 2025 patients were included (age 12.4 ± 3.8 years; 53% males; diabetes duration 5.6 ± 3.5 years; HbA1c 7.9 ± 1.1%). The incidence of SH and DKA were of 7.7 and 2.4 events/100 py, respectively. The risk of SH was higher in females (IRR = 1.44; 95%CI 1.04–1.99), in patients using rapid acting analogues as compared to regular insulin (IRR = 1.48; 95%CI 0.97–2.26) and lower for patients using long acting analogues as compared to NPH insulin (IRR = 0.40; 95%CI 0.19–0.85). No correlations were found between SH and HbA1c levels. The risk of DKA was higher in patients using rapid acting analogues (IRR = 4.25; 95%CI 1.01–17.86) and increased with insulin units needed (IRR = 7.66; 95%CI 2.83–20.74) and HbA1c levels (IRR = 1.63; 95%CI 1.36–1.95). Mother's age was inversely associated with the risk of both SH (IRR = 0.95; 95%CI 0.92–0.98) and DKA (IRR = 0.94; 95%CI 0.88–0.99). When accounting for center effect, the risk of SH associated with the use of rapid acting insulin analogues was attenuated (IRR = 1.48; 95%CI 0.97–2.26); 33% and 16% of the residual variance in SH and DKA risk was explained by center effect. Conclusion The risk of SH and DKA is mainly associated with treatment modalities and strongly depends on the practice of specialist centers.

There are no comments yet on this publication. Be the first to share your thoughts.