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Published on: June 11, 2012
Continuous subcutaneous insulin infusion attenuated glycemic instability in preschool children with type 1 diabetes
Ramin Alemzadeh1, Paola Palma-Sisto, M Holzum
1Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin, USA. ralemzad@mcw.edu
Insights
Continuous subcutaneous insulin infusion (CSII) improved glycemic instability in preschool children with type 1 diabetes mellitus (DM). This therapy enhanced glycemic control without affecting hypoglycemia or quality of life compared to flexible multiple daily insulin (FMDI).
Area of Science:
- Pediatric Endocrinology
- Metabolic Disorders
- Diabetes Management
Background:
- Continuous subcutaneous insulin infusion (CSII) is hypothesized to improve glycemic control and quality of life in children with type 1 diabetes mellitus (DM) compared to traditional insulin injection regimens.
- Evaluating the efficacy of CSII in a pediatric population, specifically preschool-aged children, is crucial for optimizing diabetes management strategies.
Purpose of the Study:
- To assess the impact of CSII on glycemic control indices, including hemoglobin A1c (HbA1c), mean blood glucose (MBG), and mean amplitude of glycemic excursion (MAGE).
- To evaluate the frequency and duration of hypoglycemic events in preschool children with DM using CSII.
- To determine the effect of CSII on the quality of life of young children with DM, as perceived by their parents.
Main Methods:
- A cohort of 14 preschool children (3.9 +/- 0.8 years) with type 1 DM were transitioned from flexible multiple daily insulin (FMDI) to CSII.
- Glycemic control was monitored quarterly for one year using HbA1c and continuous glucose monitoring (CGM) to determine MBG, MAGE, and hypoglycemic events.
- Parental quality of life questionnaires (TAPQoL) were administered at baseline and after one year of CSII therapy.
Main Results:
- CSII significantly reduced MAGE (210 +/- 31 vs. 168 +/- 22 mg/dL, P < 0.005), indicating improved glycemic stability.
- No significant changes were observed in HbA1c, MBG, or the frequency and duration of hypoglycemic events compared to FMDI.
- Quality of life scores, as assessed by parental questionnaires, remained unchanged after the transition to CSII.
Conclusions:
- CSII effectively improves glycemic instability in preschool children with type 1 DM without negatively impacting HbA1c or hypoglycemia.
- CSII represents a viable alternative to FMDI therapy for managing type 1 DM in young children, offering improved glycemic control.
- While CSII enhances glycemic stability, it does not alter parental perception of their child's quality of life in this age group.
Background/Aims:
Continuous subcutaneous insulin infusion (CSII) is believed to decrease glycemic instability and hypoglycemia while increasing quality of life compared to insulin injection regimens. To evaluate indices of glycemic control and impact on quality of life, we studied a group of preschool children with type 1 diabetes mellitus (DM) on CSII.
Methods:
Fourteen patients (eight girls and six boys) 3.9 +/- 0.8 years old with DM duration of 2.0 +/- 0.8 years were transitioned from flexible multiple daily insulin (FMDI) (pre-meal aspart and bedtime glargine) to CSII. Patients were evaluated with hemoglobin A(1c) (HbA(1c)) and continuous glucose monitoring quarterly for 1 year. Mean blood glucose (MBG), mean amplitude of glycemic excursion (MAGE), and hypoglycemic events (blood glucose <60 mg/dL) were determined. Patients' parents completed quality of life [TNO-AZL Preschool Children Quality of Life (TAPQoL)] questionnaires for their children at baseline and 1.0 year.
Results:
The total daily insulin and the bolus:basal ratio did not change during CSII (0.72 +/- 0.21 vs. 0.74 +/- 0.16 U/kg/day and 2.1 +/- 0.61 vs. 2.40 +/- 0.58 U/kg/day, respectively). There was no change in HbA(1c) (8.0 +/- 0.50% vs. 7.8 +/- 0.40%) or frequency of hypoglycemia (moderate, 92.3 vs. 73.1 events/100 patient-years; severe, 22.5 vs. 17.5 events/100 patient-years). The MBG (213 +/- 94 vs. 185 +/- 79 mg/dL) and frequency (1.9 +/- 1.6 vs. 2.1 +/- 2.2) and duration (nocturnal, 135 +/- 141 vs. 120 +/- 103 min; total, 267 +/- 222 vs. 189 +/- 148 min) of hypoglycemic events did not decrease, whereas MAGE was reduced on CSII (210 +/- 31 vs. 168 +/- 22 mg/dL, P < 0.005). The quality of life subscales on the TAPQoL questionnaire did not change on CSII.
Conclusions:
CSII improved glycemic instability without reducing HbA(1c) or frequency and duration of hypoglycemic events and altering the parent's perception of his or her child's quality of life. CSII improves glycemic instability and is an effective alternative to FMDI therapy in young children with type 1 DM.
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