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Published on: June 11, 2012
Continuous subcutaneous insulin infusion in diabetes mellitus. A year's prospective trial
Insights
Continuous subcutaneous insulin infusion improved glycemic control in children with diabetes, despite some technical challenges. This method offers an acceptable way to manage diabetes in pediatric patients, enhancing their well-being.
Area of Science:
- Pediatric Endocrinology
- Metabolic Disorders
Background:
- Type 1 diabetes management in children requires effective strategies for glycemic control.
- Conventional treatments often present challenges in achieving optimal blood glucose levels.
Purpose of the Study:
- To compare continuous subcutaneous insulin infusion (CSII) with intensified conventional treatment (ICT) in pediatric patients.
- To evaluate the efficacy and safety of CSII in improving glycemic control and well-being.
Main Methods:
- A 12-month prospective trial involving 13 children (aged 8-16 years) comparing CSII and ICT.
- Data collection included plasma glucose, M values, and glycosylated hemoglobin levels.
Main Results:
- CSII group achieved significantly improved glycemic control (mean glucose 9.8 mmol/l, HbA1c 9.1%) compared to baseline and ICT group (mean glucose 15.5 mmol/l, HbA1c 10.4%).
- Withdrawals occurred in both groups due to technical dissatisfaction; however, children on CSII reported improved well-being.
- CSII group experienced increased diabetic ketoacidosis and subcutaneous abscesses, but no difference in serious hypoglycemia incidence.
Conclusions:
- Continuous subcutaneous insulin infusion is an acceptable method for improving glycemic control in some children with diabetes.
- While CSII shows promise, careful monitoring for potential complications like abscesses and ketoacidosis is necessary.
Abstract:
Thirteen children aged between 8 and 16 years were entered into a 12 month prospective trial comparing continuous subcutaneous insulin infusion with intensified conventional treatment. Two of seven children on insulin infusion withdrew after eight and nine weeks, and three of six children on conventional treatment withdrew after four to eight weeks. Withdrawals in both groups were related to dissatisfaction with the techniques. The group on insulin infusion treatment achieved a mean plasma glucose of 9.8 mmol/l (176.4 mg/100 ml), a median M value of 50 mmol/l (900 mg/100 ml) and a mean glycosylated haemoglobin of 9.1% during the year. This represents a significant improvement compared with the previous values, and also when compared with the conventional treatment group whose trial values of a mean plasma glucose of 15.5 mmol/l (279 mg/100 ml), median M value of 167 mmol/l (3006 mg/100 ml), and glycosylated haemoglobin of 10.4% were not significantly different from those before the trial. Two children on insulin infusion developed subcutaneous abscesses in the early months. There was an increased incidence of diabetic ketoacidosis in this group, but no difference in the incidence of serious hypoglycaemia between the two groups. The children reported improved well-being when using insulin infusion and continued with the technique after the trial finished. Insulin infusion offers an acceptable means of improving glycaemic control for some diabetic children.
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