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Published on: June 11, 2012
Continuous insulin infusion in hyperglycaemic extremely-low- birth-weight neonates
Sze May Ng1, Judith E May, Anthony J B Emmerson
1Neonatal Medical Unit, St Mary's Hospital, Manchester, UK. ngszemay@yahoo.com
Insights
Continuous insulin infusion effectively treats neonatal hyperglycemia. Extremely-low-birth-weight infants require longer treatment durations and higher insulin doses compared to larger neonates.
Area of Science:
- Neonatalogy
- Endocrinology
- Pediatric Intensive Care
Background:
- Neonatal hyperglycemia is often linked to impaired gluconeogenesis inhibition and insulin resistance in premature infants.
- Understanding glucose regulation is crucial for managing hyperglycaemia in vulnerable newborns.
Purpose of the Study:
- To compare the effectiveness and response rate of continuous insulin infusion for hyperglycaemic neonates.
- To evaluate outcomes in extremely-low-birth-weight (ELBW) neonates (< or =1,000 g) versus larger birth weight (LBW) neonates (>1,000 g).
Main Methods:
- 115 neonates with hyperglycemia were treated with a standard exogenous insulin infusion protocol.
- Continuous insulin infusion efficiency was assessed by comparing ELBW infants to LBW infants.
- Data collected included duration of infusion, insulin dosage, and blood glucose levels.
Main Results:
- ELBW neonates required significantly longer insulin infusion durations (p < 0.0001).
- ELBW neonates needed significantly higher average insulin infusion rates (units/kg/h) (p < 0.0001).
- No significant differences were observed in dextrose tolerance, age at infusion initiation, or average blood glucose.
Conclusions:
- Continuous insulin infusion is a safe and effective treatment for persistent neonatal hyperglycemia.
- ELBW neonates exhibit a slower response to insulin therapy and require higher doses.
- Tailored treatment protocols may be necessary to optimize glucose normalization in ELBW infants.
Background:
The inability of the newborn to inhibit gluconeogenesis in response to a glucose infusion leading to insulin resistance has been postulated as an important cause of hyperglycaemia observed in premature infants.
Aim:
The aim of this study was to determine the efficiency and rate of response to continuous insulin infusion in improving glucose tolerance in hyperglycaemic extremely-low-birth-weight (ELBW) neonates (< or =1,000 g) compared to neonates with birth weight >1,000 g (LBW).
Methods:
We included in the study 115 consecutive neonates in the neonatal intensive care unit who developed hyperglycaemia from January 2000 to December 2001. A standard protocol for the use of exogenous insulin infusions was commenced for all hyperglycaemic neonates. The efficiency of continuous insulin infusion was compared in two groups of infants: ELBW < or =1,000 g compared with neonates with birth weight >1,000 g (LBW).
Results:
The duration (hours) of insulin infusion required to normalise blood glucose level was significantly longer in the ELBW group compared to LBW group (p < 0.0001). Average insulin infusion (units/kg/h) required to maintain normoglycaemia was also significantly higher in the ELBW group (p < 0.0001). No significant difference was found in the mean amount of intravenous dextrose tolerated, mean postnatal age (hours) at which infusions were initiated and the average blood glucose recorded. ELBW infants were more likely to receive steroid administration, have surgery, higher CRIB scores and sepsis.
Conclusion:
Continuous insulin infusion was relatively safe and effective in the treatment of persistent hyperglycaemia in premature neonates. No serious adverse side effects of insulin therapy were noted. With the current protocol for use of exogenous insulin infusion at our unit, the response to treatment was significantly slower in the ELBW neonates. The dose of insulin infusion required to maintain normoglycaemia was also higher in this group of neonates. There may be a need for different treatment schedules for this subgroup of neonates so that normalisation of blood glucose can be achieved earlier.
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