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[Cyclic parenteral nutrition in children and glucose metabolism]

Archives Francaises De Pediatrie
|August 1, 1985
PubMed

Insights

Cyclic perfusion in children receiving parenteral nutrition showed good glucose regulation. However, it led to increased insulin secretion, suggesting potential long-term risks that may be mitigated by adjusting nutrient delivery.

Area of Science:

  • Pediatrics
  • Endocrinology
  • Metabolic Research

Background:

  • Prolonged parenteral nutrition (PN) is critical for children unable to achieve adequate oral intake.
  • Understanding the impact of PN delivery methods on glucose metabolism and insulin response is essential for optimizing patient care.

Purpose of the Study:

  • To investigate the effects of cyclic perfusion during prolonged parenteral nutrition on glucose metabolism and insulin secretion in pediatric patients.
  • To assess glycemic control using glycosylated hemoglobin (HbA1c) and evaluate insulin production via urinary C-peptide excretion.

Main Methods:

  • Studied 10 children receiving prolonged parenteral nutrition.
  • Monitored glycosylated hemoglobin (HbA1c) levels to assess long-term glycemia.
  • Measured urinary C-peptide excretion to evaluate insulin secretion in response to cyclic perfusion.
  • Compared results with control groups.

Main Results:

  • Good glycemic regulation was indicated by the absence of glycosuria and acceptable HbA1c levels (mean: 4.4 +/- 0.7%).
  • A tenfold increase in urinary C-peptide excretion (mean: 47.2 +/- 33.3 nmol/m2-1) compared to controls demonstrated significant insulin hypersecretion.
  • This hypersecretion was attributed to the high rate of glucose infusion during cyclic perfusion.

Conclusions:

  • Cyclic perfusion in pediatric parenteral nutrition effectively maintains glycemic control but induces significant insulin hypersecretion.
  • This insulin hypersecretion may pose long-term health risks.
  • Optimizing PN by limiting glucose to energy requirements for growth and incorporating approximately 30% lipid emulsion may reduce insulin hypersecretion.

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