Maltodextrin May Be a Promising Treatment Modality After Near-total Pancreatectomy in Infants Younger Than Six Months

Yasemin Denkboy Öngen1, Erdal Eren1, Halil Sağlam1

  • 1Bursa Uludağ University Faculty of Medicine, Department of Pediatric Endocrinology, Bursa, Turkey

Insights

Persistent hypoglycemia in infants with congenital hyperinsulinism (CHI) is difficult to manage. Adding maltodextrin to the diet successfully controlled hypoglycemia in a CHI infant post-pancreatectomy.

Area of Science:

  • Endocrinology
  • Pediatric Gastroenterology
  • Nutritional Science

Background:

  • Congenital hyperinsulinism (CHI) presents a significant challenge in infant metabolic management.
  • Persistent hypoglycemia affects nearly half of CHI cases, often persisting after near-total pancreatectomy.
  • Maltodextrin is suggested for infants under six months, but its efficacy in persistent hypoglycemia remains unclear.

Observation:

  • A male infant diagnosed with congenital hyperinsulinism (CHI) exhibited persistent, severe hypoglycemia.
  • The infant's condition remained refractory to multiple medical therapies and a near-total pancreatectomy.
  • Hypoglycemic episodes were monitored closely to assess dietary interventions.

Findings:

  • Dietary supplementation with maltodextrin was introduced to manage the infant's persistent hypoglycemia.
  • The addition of maltodextrin to the infant's nutritional regimen led to successful control of hypoglycemic episodes.
  • This intervention demonstrated a significant improvement in metabolic stability.

Implications:

  • Maltodextrin may be an effective therapeutic option for managing refractory hypoglycemia in infants with CHI.
  • This case highlights the potential role of specific carbohydrate supplementation in complex metabolic disorders.
  • Further research is warranted to confirm maltodextrin's efficacy and optimal use in pediatric congenital hyperinsulinism.

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