Interventions for treatment of neonatal hyperglycemia in very low birth weight infants

Marcela Bottino1, Richard M Cowett, John C Sinclair

  • 1(Formerly, Fellow, Division of Neonatology, Department of Pediatrics, McMaster University, Hamilton, Ontario, Canada), Avenida Senador Danton Jobim, 150/404 Barra da Tijuca, Rio de Janeiro, Brazil, 22631-060.

Insights

Treatment for hyperglycemia in very low birth weight (VLBW) neonates lacks sufficient evidence. Current studies are too small to determine if interventions improve outcomes or if hyperglycemia causes adverse effects.

Area of Science:

  • Neonatalogy
  • Pediatric Endocrinology
  • Clinical Trials

Background:

  • Early neonatal hyperglycemia is common in very low birth weight (VLBW) neonates.
  • Hyperglycemia in VLBW neonates is associated with increased risks of death and major morbidities.
  • The causal role of hyperglycemia and the efficacy of its treatment remain uncertain.

Purpose of the Study:

  • To evaluate the clinical outcomes of interventions for neonatal hyperglycemia in VLBW infants receiving parenteral nutrition.
  • To synthesize evidence from randomized controlled trials on the treatment of hyperglycemia in this vulnerable population.

Main Methods:

  • Systematic review of randomized and quasi-randomized controlled trials.
  • Searched major databases (CENTRAL, MEDLINE, EMBASE, CINAHL) and conference abstracts.
  • Data extraction and quality assessment by two independent reviewers.

Main Results:

  • Only two small randomized trials (n=24 and n=23) met eligibility criteria.
  • Insulin infusion showed no significant effect on mortality or sepsis in one trial.
  • Insulin infusion did not significantly impact major morbidities in the second trial but increased energy and glucose intake.

Conclusions:

  • Insufficient evidence exists from randomized trials to determine the effects of treating hyperglycemia on mortality or major morbidities in VLBW neonates.
  • It remains unclear if hyperglycemia causes adverse outcomes or the optimal treatment strategy.
  • Larger, adequately powered randomized trials are needed to guide clinical practice.
Abstract

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