Brain mass estimation by head circumference and body mass methods in neonatal glycaemic modelling and control

Comput Methods Programs Biomed. 2014 Jul;115(2):47-54. doi: 10.1016/j.cmpb.2014.03.006. Epub 2014 Apr 4.

Abstract

Introduction: Hyperglycaemia is a common complication of stress and prematurity in extremely low-birth-weight infants. Model-based insulin therapy protocols have the ability to safely improve glycaemic control for this group. Estimating non-insulin-mediated brain glucose uptake by the central nervous system in these models is typically done using population-based body weight models, which may not be ideal.

Method: A head circumference-based model that separately treats small-for-gestational-age (SGA) and appropriate-for-gestational-age (AGA) infants is compared to a body weight model in a retrospective analysis of 48 patients with a median birth weight of 750g and median gestational age of 25 weeks. Estimated brain mass, model-based insulin sensitivity (SI) profiles, and projected glycaemic control outcomes are investigated. SGA infants (5) are also analyzed as a separate cohort.

Results: Across the entire cohort, estimated brain mass deviated by a median 10% between models, with a per-patient median difference in SI of 3.5%. For the SGA group, brain mass deviation was 42%, and per-patient SI deviation 13.7%. In virtual trials, 87-93% of recommended insulin rates were equal or slightly reduced (Δ<0.16mU/h) under the head circumference method, while glycaemic control outcomes showed little change.

Conclusion: The results suggest that body weight methods are not as accurate as head circumference methods. Head circumference-based estimates may offer improved modelling accuracy and a small reduction in insulin administration, particularly for SGA infants.

Keywords: Brain mass; Central nervous system; Glycaemic control; Insulin therapy; Physiological modelling; Preterm infants.

MeSH terms

  • Birth Weight
  • Blood Glucose / metabolism
  • Brain / pathology*
  • Cohort Studies
  • Computer Simulation
  • Female
  • Head
  • Humans
  • Hyperglycemia / blood
  • Hyperglycemia / drug therapy*
  • Hyperglycemia / pathology*
  • Infant, Extremely Low Birth Weight
  • Infant, Extremely Premature
  • Infant, Newborn
  • Insulin / administration & dosage
  • Insulin / therapeutic use*
  • Insulin Resistance
  • Male
  • Models, Biological*
  • Organ Size
  • Retrospective Studies

Substances

  • Blood Glucose
  • Insulin