PEDIATRICS Vol. 108 No. 5 November 2001, pp. 1187-1192
Glucose Monitoring With Long-Term Subcutaneous Microdialysis in Neonates
Received Aug 30, 2000; accepted Jul 9, 2001.
,
From the * Children's Hospital of the Technical University
Munich, Children's Clinic, Munich, Germany; Background. Microdialysis is a new
approach for continuous monitoring of small molecules in the
extracellular space, and hypoglycemia is a common problem in neonatal
intensive care. The objective of this study was to evaluate
subcutaneous microdialysis for long-term glucose monitoring in neonatal
intensive care. We determined the relative recovery of the
microdialysis system in vitro and in vivo, the stability of the
relative recovery in vivo during long-term microdialysis, and the
correlation between blood and dialysate concentrations of glucose and
urea. Furthermore, we evaluated the sensitivity and specificy of
subcutaneous microdialysis for the diagnosis of hypoglycemia.
Patient and Methods. Thirteen infants (10 neonates) with
gestational ages of 30.2 to 45.6 weeks were investigated by
microdialysis of subcutaneous adipose tissue and blood sampling.
Subcutaneous microdialysis was performed for a median (range) duration
of 9 (4-16) days.
Results. The application was safe, even in extremely low
birth weight infants (<1000 g) with scanty subcutaneous adipose
tissue. The mean ± standard deviation of the relative recovery in vitro
was 101 ± 3% for glucose and 100 ± 2% for urea. Using
urea as the internal standard, the mean relative recovery in vivo was 96.4 ± 12.7% at the beginning and remained constant up to 16 days. The correlation between microdialysate and blood was significant for
glucose (r = 0.88) and urea (r = 0.98). Subcutaneous microdialysis allowed the detection of
asymptomatic hypoglycemias. The diagnostic sensitivity of a dialysate
glucose Conclusions. Subcutaneous microdialysis is a safe method,
well suited for long-term glucose monitoring in neonates during
intensive care. Subcutaneous microdialysis can be used to reduce blood
loss and painful stress resulting from diagnostic blood sampling in
high-risk neonates.
Dr. v. Hauner
Children's Hospital, Children's Hospital of the Ludwig Maximilian
University Munich, Munich, Germany; and § Department for Medical
Statistics and Epidemiology of the Technical University Munich, Munich,
Germany.
2.9 mM to predict a blood glucose level
2.8 mM was 92.3%,
with 88.1% specificy. The positive predictive value with a 13.4%
prevalence of a blood glucose
2.8 mM was 54.5%, with a negative
predictive value of 98.7% and an accuracy of 88.7%.
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