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Continuous glucose monitoring in neonates: a review
Christopher J D McKinlay1,2, J Geoffrey Chase3, Jennifer Dickson3
1Liggins Institute, University of Auckland, Private Bag 92019, Victoria St West, Auckland, 1142 New Zealand.
Insights
Continuous glucose monitoring (CGM) offers insights into neonatal glucose metabolism but faces technical challenges in preterm infants. Further research is needed before routine clinical use for neonatal glycaemic control.
Area of Science:
- Neonatalogy
- Endocrinology
- Medical Devices
Background:
- Continuous glucose monitoring (CGM) is established for diabetes management but its neonatal application is less clear.
- Neonatal glucose instability is linked to adverse neurodevelopmental outcomes.
- CGM could personalize treatment and reduce blood tests for neonates.
Purpose of the Study:
- To evaluate the current role and limitations of CGM in neonatal glycaemic control.
- To identify technical challenges hindering routine CGM use in neonates.
- To assess the potential of CGM for improving neonatal neurodevelopmental outcomes.
Main Methods:
- Review of current literature on CGM in neonatal care.
- Analysis of technical limitations of existing CGM devices for neonates.
- Discussion of calibration, accuracy, and data interpretation challenges.
Main Results:
- CGM provides valuable data on neonatal glucose metabolism, especially in preterm infants.
- Current devices have limitations in accuracy at low/changing glucose levels and require neonatal-specific calibration.
- Sensor drift and the need for outcome-related metrics are significant issues.
Conclusions:
- CGM is currently best suited for research in neonatal glycaemia.
- Technical improvements are necessary before widespread clinical adoption.
- Randomized trials are required to demonstrate clinical benefit for routine neonatal care.
Abstract:
Continuous glucose monitoring (CGM) is well established in the management of diabetes mellitus, but its role in neonatal glycaemic control is less clear. CGM has provided important insights about neonatal glucose metabolism, and there is increasing interest in its clinical use, particularly in preterm neonates and in those in whom glucose control is difficult. Neonatal glucose instability, including hypoglycaemia and hyperglycaemia, has been associated with poorer neurodevelopment, and CGM offers the possibility of adjusting treatment in real time to account for individual metabolic requirements while reducing the number of blood tests required, potentially improving long-term outcomes. However, current devices are optimised for use at relatively high glucose concentrations, and several technical issues need to be resolved before real-time CGM can be recommended for routine neonatal care. These include: 1) limited point accuracy, especially at low or rapidly changing glucose concentrations; 2) calibration methods that are designed for higher glucose concentrations of children and adults, and not for neonates; 3) sensor drift, which is under-recognised; and 4) the need for dynamic and integrated metrics that can be related to long-term neurodevelopmental outcomes. CGM remains an important tool for retrospective investigation of neonatal glycaemia and the effect of different treatments on glucose metabolism. However, at present CGM should be limited to research studies, and should only be introduced into routine clinical care once benefit is demonstrated in randomised trials.
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