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Published on: June 11, 2012
Glycemic variability and reference percentiles in very low birth weight preterm infants using continuous glucose
Irene Gutiérrez-Rosa1, Manuel Lubián-Gutiérrez1,2, Carmen Rodríguez-Barrios1,2
1Biomedical Research and Innovation Institute of Cádiz (INiBICA), Puerta del Mar University Hospital, Cádiz, Spain.
Insights
Managing blood glucose in very-low-birth-weight preterm infants is complex. This study provides gestational-age-specific glucose reference ranges for the first 14 days, aiding individualized care for these vulnerable infants.
Area of Science:
- Neonatal Medicine
- Pediatric Endocrinology
- Metabolic Adaptation
Background:
- Glycemic control is challenging in very-low-birth-weight preterm infants due to immature glucose homeostasis.
- The first two weeks of life are critical for metabolic adaptation, showing high glucose variability.
- Continuous glucose monitoring is essential for tracking trends in this vulnerable population.
Purpose of the Study:
- To describe daily glucose patterns and variability in preterm infants during the first 14 postnatal days.
- To generate gestational-age-specific reference percentiles for clinically stable preterm infants.
- To support individualized glucose management strategies in neonatal intensive care.
Main Methods:
- A prospective observational study involving 103 clinically stable preterm infants (24-32 weeks gestational age).
- Continuous glucose monitoring was performed during the first 14 days of life.
- Infants were classified into three gestational age groups for analysis.
Main Results:
- Mean glucose concentrations and variability decreased with postnatal age across all groups.
- Infants born at 24-26 weeks showed higher mean glucose and greater variability compared to more mature groups.
- Gestational-age-specific reference percentiles for glucose levels were established for days 1 and 14.
Conclusions:
- Glucose levels and variability naturally decrease in preterm infants during the first two weeks of life.
- The least mature preterm infants (24-26 weeks) exhibit higher and more variable glucose concentrations.
- These gestational-age-specific reference percentiles derived from continuous monitoring can inform personalized glucose management.
Abstract:
Glycemic control in very-low-birth-weight preterm infants is challenging due to the immaturity of glucose homeostasis during the early postnatal period. The first two weeks of life represent a critical window of metabolic adaptation, characterized by high variability and gradual stabilization of glucose levels; continuous monitoring during this period is therefore essential to capture clinically relevant trends. We aimed to describe daily glucose patterns and variability during the first 14 days and to generate gestational-age-specific reference percentiles for clinically stable preterm infants. A prospective observational study was conducted in a tertiary neonatal intensive care unit (2021-2024), with continuous glucose monitoring during the first 14 days of life. Of 203 eligible infants, 103 clinically stable preterm infants without major comorbidities were included and classified into three gestational age groups (24-26, 27-29, and 30-32 weeks). The median number of glucose readings per infant was 2,557 [1,681-2,959]. Mean glucose concentrations declined over the first two weeks in all groups, with the largest decrease during the initial 72 hours. Infants born at 24-26 weeks had higher mean glucose on day 1 (156.5 ± 47.2 mg/dL) and day 14 (121.4 ± 21.8 mg/dL), and greater variability than those born at 27-29 and 30-32 weeks. Reference percentiles reflected these differences: on day 1, the fifth to ninety-fifth percentiles were 92-245 mg/dL for 24-26 weeks, 65-168 mg/dL for 27-29 weeks, and 67-148 mg/dL for 30-32 weeks; by day 14, they were 73-185, 67-150, and 58-136 mg/dL, respectively.In summary, glucose concentrations and variability decreased with postnatal age, and the least mature infants exhibited higher and more variable values. These gestational-age-specific reference percentiles, derived from continuous monitoring may support individualized glucose management in neonatal intensive care.
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