Real-time continuous glucose monitoring reduces the duration of hypoglycemia episodes: a randomized trial in very low birth weight neonates

Florence Uettwiller, Aude Chemin, Elisabeth Bonnemaison, Géraldine Favrais, Elie Saliba, François Labarthe, Florence Uettwiller, Aude Chemin, Elisabeth Bonnemaison, Géraldine Favrais, Elie Saliba, François Labarthe

Abstract

Objectives: Hypoglycemia is frequent in very low birth weight (VLBW) neonates and compromises their neurological outcome. The aim of this study was to compare real-time continuous glucose monitoring system (RT-CGMS) to standard methods by intermittent capillary blood glucose testing in detecting and managing hypoglycemia.

Study design: Forty-eight VLBW neonates were enrolled in this prospective study. During their 3 first days of life, their glucose level was monitored either by RT-CGMS (CGM-group), or by intermittent capillary glucose testing (IGM-group) associated with a blind-CGMS to detect retrospectively missed hypoglycemia. Outcomes were the number and duration of hypoglycemic (≤ 50 mg/dl) episodes per patient detected by CGMS.

Results: Forty-three monitorings were analyzed (IGM n = 21, CGM n = 22), with a median recording time of 72 hours. In the IGM group, blind-CGMS revealed a significantly higher number of hypoglycemia episodes than capillary blood glucose testing (1.2 ± 0.4 vs 0.4 ± 0.2 episode/patient, p<0.01). In the CGM-group, the use of RT-CGMS made it possible (i) to detect the same number of hypoglycemia episodes as blind-CGMS (1.2 ± 0.4 episode/patient), (ii) to adapt the glucose supply in neonates with hypoglycemia (increased supply during days 1 and 2), and (iii) to significantly reduce the duration of hypoglycemia episodes per patient (CGM 44[10-140] min versus IGM 95[15-520] min, p<0.05). Furthermore, it reduced the number of blood samples (CGM 16.9 ± 1.0 vs IGM 21.9 ± 1.0 blood sample/patient, p<0.001).

Conclusion: RT-CGMS played a beneficial role in managing hypoglycemia in VLBW neonates by adjusting the carbohydrate supply to the individual needs and by reducing the duration of hypoglycemia episodes. The clinical significance of the biological differences observed in our study need to be explored.

Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Figure 1. Flow chart.
Figure 1. Flow chart.
CGM: continuous glucose monitoring. IGM: intermittent glucose monitoring.
Figure 2. Number of hypoglycemic episodes per…
Figure 2. Number of hypoglycemic episodes per patient in the IGM-group and examples of hypoglycemic episodes.
Number of hypoglycemic episodes per patient detected by capillary blood glucose testing or continuous glucose monitoring in the IGM-group (A) and examples of hypoglycemic episodes (B and C). In 21 patients from the IGM-group, glucose level was monitored by capillary blood glucose testing performed every 4 hours and by blind continuous glucose monitoring system (CGMS, Guardian Clinical, Medtronic) that was analyzed retrospectively. Hypoglycemia was defined by a glucose level ≤50mg/dL. Number of hypoglycemia episodes per patient are expressed as mean ± SE; **p

Figure 3. Comparison between IGM- and CGM-group:…

Figure 3. Comparison between IGM- and CGM-group: number of heel pricks, number and duration of…

Figure 3. Comparison between IGM- and CGM-group: number of heel pricks, number and duration of hypoglycemic episodes per patient.
Number of heel pricks per patient for capillary blood glucose testing (A), number (B) and duration (C) of hypoglycemic episodes per patient. Results are expressed as mean ± SE (A and B) or as median, 25% and 75% percentiles (box) and extreme values (whisker) (C) *p

Figure 4. Daily carbohydrate supplies in IGM-…

Figure 4. Daily carbohydrate supplies in IGM- and CGM-group.

Results, expressed as mean ± SE,…

Figure 4. Daily carbohydrate supplies in IGM- and CGM-group.
Results, expressed as mean ± SE, represent daily carbohydrate supplies during the first 4 days of life in IGM versus CGM-group (A), and in patients with (HYPO) versus without (NORMO) hypoglycemia in each group (B and C); *p
Similar articles
Cited by
References
    1. Cornblath M, Schwartz R (1993) Hypoglycemia in the neonate. J Pediatr Endocrinol 6: 113–129. - PubMed
    1. Vannucci RC VS (2000) Glucose metabolism in the developing brain. Semin Perinatol 24: 107–115. 10.1053/sp.2000.6361 - DOI - PubMed
    1. Wieloch T (1985) Hypoglycemia-induced neuronal damage prevented by an N-methyl-D-aspartate antagonist. Science 230: 681–683. 10.1126/science.2996146 - DOI - PubMed
    1. Wayenberg JL, Cavedon C, Ghaddhab C, Lefevre N, Bottari SP (2011) Early transient hypoglycemia is associated with increased albumin nitration in the preterm infant. Neonatology 100: 387–397. 10.1159/000326936 - DOI - PubMed
    1. McGowan JE, Chen L, Gao D, Trush M, Wei C (2006) Increased mitochondrial reactive oxygen species production in newborn brain during hypoglycemia. Neurosci Lett 399: 111–114. 10.1016/j.neulet.2006.01.034 - DOI - PubMed
Show all 28 references
Publication types
MeSH terms
Related information
Grant support
The authors have no support or funding to report.
[x]
Cite
Copy Download .nbib
Format: AMA APA MLA NLM

NCBI Literature Resources

MeSH PMC Bookshelf Disclaimer

The PubMed wordmark and PubMed logo are registered trademarks of the U.S. Department of Health and Human Services (HHS). Unauthorized use of these marks is strictly prohibited.

Follow NCBI
Figure 3. Comparison between IGM- and CGM-group:…
Figure 3. Comparison between IGM- and CGM-group: number of heel pricks, number and duration of hypoglycemic episodes per patient.
Number of heel pricks per patient for capillary blood glucose testing (A), number (B) and duration (C) of hypoglycemic episodes per patient. Results are expressed as mean ± SE (A and B) or as median, 25% and 75% percentiles (box) and extreme values (whisker) (C) *p

Figure 4. Daily carbohydrate supplies in IGM-…

Figure 4. Daily carbohydrate supplies in IGM- and CGM-group.

Results, expressed as mean ± SE,…

Figure 4. Daily carbohydrate supplies in IGM- and CGM-group.
Results, expressed as mean ± SE, represent daily carbohydrate supplies during the first 4 days of life in IGM versus CGM-group (A), and in patients with (HYPO) versus without (NORMO) hypoglycemia in each group (B and C); *p
Similar articles
Cited by
References
    1. Cornblath M, Schwartz R (1993) Hypoglycemia in the neonate. J Pediatr Endocrinol 6: 113–129. - PubMed
    1. Vannucci RC VS (2000) Glucose metabolism in the developing brain. Semin Perinatol 24: 107–115. 10.1053/sp.2000.6361 - DOI - PubMed
    1. Wieloch T (1985) Hypoglycemia-induced neuronal damage prevented by an N-methyl-D-aspartate antagonist. Science 230: 681–683. 10.1126/science.2996146 - DOI - PubMed
    1. Wayenberg JL, Cavedon C, Ghaddhab C, Lefevre N, Bottari SP (2011) Early transient hypoglycemia is associated with increased albumin nitration in the preterm infant. Neonatology 100: 387–397. 10.1159/000326936 - DOI - PubMed
    1. McGowan JE, Chen L, Gao D, Trush M, Wei C (2006) Increased mitochondrial reactive oxygen species production in newborn brain during hypoglycemia. Neurosci Lett 399: 111–114. 10.1016/j.neulet.2006.01.034 - DOI - PubMed
Show all 28 references
Publication types
MeSH terms
Related information
Grant support
The authors have no support or funding to report.
[x]
Cite
Copy Download .nbib
Format: AMA APA MLA NLM
Figure 4. Daily carbohydrate supplies in IGM-…
Figure 4. Daily carbohydrate supplies in IGM- and CGM-group.
Results, expressed as mean ± SE, represent daily carbohydrate supplies during the first 4 days of life in IGM versus CGM-group (A), and in patients with (HYPO) versus without (NORMO) hypoglycemia in each group (B and C); *p

References

    1. Cornblath M, Schwartz R (1993) Hypoglycemia in the neonate. J Pediatr Endocrinol 6: 113–129.
    1. Vannucci RC VS (2000) Glucose metabolism in the developing brain. Semin Perinatol 24: 107–115. 10.1053/sp.2000.6361
    1. Wieloch T (1985) Hypoglycemia-induced neuronal damage prevented by an N-methyl-D-aspartate antagonist. Science 230: 681–683. 10.1126/science.2996146
    1. Wayenberg JL, Cavedon C, Ghaddhab C, Lefevre N, Bottari SP (2011) Early transient hypoglycemia is associated with increased albumin nitration in the preterm infant. Neonatology 100: 387–397. 10.1159/000326936
    1. McGowan JE, Chen L, Gao D, Trush M, Wei C (2006) Increased mitochondrial reactive oxygen species production in newborn brain during hypoglycemia. Neurosci Lett 399: 111–114. 10.1016/j.neulet.2006.01.034
    1. Imai T, Kondo M, Isobe K, Itoh S, Onishi S (1996) Cerebral energy metabolism in insulin induced hypoglycemia in newborn piglets: in vivo 31P-nuclear magnetic resonance spectroscopy. Acta Paediatr Jpn 38: 343–347. 10.1111/j.1442-200X.1996.tb03503.x
    1. Lucas A, Morley R, Cole TJ (1988) Adverse neurodevelopmental outcome of moderate neonatal hypoglycaemia. Bmj 297: 1304–1308. 10.1136/bmj.297.6659.1304
    1. Besson Duvanel C, Fawer CL, Cotting J, Hohlfeld P, Matthieu JM (1999) Long-term effects of neonatal hypoglycemia on brain growth and psychomotor development in small-for-gestational-age preterm infants. J Pediatr 134: 492–498. 10.1016/S0022-3476(99)70209-X
    1. Anderson JM, Milner RD, Strich SJ (1967) Effects of neonatal hypoglycaemia on the nervous system: a pathological study. J Neurol Neurosurg Psychiatry 30: 295–310. 10.1136/jnnp.30.4.295
    1. Fluge G (1975) Neurological findings at follow-up in neonatal hypoglycaemia. Acta Paediatr Scand 64: 629–634. 10.1111/j.1651-2227.1975.tb03835.x
    1. Khan MR, Maheshwari PK, Shamim H, Saleem AF, Ahmed S, et al. (2012) Neurodevelopmental outcomes of premature infants at a tertiary care center in pakistan. Pediatr Neurol 47: 109–113. 10.1016/j.pediatrneurol.2012.05.010
    1. Yalnizoglu D, Haliloglu G, Turanli G, Cila A, Topcu M (2007) Neurologic outcome in patients with MRI pattern of damage typical for neonatal hypoglycemia. Brain Dev 29: 285–292. 10.1016/j.braindev.2006.09.011
    1. Barkovich AJ, Ali FA, Rowley HA, Bass N (1998) Imaging patterns of neonatal hypoglycemia. AJNR Am J Neuroradiol 19: 523–528.
    1. Cornblath M, Hawdon JM, Williams AF, Aynsley-Green A, Ward-Platt MP, et al. (2000) Controversies regarding definition of neonatal hypoglycemia: suggested operational thresholds. Pediatrics 105: 1141–1145. 10.1542/peds.105.5.1141
    1. Koh TH, Aynsley-Green A, Tarbit M, Eyre JA (1988) Neural dysfunction during hypoglycaemia. Arch Dis Child 63: 1353–1358. 10.1136/adc.63.11.1353
    1. Rozance PJ, Hay WW Jr. (2010) Describing hypoglycemia--definition or operational threshold? Early Hum Dev 86: 275–280. 10.1016/j.earlhumdev.2010.05.002
    1. Harris DL, Weston PJ, Harding JE (2012) Incidence of neonatal hypoglycemia in babies identified as at risk. J Pediatr 161: 787–791. 10.1016/j.jpeds.2012.05.022
    1. Tamborlane WV, Beck RW, Bode BW, Buckingham B, Chase HP, et al. (2008) Continuous glucose monitoring and intensive treatment of type 1 diabetes. N Engl J Med 359: 1464–1476. 10.1056/NEJMoa0805017
    1. Harris DL, Battin MR, Weston PJ, Harding JE (2010) Continuous glucose monitoring in newborn babies at risk of hypoglycemia. J Pediatr 157: 198–202 e191 10.1016/j.jpeds.2010.02.003
    1. Beardsall K, Ogilvy-Stuart AL, Ahluwalia J, Thompson M, Dunger DB (2005) The continuous glucose monitoring sensor in neonatal intensive care. Arch Dis Child Fetal Neonatal Ed 90: F307–310.
    1. Iglesias Platas I, Thio Lluch M, Pociello Alminana N, Morillo Palomo A, Iriondo Sanz M, et al. (2009) Continuous glucose monitoring in infants of very low birth weight. Neonatology 95: 217–223. 10.1159/000165980
    1. Lubchenco LO, Bard H (1971) Incidence of hypoglycemia in newborn infants classified by birth weight and gestational age. Pediatrics 47: 831–838.
    1. Hulzebos CV, Sauer PJ (2007) Energy requirements. Semin Fetal Neonatal Med 12: 2–10. 10.1016/j.siny.2006.10.008
    1. Forsyth JS, Murdock N, Crighton A (1995) Low birthweight infants and total parenteral nutrition immediately after birth. III. Randomised study of energy substrate utilisation, nitrogen balance, and carbon dioxide production. Arch Dis Child Fetal Neonatal Ed 73: F13–16.
    1. Calhoun P, Lum J, Beck RW, Kollman C (2013) Performance comparison of the medtronic sof-sensor and enlite glucose sensors in inpatient studies of individuals with type 1 diabetes. Diabetes Technol Ther 15: 758–761. 10.1089/dia.2013.0042
    1. Beardsall K, Costeloe K, Dunger DB (2012) Hyperglycemia in the newborn--clinical guidelines are needed but must be based on correct reporting of the data. JPEN J Parenter Enteral Nutr 36: 378; author reply 379.
    1. Beardsall K (2010) Measurement of glucose levels in the newborn. Early Hum Dev 86: 263–267. 10.1016/j.earlhumdev.2010.05.005
    1. Keenan DB, Cartaya R, Mastrototaro JJ (2010) Accuracy of a new real-time continuous glucose monitoring algorithm. J Diabetes Sci Technol 4: 111–118. 10.1177/193229681000400114

Source: PubMed

3
S'abonner