Am J Perinatol 2024; 41(11): 1484-1494
DOI: 10.1055/a-2107-1985
Original Article

Factors Associated with Need for Intravenous Glucose Infusion for the Treatment of Early Neonatal Hypoglycemia in Late Preterm and Term Neonates

1   Division of Neonatal-Perinatal Medicine, Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, Texas
,
Lisa M. Scheid
1   Division of Neonatal-Perinatal Medicine, Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, Texas
,
L Steven Brown
2   Department of Research, Parkland Health and Hospital System, Dallas, Texas
,
Patti J. Burchfield
1   Division of Neonatal-Perinatal Medicine, Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, Texas
,
1   Division of Neonatal-Perinatal Medicine, Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, Texas
› Institutsangaben
Funding This study was funded by the George L. MacGregor Professorship of the University of Texas Southwestern Medical Center awarded to Dr. Rosenfeld.
The datasets generated and/or analyzed during the current study are available from the corresponding author upon reasonable request.

Abstract

Objective The aim of this study was to determine which late-preterm (35–36 weeks' gestational age [GA]) and term neonates with early-onset hypoglycemia in the first 72 hours postnatal required a continuous glucose infusion to achieve and successfully maintain euglycemia.

Study Design This is a retrospective cohort study of late preterm and term neonates born in 2010–2014 and admitted to the Mother-Baby Unit at Parkland Hospital who had laboratory-proven blood glucose concentration < 40 mg/dL (2.2 mmol/L) during the first 72 hours of life. Among the subgroup needing intravenous (IV) glucose infusion, we analyzed which factors predicted a maximum glucose infusion rate (GIR) ≥ 10 mg/kg/min. The entire cohort was randomly divided into a derivation cohort (n = 1,288) and a validation cohort (n = 1,298).

Results In multivariate analysis, the need for IV glucose infusion was associated with small size for GA, low initial glucose concentration, early-onset infection, and other perinatal variables in both cohorts. A GIR ≥ 10 mg/kg/min was required in 14% of neonates with blood glucose value < 20 mg/dL during the first 3 hours of observation. The likelihood of a GIR ≥ 10 mg/kg/min was associated with lower initial blood glucose value and lower umbilical arterial pH.

Conclusion Need for IV glucose infusion was associated with small size for GA, low initial glucose concentration, early-onset infection, and variables associated with perinatal hypoxia–asphyxia. The likelihood of a maximum GIR ≥ 10 mg/kg/min was greater in neonates with lower blood glucose value during the first 3 hours of observation and lower umbilical arterial pH.

Key Points

  • We studied 51,973 neonates ≥ 35 weeks' GA.

  • We established a model predicting the need for IV glucose.

  • We also predicted the need for a high rate of IV glucose.

Authors' Contributions

All authors reviewed, edited, and approved the manuscript as written. Drs. Scheid and Rosenfeld designed the study. Dr. Brion wrote the first version of the manuscript. Mr. Brown conducted statistical analyses.


Supplementary Material



Publikationsverlauf

Eingereicht: 15. Februar 2023

Angenommen: 31. Mai 2023

Accepted Manuscript online:
07. Juni 2023

Artikel online veröffentlicht:
29. Juli 2023

© 2023. Thieme. All rights reserved.

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333 Seventh Avenue, 18th Floor, New York, NY 10001, USA

 
  • References

  • 1 McGowan JE. Neonatal hypoglycemia. Pediatr Rev 1999; 20: e6-e15
  • 2 Cornblath M, Hawdon JM, Williams AF. et al. Controversies regarding definition of neonatal hypoglycemia: suggested operational thresholds. Pediatrics 2000; 105 (05) 1141-1145
  • 3 Harris DL, Weston PJ, Harding JE. Incidence of neonatal hypoglycemia in babies identified as at risk. J Pediatr 2012; 161 (05) 787-791
  • 4 Williams AF. Hypoglycaemia of the newborn: a review. Bull World Health Organ 1997; 75 (03) 261-290
  • 5 Cornblath M, Ichord R. Hypoglycemia in the neonate. Semin Perinatol 2000; 24 (02) 136-149
  • 6 Dyer JS, Rosenfeld CR. Metabolic imprinting by prenatal, perinatal, and postnatal overnutrition: a review. Semin Reprod Med 2011; 29 (03) 266-276
  • 7 Adamkin DH. Committee on Fetus and Newborn. Postnatal glucose homeostasis in late-preterm and term infants. Pediatrics 2011; 127 (03) 575-579
  • 8 Lilien LD, Grajwer LA, Pildes RS. Treatment of neonatal hypoglycemia with continuous intravenous glucose infusion. J Pediatr 1977; 91 (05) 779-782
  • 9 Lilien LD, Pildes RS, Srinivasan G, Voora S, Yeh TF. Treatment of neonatal hypoglycemia with minibolus and intraveous glucose infusion. J Pediatr 1980; 97 (02) 295-298
  • 10 Hay Jr. WW, Raju TNK, Higgins RD, Kalhan SC, Devaskar SU. Knowledge gaps and research needs for understanding and treating neonatal hypoglycemia: workshop report from Eunice Kennedy Shriver National Institute of Child Health and Human Development. J Pediatr 2009; 155 (05) 612-617
  • 11 VanHaltren K, Malhotra A. Characteristics of infants at risk of hypoglycaemia secondary to being ‘infant of a diabetic mother’. J Pediatr Endocrinol Metab 2013; 26 (9–10): 861-865
  • 12 Lord K, De León DD. Hyperinsulinism in the neonate. Clin Perinatol 2018; 45 (01) 61-74
  • 13 Sigal WM, Alzahrani O, Guadalupe GM. et al. Natural history and neurodevelopmental outcomes in perinatal stress induced hyperinsulinism. Front Pediatr 2022; 10: 999274
  • 14 Scheid LM, Brown LS, Clark C, Rosenfeld CR. Data electronically extracted from the electronic health record require validation. J Perinatol 2019; 39 (03) 468-474
  • 15 Dietzen DJ, Wilhite TR, Rasmussen M, Sheffield M. Point-of-care glucose analysis in neonates using modified quinoprotein glucose dehydrogenase. Diabetes Technol Ther 2013; 15 (11) 923-928
  • 16 Olsen IE, Groveman SA, Lawson ML, Clark RH, Zemel BS. New intrauterine growth curves based on United States data. Pediatrics 2010; 125 (02) e214-e224
  • 17 Olsen IE, Lawson ML, Ferguson AN. et al. BMI curves for preterm infants. Pediatrics 2015; 135 (03) e572-e581
  • 18 Lubchenco LO, Hansman C, Boyd E. Intrauterine growth in length and head circumference as estimated from live births at gestational ages from 26 to 42 weeks. Pediatrics 1966; 37 (03) 403-408
  • 19 Sanchez AM, Jimenez JM, Manroe BL, Rosenfeld CR, Tyson TE. Systems approach to the evaluation of maternal and neonatal care. Paper presented at: Proceedings of the 12th Hawaii International Conference on System Sciences. Selected Papers in Medical Information Processing. 1979 ;III: 140-151
  • 20 Kaiser JR, Tilford JM, Simpson PM, Salhab WA, Rosenfeld CR. Hospital survival of very-low-birth-weight neonates from 1977 to 2000. J Perinatol 2004; 24 (06) 343-350
  • 21 Peduzzi P, Concato J, Kemper E, Holford TR, Feinstein AR. A simulation study of the number of events per variable in logistic regression analysis. J Clin Epidemiol 1996; 49 (12) 1373-1379
  • 22 Le HT, Harris NS, Estilong AJ, Olson A, Rice MJ. Blood glucose measurement in the intensive care unit: what is the best method?. J Diabetes Sci Technol 2013; 7 (02) 489-499
  • 23 Pandey R, Scheid LM. Lower versus traditional treatment threshold for neonatal hypoglycaemia: no difference between the groups at 18 months of age, awaiting long-term outcomes. Acta Paediatr 2020; 109 (10) 2164-2165
  • 24 Shah R, Harding J, Brown J, McKinlay C. Neonatal glycaemia and neurodevelopmental outcomes: a systematic review and meta-analysis. Neonatology 2019; 115 (02) 116-126
  • 25 Sivarajan M, Schneider JH, Johnson KA. et al. Decreasing early hypoglycemia frequency in at-risk newborns after implementing a new hypoglycemia screening algorithm. J Perinatol 2021; 41 (12) 2840-2846
  • 26 Rozance PJ. Hypoglycemia in the newborn and neurodevelopmental outcomes in childhood. JAMA 2022; 327 (12) 1135-1137
  • 27 van Kempen AAMW, Eskes PF, Nuytemans DHGM. et al; HypoEXIT Study Group. Lower versus traditional treatment threshold for neonatal hypoglycemia. N Engl J Med 2020; 382 (06) 534-544
  • 28 Rawat M, Chandrasekharan P, Turkovich S. et al. Oral dextrose gel reduces the need for intravenous dextrose therapy in neonatal hypoglycemia. Biomed Hub 2016; 1 (03) 1-9
  • 29 Makker K, Alissa R, Dudek C, Travers L, Smotherman C, Hudak ML. Glucose gel in infants at risk for transitional neonatal hypoglycemia. Am J Perinatol 2018; 35 (11) 1050-1056
  • 30 Ponnapakkam AP, Stine CN, Ahmad KA. et al. Evaluating the effects of a neonatal hypoglycemia bundle on NICU admission and exclusive breastfeeding. J Perinatol 2020; 40 (02) 344-351
  • 31 Stanzo K, Desai S, Chiruvolu A. Effects of dextrose gel in newborns at risk for neonatal hypoglycemia in a baby-friendly hospital. J Obstet Gynecol Neonatal Nurs 2020; 49 (01) 55-64
  • 32 Edwards T, Liu G, Hegarty JE, Crowther CA, Alsweiler J, Harding JE. Oral dextrose gel to prevent hypoglycaemia in at-risk neonates. Cochrane Database Syst Rev 2021; 5 (05) CD012152
  • 33 Edwards T, Alsweiler JM, Crowther CA. et al. Prophylactic oral dextrose gel and neurosensory impairment at 2-year follow-up of participants in the hPOD randomized trial. JAMA 2022; 327 (12) 1149-1157