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Neonatal
Hypoglycemia
Lead Author
VC Manoj
Co-authors
Mamta Jajoo, Nilesh Rao
Indian Academy of Pediatrics (IAP)
STANDARD
TREATMENT
GUIDELINES 2022
Remesh Kumar R
IAP President 2022
Upendra Kinjawadekar
IAP President-Elect 2022
Piyush Gupta
IAP President 2021
Vineet Saxena
IAP HSG 2022–2023
Under the Auspices of the
IAP Action Plan 2022
© Indian Academy of Pediatrics
IAP Standard Treatment Guidelines Committee
Chairperson
Remesh Kumar R
IAP Coordinator
Vineet Saxena
National Coordinators
SS Kamath, Vinod H Ratageri
Member Secretaries
Krishna Mohan R, Vishnu Mohan PT
Members
Santanu Deb, Surender Singh Bisht, Prashant Kariya,
Narmada Ashok, Pawan Kalyan
Neonatal Hypoglycemia
1
;
; Hypoglycemia is low level of plasma or blood glucose in the neonate.
;
; In healthy term neonates, there is a transient, physiological fall in the blood glucose
concentration with a nadir at 60–90 minutes after birth, without any symptoms later rising
to levels above 60 mg/dL by 4 hours.
;
; Breastfed infants may tolerate lower blood sugar levels because of bioavailable alternate
fuels like ketone bodies, thus facilitating adaptation during transition.
Introduction
Clinical
Manifestations
of
Hypoglycemia
in
Neonate
2
;
; It is prudent to prevent recurrent and persistent hypoglycemia due to associations with
seizures, poor visual motor, and executive function at 4–5 years of age, however there is
no clear association between asymptomatic hypoglycemia, treatment for the same and
poor neurodevelopment.
Adrenergic
;
; Tachypnea
;
; Tachycardia
;
; Poor suck
;
; Poor feeding
;
; Pallor
;
; Temperature instability
;
; Sweating
Neuroglycopenic
;
; Lethargy and hypotonia
;
; Apnea or irregular
breathing efforts
;
; Cyanosis
;
; Seizures
Neonatal Hypoglycemia
4
Need
for
Further
Workup
Infant with persistent hypoglycemia for >72 hours or severe hypoglycemia >10–12 mg/kg/
min glucose requirement.
Highly controversial and there is a lack of consensus at present.
Operational threshold cutoffs (indicate the need to intervene) providing reasonable margin of
safety in late preterm and term at-risk neonates are as follows:
Symptomatic: Blood sugar <40 mg/dL
Asymptomatic:
;
; Less than 4 hours of age—25 mg/dL
;
; 4–24 hours of age—35 mg/dL
;
; 24–48 hours—45 mg/dL
;
; More than 48 hours—60 mg/dL
There is paucity of literature on preterm neonates <34 weeks GA and hence prudent to maintain
blood glucose levels >50 mg/dL.
Definition
;
; Testingiswarrantedonlyforat-riskneonatesandisnotneededforhealthytermnewborns.
;
; Point-of-caretestingusingreagentstripsisrapid,bedside,convenient,andcost-effective.
;
; Blood glucose measured by strip is 15% lesser than plasma glucose. In case of low blood
glucose, a laboratory sample for blood glucose estimation should be sent.
;
; A delay in testing of sample after collection can lead to a blood glucose reduction of up
to 6 mg/dL/hour.
Testing
Neonatal Hypoglycemia
5
Etiology
Gestation Age >35 Weeks
All infants:
;
; Skin-to-skin care, keep warm
;
; Promote breastfeeding within first hour of birth
;
; Infants should continue breastfeeding on cue
;
; Not to give water or glucose water or formula may interfere with normal metabolic
compensatory mechanisms
At risk infants:
Symptomatic and blood glucose < 40 mg/dL: Start intravenous (IV) glucose
Symptomatic with blood glucose < 25 mg/dL: Give bolus IV dextrose 10% 1–2 mL/kg followed
by infusion at the rate of 5–8 mg/kg/min.
;
; Target glucose > 50 mg/dL
;
; Continue breastfeeding frequently
;
; Recheck plasma glucose within 30 minutes
Asymptomatic: <40 mg/dL and <4 hours of age:
;
; Start breastfeeding within half an hour
;
; Recheck blood glucose before next feeding
;
; Continue skin-to-skin care
;
; Intensify breastfeeding
;
; Evaluate for other underlying illnesses
;
; If glucose <35 mg/dL start IV glucose therapy
;
; Target blood glucose > 50 mg/dL
;
; Recheck until three normal levels
;
; Check glucose levels once at 24 hours of age in babies like small for gestational age (SGA)/
low birth weight (LBW)/preterm
Management
Decreased production/stores
Prematurity, intrauterine growth
restriction (IUGR), delayed feeding,
growth hormone (GH) and cortisol
deficiency, inborn errors of
metabolism (IEM)
Increased utilization
Infant of diabetic mother, large
for gestational age (LGA), sepsis,
asphyxia, hypothermia, polycythemia,
hyperinsulinemia, maternal beta blockers,
oral hypoglycemics
Neonatal Hypoglycemia
6
;
; Rate of start of IV fluids: Use graded approach
;
; IUGR: 5–7 mg/kg/min
;
; Mother with infants of diabetic mothers (IDM)/LGA infants: 3–5 mg/kg/min
;
; Infant with other risk group: 4–6 mg/kg/min
;
; Glucose infusion >12 mg/kg/min: Consider for further interventions
;
; Maximum dextrose concentration through peripheral IV cannula and central venous catheter
is 12.5% and 25%, respectively
Parenteral
Therapy
Infant with persistent hypoglycemia for >72 hours or requiring IV therapy for symptomatic
or asymptomatic low glucose levels should only be discharged if glucose level maintained
above 70 mg/dL through several feed-fast cycles.
Discharge
Criteria
Neurodevelopment
Outcome
Due to the potential deleterious effects on the neonatal brain, it is recommended to treat
symptomatic hypoglycemia and prevent recurrent and persistent hypoglycemic episodes.
In asymptomatic hypoglycemia, although there is not much evidence for adverse
outcomes, there are concerns about poor literacy scores and lower visual motor, executive
function with recurrent or severe hypoglycemia.
In preterm neonates, associations have been reported between recurrent low sugars
and lower bailey scores, developmental and cognitive delays. More research is needed in
this group of neonates.
Neonatal Hypoglycemia
7
;
; Adamkin DH, Polin RA. Imperfect Advice: Neonatal Hypoglycemia. J Pediatr. 2016;
176:195-6.
;
; Committee on Fetus and Newborn, Adamkin DH. Postnatal glucose homeostasis in late-
preterm and term infants. Pediatrics. 2011;127:575-9.
;
; Goode RH, Rettiganti M, Li J, Lyle RE, Whiteside-Mansell L, Barrett KW, et al.
Developmental Outcomes of Preterm Infants with Neonatal Hypoglycemia. Pediatrics.
2016;138(6):e20161424.
;
; McKinlay CJD, Alsweiler JM, Anstice NS, Burakevych N, Chakraborty A, Chase JG, et al.
Association of Neonatal Glycemia with Neurodevelopmental Outcomes at 4.5 Years.
JAMA Pediatr. 2017;171:972-83.
;
; Stanley CA, Rozance PJ, Thornton PS, De Leon DD, Harris D, Haymond MW, et al. Re-
evaluating “transitional neonatal hypoglycemia”: mechanism and implications for
management. J Pediatr. 2015;166:1520-5.e1.
;
; Thornton PS, Stanley CA, De Leon DD, Harris D, Haymond MW, Hussain K, et al.
RecommendationsfromthePediatricEndocrineSocietyforEvaluationandManagement
of Persistent Hypoglycemia in Neonates, Infants, and Children. J Pediatr. 2015;167:
238-45.
Further
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Ch-01-NEONATAL-HYPOGLYCEMIA.pdf

  • 1. Neonatal Hypoglycemia Lead Author VC Manoj Co-authors Mamta Jajoo, Nilesh Rao Indian Academy of Pediatrics (IAP) STANDARD TREATMENT GUIDELINES 2022 Remesh Kumar R IAP President 2022 Upendra Kinjawadekar IAP President-Elect 2022 Piyush Gupta IAP President 2021 Vineet Saxena IAP HSG 2022–2023 Under the Auspices of the IAP Action Plan 2022
  • 2. © Indian Academy of Pediatrics IAP Standard Treatment Guidelines Committee Chairperson Remesh Kumar R IAP Coordinator Vineet Saxena National Coordinators SS Kamath, Vinod H Ratageri Member Secretaries Krishna Mohan R, Vishnu Mohan PT Members Santanu Deb, Surender Singh Bisht, Prashant Kariya, Narmada Ashok, Pawan Kalyan
  • 3. Neonatal Hypoglycemia 1 ; ; Hypoglycemia is low level of plasma or blood glucose in the neonate. ; ; In healthy term neonates, there is a transient, physiological fall in the blood glucose concentration with a nadir at 60–90 minutes after birth, without any symptoms later rising to levels above 60 mg/dL by 4 hours. ; ; Breastfed infants may tolerate lower blood sugar levels because of bioavailable alternate fuels like ketone bodies, thus facilitating adaptation during transition. Introduction Clinical Manifestations of Hypoglycemia in Neonate 2 ; ; It is prudent to prevent recurrent and persistent hypoglycemia due to associations with seizures, poor visual motor, and executive function at 4–5 years of age, however there is no clear association between asymptomatic hypoglycemia, treatment for the same and poor neurodevelopment. Adrenergic ; ; Tachypnea ; ; Tachycardia ; ; Poor suck ; ; Poor feeding ; ; Pallor ; ; Temperature instability ; ; Sweating Neuroglycopenic ; ; Lethargy and hypotonia ; ; Apnea or irregular breathing efforts ; ; Cyanosis ; ; Seizures
  • 4. Neonatal Hypoglycemia 4 Need for Further Workup Infant with persistent hypoglycemia for >72 hours or severe hypoglycemia >10–12 mg/kg/ min glucose requirement. Highly controversial and there is a lack of consensus at present. Operational threshold cutoffs (indicate the need to intervene) providing reasonable margin of safety in late preterm and term at-risk neonates are as follows: Symptomatic: Blood sugar <40 mg/dL Asymptomatic: ; ; Less than 4 hours of age—25 mg/dL ; ; 4–24 hours of age—35 mg/dL ; ; 24–48 hours—45 mg/dL ; ; More than 48 hours—60 mg/dL There is paucity of literature on preterm neonates <34 weeks GA and hence prudent to maintain blood glucose levels >50 mg/dL. Definition ; ; Testingiswarrantedonlyforat-riskneonatesandisnotneededforhealthytermnewborns. ; ; Point-of-caretestingusingreagentstripsisrapid,bedside,convenient,andcost-effective. ; ; Blood glucose measured by strip is 15% lesser than plasma glucose. In case of low blood glucose, a laboratory sample for blood glucose estimation should be sent. ; ; A delay in testing of sample after collection can lead to a blood glucose reduction of up to 6 mg/dL/hour. Testing
  • 5. Neonatal Hypoglycemia 5 Etiology Gestation Age >35 Weeks All infants: ; ; Skin-to-skin care, keep warm ; ; Promote breastfeeding within first hour of birth ; ; Infants should continue breastfeeding on cue ; ; Not to give water or glucose water or formula may interfere with normal metabolic compensatory mechanisms At risk infants: Symptomatic and blood glucose < 40 mg/dL: Start intravenous (IV) glucose Symptomatic with blood glucose < 25 mg/dL: Give bolus IV dextrose 10% 1–2 mL/kg followed by infusion at the rate of 5–8 mg/kg/min. ; ; Target glucose > 50 mg/dL ; ; Continue breastfeeding frequently ; ; Recheck plasma glucose within 30 minutes Asymptomatic: <40 mg/dL and <4 hours of age: ; ; Start breastfeeding within half an hour ; ; Recheck blood glucose before next feeding ; ; Continue skin-to-skin care ; ; Intensify breastfeeding ; ; Evaluate for other underlying illnesses ; ; If glucose <35 mg/dL start IV glucose therapy ; ; Target blood glucose > 50 mg/dL ; ; Recheck until three normal levels ; ; Check glucose levels once at 24 hours of age in babies like small for gestational age (SGA)/ low birth weight (LBW)/preterm Management Decreased production/stores Prematurity, intrauterine growth restriction (IUGR), delayed feeding, growth hormone (GH) and cortisol deficiency, inborn errors of metabolism (IEM) Increased utilization Infant of diabetic mother, large for gestational age (LGA), sepsis, asphyxia, hypothermia, polycythemia, hyperinsulinemia, maternal beta blockers, oral hypoglycemics
  • 6. Neonatal Hypoglycemia 6 ; ; Rate of start of IV fluids: Use graded approach ; ; IUGR: 5–7 mg/kg/min ; ; Mother with infants of diabetic mothers (IDM)/LGA infants: 3–5 mg/kg/min ; ; Infant with other risk group: 4–6 mg/kg/min ; ; Glucose infusion >12 mg/kg/min: Consider for further interventions ; ; Maximum dextrose concentration through peripheral IV cannula and central venous catheter is 12.5% and 25%, respectively Parenteral Therapy Infant with persistent hypoglycemia for >72 hours or requiring IV therapy for symptomatic or asymptomatic low glucose levels should only be discharged if glucose level maintained above 70 mg/dL through several feed-fast cycles. Discharge Criteria Neurodevelopment Outcome Due to the potential deleterious effects on the neonatal brain, it is recommended to treat symptomatic hypoglycemia and prevent recurrent and persistent hypoglycemic episodes. In asymptomatic hypoglycemia, although there is not much evidence for adverse outcomes, there are concerns about poor literacy scores and lower visual motor, executive function with recurrent or severe hypoglycemia. In preterm neonates, associations have been reported between recurrent low sugars and lower bailey scores, developmental and cognitive delays. More research is needed in this group of neonates.
  • 7. Neonatal Hypoglycemia 7 ; ; Adamkin DH, Polin RA. Imperfect Advice: Neonatal Hypoglycemia. J Pediatr. 2016; 176:195-6. ; ; Committee on Fetus and Newborn, Adamkin DH. Postnatal glucose homeostasis in late- preterm and term infants. Pediatrics. 2011;127:575-9. ; ; Goode RH, Rettiganti M, Li J, Lyle RE, Whiteside-Mansell L, Barrett KW, et al. Developmental Outcomes of Preterm Infants with Neonatal Hypoglycemia. Pediatrics. 2016;138(6):e20161424. ; ; McKinlay CJD, Alsweiler JM, Anstice NS, Burakevych N, Chakraborty A, Chase JG, et al. Association of Neonatal Glycemia with Neurodevelopmental Outcomes at 4.5 Years. JAMA Pediatr. 2017;171:972-83. ; ; Stanley CA, Rozance PJ, Thornton PS, De Leon DD, Harris D, Haymond MW, et al. Re- evaluating “transitional neonatal hypoglycemia”: mechanism and implications for management. J Pediatr. 2015;166:1520-5.e1. ; ; Thornton PS, Stanley CA, De Leon DD, Harris D, Haymond MW, Hussain K, et al. RecommendationsfromthePediatricEndocrineSocietyforEvaluationandManagement of Persistent Hypoglycemia in Neonates, Infants, and Children. J Pediatr. 2015;167: 238-45. Further Reading