Neonatal hypoglycemia: Difference between revisions

Line 19: Line 19:
**Intra-uterine growth retardation
**Intra-uterine growth retardation
**Glycogen storage disease
**Glycogen storage disease
**Inborn errors (e.g., fructose intolerance)
**[[Inborn errors of metabolism]] (e.g., fructose intolerance)
**Prematurity
**Prematurity
**Prolonged fasting without IV glucose
**Prolonged fasting without IV glucose
Line 33: Line 33:
*Other endocrine abnormalities:
*Other endocrine abnormalities:
**Pan-hypopituitarism
**Pan-hypopituitarism
**Hypothyroidism
**[[Hypothyroidism]]
**Adrenal insufficiency
**[[Adrenal insufficiency]]
*Increased glucose utilization:
*Increased glucose utilization:
**Cold stress
**Cold stress
**Increased work of breathing
**Increased work of breathing
**Sepsis
**[[Sepsis]]
**Perinatal asphyxia
**Perinatal asphyxia
*Miscellaneous conditions:
*Miscellaneous conditions:
**Polycythemia
**Polycythemia
**Congenital heart disease
**[[Congenital heart disease]]
**CNS abnormalities
**CNS abnormalities
   
   
===Persistent===
===Persistent===
*Too much insulin:
*Too much insulin:
**idiopathic, asphyxia, rhesus dx, Beckwith-Weiderman, Nesiodoblastosis (autosomal recessive hyperinsulinism)
**idiopathic, asphyxia, rhesus diagnoses, Beckwith-Weiderman, Nesiodoblastosis (autosomal recessive hyperinsulinism)
*Not enough anti-insulin:
*Not enough anti-insulin:
**hypopit, adrenal hyperplasia
**hypopituitarism, adrenal hyperplasia
*Inborn errors of metabolism:
*[[Inborn errors of metabolism]]
**glycogen storage dz, fatty oxidation errors
**glycogen storage disease, fatty oxidation errors


==Diagnosis==
==Diagnosis==

Revision as of 02:12, 13 July 2016

Background

  • 3 births per 1000 with hypoglycemia

Risks

  • Maternal DM (hyperinsulin)
  • Premies (cannot store glycogen)
  • Sick kids (depleted glycogen)
  • Growth restricted babies (depleted glycogen)
  • Macrosomic kids

Clinical Features

  • Jitteriness and irritability
  • Apnea and cyanosis
  • Hypotonia
  • Convulsions

Differential DIagnosis

  • Decreased substrate availability
    • Intra-uterine growth retardation
    • Glycogen storage disease
    • Inborn errors of metabolism (e.g., fructose intolerance)
    • Prematurity
    • Prolonged fasting without IV glucose
  • Hyperinsulinemia:
    • Infant of diabetic mother
    • Islet cell hyperplasia
    • Erythroblastosis fetalis
    • Exchange transfusion
    • Beckwith-Wiedemann Syndrome
    • Maternal �-mimetic tocolytic agents
    • ?High? umbilical arterial catheter
    • Abrupt cessation of IV glucose
  • Other endocrine abnormalities:
  • Increased glucose utilization:
    • Cold stress
    • Increased work of breathing
    • Sepsis
    • Perinatal asphyxia
  • Miscellaneous conditions:

Persistent

  • Too much insulin:
    • idiopathic, asphyxia, rhesus diagnoses, Beckwith-Weiderman, Nesiodoblastosis (autosomal recessive hyperinsulinism)
  • Not enough anti-insulin:
    • hypopituitarism, adrenal hyperplasia
  • Inborn errors of metabolism
    • glycogen storage disease, fatty oxidation errors

Diagnosis

  • Blood glucose level
    • blood glucose <40 mg/dL (preterm infants repeated levels below <50)

There is a normal fall in glucose @ 2-4hr of life

Management

Pediatric Hypoglycemia Dextrose Chart

Category Age Glucose Treatment Initial IV Bolus Maintenance Dose
Neonatal <2mo <40 D10W 2.5-5 mL/kg 6 mL/kg/h
Pediatric 2mo-8yrs <60 D25W 2 mL/kg

D10W:

  • 6 mL/kg/h for first 10 kg
  • + 3 mL/kg/h for 11–20 kg
  • + 1.5 mL/kg/h for each additional kg >20 kg
Adult >8yrs <70 D50W 50mL (1 amp) OR 1 mL/kg
  • Consider diluting the D25W or D50W bolus, with NS 1-to-1, as those concentrations may be sclerosing to veins
  • Recheck 5 minutes after dose and repeat dose if low.
  • Consider glucagon IM/SQ if IV access is not readily available
  • Glucometer reading 20-40 mg/dL, infant is term and is able to feed:
    • Draw blood for stat blood glucose.
    • Feed 5 mL/kg of D5W.
    • Repeat blood glucose or Glucometer 20 min after feeding.
  • Glucometer reading:
    • <20 mg/dL or
    • <40 mg/dL and NPO or preterm or
    • <40 mg/dL after feeding or
    • <40 mg/dL and symptomatic
      • Draw blood for stat glucose measurement.
      • Give IV bolus of 2-3 mL/kg of D10W.
      • Begin continuous infusion of D10W at 4-6 mg/kg/min.
      • If infant of diabetic mother, begin D10W at 8-10 mg/kg/min (100-125 cc/kg/d).
      • Repeat blood glucose in 20 min and pursue treatment until blood sugar >40 mg/dL.
  • For persistent hypoglycemia despite above measures:
    • Increase rate of glucose infusion stepwise in 2 mg/kg/min*increments up to 12-15 mg/kg/min glucose. Use increased volume with caution in infants where volume overload is a concern. Maximal concentration of glucose in peripheral IV is D12.5.
    • If infant requires IV dextrose concentrations >12.5%, insert central venous catheter.
    • Do not use D25W or D50W IV or large IV volume boluses as this creates rebound hypoglycemia in infants who are hyperinsulinemic. In addition, administration of D25W or D50W can cause dangerous increase in plasma osmolarity.
  • If hypoglycemia is not controlled with above measures: Obtain Endocrine Consult to guide further diagnostic evaluation and management. While awaiting consult, send blood (while blood sugar is low) for glucose, plasma cortisol, growth hormone and insulin concentrations. Further management may include glucocorticoids, diazoxide, somatostatin or pancreatectomy.
  • Weaning IV dextrose infusion: When blood glucose has been stable for 12-24 h, begin decreasing IV infusion by 1-2 mL/hr q3-4 hours if blood glucose remains �60 mg/dL.

Calculate rate of glucose administration

Use either of the following formulas:

  • (% glucose x mL/kg/d)/144 = glucose infusion rate (mg/kg/min)
  • (% glucose x mL/h)/(6 x body weight in kg) = glucose infusion rate (mg/kg/min)

Persistent Hypoglycemia

  • Check insulin, GH, cortisol
  • Increase volume by 30cc/kg/d
  • Increase glucose to 12.5%
  • Glucagon infusion

If continues for >7 d: send insulin, cortisol, growth hormone

Disposition

See Also

References