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•Hypocalcemia is a common 
metabolic problem in newborns. 
• The diagnosis, clinical 
manifestations, and treatment of 
neonatal hypocalcemia will be 
reviewed.
• Patient born preterm at 34 weeks 
•Normal spontaneous vaginal 
delivery 
• Birth Weight: 2050 g 
• APGAR 8
• 28 year old G1P0 
• Irrelevant medical History 
•Denies smoking 
•No medication use 
•No HTN, no DM 
•Negative serologic studies
• Irritable, with weak cry 
• +ve hypertelorism 
• jaw held tightly closed 
• cleft palate 
• CV: RR, systolic murmur 
• Extremities: hypertonic
• CBC: WNL 
• CMP: WNL except Ca 
• Ca: 6.0 mg/dL 
• P: 9.2 mg/dL (4.5-9.0) 
•Mg: 1.5 mEq/L (1.3-2.0) 
• PTH: 44 pg/mL (N 40-100)
•2D Echo reveals a small VSD 
•Hypoplastic thymus
•Hypocalcemia 
•Hypoparathyroidism 
•VSD 
•Hypoplastic thymus
• Plasma calcium totals 2.4 mM (9.4 
mg/dl) 
– Free calcium is 1.2 mM
– Albumin 
– Blood pH 
– Serum phosphate 
– Serum magnesium 
– Serum bicarbonate
Hormone Effect Bone Gut Kidney 
PTH  Ca  Po4 Increases 
Osteoclasts 
Indirect 
via Vit. D 
Ca reab 
Po4 exr. 
Vit D3  Ca  Po4 No direct 
action 
 Ca  Po4 
absorption 
No direct 
effect 
Calcitonin  Ca  Po4 Inhibits 
Osteoclasts 
No direct 
effect 
Ca & Po4 
excretion
• Ca messenger system – regulates cell 
function 
• Activates cellular enzyme cascades 
• Smooth muscle and myocardial 
contraction 
•Nerve impulse conduction 
• Secretory activity of glands
• Neuromuscular 
excitability 
• Tetany 
• Seizures 
• Stridor or cyanosis 
from laryngospasm 
• Hypotension 
• Impaired cardiac 
contractility
•May be unspecific 
– Asymptomatic 
– Lethargy 
– Poor feeding 
– Vomiting 
– Abdominal distention
• Fetus: Ca and P concentration 
higher than mother plasma, s Ca 
falls at 24 hrs. 
•Neonates: Ca lower than children at 
2nd and 3th day 
• Return to normal by 5-10 days
•Total serum Ca less than: 
– 7.0 mg/dL in Preterm infants 
– 8.0 mg/dL in Term newborns 
– 8.8 mg/dL in children
Early neonatal hypocalcemia (48-72 hours) 
Prematurity 
Poor intake, hypoalbuminemia, ↓ responsiveness 
to vit D 
Birth asphyxia 
Delayed feeding, ↑ calcitonin, endogenous 
phosphate load , alkali therapy 
Infant of diabetic mother 
Mg depletion functional hypoparathyroidis→ m → 
↓ Ca 
IUGR
Late neonatal hypocalcemia (Full 
term) 
•Exogenous phosphate load 
•Mg deficiency 
•Transient hypoparathyroidism of 
newborn 
•Congenital Hypoparathyroidism 
•Maternal Vit D deficiency 
•Maternal Hyperparathyroidism 
•Gentamycin
Bicarbonate infusion → metabolic 
alkalosis 
Transfusion with citrated blood→ 
formation of Ca complexes, ↓ Ca++ 
Lipid infusions → Ca complexes with 
FFAs → ↓ Ca++ 
Phototherapy for hyperbilirubinemia 
Acute renal failure → 
hyperphosphatemia 
Rotavirus infection
• ↓ Mg → impaired PTH secretion & 
resistance to PTH → hypocalcemia 
•Usually idiopathic & transient 
•May be secodary to disorders of 
intestinal and/or renal tubular Mg 
transport
• Antagonizes PTH secretion or 
actions → ↑ Ca & P deposition in 
bones → hypocalcemia.
Cardiac defects, Abnormal facies, 
Thymic hypoplasia, Cleft palate, and 
Hypocalcemia caused by 
Chromosome 22 deletion 
DiGeorge Syndrome is a severe 
phenotype of this group of related 
disorders. 
FISH establishes the diagnosis.
•What is the diagnosis? 
•How could we confirm the 
diagnosis?
• Total Ca 
• Ionized Ca 
• Phosphorus 
•Magnesium 
• PTH 
• Vitamin D 
• Liver function 
• Renal function
Only in infants with risk factors 
Measure Ca at 24, and 48 hrs of age. 
Measure Ca in infants with congenital 
heart ds. 
Ionized Ca should be the primary 
measurement.
1. Depends on underlying cause & 
severity 
2. Mild asymptomatic: ↑ dietary Ca by 
initiating early feeding 
3. For infants who require parenteral 
nutrition, Ca is added to the solution . 
4. If symptomatic: treat immediately
–Ca gluconate:10 mg/kg (1 ml/kg of 
10% solution) Slowly IV 
–Start oral Calcium as soon as possible 
–Early neonatal hypocalcaemia 
normalizes in 2-3 d
Late neonatal hypocalcemia 
–Associated with ­ S-phosphate 
– Decrease phosphate intake 
–Give calcium containing phosphate 
binder 
–Oral calcium gluconate 100 
mg/kg/dose 4 hourly
–Tissue necrosis/calcification if 
extravasates 
–Calcium can inhibit sinus node ® 
bradycardia + arrest 
–Avoid complete correction of 
hypocalcemia 
–Give Ca before correcting acidosis 
–If ¯ Mg – first treat & correct 
hypomagnesemia
Neonatal hy po calcemia

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Neonatal hy po calcemia

  • 1.
  • 2. •Hypocalcemia is a common metabolic problem in newborns. • The diagnosis, clinical manifestations, and treatment of neonatal hypocalcemia will be reviewed.
  • 3.
  • 4. • Patient born preterm at 34 weeks •Normal spontaneous vaginal delivery • Birth Weight: 2050 g • APGAR 8
  • 5. • 28 year old G1P0 • Irrelevant medical History •Denies smoking •No medication use •No HTN, no DM •Negative serologic studies
  • 6. • Irritable, with weak cry • +ve hypertelorism • jaw held tightly closed • cleft palate • CV: RR, systolic murmur • Extremities: hypertonic
  • 7. • CBC: WNL • CMP: WNL except Ca • Ca: 6.0 mg/dL • P: 9.2 mg/dL (4.5-9.0) •Mg: 1.5 mEq/L (1.3-2.0) • PTH: 44 pg/mL (N 40-100)
  • 8. •2D Echo reveals a small VSD •Hypoplastic thymus
  • 10.
  • 11.
  • 12. • Plasma calcium totals 2.4 mM (9.4 mg/dl) – Free calcium is 1.2 mM
  • 13. – Albumin – Blood pH – Serum phosphate – Serum magnesium – Serum bicarbonate
  • 14.
  • 15.
  • 16. Hormone Effect Bone Gut Kidney PTH  Ca  Po4 Increases Osteoclasts Indirect via Vit. D Ca reab Po4 exr. Vit D3  Ca  Po4 No direct action  Ca  Po4 absorption No direct effect Calcitonin  Ca  Po4 Inhibits Osteoclasts No direct effect Ca & Po4 excretion
  • 17. • Ca messenger system – regulates cell function • Activates cellular enzyme cascades • Smooth muscle and myocardial contraction •Nerve impulse conduction • Secretory activity of glands
  • 18. • Neuromuscular excitability • Tetany • Seizures • Stridor or cyanosis from laryngospasm • Hypotension • Impaired cardiac contractility
  • 19. •May be unspecific – Asymptomatic – Lethargy – Poor feeding – Vomiting – Abdominal distention
  • 20.
  • 21. • Fetus: Ca and P concentration higher than mother plasma, s Ca falls at 24 hrs. •Neonates: Ca lower than children at 2nd and 3th day • Return to normal by 5-10 days
  • 22. •Total serum Ca less than: – 7.0 mg/dL in Preterm infants – 8.0 mg/dL in Term newborns – 8.8 mg/dL in children
  • 23.
  • 24. Early neonatal hypocalcemia (48-72 hours) Prematurity Poor intake, hypoalbuminemia, ↓ responsiveness to vit D Birth asphyxia Delayed feeding, ↑ calcitonin, endogenous phosphate load , alkali therapy Infant of diabetic mother Mg depletion functional hypoparathyroidis→ m → ↓ Ca IUGR
  • 25. Late neonatal hypocalcemia (Full term) •Exogenous phosphate load •Mg deficiency •Transient hypoparathyroidism of newborn •Congenital Hypoparathyroidism •Maternal Vit D deficiency •Maternal Hyperparathyroidism •Gentamycin
  • 26. Bicarbonate infusion → metabolic alkalosis Transfusion with citrated blood→ formation of Ca complexes, ↓ Ca++ Lipid infusions → Ca complexes with FFAs → ↓ Ca++ Phototherapy for hyperbilirubinemia Acute renal failure → hyperphosphatemia Rotavirus infection
  • 27. • ↓ Mg → impaired PTH secretion & resistance to PTH → hypocalcemia •Usually idiopathic & transient •May be secodary to disorders of intestinal and/or renal tubular Mg transport
  • 28. • Antagonizes PTH secretion or actions → ↑ Ca & P deposition in bones → hypocalcemia.
  • 29. Cardiac defects, Abnormal facies, Thymic hypoplasia, Cleft palate, and Hypocalcemia caused by Chromosome 22 deletion DiGeorge Syndrome is a severe phenotype of this group of related disorders. FISH establishes the diagnosis.
  • 30.
  • 31. •What is the diagnosis? •How could we confirm the diagnosis?
  • 32. • Total Ca • Ionized Ca • Phosphorus •Magnesium • PTH • Vitamin D • Liver function • Renal function
  • 33. Only in infants with risk factors Measure Ca at 24, and 48 hrs of age. Measure Ca in infants with congenital heart ds. Ionized Ca should be the primary measurement.
  • 34. 1. Depends on underlying cause & severity 2. Mild asymptomatic: ↑ dietary Ca by initiating early feeding 3. For infants who require parenteral nutrition, Ca is added to the solution . 4. If symptomatic: treat immediately
  • 35. –Ca gluconate:10 mg/kg (1 ml/kg of 10% solution) Slowly IV –Start oral Calcium as soon as possible –Early neonatal hypocalcaemia normalizes in 2-3 d
  • 36. Late neonatal hypocalcemia –Associated with ­ S-phosphate – Decrease phosphate intake –Give calcium containing phosphate binder –Oral calcium gluconate 100 mg/kg/dose 4 hourly
  • 37. –Tissue necrosis/calcification if extravasates –Calcium can inhibit sinus node ® bradycardia + arrest –Avoid complete correction of hypocalcemia –Give Ca before correcting acidosis –If ¯ Mg – first treat & correct hypomagnesemia

Editor's Notes

  1. Chvostek sign: twitch at ipsilateral corner of mouth with a light tap over the facial nerve just below the maxilla Trousseau sign: carpal spasm in hand produced by inflating a BP cuff around an arm and maintaining pressure at just above systolic for 3-5 mins Seizures are anticonvulsant-resistant
  2. Ca concentration falls 0.8 mg/dL for every 1.0 g/dL decrease in albumin concentration Acidemia releases Ca from albumin, alkalosis increases binding