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Severe hypercalcemia associated with hypophosphatemia in very premature infants: a case report
Nicola Improda1,2, Francesca Mazzeo3, Alessandro Rossi4
1Department of Translational Medical Sciences, Section of Pediatrics, Federico II University of Naples, Naples, Italy. nicolaimproda@gmail.com.
Insights
Severe hypercalcemia in newborns, though rare, can occur with hypophosphatemia. Prompt phosphate (PO4) infusion is crucial for managing this condition, alongside careful monitoring of calcium (Ca) levels.
Area of Science:
- Neonatology
- Pediatric Endocrinology
- Biochemistry
Background:
- Severe hypercalcemia is a rare neonatal condition with potential sequelae.
- Hypophosphatemia in infants can stem from intrauterine malnutrition, sepsis, or high-energy parenteral nutrition (PN).
- The mechanism linking hypophosphatemia to severe hypercalcemia in neonates remains unclear, and phosphate (PO4) and calcium (Ca) monitoring in preterm infants is debated.
Observation:
- A preterm infant (29 weeks gestation) with intrauterine growth retardation (IUGR) presented with sustained severe hypercalcemia (corrected Ca up to 24 mg/dl).
- The hypercalcemia was attributed to hypophosphatemia during phosphorus-free PN.
- Initial treatments including hyperhydration and furosemide were ineffective, but hypercalcemia resolved with PO4 infusion.
Findings:
- Hypophosphatemic hypercalcemia in a neonate responded effectively to phosphate (PO4) infusion.
- The infant later experienced symptomatic hypocalcemia, potentially worsened by albumin infusion.
- Normalization of parathyroid hormone (PTH) and alkaline phosphatase (ALP) was observed post-treatment.
Implications:
- Clinicians must recognize the risk of severe, life-threatening hypercalcemia in neonates with or at risk for hypophosphatemia.
- Phosphate (PO4) infusion is the primary management strategy for hypophosphatemic hypercalcemia.
- Close monitoring of both calcium (Ca) and phosphate (PO4) levels is essential during treatment.
Background:
Severe hypercalcemia is rare in newborns; even though often asymptomatic, it may have important sequelae. Hypophosphatemia can occur in infants experiencing intrauterine malnutrition, sepsis and early high-energy parenteral nutrition (PN) and can cause severe hypercalcemia through an unknown mechanism. Monitoring and supplementation of phosphate (PO4) and calcium (Ca) in the first week of life in preterm infants are still debated.
Case Presentation:
We report on a female baby born at 29 weeks' gestation with intrauterine growth retardation (IUGR) experiencing sustained severe hypercalcemia (up to 24 mg/dl corrected Ca) due to hypophosphatemia while on phosphorus-free PN. Hypercalcemia did not improve after hyperhydration and furosemide but responded to infusion of PO4. Eventually, the infant experienced symptomatic hypocalcaemia (ionized Ca 3.4 mg/dl), likely exacerbated by contemporary infusion of albumin. Subsequently, a normalization of both parathyroid hormone (PTH) and alkaline phosphatase (ALP) was observed.
Conclusions:
Although severe hypercalcemia is extremely rare in neonates, clinicians should be aware of the possible occurrence of this life-threatening condition in infants with or at risk to develop hypophosphatemia. Hypophosphatemic hypercalcemia can only be managed with infusion of PO4, with strict monitoring of Ca and PO4 concentrations.
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