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Impact of intercurrent illness on calcium homeostasis in children with hypoparathyroidism: a case series
Insights
Intercurrent illnesses can cause symptomatic hypocalcaemia in children with hypoparathyroidism, requiring increased alfacalcidol and calcium doses. Careful monitoring and dose reduction are crucial post-illness to prevent hypercalcemia.
Area of Science:
- Pediatric Endocrinology
- Metabolic Bone Diseases
- Genetics
Background:
- Hypoparathyroidism is a condition characterized by low calcium levels (hypocalcaemia).
- Standard treatment involves active vitamin D analogues and calcium supplements.
- The effect of intercurrent illnesses on calcium balance in children with hypoparathyroidism is not well-documented.
Purpose of the Study:
- To describe the impact of intercurrent illnesses on calcium homeostasis in children with hypoparathyroidism.
- To highlight the need for adjusted treatment during and after illness.
Main Methods:
- Case series describing three infants with hypoparathyroidism.
- Treatment adjustments with alfacalcidol and calcium supplements during illness.
- Monitoring of serum calcium and urinary calcium levels.
Main Results:
- Intercurrent respiratory or gastrointestinal illnesses precipitated symptomatic hypocalcaemia in three infants.
- Alfacalcidol and calcium doses were increased up to threefold to manage hypocalcaemia.
- Resolution of illness led to hypercalcaemia and hypercalciuria, requiring dose reduction.
Conclusions:
- Intercurrent illnesses can destabilize calcium homeostasis in pediatric hypoparathyroidism.
- Dosage adjustments of alfacalcidol and calcium are necessary during illness.
- Close monitoring and timely reduction of treatment are essential post-illness to prevent complications like hypercalcaemia and nephrocalcinosis.
Background:
Hypoparathyroidism is characterised by hypocalcaemia, and standard management is with an active vitamin D analogue and adequate oral calcium intake (dietary and/or supplements). Little is described in the literature about the impact of intercurrent illnesses on calcium homeostasis in children with hypoparathyroidism.
Methods:
We describe three children with hypoparathyroidism in whom intercurrent illnesses led to hypocalcaemia and escalation of treatment with alfacalcidol (1-hydroxycholecalciferol) and calcium supplements.
Results:
Three infants managed with standard treatment for hypoparathyroidism (two with homozygous mutations in GCMB2 gene and one with Sanjad-Sakati syndrome) developed symptomatic hypocalcaemia (two infants developed seizures) following respiratory or gastrointestinal illnesses. Substantial increases in alfacalcidol doses (up to three times their pre-illness doses) and calcium supplementation were required to achieve acceptable serum calcium concentrations. However, following resolution of illness, these children developed an increase in serum calcium and hypercalciuria, necessitating rapid reduction to pre-illness dosages of alfacalcidol and oral calcium supplementation.
Conclusion:
Intercurrent illness may precipitate symptomatic hypocalcaemia in children with hypoparathyroidism, necessitating increase in dosages of alfacalcidol and calcium supplements. Close monitoring is required on resolution of the intercurrent illness, with timely reduction of dosages of active analogues of vitamin D and calcium supplements to prevent hypercalcaemia, hypercalciuria and nephrocalcinosis.
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