Treatment of Vitamin D Deficiency in Children
Recommended Treatment Regimen
For children presenting with symptomatic vitamin D deficiency, initiate treatment with 2,000 IU of oral vitamin D3 (cholecalciferol) daily for 12 weeks, along with concurrent calcium supplementation of 250-500 mg/day. 1
Alternative dosing regimens that achieve equivalent outcomes include 50,000 IU of vitamin D every other week for 12 weeks or 4,000 IU daily for 12 weeks. 1, 2, 3
Initial Treatment Phase (Loading Dose)
Standard Dosing Options
- Daily regimen: 2,000-4,000 IU of vitamin D3 orally for 12 weeks 1, 2, 4
- Intermittent high-dose regimen: 50,000 IU every 2 weeks for 12 weeks 1, 3
- Weekly regimen: 50,000 IU weekly for 8-12 weeks (alternative for severe deficiency) 5
Concurrent Calcium Supplementation
- Administer 250-500 mg/day of elemental calcium during the treatment phase to support bone mineralization and prevent hypocalcemia 1
- This is particularly critical in children with low ionized calcium or elevated parathyroid hormone (PTH) at baseline 1
Treatment Goals
- Achieve serum 25(OH)D levels above 20 ng/mL (50 nmol/L) 1, 5
- Target range for sufficiency is >50 nmol/L 1
Maintenance Phase (After Initial 12 Weeks)
Age-Specific Maintenance Dosing
- Infants 0-12 months: 400 IU/day 1, 6, 5
- Children and adolescents 1-18 years: 600 IU/day 1, 6, 5
- Preterm infants on parenteral nutrition: 200-1,000 IU/day (or 80-400 IU/kg/day) 1
Monitoring Strategy
Initial Assessment
Before starting treatment, evaluate:
- Serum 25(OH)D level (to confirm deficiency) 1
- Serum calcium, phosphorus, and alkaline phosphatase (to assess for metabolic bone disease) 1, 2
- Parathyroid hormone (PTH) level (to evaluate secondary hyperparathyroidism) 1, 2
- Ionized calcium (more accurate than total calcium, especially if hypoalbuminemia present) 7
- Clinical assessment for rickets manifestations (bowing of legs, rachitic rosary, delayed fontanelle closure) 1
Follow-Up Monitoring
- At 4 weeks: Check serum calcium and 25(OH)D to assess early response 2
- At 12 weeks: Recheck 25(OH)D, calcium, phosphorus, alkaline phosphatase, and PTH to confirm normalization 1, 2
- After normalization: Monitor 25(OH)D levels every 6-12 months, especially during winter months when sun exposure is limited 1
- Urine calcium:creatinine ratio: Monitor if hypercalciuria is suspected 2
Special Population Considerations
Children with Nephrotic Syndrome
- These children have massive urinary losses of vitamin D-binding protein, leading to low 25(OH)D levels despite normal vitamin D stores 7
- Monitor ionized calcium, 25(OH)D3, and PTH levels closely 7, 1
- Supplement with oral cholecalciferol or calcifediol plus calcium (250-500 mg/day) when 25(OH)D is low, ionized calcium is low, or PTH is elevated 7, 1
Children with Chronic Kidney Disease (CKD)
- Optimal dosing for children with CKD stages 3-5 is not well-established 1
- Monitor calcium and phosphorus closely to avoid hypercalcemia 1
- In advanced CKD with GFR <20 mL/min/1.73 m², there may be less benefit from ergocalciferol supplementation due to impaired renal conversion to active vitamin D 7
Children with Overweight/Obesity
- These children are at increased risk for vitamin D deficiency and may require higher doses 4
- Both 4,000 IU/day and 6,000 IU/day are effective and safe, with higher doses achieving sufficiency more rapidly 4
Vitamin D Formulation Selection
Cholecalciferol (vitamin D3) is preferred over ergocalciferol (vitamin D2) due to higher bioefficacy. 1
- Vitamin D3 has superior bioavailability and maintains higher 25(OH)D levels compared to vitamin D2 1
- However, both formulations are effective when used in equivalent doses 3
Safety Considerations and Upper Limits
Age-Specific Upper Tolerable Limits
- 0-6 months: 1,000 IU/day maximum 1
- 7-12 months: 1,500 IU/day maximum 1
- 1-3 years: 2,500 IU/day maximum 1
- 4-8 years: 3,000 IU/day maximum 1
- 9-18 years: 4,000 IU/day maximum 1
Monitoring for Toxicity
- Prolonged daily intake up to 10,000 IU appears safe in most children 1
- Serum concentrations >375 nmol/L are associated with acute hypercalcemia and hyperphosphatemia 1
- Mild, asymptomatic hypercalcemia may occur in 34-51% of treated children but typically resolves spontaneously without intervention 2, 4
- Hypercalciuria occurs in approximately 5.7% of children on daily vitamin D therapy and resolves spontaneously 2
Critical Pitfalls to Avoid
Do Not Use Active Vitamin D Analogs for Nutritional Deficiency
Calcitriol or other 1-hydroxylated vitamin D sterols (such as alfacalcidol) should NOT be used to treat nutritional vitamin D deficiency. 7, 1
- These active forms are reserved for specific conditions like CKD with impaired renal conversion or hypoparathyroidism 7
- Using active vitamin D for nutritional deficiency increases risk of hypercalcemia without addressing the underlying nutritional problem 7
Ensure Treatment Adherence
- Inconsistent supplementation is a common cause of treatment failure 1
- Consider intermittent high-dose regimens (50,000 IU every 2 weeks) if daily adherence is a concern 1, 3
- Both daily and intermittent regimens achieve equivalent outcomes when cumulative doses are similar 2, 3
Avoid Excessive Supplementation
- While vitamin D toxicity is rare at recommended doses, excessive supplementation can lead to hypercalcemia and nephrocalcinosis 1
- Do not exceed age-appropriate upper tolerable limits without specific clinical indication and close monitoring 1