Treatment of Vitamin D Deficiency
For vitamin D deficiency (25(OH)D <20 ng/mL), prescribe ergocalciferol or cholecalciferol 50,000 IU once weekly for 8-12 weeks, followed by maintenance therapy with 1,500-2,000 IU daily to achieve and maintain levels ≥30 ng/mL. 1, 2
Defining the Problem
- Deficiency is defined as serum 25(OH)D <20 ng/mL and requires treatment 1, 2
- Severe deficiency (<10-12 ng/mL) significantly increases risk for osteomalacia and rickets, demanding urgent treatment 1, 2
- Insufficiency (20-30 ng/mL) warrants treatment in patients with osteoporosis, fracture risk, falls, or elderly status 2
- The target level is ≥30 ng/mL for optimal bone health and anti-fracture efficacy 1, 2
Loading Phase Protocol
Cholecalciferol (vitamin D3) is strongly preferred over ergocalciferol (vitamin D2) because it maintains serum levels longer and has superior bioavailability 1, 2
- Administer 50,000 IU once weekly for 8-12 weeks for documented deficiency 1, 2
- For severe deficiency (<10 ng/mL) with symptoms or high fracture risk, consider 50,000 IU weekly for 12 weeks 1
- This cumulative dose (400,000-600,000 IU over 8-12 weeks) is necessary to replenish vitamin D stores 3
Maintenance Phase
After completing the loading phase, transition to one of these regimens:
- 1,500-2,000 IU daily (preferred for consistent levels) 1, 2
- 50,000 IU monthly (equivalent to ~1,600 IU daily; may improve adherence) 1, 2
- For elderly patients (≥65 years), use 800-1,000 IU daily minimum to reduce fall and fracture risk 1, 2
Essential Co-Interventions
- Ensure 1,000-1,500 mg calcium daily from diet plus supplements—adequate calcium is necessary for clinical response to vitamin D therapy 1, 2
- Take calcium supplements in divided doses of ≤600 mg for optimal absorption 1, 2
- Recommend weight-bearing exercise 30 minutes, 3 days per week 1
Monitoring Protocol
- Recheck 25(OH)D levels at 3 months after starting maintenance therapy to confirm adequate response 1, 2
- If using intermittent dosing (weekly or monthly), measure levels just prior to the next scheduled dose 1
- Continue monitoring every 3-6 months until stable levels ≥30 ng/mL are achieved 1, 2
- The upper safety limit is 100 ng/mL—do not exceed this threshold 1, 2
Special Populations
Chronic Kidney Disease (CKD)
- For CKD stages 3-4 (GFR 20-60 mL/min/1.73m²), use standard nutritional vitamin D (ergocalciferol or cholecalciferol) 1, 2
- CKD patients are at particularly high risk due to reduced sun exposure, dietary restrictions, and urinary losses 1
Malabsorption Syndromes
- For patients with inflammatory bowel disease, post-bariatric surgery, pancreatic insufficiency, or short-bowel syndrome, intramuscular vitamin D3 50,000 IU is the preferred route 1
- IM administration results in significantly higher 25(OH)D levels and lower rates of persistent deficiency compared to oral supplementation 1
- When IM is unavailable, use substantially higher oral doses: 4,000-5,000 IU daily for 2 months 1
Elderly and High-Risk Groups
- Dark-skinned or veiled individuals with limited sun exposure should receive 800 IU daily without baseline testing 1, 2
- Institutionalized individuals should receive 800 IU daily 2
Critical Pitfalls to Avoid
- Never use active vitamin D analogs (calcitriol, alfacalcidol, doxercalciferol, paricalcitol) to treat nutritional vitamin D deficiency—they do not correct 25(OH)D levels and bypass regulatory mechanisms 1, 2
- Avoid single very large doses (>300,000 IU) as they may be inefficient or potentially harmful 1, 2
- Do not supplement patients with normal vitamin D levels—benefits are only seen in those with documented deficiency 1
- Correct vitamin D deficiency before initiating bisphosphonates to prevent hypocalcemia 2
Safety Considerations
- Daily doses up to 4,000 IU are generally safe for adults 1, 2, 4
- Toxicity is rare, typically occurring only with prolonged doses >10,000 IU daily, and manifests as hypercalcemia, hyperphosphatemia, and suppressed parathyroid hormone 1, 2
- Monitor for hypercalcemia, especially in CKD patients 2
- Thiazide diuretics can cause hypercalcemia in patients receiving vitamin D therapy 4