Iron Infusion Administration Guidelines for Severe Iron Deficiency
For severe iron deficiency, administer a single IV dose of 1000 mg iron as ferric carboxymaltose over 15 minutes, with follow-up iron status evaluation after 3 months to determine if additional treatment is needed. 1
Diagnosis Confirmation
Before administering iron infusion, confirm iron deficiency using these criteria:
- Serum ferritin <100 μg/L (absolute iron deficiency), or
- Serum ferritin 100-299 μg/L with transferrin saturation (TSAT) <20% (functional iron deficiency) 1
- Complete evaluation should include: plasma iron, transferrin, TSAT, ferritin, CRP, and red blood cell morphology 1
Dosing Protocol
First-line Treatment:
- Single dose approach: 1000 mg of iron as ferric carboxymaltose infused over 15 minutes 1, 2
- For patients <50 kg: Use weight-based dosing at 15 mg/kg body weight 2
Alternative Dosing Options:
- Split dosing: 750 mg in two doses separated by at least 7 days (total 1500 mg) for patients ≥50 kg 2
- For patients with heart failure and iron deficiency, follow specific dosing based on weight and hemoglobin level 2:
- <70 kg with Hb <10 g/dL: 1000 mg initially, 500 mg at week 6
- ≥70 kg with Hb <10 g/dL: 1000 mg initially, 1000 mg at week 6
Administration Method
- Administer as undiluted slow IV push or diluted infusion 2
- For infusion: Dilute up to 1000 mg in no more than 250 mL of sterile 0.9% sodium chloride 1, 2
- Ensure concentration is not less than 2 mg iron/mL 2
- Monitor for extravasation during administration 2
- Observe patient for at least 30 minutes following injection to monitor for hypersensitivity reactions 1
Monitoring and Follow-up
- Re-evaluate iron status 3 months after infusion 1
- Avoid early re-evaluation (within 4 weeks) as ferritin levels are falsely elevated immediately after IV iron administration 1
- If iron deficiency persists or recurs, provide additional iron repletion as needed 1
- Monitor serum phosphate levels, particularly in patients receiving ferric carboxymaltose, as hypophosphatemia occurs in 50-74% of patients 3, 4
Important Precautions
Contraindications:
- Hypersensitivity to ferric carboxymaltose or any components
- Known serious hypersensitivity to other parenteral iron products
- Anemia not attributed to iron deficiency
- Evidence of iron overload 1
Cautions:
- Use with caution in patients with acute or chronic infection
- Higher risk of hypersensitivity in patients with drug allergies, asthma, eczema, or atopic allergies
- Higher risk in patients with immune or inflammatory conditions 1
- Monitor for hypophosphatemia, especially with ferric carboxymaltose, which may cause persistent fatigue despite anemia correction 4
Special Populations
- For chronic kidney disease patients: Consider IV iron when TSAT <20% and ferritin <100 ng/mL 1, 5
- For patients with heart failure and reduced ejection fraction: IV iron is recommended when ferritin <100 μg/L or ferritin 100-299 μg/L with TSAT <20% 1
- For inflammatory conditions: IV iron is preferred over oral iron due to poor absorption and efficacy of oral iron in inflammatory states 6
By following these guidelines, you can effectively treat severe iron deficiency while minimizing risks and optimizing patient outcomes in terms of morbidity, mortality, and quality of life.