Iron Sucrose Dosing for Severe Iron-Deficiency Anemia
Immediate Dosing Recommendation
For an adult with severe iron-deficiency anemia (hemoglobin 3.8 g/dL), administer iron sucrose 200 mg intravenously over 10 minutes without dilution, repeated 2–3 times weekly until the calculated total iron deficit is met, typically requiring 10–15 doses (2000–3000 mg total) over 4–6 weeks. 1, 2
Calculating Total Iron Requirement Using the Ganzoni Formula
The Ganzoni formula calculates total iron deficit as: Body weight (kg) × [target Hb - actual Hb (g/dL)] × 0.24 + 500 mg. 2
Practical Example for Severe Anemia (Hb 3.8 g/dL):
- For a 70 kg patient with Hb 3.8 g/dL targeting 12 g/dL (women) or 13 g/dL (men):
- Women: 70 × (12 - 3.8) × 0.24 + 500 = 1,882 mg total
- Men: 70 × (13 - 3.8) × 0.24 + 500 = 2,048 mg total
- Add an additional 500 mg when Hb <7.0 g/dL, bringing the total to approximately 2,400–2,550 mg. 2
Translating to Number of Iron Sucrose Doses:
Administration Protocol
Dose Per Infusion:
Infusion Rate:
- Administer 200 mg undiluted as IV push over 10 minutes 1, 4
- Alternative: 200 mg diluted in 150 mL normal saline infused over 30 minutes 5
- The 10-minute undiluted push is preferred for efficiency and is FDA-approved 3, 1
Frequency:
- Give 200 mg doses 2–3 times weekly (with at least 48 hours between doses) 1, 2
- Maximum weekly dose: 500 mg 3
- For severe anemia requiring rapid repletion, the 3-times-weekly schedule is optimal 1, 2
Total Treatment Duration:
Monitoring and Expected Response
Baseline Assessment:
During Treatment:
- Recheck hemoglobin every 4 weeks until normalized 3
- Do not recheck iron studies (ferritin, TSAT) until ≥4 weeks after the final infusion, as circulating iron falsely elevates assay results 2
Expected Hemoglobin Response:
- Hemoglobin should increase by ≥2 g/dL within 4 weeks of completing the full iron sucrose course 1, 2, 6
- In severe anemia (Hb 3.8 g/dL), expect incremental rises of 0.5–1.0 g/dL per week during active treatment 6
Target Iron Parameters After Repletion:
- TSAT ≥20% and ferritin ≥100 ng/mL 1
- Maintain TSAT <50% and ferritin <800 ng/mL (preferably ≤500 ng/mL) to avoid iron overload 1
Long-Term Surveillance:
- After hemoglobin normalizes, monitor complete blood count every 3 months for the first year, then every 6 months for 2–3 years to detect recurrent anemia 3, 1
Safety Considerations and Contraindications
Absolute Contraindications:
- Active bacteremia or uncontrolled infection—withhold iron sucrose until infection is resolved 1
- Known hypersensitivity to iron sucrose or excipients 1
Relative Contraindications:
- Acute or chronic infection may be acceptable after risk-benefit assessment if treating iron-deficiency anemia is critical 1
Adverse Event Profile:
- Hypersensitivity reactions occur in approximately 0.5% of recipients 1
- Anaphylactic reactions are extremely rare (<1:200,000 administrations) 1
- Common minor side effects: arthralgia, hypotension, injection site reactions 1
- Clinically relevant hypophosphatemia is rare with iron sucrose (≈1%), markedly lower than the 58% incidence with ferric carboxymaltose 1
Resuscitation Preparedness:
Critical Pitfalls to Avoid
Underdosing:
- The most common error is stopping after 2–3 doses when patients need 12–13 doses to fully replete iron stores in severe anemia. 2
- Always calculate total iron deficit using the Ganzoni formula before starting treatment 2
Premature Iron Studies:
- Do not recheck ferritin or TSAT until ≥4 weeks after the final dose, as immediate post-infusion levels are falsely elevated and clinically meaningless 2
Concurrent Oral Iron:
- Do not give oral iron simultaneously with IV iron therapy—it provides no additional benefit and increases gastrointestinal side effects 2
Iron Overload Risk:
- Stop further iron supplementation once TSAT reaches 50% or ferritin reaches 800 ng/mL 1
Infection Management:
Management of Treatment Failure
If hemoglobin fails to rise by ≥2 g/dL within 4 weeks after completing the full iron sucrose course, evaluate for:
- Ongoing blood loss (gastrointestinal, menstrual, urinary) 1
- Chronic inflammation or malignancy (elevated CRP, ESR) 1
- Bone marrow disorders (consider bone marrow biopsy) 1
- Other non-iron-deficiency causes of anemia (B12/folate deficiency, hemolysis, renal disease) 1
Comparison with Alternative IV Iron Formulations
While iron sucrose requires multiple infusions, it offers distinct advantages in severe anemia:
| Formulation | Max Single Dose | Infusion Time | Doses for 2,400 mg | Hypophosphatemia Risk |
|---|---|---|---|---|
| Iron sucrose | 200 mg | 10 min | 12 doses | Low (≈1%) [1] |
| Ferric carboxymaltose | 1,000 mg | 15 min | 2–3 doses | High (≈58%) [1] |
| Ferric derisomaltose | 1,000 mg | 15–30 min | 2–3 doses | Moderate (≈4%) [1] |
Iron sucrose is preferred when:
- The patient requires repeat infusions within a 3-month interval to minimize hypophosphatemia risk 1
- Cost considerations dominate and the healthcare setting can accommodate multiple clinic visits 1
- The patient is on hemodialysis (iron sucrose can be administered directly through the dialysis circuit) 1
Special Considerations for Severe Anemia (Hb 3.8 g/dL)
Transfusion Decision:
- With hemoglobin 3.8 g/dL, assess for hemodynamic instability, angina, or severe symptoms requiring urgent transfusion before initiating iron therapy alone
- If the patient is stable, iron sucrose can be started immediately while monitoring closely 6
Accelerated Dosing:
- In stable severe anemia, administer 200 mg three times weekly (Monday/Wednesday/Friday schedule) to achieve more rapid repletion 1, 2