Treatment of Low Ferritin and Iron Deficiency
Iron deficiency should be treated when associated with anemia and/or low ferritin levels, with oral iron as first-line therapy (100-200 mg elemental iron daily) for most patients, while intravenous iron is reserved for specific clinical scenarios including intolerance to oral iron, malabsorption conditions, active inflammation, hemoglobin <100 g/L, or ongoing blood loss. 1
Diagnostic Thresholds
- Ferritin <30 ng/mL indicates iron deficiency in individuals without inflammatory conditions 2
- Transferrin saturation <20% serves as an alternative diagnostic marker 2
- In inflammatory conditions (IBD, CKD, heart failure), iron deficiency may exist with ferritin between 30-100 ng/mL; use transferrin saturation or hepcidin for confirmation 1
- All ferritin measurements should exclude acute inflammation by checking C-reactive protein, as ferritin is falsely elevated during inflammation 1, 3
First-Line Treatment: Oral Iron
Oral iron supplementation is the initial treatment for most patients with iron deficiency 1, 2:
- Dosage: 100-200 mg elemental iron daily in divided doses 1
- Standard formulation: Ferrous sulfate 324 mg (65 mg elemental iron) daily 4
- Alternate-day dosing (every other day) shows better iron absorption and fewer gastrointestinal side effects than daily dosing 1
- Avoid exceeding 100 mg elemental iron per day in IBD patients to minimize mucosal harm 1
Oral Iron Indications
- Mild anemia with clinically inactive disease 1
- No previous intolerance to oral iron 1
- Hemoglobin >100 g/L 1
- Absence of malabsorption conditions 1
Enhancing Oral Iron Absorption
- Co-administer vitamin C (250-500 mg) with iron to enhance absorption 1
- Avoid tea, coffee, and calcium supplements around iron dosing times 1
- Integrate heme iron sources (red meat) into diet 1, 3
Intravenous Iron Therapy
IV iron should be considered as first-line treatment in the following scenarios 1:
Absolute Indications
- Active inflammatory bowel disease with compromised absorption 1
- Hemoglobin <100 g/L 1
- Previous intolerance to oral iron (nausea, constipation, diarrhea) 1
- Malabsorption conditions: celiac disease, post-bariatric surgery, atrophic gastritis 1, 2
- Ongoing blood loss not responding to oral iron 1
- Second and third trimesters of pregnancy 2
- Chronic inflammatory conditions: CKD, heart failure, cancer 1, 2
- Need for rapid iron repletion (e.g., preoperative patient blood management) 1
IV Iron Dosing by Body Weight and Hemoglobin 1
| Hemoglobin Level | Body Weight <70 kg | Body Weight ≥70 kg |
|---|---|---|
| 100-120 g/L (women) or 100-130 g/L (men) | 1000 mg | 1500 mg |
| 70-100 g/L | 1500 mg | 2000 mg |
IV Iron Formulations
- Ferric carboxymaltose: 1000 mg single dose over 15 minutes, best studied formulation 1
- Iron sucrose: 200 mg over 10 minutes, requires multiple administrations 1
- Low molecular weight iron dextran: allows large single doses but requires test dose due to anaphylaxis risk 1
- Avoid high molecular weight iron dextran (highest anaphylaxis risk) 1
Safety Considerations
- Anaphylactic reactions occur in <1:250,000 administrations with modern formulations 1
- Resuscitation facilities must be available during IV iron infusion 1
- Test dose of 25 mg required for iron dextran only 1
Monitoring Treatment Response
- Repeat blood tests at 8-10 weeks after initiating treatment, not earlier after IV iron as ferritin is falsely elevated 1, 3
- Measure hemoglobin, ferritin, and transferrin saturation 1
- Do not recheck ferritin immediately after IV iron due to falsely high levels 1
Maintenance and Prevention
After successful treatment, monitor for recurrence 1:
- Every 3 months for the first year, then every 6-12 months 1, 3
- Re-treat with IV iron when ferritin drops <100 ng/mL or hemoglobin falls below 12 g/dL (women) or 13 g/dL (men) 1
- Rapid recurrence of iron deficiency suggests ongoing blood loss or subclinical inflammation requiring further investigation 1
Critical Safety Warnings
- Never supplement iron when ferritin is normal or elevated (potentially harmful) 1, 3
- Upper safety limits: transferrin saturation should not chronically exceed 50% and ferritin should not exceed 800 ng/mL 1
- In critically ill patients with inflammation, hepcidin is more reliable than transferrin saturation for diagnosing iron deficiency 1
- One study showed 1 g ferric carboxymaltose in critically ill patients reduced hospital stay and 90-day mortality 1