When to Offer Intravenous Iron Infusion in Pregnancy
Intravenous iron should be offered to pregnant women with iron-deficiency anemia when oral iron has failed after 4 weeks, when oral iron is not tolerated, when hemoglobin is severely low (<9.0 g/dL), or when rapid correction is needed in the second or third trimester. 1
Diagnostic Confirmation Before IV Iron
Before considering IV iron, confirm true iron-deficiency anemia:
- Serum ferritin ≤15 μg/L in an anemic pregnant woman confirms iron deficiency with 98% specificity 2
- Hemoglobin thresholds for anemia in pregnancy are <11 g/dL in the first and third trimesters, and <10.5 g/dL in the second trimester 3
- Verify compliance with oral iron and absence of acute illness before declaring oral iron failure 1
- Consider alternative diagnoses (thalassemia, sickle cell trait) in women of African, Mediterranean, or Southeast Asian ancestry who do not respond to oral iron 1
Specific Indications for IV Iron
IV iron is indicated in the following clinical scenarios:
Primary Indications
- Failure of oral iron therapy after at least 4 weeks of treatment, defined as hemoglobin failing to rise by ≥1 g/dL 1
- Intolerance to oral iron preparations despite trying alternative formulations (ferrous gluconate, fumarate, or liquid preparations) 4, 1
- Severe anemia with hemoglobin <9.0 g/dL requiring physician referral and consideration of rapid correction 1
- Advanced pregnancy (third trimester) when there is insufficient time for oral iron to adequately replenish maternal and fetal iron stores 5, 6
Secondary Indications
- Impaired iron absorption due to conditions such as celiac disease or post-bariatric surgery 6
- Ongoing blood loss where oral iron cannot keep pace with losses 6
- Clinical need for rapid and efficient treatment when time is limited before delivery 5
Preferred IV Iron Preparation
Ferric carboxymaltose (Injectafer) is the preferred agent based on clinical trial evidence in pregnancy and postpartum populations 1:
- Dosing: 15 mg/kg body weight up to maximum 750 mg per dose 1
- Administration: Two doses separated by at least 7 days, for cumulative dose up to 1,500 mg 1
- Infusion time: 15 minutes, significantly more convenient than older preparations 1
Alternative Preparations
- Iron sucrose (Venofer): Maximum 200 mg per dose, 10-minute infusion 1
- Iron dextran (Cosmofer): Can give total dose in single 6-hour infusion but carries 0.6-0.7% risk of serious reactions including anaphylaxis 1
Timing Considerations
Gestational age matters for IV iron decisions:
- IV iron is safe and effective in the second and third trimesters 7
- In the third trimester, IV iron is preferred when hemoglobin is <8 g/dL at any time, as oral iron has little expectation of delivering adequate iron to the fetus 7
- Avoid ferritin measurement within 4 weeks after IV iron infusion, as circulating iron interferes with the assay and produces falsely elevated results 2
Monitoring Response
After IV iron administration:
- Reassess hemoglobin at 2-4 weeks: Expected increase of ≥1 g/dL 1
- Once hemoglobin normalizes for gestational age, decrease to maintenance dose of 30 mg/day oral iron 1
- Recheck ferritin 4-8 weeks after initiating any iron therapy to determine if stores have been restored 2
Common Pitfalls to Avoid
- Do not rely on hemoglobin alone to diagnose iron deficiency—ferritin is the most specific indicator of depleted iron stores 2
- Do not assume compliance with oral iron—treatment failure is most commonly due to poor adherence 4
- Do not measure ferritin during inflammation or infection, as it is an acute phase reactant and may be falsely elevated, masking true iron deficiency 2
- Do not delay IV iron in severe anemia (<9.0 g/dL) or late pregnancy when oral iron is unlikely to be effective in time 1, 7
Safety Profile
- Anaphylactic reactions are extremely rare with non-dextran products, but close surveillance during administration is recommended for all IV iron products 5
- IV iron preparations with complex carbohydrate cores that bind elemental iron more tightly have excellent safety profiles 7
- Ferric carboxymaltose has been studied in well-controlled clinical trials in pregnancy and postpartum and should be preferred for safety reasons 5