How much does ferrous carboxymaltose (intravenous iron formulation) increase ferritin storage?

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Ferric Carboxymaltose Ferritin Storage Increase

Ferric carboxymaltose increases ferritin storage by approximately 218-735 ng/mL depending on the clinical population and cumulative dose administered, with the most robust data showing mean increases of 264 ng/mL in iron-deficient anemia patients and 735 ng/mL in chronic kidney disease patients after cumulative doses of 1,000-1,500 mg. 1

Magnitude of Ferritin Increase by Clinical Population

Iron Deficiency Anemia (General Population)

  • Mean ferritin increase of 264.2 ± 224.2 ng/mL in patients intolerant to oral iron (Cohort 1) at Day 35 after cumulative doses up to 1,500 mg 1
  • Mean ferritin increase of 218.2 ± 211.4 ng/mL in patients with unsatisfactory response to oral iron (Cohort 2) at Day 35 1
  • These increases occurred from baseline ferritin levels that were already in the "sufficient" range (321-460 ng/mL), demonstrating robust storage replenishment 2

Chronic Kidney Disease (Non-Dialysis Dependent)

  • Mean ferritin increase of 734.7 ± 337.8 ng/mL prior to Day 56 after ferric carboxymaltose administration 1
  • This represents the highest magnitude of ferritin increase documented across clinical populations 1
  • Baseline ferritin in this population was approximately 100-300 ng/mL 3

Cancer-Related Anemia

  • Mean ferritin increase of 1,200 ng/mL from baseline of 190 ng/mL after 1,100 mg cumulative dose over 16 weeks 2
  • Mean ferritin increase of 1,265.5 ng/mL from baseline of 460.5 ng/mL after 937.5 mg cumulative dose 2
  • These dramatic increases occurred in patients receiving concurrent erythropoiesis-stimulating agents 2

Heart Failure with Iron Deficiency

  • Mean ferritin increase of 269 ng/mL (95% CI: 229-309) from baseline to Week 24 in the CONFIRM-HF trial 1
  • Baseline ferritin was 57 ng/mL in this population, representing true iron deficiency 1

Dose-Response Relationship

Standard Dosing Regimen

  • Maximum single dose of 1,000 mg iron administered over minimum 15 minutes 2, 1
  • Typical cumulative dose of 1,000-1,500 mg given as two doses separated by at least 7 days 1
  • The ferritin response is dose-dependent, with higher cumulative doses producing greater storage replenishment 4

Time Course of Ferritin Elevation

  • Ferritin levels increase markedly and rapidly following IV ferric carboxymaltose administration 2
  • Peak ferritin elevation occurs within the first 4 weeks post-administration 2
  • Critical monitoring caveat: Ferritin cannot be used as an accurate indicator of iron status within 4 weeks of IV iron administration due to acute-phase reactant effects 2

Clinical Context and Practical Implications

When to Reassess Iron Status

  • Re-evaluate iron parameters (ferritin and TSAT) 3 months after initial treatment, not earlier 2, 5, 6
  • Early re-evaluation within 4 weeks should be avoided as ferritin levels are artificially elevated and unreliable 2, 6
  • For chronic conditions like heart failure, consider routine iron status evaluation 1-2 times per year 2, 6

Transferrin Saturation Changes

  • Ferric carboxymaltose also increases transferrin saturation by 13-30% depending on population 1
  • In iron deficiency anemia patients: TSAT increased by 13-20% 1
  • In chronic kidney disease patients: TSAT increased by 30% 1

Hemoglobin Response Correlation

  • The ferritin increase correlates with hemoglobin improvements of 0.6-2.9 g/dL depending on baseline severity and clinical condition 1
  • A single dose of 1,000 mg produces mean hemoglobin increase of 8 g/L over 8 days 2
  • Reticulocytosis occurs at 3-5 days after administration, indicating active erythropoiesis 2

Population-Specific Considerations

  • Inflammatory conditions (IBD, cancer, heart failure): Hepcidin activation impairs oral iron absorption, making IV ferric carboxymaltose particularly effective at overcoming this barrier 2, 5
  • Chronic kidney disease: Demonstrates the highest magnitude ferritin response, likely due to baseline severe depletion and impaired oral absorption 1, 3
  • Cancer patients on ESAs: Show dramatic ferritin increases (>1,000 ng/mL) but require monitoring to avoid iron overload (hold if ferritin >1,000 ng/mL) 2

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

A randomized controlled trial comparing intravenous ferric carboxymaltose with oral iron for treatment of iron deficiency anaemia of non-dialysis-dependent chronic kidney disease patients.

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2011

Guideline

Iron Deficiency Anemia Treatment with Ferric Carboxymaltose

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Ferric Carboxymaltose Dosing in Heart Failure with Anemia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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