What is the recommended ferritin level range in patients with Chronic Kidney Disease (CKD)?

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Last updated: September 15, 2025View editorial policy

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Recommended Ferritin Level Range in Chronic Kidney Disease (CKD)

For patients with CKD, ferritin levels should be maintained at >100 ng/mL for non-dialysis and peritoneal dialysis patients, and >200 ng/mL for hemodialysis patients, with an upper limit of 500 ng/mL, while maintaining transferrin saturation (TSAT) >20%. 1, 2

Ferritin Targets by CKD Category

Non-Dialysis CKD and Peritoneal Dialysis Patients:

  • Lower limit: >100 ng/mL 1, 2
  • Upper limit: 500 ng/mL 1
  • TSAT should be maintained >20% 1, 2

Hemodialysis Patients:

  • Lower limit: >200 ng/mL 1, 2
  • Upper limit: 500 ng/mL 1
  • TSAT should be maintained >20% 1, 2

Iron Therapy Recommendations

When to Initiate Iron Therapy:

  • For non-dialysis and peritoneal dialysis CKD patients: When ferritin is <100 ng/mL or TSAT is <20% 1
  • For hemodialysis patients: When ferritin is <200 ng/mL or TSAT is <20% 1, 2

Route of Administration:

  • Hemodialysis patients: IV iron is recommended 2
  • Non-dialysis CKD: Either IV iron or a 1-3 month trial of oral iron 1

Monitoring Recommendations

  • Iron status (TSAT and ferritin) should be evaluated at least every 3 months during ESA therapy 1, 2
  • More frequent monitoring is recommended when:
    • Initiating or increasing ESA dose
    • Following blood loss
    • After a course of IV iron
    • When iron stores may become depleted 1

Special Considerations

High Ferritin Levels:

  • Ferritin levels >500 ng/mL with low TSAT (<20%) may indicate functional iron deficiency or inflammation rather than iron overload 1, 3
  • The safety of administering IV iron to patients with ferritin >500 ng/mL is uncertain, but preliminary evidence suggests it may increase hemoglobin in patients with low TSAT 1
  • In the DRIVE study, IV iron improved hemoglobin levels in patients with ferritin 500-1200 ng/mL and TSAT <25% 1

Iron Overload Concerns:

  • Moderate hyperferritinemia (500-2000 ng/mL) is often due to non-iron-related conditions including inflammation, malnutrition, liver disease, and infection 3
  • Conventional iron markers (ferritin, TSAT) may not accurately reflect body iron stores in CKD patients 4
  • Historical cases of hemochromatosis in dialysis patients typically had ferritin levels >2000 ng/mL 3

Common Pitfalls to Avoid

  1. Relying solely on ferritin levels: Both ferritin and TSAT should be used together to assess iron status, as ferritin can be elevated due to inflammation 1, 3

  2. Withholding iron based only on ferritin levels: Patients with high ferritin but low TSAT may still benefit from iron therapy 1

  3. Ignoring patient's clinical status: Iron therapy decisions should consider hemoglobin levels, ESA dose, and overall clinical status in addition to iron markers 1

  4. Overlooking functional iron deficiency: This can occur despite normal or elevated ferritin levels due to increased hepcidin in CKD 5

  5. Excessive iron supplementation: Potential risks include iron overload, increased infection risk, and oxidative stress 6

By following these guidelines for ferritin targets and monitoring, clinicians can optimize anemia management in CKD patients while minimizing risks associated with both iron deficiency and iron overload.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Anemia Management in End-Stage Renal Disease (ESRD) Patients

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

The fascinating but deceptive ferritin: to measure it or not to measure it in chronic kidney disease?

Clinical journal of the American Society of Nephrology : CJASN, 2006

Research

Serum iron markers are inadequate for guiding iron repletion in chronic kidney disease.

Clinical journal of the American Society of Nephrology : CJASN, 2011

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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