KDOQI US Commentary on the KDIGO 2026 Clinical Practice Guideline for the Management of Anemia in CKD

Diana I Jalal1, Nisha Bansal2, Monique E Cho3

  • 1Carver College of Medicine, University of Iowa, Iowa City, Iowa.

Insights

Anemia management in chronic kidney disease (CKD) is evolving. The KDOQI work group supports KDIGO 2026 guidelines, favoring IV iron and ESAs for anemia in CKD patients in the US.

Area of Science:

  • Nephrology
  • Hematology
  • Pharmacology

Background:

  • Anemia is a common complication of chronic kidney disease (CKD), worsening with disease progression.
  • The Kidney Disease: Improving Global Outcomes (KDIGO) released updated 2026 guidelines for managing anemia in CKD patients.
  • Previous KDIGO guidelines and conferences addressed iron management and hypoxia-inducible factor-prolyl hydroxylase inhibitor (HIF-PHI) use.

Purpose of the Study:

  • To provide perspective on implementing the KDIGO 2026 anemia guideline in US clinical practice.
  • To align with KDIGO recommendations while addressing US-specific considerations.
  • To offer commentary on specific aspects of anemia management in CKD.

Main Methods:

  • Review of the KDIGO 2026 clinical practice guideline for anemia in CKD.
  • Convening of a Kidney Disease Outcomes Quality Initiative (KDOQI) work group.
  • Analysis of US-specific factors influencing guideline implementation.

Main Results:

  • General agreement with KDIGO recommendations, including proactive intravenous (IV) iron use in hemodialysis patients.
  • Preference for erythropoiesis-stimulating agents (ESAs) over HIF-PHIs as first-line therapy due to familiarity with ESA safety.
  • Identification of US-specific issues: higher ferritin targets, limited HIF-PHI availability, and payment barriers.

Conclusions:

  • The KDOQI work group supports the KDIGO 2026 guideline for anemia in CKD.
  • US implementation requires addressing unique challenges, including therapeutic agent choices and iron management.
  • Further discussion is needed on IV iron, hypophosphatemia, iron repletion, HIF-PHI benefits, and transfusion risks.

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