Anemia management in chronic kidney disease and dialysis: a narrative review

Curr Opin Nephrol Hypertens. 2017 May;26(3):214-218. doi: 10.1097/MNH.0000000000000317.

Abstract

Purpose of review: This review describes the current state of anemia management with erythropoietin (EPO)-stimulating agents and iron supplementation in both chronic kidney disease and dialysis patients, with a focus on novel therapies.

Recent findings: We review the benefits and risks of EPO-stimulating agents, focusing on health-related quality of life and the uncertainties regarding optimal iron utilization in patients with kidney disease. We discuss novel therapies for iron supplementation including iron-based phosphate binders and dialysate iron delivery as well as alternatives to EPO-stimulating agents including hypoxia-inducible factor prolyl hydroxylase inhibitors.

Summary: Individualization of hemoglobin targets using EPO-stimulating agents and iron supplementation may be considered in younger, healthier patients with kidney disease to improve health-related quality of life. Optimal iron utilization in kidney disease patients is unclear, but novel iron base phosphate binders and dialysate iron delivery may play a role in intravenous iron avoidance and its potential complications. Phase 3 randomized controlled trials of hypoxia-inducible factor prolyl hydroxylase inhibitors are ongoing and are promising new alternatives to EPO-stimulating agents and their known adverse effects.

Publication types

  • Review

MeSH terms

  • Anemia / drug therapy*
  • Anemia / etiology
  • Dialysis Solutions / chemistry
  • Enzyme Inhibitors / therapeutic use
  • Hematinics / therapeutic use*
  • Humans
  • Hypoxia-Inducible Factor-Proline Dioxygenases / antagonists & inhibitors
  • Iron / administration & dosage
  • Iron / therapeutic use*
  • Quality of Life
  • Renal Dialysis
  • Renal Insufficiency, Chronic / complications
  • Renal Insufficiency, Chronic / therapy*

Substances

  • Dialysis Solutions
  • Enzyme Inhibitors
  • Hematinics
  • Iron
  • Hypoxia-Inducible Factor-Proline Dioxygenases