4.6 Article

Anemia and iron deficiency among chronic kidney disease Stages 3-5ND patients in the Chronic Kidney Disease Outcomes and Practice Patterns Study: often unmeasured, variably treated

Journal

CLINICAL KIDNEY JOURNAL
Volume 13, Issue 4, Pages 613-624

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/ckj/sfz091

Keywords

anemia; chronic kidney disease; erythropoiesis-stimulating agents; iron deficiency; iron supplementation

Funding

  1. Agence Nationale de la Recherche through the 2010 'Cohortes-Investissements d'Avenir' program
  2. 2010 national Programme Hospitalier de Recherche Clinique
  3. Amgen
  4. Fresenius Medical Care
  5. GlaxoSmithKline (GSK)
  6. Lilly France
  7. Otsuka Pharmaceutical
  8. Baxter
  9. Merck Sharp & Dohme-Chibret (MSD France)
  10. Sanofi-Genzyme
  11. WiNe (Wissenschaftliches Institut fur Nephrologie) of the Verband Deutsche Nierenzentren
  12. Keryx
  13. Japan Agency for Medical Research and Development (AMED)

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Background. International variation in anemia assessment and management practices in chronic kidney disease (CKD) is poorly understood. Methods. We performed a cross-sectional analysis of anemia laboratory monitoring, prevalence and management in the prospective Chronic Kidney Disease Outcomes and Practice Patterns Study (CKDopps). A total of 6766 participants with CKD Stages 3a-5ND from nephrology clinics in Brazil, France, Germany and the USA were included. Results. Among patients with anemia (hemoglobin <12 g/dL), 36-58% in Brazil, the USA and Germany had repeat hemoglobin measured and 40-61% had iron indices measured within 3 months of the index hemoglobin measurement. Anemia was more common in the USA and Brazil than in France and Germany across CKD stages. Higher ferritin and lower iron saturation (TSAT) levels were observed with lower hemoglobin levels, and higher ferritin with more advanced CKD. The proportion of anemic patients with ferritin <100 ng/mL or TSAT <20% ranged from 42% in Brazil to 53% in France and Germany, and of these patients, over 40% in Brazil, Germany and the USA, compared with 27% in France, were treated with oral or intravenous iron within 3 months after hemoglobin measurement. The proportion of patients with hemoglobin <10 g/dL treated with erythropoiesis-stimulating agents ranged from 28% in the USA to 57% in Germany. Conclusions. Hemoglobin and iron stores are measured less frequently than per guidelines. Among all regions, there was a substantial proportion of anemic patients with iron deficiency who were not treated with iron, highlighting an area for practice improvement in CKD care.

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