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ALL / Nephrology

Chronic kidney disease: anaemia

Chronic kidney disease: anaemia

Patients with chronic kidney disease (CKD) may develop anaemia due to a variety of factors, the most significant of which is reduced erythropoietin levels. This is usually a normochromic normocytic anaemia and becomes apparent when the GFR is less than 35 ml/min (other causes of anaemia should be considered if the GFR is > 60 ml/min). Anaemia in CKD predisposes to the development of left ventricular hypertrophy - associated with a three fold increase in mortality in renal patients

Causes of anaemia in renal failure
  • reduced erythropoietin levels
    • the most significant factor in CKD causing anaemia
    • CKD is associated with a decrease in the production of erythropoietin, a hormone produced by the kidneys that stimulates erythropoiesis in the bone marrow
    • reduced erythropoietin levels → diminished red blood cell production
  • reduced absorption of iron
    • hepcidin is an acute-phase reactant
    • in CKD, hepcidin levels are often increased due to inflammation and reduced renal clearance
    • elevated hepcidin levels lead to decreased iron absorption from the gut and impaired release of stored iron from macrophages and hepatocytes, reducing the iron available for erythropoiesis
    • additionally, metabolic acidosis, a common condition in CKD, can inhibit the conversion of ferric iron (Fe³) to its absorbable form, ferrous iron (Fe²), in the duodenum → reduced iron absorption.
  • reduced erythropoiesis due to toxic effects of uraemia on bone marrow
  • anorexia/nausea due to uraemia
  • reduced red cell survival (especially in haemodialysis)
  • blood loss due to capillary fragility and poor platelet function
  • stress ulceration leading to chronic blood loss

Management
  • the 2011 NICE guidelines suggest a target haemoglobin of 10 - 12 g/dl
  • determination and optimisation of iron status should be carried out prior to the administration of erythropoiesis-stimulating agents (ESA).
    • oral iron should be offered for patients who are not on ESAs or haemodialysis. If target Hb levels are not reached within 3 months then patients should be switched to IV iron
    • patients on ESAs or haemodialysis generally require IV iron
  • ESAs such as erythropoietin and darbepoetin should be used in those 'who are likely to benefit in terms of quality of life and physical function'
+PassMedicine Notes

Patients with chronic kidney disease (CKD) may develop anaemia due to a variety of factors, the most significant of which is reduced erythropoietin levels. This is usually a normochromic normocytic anaemia and becomes apparent when the GFR is less than 35 ml/min (other causes of anaemia should be considered if the GFR is > 60 ml/min). Anaemia in CKD predisposes to the development of left ventricular hypertrophy - associated with a three fold increase in mortality in renal patients

Causes of anaemia in renal failure
  • reduced erythropoietin levels
    • the most significant factor in CKD causing anaemia
    • CKD is associated with a decrease in the production of erythropoietin, a hormone produced by the kidneys that stimulates erythropoiesis in the bone marrow
    • reduced erythropoietin levels --> diminished red blood cell production
  • reduced absorption of iron
    • hepcidin is an acute-phase reactant
    • in CKD, hepcidin levels are often increased due to inflammation and reduced renal clearance
    • elevated hepcidin levels lead to decreased iron absorption from the gut and impaired release of stored iron from macrophages and hepatocytes, reducing the iron available for erythropoiesis
    • additionally, metabolic acidosis, a common condition in CKD, can inhibit the conversion of ferric iron (Fe³) to its absorbable form, ferrous iron (Fe²), in the duodenum --> reduced iron absorption.
  • reduced erythropoiesis due to toxic effects of uraemia on bone marrow
  • anorexia/nausea due to uraemia
  • reduced red cell survival (especially in haemodialysis)
  • blood loss due to capillary fragility and poor platelet function
  • stress ulceration leading to chronic blood loss
Management
  • the 2011 NICE guidelines suggest a target haemoglobin of 10 - 12 g/dl
  • determination and optimisation of iron status should be carried out prior to the administration of erythropoiesis-stimulating agents (ESA).
    • oral iron should be offered for patients who are not on ESAs or haemodialysis. If target Hb levels are not reached within 3 months then patients should be switched to IV iron
    • patients on ESAs or haemodialysis generally require IV iron
  • ESAs such as erythropoietin and darbepoetin should be used in those 'who are likely to benefit in terms of quality of life and physical function'


Media
Chronic kidney disease
Osmosis - YouTube
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Chronic kidney disease
Rhesus Medicine - YouTube
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