Highlighter is on. Drag to highlight text. Click a highlight to remove it.
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 patientsCauses 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
- 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'
