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Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
[Parenteral iron therapy in chronic kidney disease or chronic heart failure]
Michele F Eisenga1, Adry Diepenbroek, Dorine W Swinkels
1Universitair Medisch Centrum Groningen, Groningen.
Insights
Iron deficiency is common in chronic kidney disease and heart failure, impacting quality of life. Parenteral iron therapy improves symptoms in heart failure, regardless of hemoglobin levels.
Area of Science:
- Nephrology
- Cardiology
- Hematology
Background:
- Iron deficiency and anemia are prevalent in chronic kidney disease (CKD) and chronic heart failure (CHF).
- These conditions are linked to reduced quality of life and increased mortality.
- Current anemia treatments with erythropoietic growth factors show limited efficacy.
Purpose of the Study:
- To investigate the role of iron deficiency in CKD and CHF.
- To evaluate the effectiveness of parenteral iron therapy in managing iron deficiency symptoms.
Main Methods:
- Review of existing literature on iron metabolism in CKD and CHF.
- Analysis of the impact of chronic inflammation on iron regulation via hepcidin.
- Assessment of parenteral iron therapy's effects on CHF symptoms.
Main Results:
- Chronic inflammation in CKD elevates hepcidin, hindering iron absorption and utilization.
- Both absolute and functional iron deficiency occur, with ferritin levels not always indicative of tissue iron status.
- Parenteral iron therapy alleviates iron deficiency symptoms in CHF patients, independent of hemoglobin changes.
Conclusions:
- Iron deficiency is a significant issue in CKD and CHF, requiring focused management.
- Parenteral iron is beneficial for CHF symptoms, but long-term outcomes require further study.
- Understanding iron dysregulation, particularly hepcidin's role, is crucial for effective treatment strategies.
Abstract:
Iron deficiency and anaemia occur frequently in patients with chronic kidney disease (CKD) or chronic heart failure (CHF) and are associated with lower quality of life and higher mortality. Treating anaemia with erythropoietic growth factors produces no improvement. In recent years, the focus has therefore shifted to correction of iron deficiency. Chronic inflammation in CKD increases the production of hepcidin, which blocks iron absorption from the intestine and leads to less efficient re-use of iron from the macrophages. In absolute iron deficiency the body's iron stores are depleted, whereas in functional iron deficiency the supply of iron is not sufficient to meet demand from the bone marrow. Normal or high ferritin levels do not exclude iron deficiency at tissue level. The iron saturation fraction is a more useful indicator. Parenteral iron therapy ameliorates in CHF the symptoms of iron deficiency, irrespective of the effect on haemoglobin levels. The long-term effects of intravenous iron on mortality and morbidity are still unknown.
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