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Practical Guidance for Diagnosing and Treating Iron Deficiency in Patients with Heart Failure: Why, Who and How?
Andrew Sindone1, Wolfram Doehner2,3,4,5, Nicolas Manito6,7
1Heart Failure Unit, Department of Cardiac Rehabilitation, Concord Repatriation General Hospital, Concord, NSW 2139, Australia.
Insights
Iron deficiency (ID) in heart failure (HF) patients, even without anemia, worsens quality of life and increases mortality risk. Intravenous iron effectively treats ID, improving HF symptoms and reducing hospitalizations.
Area of Science:
- Cardiology
- Hematology
- Internal Medicine
Background:
- Iron deficiency (ID) is a common comorbidity in heart failure (HF) patients.
- ID negatively impacts quality of life, exercise capacity, and mortality risk in HF, independent of anemia.
- ID is under-recognized but easily diagnosed and managed.
Purpose of the Study:
- To review the epidemiology and pathophysiology of ID in heart failure with reduced ejection fraction (HFrEF).
- To provide practical guidance on screening, diagnosing, and treating ID in HFrEF patients.
- To highlight the 2021 European Society of Cardiology (ESC) guidelines on HF regarding ID management.
Main Methods:
- Review of prospective randomized controlled trials and recent trial data.
- Summary of epidemiological and pathophysiological findings.
- Guidance based on current clinical guidelines and evidence.
Main Results:
- Intravenous iron (ferric carboxymaltose [FCM]) improves HF symptoms, exercise capacity, and quality of life in HFrEF patients with ID.
- FCM therapy reduces subsequent HF hospitalizations after acute decompensated HF.
- Early diagnosis and treatment of ID are crucial for better patient outcomes.
Conclusions:
- ID is a significant and treatable condition in HFrEF.
- Intravenous iron therapy is recommended for symptomatic HFrEF patients with ID.
- Adherence to updated guidelines ensures optimal management of ID in HF.
Abstract:
Iron deficiency (ID) is a comorbid condition frequently seen in patients with heart failure (HF). Iron has an important role in the transport of oxygen, and is also essential for skeletal and cardiac muscle, which depend on iron for oxygen storage and cellular energy production. Thus, ID per se, even without anaemia, can be harmful. In patients with HF, ID is associated with a poorer quality of life (QoL) and exercise capacity, and a higher risk of hospitalisations and mortality, even in the absence of anaemia. Despite its negative clinical consequences, ID remains under-recognised. However, it is easily diagnosed and managed, and the recently revised 2021 European Society of Cardiology (ESC) guidelines on HF provide specific recommendations for its diagnosis and treatment. Prospective randomised controlled trials in patients with symptomatic HF with reduced ejection fraction (HFrEF) show that correction of ID using intravenous iron (principally ferric carboxymaltose [FCM]) provides improvements in symptoms of HF, exercise capacity and QoL, and a recent trial demonstrated that FCM therapy following hospitalisation due to acute decompensated HF reduced the risk of subsequent HF hospitalisations. This review provides a summary of the epidemiology and pathophysiology of ID in HFrEF, and practical guidance on screening, diagnosing, and treating ID.
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