Practical Guidance for Diagnosing and Treating Iron Deficiency in Patients with Heart Failure: Why, Who and How?
Andrew P SindoneWolfram DöhnerNicolas ManitoTheresa McDonaghAlain Cohen-SolalThibaud DamyJulio NunezOtmar PfisterPeter van der MeerJosep Comín ColetPublished in: Journal of clinical medicine (2022)
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.
Keyphrases
- iron deficiency
- acute heart failure
- heart failure
- liver failure
- physical activity
- high intensity
- risk factors
- cardiovascular disease
- study protocol
- stem cells
- skeletal muscle
- cardiovascular events
- high dose
- cardiac surgery
- coronary artery disease
- phase ii
- mesenchymal stem cells
- bone marrow
- acute kidney injury
- extracorporeal membrane oxygenation
- acute respiratory distress syndrome
- phase iii
- drug induced