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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
Iron chelation therapy in the management of transfusion-related cardiac iron overload
1University of Campinas, São Paulo, Brazil. jlaraf@fcm.unicamp.br
Insights
Iron overload in patients receiving chronic transfusions can harm the heart. This review examines iron chelators like deferoxamine, deferiprone, and deferasirox to manage cardiac iron overload and improve patient outcomes.
Area of Science:
- Cardiology
- Hematology
- Pharmacology
Background:
- Chronic transfusion therapy can lead to iron overload, a significant cause of morbidity and mortality.
- Excessive iron accumulation in the heart can cause left ventricular dysfunction.
- Accurate monitoring and treatment are crucial for managing cardiac complications in these patients.
Purpose of the Study:
- To review recent studies on iron chelation therapy for managing cardiac iron overload in chronically transfused patients.
- To assess the effectiveness of deferoxamine, deferiprone, and deferasirox in removing cardiac iron.
- To identify optimal treatment strategies based on patient characteristics and cardiac iron status.
Main Methods:
- Systematic review of recent clinical studies on iron chelators.
- Analysis of data linking patient characteristics, clinical settings, and drug dosing.
- Stratification of patients based on cardiac iron overload and ventricular function.
Main Results:
- The review summarizes findings on deferoxamine, deferiprone, and deferasirox in treating cardiac iron overload.
- Identified specific patient scenarios and dosing regimens for each chelator.
- Highlighted the importance of tailoring treatment to individual patient profiles.
Conclusions:
- Iron chelation therapy is essential for preventing and reversing myocardial iron overload.
- Personalized treatment approaches, considering patient stratification, are key for managing transfusion-related cardiac iron overload.
- Further research can refine management strategies for optimal cardiac outcomes.
Abstract:
Iron overload is one of the major causes of morbidity and death in patients undergoing chronic transfusion therapy. Furthermore, excessive iron accumulation in the heart may result in impaired left ventricular dysfunction. With accurate monitoring techniques and treatment regimens, progression of heart complications can be followed, and their natural history changed. Iron chelation therapy is the mainstay of prevention and reversal of myocardial iron overload. Despite recent appraisals of general chelating strategies, the management of iron chelation in chronically transfused patients with a focus on the heart has not been extensively assessed. New studies published in the past couple of years have provided important new data in this topic and therefore this review summarizes the major studies that examined the removal of iron from the heart with the iron chelators: deferoxamine, deferiprone, and deferasirox. Since chronically transfused patients and their cardiac clinical presentations vary widely, this review tries to identify--with each drug--the precise scenarios evaluated, linking patients' baseline characteristics, clinical setting, and drug intake and dosing. Ultimately, by stratifying patients according to their cardiac iron overload status and ventricular function, this review identifies possible approaches for the initial treatment and follow-up of transfusion-related cardiac iron overload.
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