AHA 2020 | AFFIRM-AHF: Ferric Carboxymaltose and Fewer Hospitalizations for Cardiac Failure

Correcting iron deficiency in patients with cardiac failure might reduce the risk of new hospitalizations according to the AFFIRM-AHF published in the Lancet and presented at AHA 2020.

The combined primary end point of death and hospitalizations was not met; yet the study showed a significant reduction of 26% in hospitalization rate.

Irrespective of the presence of anemia, iron deficiency is among the predictors of bad prognosis and is present in over 70% of patients with cardiac failure.

This new study data support the administration of intravenous ferric carboxymaltose for patients with iron deficiency (with or without anemia) and less than 50% ejection fraction. Therefore, rather than a bad prognosis factor, iron deficiency has become a changeable factor. 

AFFIRM-AHF was a multicenter study including 1108 patients hospitalized for cardiac failure. They all had iron deficiency defined as ferritin <100 μg/L, or 100–299 μg/L with transferrin saturation <20%). Mean age was 71 and mean ejection fraction was 33%. Before discharge, patients were randomized to endovenous iron vs. placebo. 


Read also: AHA 2020 | Statins: Confirmed Benefits for the Elderly.


At 52 weeks followup, cardiovascular events rate resulted similar between the branches, as was the combined end point of death and hospitalization. However, when looked at separately, new hospitalization rate saw a significant reduction of 26%.

hierro-en-ICC

Original Title: Ferric carboxymaltose for iron deficiency at discharge after acute heart failure: a multicentre, double-blind, randomised, controlled trial.

Reference: Ponikowski P et al. Lancet. 2020; Epub ahead of print y presentado en las sesiones científicas del AHA 2020.


Subscribe to our weekly newsletter

Get the latest scientific articles on interventional cardiology

More articles by this author

SMART-CHOICE 3 | Efficacy and Safety of Clopidogrel vs Aspirin Monotherapy in High Risk Patients after Percutaneous Coronary Intervention

Courtesy of Dr. Juan Manuel Pérez. After post percutaneous coronary intervention (PCI) standard duration dual antiplatelet therapy (DAPT), the optimal long term monotherapy strategy is...

Patients at High Risk of Bleeding After Coronary Angioplasty: Are Risk Assessment Tools ARC-HBR and PRECISE-DAPT Useful?

Patients undergoing coronary stenting typically receive dual antiplatelet therapy (DAPT) for 6 to 12 months, consisting of a P2Y12 receptor inhibitor and aspirin. While DAPT...

ACC-2025 Congress Second Day Key Studies

BHF PROTECT-TAVI (Kharbanda RK, Kennedy J, Dodd M, et al.)The largest randomized  trial carried out across 33 UK centers between 2020 and 2024, assessing...

ACC 2025 | API-CAT: Reduced vs. Full Dose Extended Anticoagulation in Patients with Cancer Related VTE

The risk of cancer related recurrent venous thromboembolism (VTE) will drop over time, while bleeding risk will persist. At present, it is recommended we...

LEAVE A REPLY

Please enter your comment!
Please enter your name here

Related Articles

SOLACI Sessionsspot_img

Recent Articles

Radial Patency in Coronary Procedures: Is Heparin Enough or Should We Aim for Distal Transradial Access?

Transradial access is the preferred route in most coronary procedures due to its proven reduction in mortality compared to transfemoral access. However, one of...

SMART-CHOICE 3 | Efficacy and Safety of Clopidogrel vs Aspirin Monotherapy in High Risk Patients after Percutaneous Coronary Intervention

Courtesy of Dr. Juan Manuel Pérez. After post percutaneous coronary intervention (PCI) standard duration dual antiplatelet therapy (DAPT), the optimal long term monotherapy strategy is...

RACE Trial: Effect of Balloon Pulmonary Angioplasty and Riociguat on Right Ventricular Afterload and Function in Chronic Thromboembolic Pulmonary Hypertension

Even though pulmonary endarterectomy is the treatment of choice for chronic thromboembolic pulmonary hypertension (CTEPH), up to 40% of patients are not candidates because...