Key result
Intravenous ferric carboxymaltose did not significantly reduce the primary composite of total heart failure hospitalizations and cardiovascular death compared to placebo in patients stabilized after acute heart failure with iron deficiency (RR 0.79, p=0.059).
Why the study?
Iron deficiency in acute heart failure predicts adverse outcomes, prompting a review of pathophysiological links and results from the AFFIRM-AHF trial of ferric carboxymaltose.
Does ferric carboxymaltose improve outcomes in patients stabilized after an episode of acute heart failure with concomitant iron deficiency?
Does ferric carboxymaltose improve outcomes in patients stabilized after an episode of acute heart failure with concomitant iron deficiency?
Answers are grounded in this paper and cite their sources.
This review highlights iron deficiency as a prevalent comorbidity in acute heart failure that predicts worse outcomes and discusses the AFFIRM-AHF trial of ferric carboxymaltose.
Acute heart failure (AHF) syndromes are among the most frequent causes of hospitalization in the elderly and put a heavy financial burden on healthcare systems, mainly due to high early readmission rates. The understanding of AHF has evolved over the years from a significant hemodynamic failure to a multi-organ disease in the course of which peripheral mechanisms such as dysregulated cardiorenal axis or inflammation also play essential roles. A few available observational studies investigating iron deficiency (ID) in patients hospitalized for AHF indicate that this comorbidity is more prevalent than in chronic heart failure, and iron status presents some dynamics in these subjects. ID in AHF predicts increased mortality, greater risk for early readmission and is related to prolonged hospitalization. This paper reviews the results of the first multicenter, double-blind, randomized clinical trial on ferric carboxymaltose in patients who were stabilized after an episode of AHF who had concomitant ID (AFFIRM-AHF), and potential pathophysiological links between dysregulated iron status and AHF syndromes are discussed.
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A 2021 study conducted a review in Acute heart failure with iron deficiency (n=1,100). Ferric carboxymaltose vs. Placebo was evaluated on Composite of total hospitalizations for heart failure and cardiovascular death up to 52 weeks (RR 0.79, 95% CI 0.62-1.01, p=0.059). Intravenous ferric carboxymaltose did not significantly reduce the primary composite of total heart failure hospitalizations and cardiovascular death compared to placebo in patients stabilized after acute heart failure with iron deficiency (RR 0.79, p=0.059).
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