Ferric Carboxymaltose in Patients with Acute Decompensated Heart Failure and Iron Deficiency: A Real-Life Study

Federico Capone1, Alberto Cipriani2, Leonardo Molinari1

  • 1Department of Medicine (DIMED), University of Padua, Via Giustiniani, 2, 35128 Padova, Italy.

PubMed

Insights

Iron deficiency (ID) treatment with ferric carboxymaltose (FCM) in acute decompensated heart failure (ADHF) requires achieving target doses and outpatient follow-up for clinical benefits. Inadequate dosing and short-term treatment in this ADHF cohort did not correct ID or improve outcomes.

Area of Science:

  • Cardiology
  • Hematology
  • Pharmacology

Background:

  • Iron deficiency (ID) is a common comorbidity in heart failure (HF) with reduced ejection fraction.
  • Ferric carboxymaltose (FCM) is a recommended treatment for ID in HF.
  • The clinical significance of ID screening and FCM treatment in acute decompensated heart failure (ADHF) requires real-world evaluation.

Purpose of the Study:

  • To evaluate the real-life clinical significance of iron deficiency screening and ferric carboxymaltose treatment in patients with acute decompensated heart failure (ADHF).

Main Methods:

  • A cohort of 104 ADHF patients were assessed for iron status.
  • Iron deficiency was detected in 81.1% of patients (n=73).
  • 55 patients received in-hospital ferric carboxymaltose (FCM), with only 13 reaching the target dose.

Main Results:

  • No significant differences in mortality or rehospitalization rates were observed between FCM-supplemented and unsupplemented patients.
  • Iron deficiency persisted in 75% of FCM-treated patients and 69.2% of untreated patients at follow-up.
  • Only 14.5% of FCM-supplemented patients received continued treatment after discharge.

Conclusions:

  • In this real-world ADHF cohort, ferric carboxymaltose (FCM) was often underdosed and did not effectively correct iron deficiency.
  • Achieving the target FCM dose and ensuring outpatient treatment are crucial for correcting iron deficiency and achieving long-term clinical benefits in ADHF patients.
  • Current real-life practices for FCM administration in ADHF may not yield the intended clinical improvements.

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