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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.
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.
Abstract:
Background: The correction of iron deficiency (ID) with ferric carboxymaltose (FCM) is a recommended intervention in heart failure (HF) with reduced ejection fraction. Our aim is to evaluate, in a real-life setting, the clinical significance of ID screening and FCM treatment in acute decompensated HF (ADHF). Methods: In a cohort of ADHF patients, the prevalence of ID and FCM administration were investigated. Among the 104 patients admitted for ADHF, in n = 90 (median age 84, 53.5% with preserved left ventricular ejection fraction-LVEF), a complete iron status evaluation was obtained. ID was detected in n = 73 (81.1%), 55 of whom were treated with in-hospital FCM. The target dose was reached in n = 13. Results: No significant differences were detected in terms of age, sex, comorbidities, or LVEF between the FCM-supplemented and -unsupplemented patients. During a median follow-up of 427 days (IQR 405-466) among the FCM-supplemented patients, only 14.5% received FCM after discharge; the mortality and rehospitalizations among FCM-supplemented and -unsupplemented patients were similar (p = ns). In a follow-up evaluation, ID was still present in 75.0% of the FCM-supplemented patients and in 69.2% of the unsupplemented patients (p = ns). Conclusions: In this real-life ADHF cohort, FCM was administered at lower-than-prescribed doses, thus having no impact on ID correction. The significance of our findings is that only achieving the target dose of FCM and pursuing outpatient treatment can correct ID and produce long-term clinical benefits.
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