Abstract 4363467: Real World Experience of Intravenous Iron Repletion in Children with Heart Failure

D David Newland (Seattle Children's Hospital, Seattle, Washington, United States) R Reda Ali (Seattle Children's Hospital, Seattle, Washington, United States) E Erin Albers (Seattle Children's Hospital, Seattle, Washington, United States) C Christina Hartje-Dunn (Seattle Children's Hospital, Seattle, Washington, United States) B Borah Hong (Seattle Children's Hospital, Seattle, Washington, United States) M Mariska Kemna (Seattle Children's Hospital, Seattle, Washington, United States) J Jiawen Liu (State Key Laboratory of Supramolecular Structure and Materials) N Nina Srour (Seattle Children's Hospital, Seattle, Washington, United States) B Bethany Wisotzkey (Seattle Children's Hospital, Seattle, Washington, United States) Y Yuk Law (Seattle Children's Hospital, Seattle, Washington, United States)

Abstract

Introduction: Iron deficiency (ID) is common in HF and is associated with adverse CV outcomes. There is a paucity of literature on efficacy of intravenous iron replacement (FeIV) in children with HF. Methods: Single-center observational analysis of 244 children (≤ 21 years old) with HF or post-heart transplant (HTX) who received IV iron sucrose (IS, 46%) from 2010-2018 or IV ferric carboxymaltose (FCM, 54%) from 2019-2024. Anemia was defined by World Health Organization age-specific hemoglobin cutoffs; ID was defined as iron saturation (TSAT) <20% or ferritin <100 ng/mL. Primary outcome was change in iron profile and hematological indices. Secondary outcome was change in LVEF and BNP. Exploratory outcome included baseline risk factors for anemia and composite event of HTX listing, need for MCS, or death by latest follow-up. Results: Median age at first FeIV infusion was 3.6 years (IQR 0.8-13.2); 43% were female. Diagnoses included CDM (49%), congenital heart disease (43%), and s/p HTX (8%). Total of 812 FeIV infusions were administered (67% IS; 33% FCM). Median number of infusions per patient was 4 (IQR 3–6) for IS and 1 (IQR 1–2) for FCM (p<0.01). Despite fewer infusions, the median cumulative dose was higher with FCM (19.9 vs 13.1 mg/kg; p<0.01). At baseline, 82% had TSAT <20%, 70% had ferritin <100 ng/mL, 38% had serum iron <40 mcg/dL, and 50% were anemic. Only 56% had TSAT <20% with ferritin <100 ng/mL. Mean follow-up was 255 days (SD±144). Significant increases in TSAT, ferritin, serum iron, hemoglobin, and LVEF, and decreases in BNP, were observed at most follow-up points (Table 1) (all p<0.05). Following FeIV, 81% achieved TSAT ≥20% and 80% ferritin ≥100 ng/mL. Composite event occurred in 28% at median 28 days (IQR 8-102) following first FeIV infusion; time to event occurred significantly earlier in IS vs FCM cohorts (18 vs 32 days, respectively, p=0.04). Multivariable analysis identified ferritin <100 ng/mL was independently associated with decreased risk of anemia and serum iron <40 mcg/dL as increased risk (Table 2). Older era (2010-2018), lower cumulative FeIV dose, ferritin <100 ng/mL, lower TSAT, and higher BNP were all independently associated with higher risk of composite event (Table 3). Conclusion: FeIV effectively corrects ID in children with HF and may be linked with improvements in clinical outcomes. Further studies are needed to confirm safety and clinical benefits of FeIV in pediatric HF.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (10)

D

David Newland

Seattle Children's Hospital, Seattle, Washington, United States

R

Reda Ali

Seattle Children's Hospital, Seattle, Washington, United States

E

Erin Albers

Seattle Children's Hospital, Seattle, Washington, United States

C

Christina Hartje-Dunn

Seattle Children's Hospital, Seattle, Washington, United States

B

Borah Hong

Seattle Children's Hospital, Seattle, Washington, United States

M

Mariska Kemna

Seattle Children's Hospital, Seattle, Washington, United States

J

Jiawen Liu

State Key Laboratory of Supramolecular Structure and Materials

N

Nina Srour

Seattle Children's Hospital, Seattle, Washington, United States

B

Bethany Wisotzkey

Seattle Children's Hospital, Seattle, Washington, United States

Y

Yuk Law

Seattle Children's Hospital, Seattle, Washington, United States