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March 29, 2026BMC Cardiovascular Disorders0 citationsOpen Access

Intravenous iron therapy for patients with heart failure: a meta-analysis stratified by chronic kidney disease status

YDYiran DuYLYingnan LiangJLJie Lv

Key Result

Intravenous iron therapy did not significantly reduce all-cause mortality (RR 0.94) in patients with heart failure and chronic kidney disease, despite reducing heart failure hospitalizations.

Key Points

  • This research aims to evaluate the efficacy of intravenous iron therapy in patients with heart failure, particularly considering chronic kidney disease status.
  • Conducted a meta-analysis of randomized controlled trials from multiple databases including Embase, PubMed, and Cochrane Library.
  • Included 8 randomized controlled trials with a total of 7009 participants.
  • Analyzed clinical outcomes using random-effects models to pool relative risks and mean differences.
  • IV iron therapy significantly reduced first heart failure hospitalization or cardiovascular death (RR = 0.79, P < 0.001).
  • Heart failure hospitalization or cardiovascular death was also reduced (RR = 0.85, P = 0.02).
  • Anemic patients showed a trend towards benefit regarding all-cause mortality (RR = 0.84, P = 0.06), while non-anemic patients did not.

Study Design

Type

Meta-Analysis (n=7,009)

Structured PICO

Does intravenous iron therapy reduce mortality and cardiovascular events in patients with heart failure and chronic kidney disease?

P
Population
Patients with heart failure (HF) complicated by chronic kidney disease (CKD)
I
Intervention
Intravenous (IV) iron therapy (ferric carboxymaltose, iron sucrose, or ferric derisomaltose)
C
Comparator
Placebo or control
O
Outcome
All-cause mortalityhard clinical

Intravenous iron therapy significantly reduces the risk of heart failure hospitalization or cardiovascular death in patients with concurrent heart failure and chronic kidney disease, though it does not significantly reduce all-cause mortality.

Main Result

Effect estimate: RR 0.94 (95% CI 0.81-1.10)

Absolute Event Rate: 25.2% vs 28.7%

p-value: p=0.46

Limitations

  • Some subgroups contained fewer than 10 studies
  • Further large-sample, long-term trials are needed to identify the optimal patient population and clarify the long-term safety of this therapy

Abstract

Iron deficiency is highly prevalent in patients with heart failure (HF) complicated by chronic kidney disease (CKD), yet the efficacy of intravenous (IV) iron therapy remains unclear. We performed a meta-analysis of randomized controlled trials (RCTs) retrieved from Embase, PubMed, and the Cochrane Library from inception to January 1, 2026. A total of 8 RCTs involving 7009 participants were included. Clinical outcomes were assessed by generating forest plots using the random-effects model and pooling relative risks (RRs) or mean differences (MDs). IV iron therapy showed a significantly reduced incidence of first heart failure hospitalization or cardiovascular death (RR = 0.79, 95% CI: 0.72–0.86, P < 0.001), heart failure hospitalization or cardiovascular death (RR = 0.85, 95% CI: 0.75–0.98, P = 0.02) in HF-CKD patients as compared with the control group, with significant improvements in relevant biomarkers. Subgroup analyses revealed no effect modification by CKD status. Anemia status modified the treatment effect on all-cause mortality (P = 0.04). Anemic patients exhibited a trend toward clinical benefit (RR = 0.84, 95% CI: 0.70–1.01, P = 0.06), while no such trend was observed in non-anemic patients (RR = 1.28, 95% CI: 0.90–1.81, P = 0.16). Further large-sample, long-term trials are needed to identify the optimal patient population and clarify the long-term safety of this therapy.

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Cite This Study

Du et al. (2026) conducted a meta-analysis in Heart failure complicated by chronic kidney disease (n=7,009). Intravenous iron therapy vs. Placebo / Control was evaluated on All-cause mortality (RR 0.94, 95% CI 0.81-1.10, p=0.46). Intravenous iron therapy did not significantly reduce all-cause mortality (RR 0.94) in patients with heart failure and chronic kidney disease, despite reducing heart failure hospitalizations.

synapsesocial.com/papers/69c8c371de0f0f753b39e3efhttps://doi.org/10.1186/s12872-026-05672-5
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