Key result
IV ferric carboxymaltose reduces CV hospitalizations and CV death ~14% in iron-deficient HF.
Why the study?
Does intravenous ferric carboxymaltose reduce cardiovascular hospitalizations and death in adults with heart failure and iron deficiency?
Meta-Analysis (n=4,501)
placebo-controlled
randomized
Does intravenous ferric carboxymaltose reduce cardiovascular hospitalizations and death in adults with heart failure and iron deficiency?
Answers are grounded in this paper and cite their sources.
In patients with HFrEF and iron deficiency, intravenous ferric carboxymaltose reduces the risk of cardiovascular hospitalizations but does not significantly affect mortality.
BACKGROUND AND AIMS: Whereas a beneficial effect of intravenous ferric carboxymaltose (FCM) on symptoms and exercise capacity among patients with iron deficiency and heart failure (HF) has been consistently demonstrated, the effects of treatment on clinical events remain the subject of research. This meta-analysis aimed to characterize the effects of FCM therapy on hospitalizations and mortality. METHODS: Patient-level data from randomized, placebo-controlled FCM trials including adults with HF and iron deficiency with ≥52 weeks follow-up were analysed. The co-primary efficacy endpoints were (i) composite of total/recurrent cardiovascular hospitalizations and cardiovascular death and (ii) composite of total HF hospitalizations and cardiovascular death, through 52 weeks. Key secondary endpoints included individual composite endpoint components. Event rates were analysed using a negative binomial model. Treatment-emergent adverse events were also examined. RESULTS: Three FCM trials with a total of 4501 patients were included. Ferric carboxymaltose was associated with a significantly reduced risk of co-primary endpoint 1 (rate ratio 0.86; 95% confidence interval 0.75-0.98; P = .029; Cochran Q: 0.008), with a trend towards a reduction of co-primary endpoint 2 (rate ratio 0.87; 95% confidence interval 0.75-1.01; P = .076; Cochran Q: 0.024). Treatment effects appeared to result from reduced hospitalization rates, not improved survival. Treatment appeared to have a good safety profile and was well tolerated. CONCLUSIONS: In iron-deficient patients with HF with reduced left ventricular ejection fraction, intravenous FCM was associated with significantly reduced risk of hospital admissions for HF and cardiovascular causes, with no apparent effect on mortality.
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Ponikowski et al. (2023) conducted a meta-analysis in heart failure with iron deficiency (n=4,501). Intravenous ferric carboxymaltose vs. placebo was evaluated on composite of total/recurrent cardiovascular hospitalizations and cardiovascular death (rate ratio 0.86, 95% CI 0.75-0.98, p=0.029). Intravenous ferric carboxymaltose reduced the composite of cardiovascular hospitalizations and cardiovascular death in heart failure with iron deficiency (RR 0.86; 95% CI 0.75-0.98; P=0.029).
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