Heart failure & cardiomyopathies

Hypophosphataemia Risk Associated with Ferric Carboxymaltose in Heart Failure: A Pooled Analysis of Clinical Trials

ESC Heart FailPublished Pooled analysis of clinical trials

Authors' conclusion

The risk of laboratory-assessed hypophosphataemia in HF patients treated with FCM was lower than that seen in patients in other therapeutic areas treated with FCM, and clinical events associated with hypophosphataemia are uncommon with FCM therapy in this population.

Study context

Population
Adults with iron deficiency across disease states and therapeutic areas treated with intravenous ferric carboxymaltose (FCM)
Participants
7,931 adults41 studies
Comparison
Hypophosphataemia incidence with FCM across therapeutic areas
Outcome
Post-baseline moderate or severe hypophosphataemia (serum PO4 3- <2.0 mg/dL)

Pooled result

As reported in the abstract

Further pooled results

OutcomeHFNeurologyGastrointestinalOR
Serum PO4 3- <1.0 mg/dL<0.1%4.8%4.0%
Predictor of hypophosphataemia: preserved kidney function (eGFR >60 vs <30 mL/min/1.73 m²)Strongest predictor12.2

Mean serum PO4 3- over time

Except haemodialysis-dependent chronic kidney disease (HD-CKD), mean serum PO4 3- decreased through weeks 2 to 4, then returned toward baseline and plateaued by week 8

Safety

TEAEs potentially related to hypophosphataemia (heart failure (HF) subgroup)

Lower with FCM than placebo
Lower with post-baseline PO4 3- <2 mg/dL than without

Original publication

Hypophosphataemia Risk Associated with Ferric Carboxymaltose in Heart Failure: A Pooled Analysis of Clinical Trials. ESC Heart Fail. Published 1 February 2023. doi:10.1002/ehf2.14286

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