Evidence map›Paper›PMID 37382961›Full record

Trial reportClinical journal of the American Society of Nephrology : CJASN2023

Ferric Carboxymaltose in Iron-Deficient Patients with Hospitalized Heart Failure and Reduced Kidney Function.

Iain C Macdougall, Piotr Ponikowski, Austin G Stack, David C Wheeler, Stefan D Anker, Javed Butler, Gerasimos Filippatos, Udo-Michael Göhring, Bridget-Anne Kirwan, Vasuki Kumpeson and 6 more

Registry-linked trialOpen access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Clinical journal of the American Society of Nephrology : CJASN, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02937454 (A Randomised, Double-Blind Placebo Controlled Trial Comparing the Effect of Intravenous Ferric Carboxymaltose on Hospitalisations and Mortality in Iron Deficient Patients Admitted for Acute Heart Failure), which is not on this map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02937454 phase4completednot on this map

A Randomised, Double-Blind Placebo Controlled Trial Comparing the Effect of Intravenous Ferric Carboxymaltose on Hospitalisations and Mortality in Iron Deficient Patients Admitted for Acute Heart Failure (Affirm-AHF)

TypeinterventionalSponsorVifor (International) Inc.Ran2017 to 2020Enrolled1,132ConditionsIron Deficiency, Heart FailureArmsferric carboxymaltose, Normal saline 0.9%
3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Review
  6. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 13 institutions in 9 countries.

Iain C MacdougallDepartment of Renal Medicine, King's College Hospital, London, United Kingdom.
Piotr PonikowskiInstitute of Heart Diseases, Wrocław Medical University, and Institute of Heart Diseases, University Hospital, Wrocław, Poland.
Austin G StackDepartment of Nephrology, University Hospital Limerick and School of Medicine, University of Limerick, Limerick, Ireland.
David C WheelerDepartment of Renal Medicine, University College London, London, United Kingdom.
Stefan D AnkerDepartment of Cardiology, Charité, Campus Virchow-Klinikum, Berlin, Germany.ORCID 0000-0002-0805-8683
Javed ButlerDepartment of Medicine, Baylor University Medical Center, Dallas, Texas.
Gerasimos FilippatosDepartment of Cardiology, National and Kapodistrian University of Athens School of Medicine, Athens University, Athens, Greece.ORCID 0000-0002-5640-0332
Udo-Michael GöhringCSL Vifor, Glattbrugg, Switzerland.
Bridget-Anne KirwanDepartment of Clinical Research, SOCAR Research SA, Nyon, Switzerland.
Vasuki KumpesonCSL Vifor, Glattbrugg, Switzerland.
Marco MetraDepartment of Cardiology, University and Civil Hospital, Brescia, Italy.ORCID 0000-0001-6691-8568
Giuseppe RosanoCentre for Clinical and Basic Research, Department of Medical Sciences, IRCCS San Raffaele Pisana, Rome, Italy.
Frank RuschitzkaDepartment of Cardiology, University Heart Center, University Hospital Zürich and University of Zürich, Zürich, Switzerland.ORCID 0000-0001-5972-0596
Peter van der MeerUniversity Medical Center Groningen, Department of Cardiology, Groningen, The Netherlands.
Sandra WächterCSL Vifor, Glattbrugg, Switzerland.ORCID 0009-0007-3338-6607
Ewa A JankowskaInstitute of Heart Diseases, Wrocław Medical University, and Institute of Heart Diseases, University Hospital, Wrocław, Poland.ORCID 0000-0002-9202-432
Vifor Pharma (Switzerland) · CHWroclaw Medical University · PLBaylor University Medical Center · USCharité - Universitätsmedizin Berlin · DEIstituti di Ricovero e Cura a Carattere Scientifico · ITKing's College Hospital · GBLondon School of Hygiene & Tropical Medicine · GBNational and Kapodistrian University of Athens · GRUniversity College London · GBUniversity Medical Center Groningen · NLUniversity of Brescia · ITUniversity of Limerick · IEUniversity of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundReduced kidney function is common among patients with heart failure. In patients with heart failure and/or kidney disease, iron deficiency is an independent predictor of adverse outcomes. In the AFFIRM-AHF trial, patients with acute heart failure with iron deficiency treated with intravenous ferric carboxymaltose demonstrated reduced risk of heart failure hospitalization, with improved quality of life. We aimed to further characterize the impact of ferric carboxymaltose among patients with coexisting kidney impairment.

methodsThe double-blind, placebo-controlled AFFIRM-AHF trial randomized 1132 stabilized adults with acute heart failure (left ventricular ejection fraction <50%) and iron deficiency. Patients on dialysis were excluded. The primary end point was a composite of total heart failure hospitalizations and cardiovascular death during the 52-week follow-up period. Additional end points included cardiovascular hospitalizations, total heart failure hospitalizations, and days lost to heart failure hospitalizations or cardiovascular death. For this subgroup analysis, patients were stratified according to baseline eGFR.

resultsOverall, 60% of patients had an eGFR <60 ml/min per 1.73 m 2 (the lower eGFR subgroup). These patients were significantly older, more likely to be female and to have ischemic heart failure, and had higher baseline serum phosphate levels and higher rates of anemia. For all end points, event rates were higher in the lower eGFR group. In the lower eGFR group, the annualized event rates for the primary composite outcome were 68.96 and 86.30 per 100 patient-years in the ferric carboxymaltose and placebo arms, respectively (rate ratio, 0.76; 95% confidence interval, 0.54 to 1.06). The treatment effect was similar in the higher eGFR subgroup (rate ratio, 0.65; 95% confidence interval, 0.42 to 1.02; Pinteraction = 0.60). A similar pattern was observed for all end points ( Pinteraction > 0.05).

conclusionsIn a cohort of patients with acute heart failure, left ventricular ejection fraction <50%, and iron deficiency, the safety and efficacy of ferric carboxymaltose were consistent across a range of eGFR values. CLINICAL TRIAL REGISTRY NAME AND REGISTRATION NUMBER: Study to Compare Ferric Carboxymaltose With Placebo in Patients With Acute Heart Failure and Iron Deficiency (Affirm-AHF), NCT02937454 .

Indexed as

Anemia, Iron-DeficiencyHeart FailureIron DeficienciesRenal InsufficiencyAdultFemaleFerric CompoundsHumansIronKidneyMaleMaltoseQuality of LifeStroke VolumeVentricular Function, Leftferric carboxymaltoseFerric CompoundsIronMaltose

Identifiers

PMID37382961
PMCPMC10564367
OpenAlexW4382501531

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.