Rationale and design of the AFFIRM-AHF trial: 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

dc.contributor.authorPonikowski, Piotr P.
dc.contributor.authorKirwan, Bridget Anne
dc.contributor.authorAnker, Stefan D.
dc.contributor.authorDorobanţu, Maria I.
dc.contributor.authorDrożdż, Jaroslaw
dc.contributor.authorFabien, Vincent
dc.contributor.authorFilippatos, Gerasimos S.
dc.contributor.authorHaboubi, Teba
dc.contributor.authorKeren, André
dc.contributor.authorKhintibidze, Irakli
dc.contributor.authorKragten, Hans A.
dc.contributor.authorMartínez, Felipe A.
dc.contributor.authorMcDonagh, Theresa A.
dc.contributor.authorMetra, Marco
dc.contributor.authorMiličić, Davor
dc.contributor.authorNicolau, José Carlos
dc.contributor.authorOhlsson, Marcus Andreas
dc.contributor.authorParhomenko, Alexander
dc.contributor.authorPascual-Figal, Domingo A.
dc.contributor.authorRuschitzka, Frank T.
dc.contributor.authorSim, David Kheng Leng
dc.contributor.authorSkouri, Hadi N.
dc.contributor.authorvan der Meer, Peter
dc.contributor.authorJankowska, Ewa Anita
dc.contributor.departmentInternal Medicine
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:55:41Z
dc.date.available2025-01-24T11:55:41Z
dc.date.issued2019
dc.description.abstractAims: Iron deficiency (ID) is a common co-morbidity in heart failure (HF), associated with impaired functional capacity, poor quality of life and increased morbidity and mortality. Treatment with intravenous (i.v.) ferric carboxymaltose (FCM) has shown improvements in functional capacity, symptoms and quality of life in stable HF patients with reduced ejection fraction. The effect of i.v. iron supplementation on morbidity and mortality in patients hospitalised for acute HF (AHF) and who have ID has yet to be established. The objective of the present article is to present the rationale and design of the AFFIRM-AHF trial (ClinicalTrials.gov NCT02937454) which will investigate the effect of i.v. FCM (vs. placebo) on recurrent HF hospitalisations and cardiovascular (CV) mortality in iron-deficient patients hospitalised for AHF. Methods: AFFIRM-AHF is a multicentre, randomised (1:1), double-blind, placebo-controlled trial which recruited 1100 patients hospitalised for AHF and who had iron deficiency ID defined as serum ferritin <100 ng/mL or 100–299 ng/mL if transferrin saturation <20%. Eligible patients were randomised (1:1) to either i.v. FCM or placebo and received the first dose of study treatment just prior to discharge for the index hospitalisation. Patients will be followed for 52 weeks. The primary outcome is the composite of recurrent HF hospitalisations and CV mortality. The main secondary outcomes include the composite of recurrent CV hospitalisations and CV mortality, recurrent HF hospitalisations and safety-related outcomes. Conclusion: The AFFIRM-AHF trial will evaluate, compared to placebo, the effect of i.v. FCM on morbidity and mortality in iron-deficient patients hospitalised for AHF. © 2019 The Authors. European Journal of Heart Failure © 2019 European Society of Cardiology
dc.identifier.doihttps://doi.org/10.1002/ejhf.1710
dc.identifier.eid2-s2.0-85077183438
dc.identifier.pmid31883356
dc.identifier.urihttp://hdl.handle.net/10938/31215
dc.language.isoen
dc.publisherJohn Wiley and Sons Ltd
dc.relation.ispartofEuropean Journal of Heart Failure
dc.sourceScopus
dc.subjectAcute heart failure
dc.subjectCardiovascular mortality
dc.subjectFerric carboxymaltose
dc.subjectIron deficiency
dc.subjectRecurrent heart failure hospitalizations
dc.subjectAged
dc.subjectAnemia, iron-deficiency
dc.subjectDose-response relationship, drug
dc.subjectDouble-blind method
dc.subjectFemale
dc.subjectFerric compounds
dc.subjectFollow-up studies
dc.subjectHeart failure
dc.subjectHospitalization
dc.subjectHumans
dc.subjectInjections, intravenous
dc.subjectInpatients
dc.subjectMale
dc.subjectMaltose
dc.subjectMiddle aged
dc.subjectQuality of life
dc.subjectRetrospective studies
dc.subjectSurvival rate
dc.subjectSwitzerland
dc.subjectTreatment outcome
dc.subjectFerritin
dc.subjectPlacebo
dc.subjectTransferrin
dc.subjectFerric ion
dc.subjectAdult
dc.subjectArticle
dc.subjectBody weight
dc.subjectComparative effectiveness
dc.subjectControlled study
dc.subjectDouble blind procedure
dc.subjectDrug efficacy
dc.subjectDrug safety
dc.subjectDrug screening
dc.subjectFerritin blood level
dc.subjectFollow up
dc.subjectHospital admission
dc.subjectHospital discharge
dc.subjectHospital patient
dc.subjectHuman
dc.subjectMajor clinical study
dc.subjectMorbidity
dc.subjectMulticenter study
dc.subjectOutcome assessment
dc.subjectPriority journal
dc.subjectRandomized controlled trial
dc.subjectRecurrent disease
dc.subjectTransferrin blood level
dc.subjectClinical trial
dc.subjectComplication
dc.subjectDose response
dc.subjectEpidemiology
dc.subjectIntravenous drug administration
dc.subjectIron deficiency anemia
dc.subjectMortality
dc.subjectRetrospective study
dc.titleRationale and design of the AFFIRM-AHF trial: 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
dc.typeArticle

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