WebMar 23, 2024 · The AFFIRM-AHF trial suggests that the reduction in hospitalisations for heart failure is not observed until 8–12 weeks after administration of IV iron, consistent … WebAFFIRM-AHF was designed to evaluate the effect of intravenous FCM or placebo initiated shortly before hospital discharge in patients with acute HF and iron deficiency on recurrent heart failure hospitalisations and cardiovascular death up to 52 weeks after randomisation8 HFrEF, Heart Failure with reduced Ejection Fraction
Atrial Fibrillation Follow-up Investigation of Rhythm Management
WebNov 11, 2024 · AFFIRM-AHF. Trial Description: Patients hospitalized with acute heart failure with LVEF <50% and iron deficiency were randomized to intravenous ferric carboxymaltose with dosing based on weight and hemoglobin levels vs. placebo. RESULTS • Primary outcome was composite of total heart failure hospitalizations and WebMar 14, 2015 · Treatment of symptomatic, iron-deficient HF patients with FCM over a 1-year period resulted in sustainable improvement in functional capacity, symptoms, and QoL and may be associated with risk reduction of hospitalization for worsening HF (ClinicalTrials.gov number NCT01453608). pasha is home
AFFIRMing What We Know About IV Iron in Patients with Acute …
WebAbstract Background: The recent AFFIRM-AHF trial assessing the effect of intravenous (IV) iron on outcomes in patients hospitalised with worsening heart failure who had iron … WebDec 1, 2024 · 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... WebDec 28, 2024 · 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 Piotr Ponikowski, Corresponding Author Piotr Ponikowski [email protected] tinkatuff location scarlet