PMID- 18191732 OWN - NLM STAT- MEDLINE DCOM- 20080205 LR - 20220316 IS - 1558-3597 (Electronic) IS - 0735-1097 (Linking) VI - 51 IP - 2 DP - 2008 Jan 15 TI - Effect of intravenous iron sucrose on exercise tolerance in anemic and nonanemic patients with symptomatic chronic heart failure and iron deficiency FERRIC-HF: a randomized, controlled, observer-blinded trial. PG - 103-12 LID - 10.1016/j.jacc.2007.09.036 [doi] AB - OBJECTIVES: We tested the hypothesis that intravenous iron improves exercise tolerance in anemic and nonanemic patients with symptomatic chronic heart failure (CHF) and iron deficiency. BACKGROUND: Anemia is common in heart failure. Iron metabolism is disturbed, and administration of iron might improve both symptoms and exercise tolerance. METHODS: We randomized 35 patients with CHF (age 64 +/- 13 years, peak oxygen consumption [pVO2] 14.0 +/- 2.7 ml/kg/min) to 16 weeks of intravenous iron (200 mg weekly until ferritin >500 ng/ml, 200 mg monthly thereafter) or no treatment in a 2:1 ratio. Ferritin was required to be <100 ng/ml or ferritin 100 to 300 ng/ml with transferrin saturation <20%. Patients were stratified according to hemoglobin levels (<12.5 g/dl [anemic group] vs. 12.5 to 14.5 g/dl [nonanemic group]). The observer-blinded primary end point was the change in absolute pVO2. RESULTS: The difference (95% confidence interval [CI]) in the mean changes from baseline to end of study between the iron and control groups was 273 (151 to 396) ng/ml for ferritin (p < 0.0001), 0.1 (-0.8 to 0.9) g/dl for hemoglobin (p = 0.9), 96 (-12 to 205) ml/min for absolute pVO2 (p = 0.08), 2.2 (0.5 to 4.0) ml/kg/min for pVO2/kg (p = 0.01), 60 (-6 to 126) s for treadmill exercise duration (p = 0.08), -0.6 (-0.9 to -0.2) for New York Heart Association (NYHA) functional class (p = 0.007), and 1.7 (0.7 to 2.6) for patient global assessment (p = 0.002). In anemic patients (n = 18), the difference (95% CI) was 204 (31 to 378) ml/min for absolute pVO2 (p = 0.02), and 3.9 (1.1 to 6.8) ml/kg/min for pVO2/kg (p = 0.01). In nonanemic patients, NYHA functional class improved (p = 0.06). Adverse events were similar. CONCLUSIONS: Intravenous iron loading improved exercise capacity and symptoms in patients with CHF and evidence of abnormal iron metabolism. Benefits were more evident in anemic patients. (Effect of Intravenous Ferrous Sucrose on Exercise Capacity in Chronic Heart Failure; http://www.clinicaltrials.gov/ct/show/NCT00125996; NCT00125996). FAU - Okonko, Darlington O AU - Okonko DO AD - Clinical Cardiology, NHLI, Imperial College London, London, United Kingdom. d.okonko@imperial.ac.uk FAU - Grzeslo, Agnieszka AU - Grzeslo A FAU - Witkowski, Tomasz AU - Witkowski T FAU - Mandal, Amit K J AU - Mandal AK FAU - Slater, Robert M AU - Slater RM FAU - Roughton, Michael AU - Roughton M FAU - Foldes, Gabor AU - Foldes G FAU - Thum, Thomas AU - Thum T FAU - Majda, Jacek AU - Majda J FAU - Banasiak, Waldemar AU - Banasiak W FAU - Missouris, Constantinos G AU - Missouris CG FAU - Poole-Wilson, Philip A AU - Poole-Wilson PA FAU - Anker, Stefan D AU - Anker SD FAU - Ponikowski, Piotr AU - Ponikowski P LA - eng SI - ClinicalTrials.gov/NCT00125996 PT - Comparative Study PT - Journal Article PT - Randomized Controlled Trial PT - Research Support, Non-U.S. Gov't PL - United States TA - J Am Coll Cardiol JT - Journal of the American College of Cardiology JID - 8301365 RN - 0 (Ferric Compounds) SB - IM MH - Aged MH - Analysis of Variance MH - Anemia, Iron-Deficiency/complications/diagnosis/*drug therapy/mortality MH - Chronic Disease MH - Confidence Intervals MH - Dose-Response Relationship, Drug MH - Double-Blind Method MH - Drug Administration Schedule MH - Exercise Tolerance/*drug effects MH - Female MH - Ferric Compounds/*administration & dosage MH - Follow-Up Studies MH - Heart Failure/complications/diagnosis/*drug therapy/mortality MH - Humans MH - Infusions, Intravenous MH - Male MH - Middle Aged MH - Oxygen Consumption/*drug effects/physiology MH - Probability MH - Prospective Studies MH - Reference Values MH - Risk Assessment MH - Survival Rate MH - Treatment Outcome EDAT- 2008/01/15 09:00 MHDA- 2008/02/06 09:00 CRDT- 2008/01/15 09:00 PHST- 2006/11/09 00:00 [received] PHST- 2007/08/14 00:00 [revised] PHST- 2007/09/11 00:00 [accepted] PHST- 2008/01/15 09:00 [pubmed] PHST- 2008/02/06 09:00 [medline] PHST- 2008/01/15 09:00 [entrez] AID - S0735-1097(07)03363-3 [pii] AID - 10.1016/j.jacc.2007.09.036 [doi] PST - ppublish SO - J Am Coll Cardiol. 2008 Jan 15;51(2):103-12. doi: 10.1016/j.jacc.2007.09.036.