PMID- 22348897 OWN - NLM STAT- MEDLINE DCOM- 20120720 LR - 20201216 IS - 1879-0844 (Electronic) IS - 1388-9842 (Linking) VI - 14 IP - 4 DP - 2012 Apr TI - Iron supplementation for the treatment of chronic heart failure and iron deficiency: systematic review and meta-analysis. PG - 423-9 LID - 10.1093/eurjhf/hfs017 [doi] AB - AIMS: Over half of chronic heart failure (CHF) patients are anaemic, and iron deficiency is common. Iron replacement therapy (oral or i.v.) might improve exercise capacity and quality of life (QOL). METHODS AND RESULTS: We carried out a systematic review and meta-analysis of all randomized control trials that compared iron with no therapy for CHF patients with iron deficiency, whether or not they were anaemic. We searched electronic databases as well as haematology and cardiology conferences up to August 2011. The primary outcome was the effect of iron on QOL parameters such as New York Heart Association (NYHA) class and the Minnesota Living With Heart Failure Questionnaire (MLHWFQ). Secondary outcomes included all-cause mortality, mean ejection fraction, 6 min walk distance (6MWD), hospitalizations due to any cause, iron indices, C-reactive protein levels, and adverse events. Four trials performed fulfilled the inclusion criteria. A total of 370 patients were treated with i.v. iron, compared with 224 control patients. There was significant improvement in QOL in the iron arm according to the MLWHFQ score at 26 weeks, with a weighted mean difference of -18.00 (-22.54, -13.46, I(2) = 0%]. The point estimate for improvement in NYHA class was in favour of iron. Iron reduced the number of hospitalizations and C-reactive protein levels, and increased the 6MWD and mean ejection fraction. Iron indices were significantly improved without a change in haemoglobin levels. No increase in the rate of adverse events was found. CONCLUSION: Intravenous iron therapy is associated with improved QOL parameters, reduction in hospitalizations, and increased 6MWD. Treatment with i.v. iron is safe, with no increased rate of adverse events. The results of our analysis are limited by the paucity of trials, and significant heterogeneity between trials. FAU - Avni, Tomer AU - Avni T AD - Department of Medicine E, Rabin Medical Center, Beilinson Hospital, Petah-Tikva, Israel. tomerav@clalit.org.il FAU - Leibovici, Leonard AU - Leibovici L FAU - Gafter-Gvili, Anat AU - Gafter-Gvili A LA - eng PT - Journal Article PT - Meta-Analysis PT - Review PT - Systematic Review DEP - 20120220 PL - England TA - Eur J Heart Fail JT - European journal of heart failure JID - 100887595 RN - 0 (Iron, Dietary) RN - 0 (Peptide Fragments) RN - 0 (pro-brain natriuretic peptide (1-76)) RN - 114471-18-0 (Natriuretic Peptide, Brain) RN - 9007-41-4 (C-Reactive Protein) SB - IM MH - Anemia, Iron-Deficiency/*drug therapy MH - C-Reactive Protein MH - Chi-Square Distribution MH - Confidence Intervals MH - *Dietary Supplements MH - Exercise Tolerance MH - Health Status Indicators MH - Heart Failure/*drug therapy/psychology MH - Humans MH - Infusions, Intravenous MH - Iron, Dietary/administration & dosage/adverse effects/*therapeutic use MH - Natriuretic Peptide, Brain/blood MH - Peptide Fragments/blood MH - Quality of Life/psychology MH - Surveys and Questionnaires EDAT- 2012/02/22 06:00 MHDA- 2012/07/21 06:00 CRDT- 2012/02/22 06:00 PHST- 2012/02/22 06:00 [entrez] PHST- 2012/02/22 06:00 [pubmed] PHST- 2012/07/21 06:00 [medline] AID - hfs017 [pii] AID - 10.1093/eurjhf/hfs017 [doi] PST - ppublish SO - Eur J Heart Fail. 2012 Apr;14(4):423-9. doi: 10.1093/eurjhf/hfs017. Epub 2012 Feb 20.