Erythropoietin treatment in patients with chronic heart failure: a meta-analysis.


Journal Article (Review)

BACKGROUND: Anaemia is common in patients with chronic heart failure (HF), and erythropoiesis stimulating proteins (ESPs) are frequently used for its treatment. However, recent studies in patients with malignancies and renal failure have raised concerns about the safety of these agents. OBJECTIVE: To determine whether treatment of anaemic patients with chronic HF with ESPs is associated with an effect on morbidity and mortality. DATA SOURCES: A systematic literature search in Medline, the Cochrane Controlled Trials Register Database and through July 2008 was performed. STUDY SELECTION: Randomised clinical trials comparing the effect of ESP treatment with placebo or usual care in anaemic patients with HF were included. RESULTS: Seven randomised controlled trials were identified that enrolled 650 patients, of whom 363 were treated with ESPs and 287 with placebo. ESP treatment had a significantly lower risk of HF hospitalisation (risk ratio (RR) = 0.59; 95% CI 0.41 to 0.86; p = 0.006).There was no significant difference in the mortality risk between the two groups (RR = 0.69; 95% CI 0.39 to 1.23; p = 0.21). No significant differences were observed in the occurrence of hypertension or venous thrombosis. CONCLUSIONS: In chronic HF, treatment with ESPs is not associated with a higher mortality rate or more adverse events, whereas a beneficial effect on HF hospitalisation is seen. These outcomes are in contrast with studies in cancer and kidney disease, and support a large phase III morbidity and mortality trial of anaemia correction in patients with chronic HF.

Full Text

Duke Authors

Cited Authors

  • van der Meer, P; Groenveld, HF; Januzzi, JL; van Veldhuisen, DJ

Published Date

  • August 2009

Published In

Volume / Issue

  • 95 / 16

Start / End Page

  • 1309 - 1314

PubMed ID

  • 19168472

Pubmed Central ID

  • 19168472

Electronic International Standard Serial Number (EISSN)

  • 1468-201X

Digital Object Identifier (DOI)

  • 10.1136/hrt.2008.161091


  • eng

Conference Location

  • England