Erythropoietin-receptor agonists in critically ill patients: a meta-analysis of randomized controlled trials

Ryan Zarychanski, MD, Alexis F. Turgeon, MD MSc, Lauralyn McIntyre, MD MHSc and Dean A. Fergusson, MHA PhD

From the Department of Epidemiology and Community Medicine (Zarychanski, McInytre, Fergusson), University of Ottawa; the Ottawa Health Research Institute (Zarychanski, McIntyre, Fergusson), The Ottawa Hospital, Ottawa, Ont.; and the Centre Hospitalier Affilié Universitaire de Québec Research Center, the Department of Anesthesia and the Division of Critical Care Medicine (Turgeon), Laval University, Québec City, Que.
Correspondence to: Dr. Ryan Zarychanski, Ottawa Health Research Institute, 501 Smyth Rd., Ottawa ON K1H 8L6; ryan@zarychanski.com


Introduction: Anemia and the need for red blood cell transfusions are common among patients admitted to intensive care units. Erythropoietin has been used to decrease the need for transfusions; however, its ability to improve clinical outcomes is unknown. We evaluated the effect of erythropoietin-receptor agonists on clinically important outcomes, including mortality, length of stay in hospital or intensive care unit, ventilator use, transfusion requirements and major adverse events.
Methods: To identify relevant studies, we searched electronic databases covering 1950 to 2007 (MEDLINE, EMBASE, the Cochrane Central Register of Controlled Trials and the Scopus database). We also searched conference proceedings and grey literature sources. We selected all randomized controlled trials involving critically ill patients that compared an erythropoietin-receptor agonist with a placebo or no intervention. No language restrictions were considered. Data were extracted using a standardized extraction template. We used a fixed effects model to calculate all summary measures of treatment effects.
Results: Of 673 identified records, 9 studies that investigated erythropoietin alpha met the eligibility criteria and were included in our analysis. Erythropoietin, compared with placebo or no intervention, had no statistically significant effect on overall mortality (odds ratio [OR] 0.86, 95% confidence interval [CI] 0.71–1.05, I2 = 0%). The treatment and control groups did not differ in the length of stay in hospital or intensive care unit, or in the duration of mechanical ventilation, in the 3 studies that reported these outcomes. Erythropoietin, compared with placebo, significantly reduced the odds of a patient receiving at least 1 transfusion (OR 0.73, 95% CI 0.64–0.84, I2 = 54.7%). The mean number of units of blood transfused per patient was decreased by 0.41 units in the erythropoietin group (95% CI 0.10–0.74, I2 = 79.2%). Most of the included studies were performed before the widespread adoption of a restrictive transfusion strategy. Only 1 study provided detailed reports of adverse events, and none of the studies systematically evaluated all patients for venous thromboembolism.
Interpretation: At this time, we do not recommend the routine use of erythropoietin-receptor agonists in critically ill patients. The reduction in red blood cell transfusions per patient was very small, and there is insufficient evidence to determine whether this intervention results in clinically important benefits with acceptable risks.