Anemia Management: Erythropoietic Agents

Erythropoiesis-stimulating agent administration and survival after severe traumatic brain injury: a prospective study.

Article date: 
Thursday, March 1, 2012

 

Abstract

OBJECTIVE:

To validate previous findings of the effects of erythropoiesis-stimulating agent (ESA) administration following severe traumatic brain injury.

DESIGN:

Prospective observational study of all patients with severe traumatic brain injury admitted to the surgical intensive care unit (SICU) at our institution from January 1, 2009, to December 31, 2010 (head Abbreviated Injury Scale score ≥3). Propensity scores were calculated to match patients who received ESA within 30 days after admission to patients who did not receive ESA.

Outcomes of erythropoiesis-stimulating agents in cancer patients with chemotherapy-induced anemia.

Article date: 
Sunday, January 1, 2012

 

Abstract

PURPOSE:

To assess the clinical and economic outcomes among patients with chemotherapy-induced anemia (CIA) treated with United States Food and Drug Administration-approved fixed dosing regimens of erythropoiesis-stimulating agents (ESA).

METHODS:

Effectiveness of darbepoetin-alfa in combination with intravenous iron sucrose in patients with inflammatory bowel disease and refractory anaemia: a pilot study.

Article date: 
Saturday, April 1, 2006

Summary While several studies have evaluated recombinant human erythropoietin (EPO) in the treatment of refractory anemia in inflammatory bowel disease (IBD) this is the first treatment study to determine the effectiveness of the longer half-life agent darbepoetin-alpha (DPO). In a single center, open label, single arm study the investigators recruited 20 patients with confirmed IBD and who had anemia (Hb <10 g/dL for females and <11 g/dL in males) refractory to intravenous (IV) iron therapy.

Does the use of erythropoietin reduce the risk of exposure to allogeneic blood transfusion in cardiac surgery? A systematic review and meta-analysis.

Article date: 
Monday, May 1, 2006

Summary Alghamdi and colleagues conducted what they believe to be the largest systematic review to date to investigate the effectiveness of preoperative erythropoietin (EPO) in reducing allogeneic blood transfusion exposure in patients undergoing cardiac surgery. The primary outcome measure was the number of patients transfused with allogeneic blood during the hospital stay.

Recombinant human erythropoietins and cancer patients: updated meta-analysis of 57 studies including 9353 patients.

Article date: 
Friday, March 17, 2006

Summary This systematic review of 57 trials (involving 9,353 cancer patients) published between January 1985 and April 2005 updates an earlier review covering the period between January 1985 and December 2001 (Bohlius et al).

Iron and the anaemia of chronic disease: a review and strategic recommendations.

Article date: 
Saturday, April 1, 2006

Summary This panel of international experts report on the broad impact of anemia on patients and the community. They refer to a WHO estimate that over 30% of the world’s population are anemic and 66-80% may be iron deficient.

Perioperative intravenous iron, with or without erythropoietin, plus restrictive transfusion protocol reduce the need for allogeneic blood after knee replacement surgery.

Article date: 
Saturday, July 1, 2006

Summary Garcia-Erce and colleagues have previously reported on a blood saving protocol utilizing perioperative intravenous (IV) iron and recombinant human erythropoietin (rHuEPO) in patients undergoing surgery for hip fracture (Carcia-Erce JA, et al).

Efficacy of recombinant human erythropoietin in critically ill patients admitted to a long-term acute care facility: a randomized, double-blind, placebo-controlled trial.

Article date: 
Friday, September 1, 2006

Summary This multicenter randomized controlled trial investigated the use of recombinant human erythropoietin (rHuEPO) in patients who, following their acute critical illness, are discharged from the intensive care unit (ICU) and, because of their chronic critical illness, are admitted to a long-term acute care facility (LTAC).

Double-blind, placebo-controlled study of quality of life, hematologic end points, and safety of weekly epoetin alfa in children with cancer receiving myelosuppressive chemotherapy.

Article date: 
Tuesday, August 1, 2006

Summary This multicenter (n=27) randomized, double-blind, placebo-controlled trial enrolled children with cancer (solid tumors, Hodgkin’s disease, acute lymphoblastic leukemia or non-Hodgkin’s lymphoma) and who were anemic and receiving myelosuppressive chemotherapy. The trial’s objective was to assess the effects of a once-weekly dose of epoetin alfa (EPO) on health-related quality of life (HRQOL), hemoglobin (Hb) levels and red blood cell (RBC) transfusions in this group of patients. Outcome measures also included adverse events.

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