Recombinant erythropoietin in clinical practice
- 1Phase One Clinical Trials Unit Ltd, Plymouth, UK
- 2Sydney Haematology Oncology Clinic, Hornsby, New South Wales, Australia
- 3Department of Haematology, John Radcliff Hospital, Oxford, UK
- 4Department of Renal Medicine, King’s College Hospital (Dulwich), London, UK
- Correspondence to: Dr Thomas Ng, Phase One Clinical Trials Unit Ltd, 119 Looseleigh Lane, Derriford, Plymouth PL6 5HH, UK; tsfng{at}hotmail.com
- Received 5 March 2002
- Accepted 31 December 2002
Abstract
The introduction of recombinant human erythropoietin (RHuEPO) has revolutionised the treatment of patients with anaemia of chronic renal disease. Clinical studies have demonstrated that RHuEPO is also useful in various non-uraemic conditions including haematological and oncological disorders, prematurity, HIV infection, and perioperative therapies. Besides highlighting both the historical and functional aspects of RHuEPO, this review discusses the applications of RHuEPO in clinical practice and the potential problems of RHuEPO treatment.
- G-CSF, granulocyte colony-stimulating factor
- NESP, novel erythropoiesis stimulating protein
- PRCA, pure red cell aplasia
- RBCs, red blood cells
- RHuEPO, recombinant human erythropoietin Please note that packed cell volume is used in the text
- this is equivalent to haematocrit







