Abstract
Recombinant human erythropoietin (EPO) therapy has now been approved for use in patients undergoing autologous blood donation (ABD) in Japan, the European Union, and Canada since 1993, 1994, and 1996 respectively, and for perisurgical adjuvant therapy without ABD in Canada and the US since 1966. This paper is intended to provide a framework for clinicians who will have the options of administering EPO therapy to patients undergoing surgery, and to provide a better understanding of its proper use in this setting [1].
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Goodnough, L.T. (1998). Recombinant Human Erythropoietin — could it be used in a Better Way?. In: Sibinga, C.T.S., Das, P.C., Fratantoni, J.C. (eds) Alternative Approaches to Human Blood Resources in Clinical Practice. Developments in Hematology and Immunology, vol 33. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-5619-0_7
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DOI: https://doi.org/10.1007/978-1-4615-5619-0_7
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