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INTRAVENOUS ADMINISTRATION OF EPOETIN IN HAEMODIALYSIS PATIENTS
Author(s) -
Vos JeanYves,
Upsing Louise
Publication year - 2003
Publication title -
edtna‐erca journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.381
H-Index - 27
eISSN - 1755-6686
pISSN - 1019-083X
DOI - 10.1111/j.1755-6686.2003.tb00299.x
Subject(s) - medicine , erythropoietin , epoetin alfa , route of administration , intravenous iron , dialysis , administration (probate law) , dosing , anesthesia , intensive care medicine , surgery , anemia , iron deficiency , political science , law
SUMMARY Recombinant human erythropoietin (epoetin, rHuEPO) can be administered to haemodialysis patients intravenously or subcutaneously. Although the intravenous route is the originally approved and used route of administration, subcutaneous administration has been quite common throughout Europe since the introduction of prefilled syringes. The intravenous route has been shown to be as effective as the subcutaneous route, but patients should have adequate iron stores. In addition, intravenous administration is patient‐friendly and results in fewer injections, less pain and bruising, and a minimised risk of immunogenicity. Furthermore, intravenous administration of epoetin is convenient for the nurse and is commonly used in Germany, Belgium and the USA. The purpose of this paper is to illustrate the very easy, practical ways of administering epoetin in prefilled syringes during dialysis at machine level, based on the authors' experiences in Belgium and Germany.