Skip Navigation

Nephrology Dialysis Transplantation 2005 20(Supplement 6):vi10-vi15; doi:10.1093/ndt/gfh1098
This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (5)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Besarab, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Besarab, A.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author [2005]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please email: journals.permissions@oupjournals.org

Optimizing anaemia management with subcutaneous administration of epoetin

Anatole Besarab

Division of Nephrology and Hypertension, Henry Ford Hospital, Detroit, MI, USA

Correspondence and offprint requests to: Dr Anatole Besarab, Division of Nephrology and Hypertension, Henry Ford Hospital, CFP-511, 2799 West Grand Boulevard, Detroit, MI 48201, USA. Email: abesarab{at}ghsrenal.com

European and US guidelines for renal anaemia management recommend subcutaneous (s.c.) epoetin as the preferred route of administration in pre-dialysis, peritoneal dialysis and haemodialysis patients. However, the restriction of Eprex®/Erypro® to intravenous (i.v.) administration in Europe has increased the interest of health care professionals regarding the optimal route of administration for all epoetin formulations. There are five major considerations for the ‘optimal’ route of epoetin administration: efficacy; dosing frequency; convenience; safety and tolerability; and cost. Although epoetin bioavailability is lower after s.c. administration, its efficacy is higher, owing to its prolonged elimination half-life compared with i.v. epoetin. Several studies and clinical surveys comparing s.c. and i.v. administration have demonstrated that equivalent target haemoglobin levels can be maintained at much lower doses of epoetin when administered s.c. Furthermore, s.c. epoetin dosing frequency can be reduced in some patients to once every 2 weeks, without compromising efficacy. Devices such as the Reco-Pen® have been specifically designed to facilitate self-administration of s.c. epoetin-ß. An upsurge in the incidence of pure red cell aplasia (PRCA) was linked to the epoetin-{alpha} product Eprex/Erypo in Europe, and an increase in PRCA cases of the same magnitude was not seen in patients taking other epoetin products s.c. Therefore, PRCA should not be used as an argument against s.c. administration. The reduced dose with s.c. administration of epoetin-ß provides significant cost benefits, without compromising either safety or efficacy, and may also increase patient satisfaction and compliance with treatment.

Keywords: anaemia management; cost-effectiveness; dose; epoetin, safety and tolerability; subcutaneous administration


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
The Annals of PharmacotherapyHome page
S. Bacchus, N. O'Mara, H. Manley, and S. Fishbane
Meeting New Challenges in the Management of Anemia of Chronic Kidney Disease Through Collaborative Care with Pharmacists
Ann. Pharmacother., November 1, 2009; 43(11): 1857 - 1866.
[Abstract] [Full Text] [PDF]


Home page
Am J Health Syst PharmHome page
T. C. Dowling
Prevalence, etiology, and consequences of anemia and clinical and economic benefits of anemia correction in patients with chronic kidney disease: An overview
Am. J. Health Syst. Pharm., July 1, 2007; 64(13_Supplement_8): S3 - S7.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.