Skip Navigation


NDT Advance Access originally published online on July 19, 2005
Nephrology Dialysis Transplantation 2005 20(10):2036-2042; doi:10.1093/ndt/gfi004
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
20/10/2036    most recent
gfi004v1
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 (7)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Hetzel, G. R.
Right arrow Articles by Sucker, C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hetzel, G. R.
Right arrow Articles by Sucker, C.
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


Editorial Review

The heparins: all a nephrologist should know

Gerd R. Hetzel1 and Christoph Sucker2

1 Department of Nephrology and 2 Department of Hemostasis and Transfusion Medicine, Heinrich Heine University Medical Center, Duesseldorf, Germany

Correspondence and offprint requests to: PD Dr med. Gerd Rüdiger Hetzel, Department of Nephrology, University Medical Center, Moorenstrasse 5, D-40225 Düsseldorf, Germany. Email: hetzel@med.uni-duesseldorf.de

The first 150 words of the full text of this article appear below.



   Introduction
 
For decades, the use of unfractionated heparin (UFH) has been the basic principle of anticoagulation in patients at risk of or with established thromboembolic disorders. Nowadays, low molecular weight heparins (LMWHs) are increasingly used in this setting, because they are as effective but more convenient than UFH. The advantages of LMWHs include a longer elimination half-life, a lower incidence of heparin-induced thrombocytopenia type II (HIT-II), a lower risk of osteopenia and a more predictable anticoagulant effect that reduces the need for routine laboratory monitoring. Major clinical trials have demonstrated superior therapeutic efficacy in patients with acute coronary syndrome or venous thromboembolism compared with UFH [1–3]. However, most trials excluded subjects at risk for unpredictable pharmacokinetics such as the severely obese, the very elderly and patients suffering from chronic kidney disease stage IV and V. In renal failure, the elimination half-life of all LMWHs is significantly prolonged. Thus, severe . . . [Full Text of this Article]



   Chemical structure and mechanism of action
 


   Pharmacokinetics
 


   Clinical use of heparins in patients with renal failure
 


   The problem of HIT-II
 


   Conclusion
 

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
Nephrol Dial TransplantHome page
B. Naumnik, J. Borawski, K. Pawlak, and M. Mysliwiec
Enoxaparin but not unfractionated heparin causes a dose-dependent increase in plasma TGF-{beta}1 during haemodialysis: a cross-over study
Nephrol. Dial. Transplant., June 1, 2007; 22(6): 1690 - 1696.
[Abstract] [Full Text] [PDF]