Clinical Chemistry
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Clinical Chemistry 55: 709-711, 2009. First published January 30, 2009; 10.1373/clinchem.2008.115964
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
clinchem.2008.115964v1
55/4/709    most recent
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 PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Wadelius, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wadelius, M.
(Clinical Chemistry. 2009;55:709-711.)
© 2009 American Association for Clinical Chemistry, Inc.


Point/Counterpoint

Point: Use of Pharmacogenetics in Guiding Treatment with Warfarin

Mia Wadelius1,a

1 Department of Medical Sciences, Clinical Pharmacology, Uppsala University Hospital, Uppsala, Sweden.

aAddress correspondence to the author at: Clinical Pharmacology, Uppsala University Hospital, Entrance 61, 3rd Floor, Uppsala, NA, Sweden SE-75185. Fax +46-18-6113703; e-mail mia.wadelius@medsci.uu.se.

The first 20% of the full text of this article appears below.

Warfarin is the most widely used oral anticoagulant for the treatment of thromboembolic disorders and for stroke prophylaxis. Warfarin is a problematic drug because it exhibits large interindividual variation in the required therapeutic dose, has a narrow therapeutic range, and shows multiple food and drug interactions. Its anticoagulant effect is monitored by measuring the international normalized ratio (INR), which is a function of the time required for a patient’s blood to coagulate relative to the time it takes for a reference blood sample. Although warfarin has been used in humans for more than 50 years, its main side effect—bleeding—is a leading cause of hospital admission and drug-related death(1)(2). This problem has made patients and clinicians yearn for a new efficient and safe oral anticoagulant drug that does not require frequent monitoring. In Europe, a new oral anticoagulant drug (dabigatran) claimed to have these qualities has been licensed for short-term primary prevention of venous thromboembolic events, but its effectiveness in long-term secondary thromboprophylaxis remains to be shown. Furthermore, the daily cost of dabigatran is 5 times that of warfarin therapy including INR tests. To switch all warfarin patients (currently 1% of the population in many Western countries) to dabigatran would boost . . . [Full Text of this Article]







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2009 by the American Association for Clinical Chemistry.