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  Vol. 165 No. 7, April 11, 2005 TABLE OF CONTENTS
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Low-Molecular-Weight Heparins

Do We Have the GUSTO to Identify Differences Between Alternative Formulations?

Arch Intern Med. 2005;165:722-723.

Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings.

In this issue of the ARCHIVES, Wells et al1 present data on the first randomized trial of 2 different formulations of low-molecular-weight heparin (LMWH). The question of whether these compounds are interchangeable is important for the treatment of venous thromboembolism as well as for thromboprophylaxis and treatment of acute coronary syndrome.

Low-molecular-weight heparins, first developed about 25 years ago, are a mixture of polysaccharides derived from unfractionated heparin by depolymerization. Each LMWH is prepared by a different depolymerization method—chemical, enzymatic, physical, or radiochemical. The 3 preparations currently approved by the US Food and Drug Administration for use in the United States are enoxaparin sodium, dalteparin sodium, and tinzaparin sodium. Although the molecular weight of unfractionated heparins ranges from 3000 to 30 000 Da, the LMWHs range from 2000 to 9000 Da, with a mean of around 5000 Da.2 Heparin exerts its anticoagulant action by binding to antithrombin. This complex . . . [Full Text of this Article]


AUTHOR INFORMATION
Anaadriana Zakarija, MD; Charles L. Bennett, MD, PhD, MPP


RELATED ARTICLE

A Randomized Trial Comparing 2 Low-Molecular-Weight Heparins for the Outpatient Treatment of Deep Vein Thrombosis and Pulmonary Embolism
Philip S. Wells, David R. Anderson, Marc A. Rodger, Melissa A. Forgie, Peggy Florack, Donna Touchie, Beverly Morrow, Lisa Gray, Keith O’Rourke, George Wells, Judy Kovacs, and Michael J. Kovacs
Arch Intern Med. 2005;165(7):733-738.
ABSTRACT | FULL TEXT  


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Comparison of Two Low-Molecular-Weight Heparins for DVT and PE
JWatch General 2005;2005:2-2.
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