Literature DB >> 9396637

Successors to heparin: new antithrombotic agents.

A G Turpie1.   

Abstract

New advances in antithrombotic therapy include low-molecular weight heparins (LMWHs), heparinoids, and direct thrombin inhibitors. LMWHs and heparinoids have improved pharmacologic and pharmacokinetic properties compared with standard, unfractionated heparin. LMWHs are effective in preventing venous thromboembolism in general surgical patients, orthopedic patients, and general medical patients. At equipotent antithrombotic doses, LMWHs produce less bleeding than does unfractionated heparin. When given in fixed doses subcutaneously in the treatment of venous thromboembolic disease, LMWHs have been shown to be as effective as or more effective than and safer than standard heparin given intravenously with regular monitoring. Recent studies have demonstrated that LMWHs are effective in reducing the risk of death and myocardial infarction in patients with unstable angina; they are as effective as intravenous heparin when given subcutaneously without monitoring. Preliminary data indicate that LMWHs also may be effective in improving outcomes in patients with ischemic stroke. The pharmacokinetic characteristics of LMWHs permit their use in a fixed dose administered subcutaneously without monitoring, resulting in greater clinical utility than standard heparin. The direct thrombin inhibitors have a narrow safety window, and in doses that do not produce excessive bleeding have not been shown to have greater efficacy than that of unfractionated heparin.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9396637

Source DB:  PubMed          Journal:  Am Heart J        ISSN: 0002-8703            Impact factor:   4.749


  4 in total

Review 1.  A guide to drug use during percutaneous coronary intervention.

Authors:  Joseph K Choo; John J Young; Dean J Kereiakes
Journal:  Drugs       Date:  2002       Impact factor: 9.546

2.  Serine base exchange enzyme in porcine lyophilised platelets: enzyme properties and modulation by AlF4- and different types of heparin.

Authors:  S Buratta; V Andreoli; R Mambrini; A Iorio; S Porcellati; R Mozzi
Journal:  Mol Cell Biochem       Date:  2000-01       Impact factor: 3.396

3.  Routine plasma anti-Xa monitoring is required for low-molecular-weight heparins.

Authors:  Hesham S Al-Sallami; Michael A Barras; Bruce Green; Stephen B Duffull
Journal:  Clin Pharmacokinet       Date:  2010-09       Impact factor: 6.447

Review 4.  Heparin dose during percutaneous coronary intervention: how low dare we go?

Authors:  G Niccoli; A P Banning
Journal:  Heart       Date:  2002-10       Impact factor: 5.994

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.