Literature DB >> 10980843

Low molecular weight heparin in acute coronary syndromes.

C P Cannon1.   

Abstract

Traditionally, unfractionated heparin has played an important role in the treatment of acute coronary syndromes. Low molecular weight heparin (LMWH), is a promising new type of heparin, which is fractionated to include only heparin molecules of lower molecular weight. LMWHs are administered subcutaneously and do not require monitoring of the activated partial thromboplastin time, making them much easier to use. LMWHs are combined inhibitors of both thrombin and Factor Xa inhibitors. Several recent large trials in unstable angina and non-Q wave myocardial infarction have shown that LMWH is effective, and one agent has been shown to be superior to unfractionated heparin in reducing death, myocardial infarction, or recurrent angina. They also are very low cost (approximately $50 per day) and appear to be very cost effective in the treatment of unstable angina. Thus, LMWHs appear to be the new anticoagulant agent in acute coronary syndromes.

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Year:  1999        PMID: 10980843     DOI: 10.1007/s11886-999-0024-x

Source DB:  PubMed          Journal:  Curr Cardiol Rep        ISSN: 1523-3782            Impact factor:   2.931


  37 in total

1.  Safety of high doses of low molecular weight heparin (Fragmin) in acute myocardial infarction. A dose-finding study.

Authors:  A Nesvold; F Kontny; U Abildgaard; J Dale
Journal:  Thromb Res       Date:  1991-12-01       Impact factor: 3.944

2.  Prophylaxis of fatal pulmonary embolism in general surgery using low-molecular weight heparin Cy 216: a multicentre, double-blind, randomized, controlled, clinical trial versus placebo (STEP). STEP-Study Group.

Authors:  G Pezzuoli; G G Neri Serneri; P Settembrini; G Coggi; N Olivari; G Buzzetti; S Chierichetti; A Scotti; M Scatigna; M Carnovali
Journal:  Int Surg       Date:  1989 Oct-Dec

3.  Prevention of deep vein thrombosis after elective hip surgery. A randomized trial comparing low molecular weight heparin with standard unfractionated heparin.

Authors:  M N Levine; J Hirsh; M Gent; A G Turpie; J Leclerc; P J Powers; R M Jay; J Neemeh
Journal:  Ann Intern Med       Date:  1991-04-01       Impact factor: 25.391

4.  A randomized controlled trial of a low-molecular-weight heparin (enoxaparin) to prevent deep-vein thrombosis in patients undergoing elective hip surgery.

Authors:  A G Turpie; M N Levine; J Hirsh; C J Carter; R M Jay; P J Powers; M Andrew; R D Hull; M Gent
Journal:  N Engl J Med       Date:  1986-10-09       Impact factor: 91.245

5.  Heparin-induced thrombocytopenia in patients treated with low-molecular-weight heparin or unfractionated heparin.

Authors:  T E Warkentin; M N Levine; J Hirsh; P Horsewood; R S Roberts; M Gent; J G Kelton
Journal:  N Engl J Med       Date:  1995-05-18       Impact factor: 91.245

6.  Aspirin versus heparin to prevent myocardial infarction during the acute phase of unstable angina.

Authors:  P Théroux; D Waters; S Qiu; J McCans; P de Guise; M Juneau
Journal:  Circulation       Date:  1993-11       Impact factor: 29.690

7.  The multiple complexes formed by the interaction of platelet factor 4 with heparin.

Authors:  P E Bock; M Luscombe; S E Marshall; D S Pepper; J J Holbrook
Journal:  Biochem J       Date:  1980-12-01       Impact factor: 3.857

8.  Treatment of venous thrombosis with intravenous unfractionated heparin administered in the hospital as compared with subcutaneous low-molecular-weight heparin administered at home. The Tasman Study Group.

Authors:  M M Koopman; P Prandoni; F Piovella; P A Ockelford; D P Brandjes; J van der Meer; A S Gallus; G Simonneau; C H Chesterman; M H Prins
Journal:  N Engl J Med       Date:  1996-03-14       Impact factor: 91.245

9.  Heparin binding to plasma proteins, an important mechanism for heparin resistance.

Authors:  E Young; M Prins; M N Levine; J Hirsh
Journal:  Thromb Haemost       Date:  1992-06-01       Impact factor: 5.249

10.  Risk of myocardial infarction and death during treatment with low dose aspirin and intravenous heparin in men with unstable coronary artery disease. The RISC Group.

Authors: 
Journal:  Lancet       Date:  1990-10-06       Impact factor: 79.321

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