Literature DB >> 9042557

Comparison of the efficacy and safety of low molecular weight heparins and unfractionated heparin in the initial treatment of deep venous thrombosis. An updated meta-analysis.

A Leizorovicz1.   

Abstract

The aim of this study was to determine whether treatment with low molecular weight heparin (LMWH) reduces the incidence of recurrent thromboembolic events, death, haemorrhages, and extension of thrombus more than treatment with unfractionated heparin (UFH) in patients with established deep vein thrombosis (DVT). The study design was an updated meta-analysis of results from 20 randomised controlled clinical studies comparing LMWH with UFH. The main outcomes measured included i) the incidence of thromboembolic events (DVT and/or pulmonary embolism): ii) the incidence of major haemorrhages; iii) total mortality; and iv) extension of thrombus. Statistically significant reductions in favour of LMWH were observed for mortality [common odds ratio (OR) 0.70, 95% confidence interval (CI) 0.50 to 0.98; p = 0.035]. major haemorrhage (common OR 0.59, 95% CI 0.35 to 0.98; p = 0.042) and thrombus extension (common OR 0.65, 95% CI 0.44 to 0.96; p = 0.03). A nonsignificant trend, also in favour of LMWH, was observed for the recurrence of venous thromboembolic events (common OR 0.77, 95% CI 0.55 to 1.08; p = 0.13). The results from the meta-analysis showed that LMWHs seem to have a higher benefit/risk ratio than UFH in the treatment of venous thrombosis.

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Year:  1996        PMID: 9042557     DOI: 10.2165/00003495-199600527-00006

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  19 in total

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Authors:  D W BARRITT; S C JORDAN
Journal:  Lancet       Date:  1960-06-18       Impact factor: 79.321

2.  Treatment of acute venous thromboembolism with low molecular weight heparin (Fragmin). Results of a double-blind randomized study.

Authors:  J Albada; H K Nieuwenhuis; J J Sixma
Journal:  Circulation       Date:  1989-10       Impact factor: 29.690

3.  [A new treatment of deep venous thrombosis: low molecular weight heparin fractions. Randomized study].

Authors:  R Faivre; Y Neuhart; Y Kieffer; F Apfel; D Magnin; D Didier; F Toulemonde; J P Bassand; J P Maurat
Journal:  Presse Med       Date:  1988-02-13       Impact factor: 1.228

4.  Deep vein thrombosis of the legs: new therapy by means of low molecular weight heparins.

Authors:  M Zanghi'; V Morici; M Costanzo; L Astuto; G Salanitri
Journal:  J Int Med Res       Date:  1988 Nov-Dec       Impact factor: 1.671

5.  [Treatment of deep venous thrombosis. Comparative study of a low molecular weight heparin fragment (Fragmin) by the subcutaneous route and standard heparin by the continuous intravenous route. A multicenter study].

Authors:  M Aiach; J N Fiessinger; J F Vitoux; A Derlon; G Grollier; A Le Querrec; M Gouault-Heilmann; Y Huet; A Franco; B Polack; P Pouzol; A Dubois; J F Schved; B Boneu; J Guittard; P Sie; J J Heilmann; A Kher; I Haye
Journal:  Rev Med Interne       Date:  1989 Jul-Aug       Impact factor: 0.728

6.  Comparison of efficacy and safety of low molecular weight heparins and unfractionated heparin in initial treatment of deep venous thrombosis: a meta-analysis.

Authors:  A Leizorovicz; G Simonneau; H Decousus; J P Boissel
Journal:  BMJ       Date:  1994-07-30

7.  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

8.  A comparison of low-molecular-weight heparin administered primarily at home with unfractionated heparin administered in the hospital for proximal deep-vein thrombosis.

Authors:  M Levine; M Gent; J Hirsh; J Leclerc; D Anderson; J Weitz; J Ginsberg; A G Turpie; C Demers; M Kovacs
Journal:  N Engl J Med       Date:  1996-03-14       Impact factor: 91.245

9.  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

10.  Therapeutic application of subcutaneous low-molecular-weight heparin in acute venous thrombosis.

Authors:  J Harenberg; K Huck; H Bratsch; G Stehle; C E Dempfle; K Mall; M Blauth; K H Usadel; D L Heene
Journal:  Haemostasis       Date:  1990
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  5 in total

1.  Delivery of low molecular weight heparin for prophylaxis against deep vein thrombosis using a novel, needle-less injection device (J-Tip).

Authors:  S J Hollingsworth; K Hoque; D Linnard; D G Corry; S G Barker
Journal:  Ann R Coll Surg Engl       Date:  2000-11       Impact factor: 1.891

Review 2.  Safety profile of different low-molecular weight heparins used at therapeutic dose.

Authors:  Isabelle Gouin-Thibault; Eric Pautas; Virginie Siguret
Journal:  Drug Saf       Date:  2005       Impact factor: 5.606

3.  Enoxaparin: a pharmacoeconomic review of its use in the prevention and treatment of venous thromboembolism and in acute coronary syndromes.

Authors:  David Bergqvist
Journal:  Pharmacoeconomics       Date:  2002       Impact factor: 4.981

Review 4.  Enoxaparin. A review of its clinical potential in the management of coronary artery disease.

Authors:  S Noble; C M Spencer
Journal:  Drugs       Date:  1998-08       Impact factor: 9.546

5.  Gigantic retroperitoneal hematoma as a complication of anticoagulation therapy with heparin in therapeutic doses: a case report.

Authors:  Stavros I Daliakopoulos; Andreas Bairaktaris; Dimitrios Papadimitriou; Perikles Pappas
Journal:  J Med Case Rep       Date:  2008-05-17
  5 in total

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