Literature DB >> 11096468

Deep Vein Thrombosis.

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Abstract

Initially, patients with deep vein thrombosis (DVT) should be treated with a 5- to 7-day course of heparin or low-molecular-weight heparin (LMWH). They can be administered LMWH as outpatients. Patients with extensive iliofemoral thrombosis, major pulmonary embolism, or concomitant medical illness, and those at high risk for bleeding, should be treated as inpatients. Thrombolytic therapy may be considered for patients with extensive iliofemoral thrombosis if there is no contraindication to the use of thrombolytic drugs. Oral anticoagulants can be started within 24 hours of the initiation of heparin or LMWH. Warfarin is started at a dose of 5 mg, and subsequent doses are given in amounts sufficient to achieve an international normalized ratio of 2.0 to 3.0. Inferior vena caval filters should be considered for patients with overt bleeding or for those at high risk for hemorrhage. Warfarin can be used for secondary prophylaxis in most patients. Patients in whom there are contraindications to the use of oral anticoagulants and patients in whom recurrent venous thromboembolism (VTE) develops while they are receiving therapeutic doses of warfarin can be safely and effectively treated with LMWH. Patients with idiopathic DVT should be treated with anticoagulants for at least 6 months. Those with calf DVT or proximal DVT that complicates surgery or medical illness can be treated with anticoagulants for 6 weeks and 3 months, respectively, provided that there are no ongoing risk factors for recurrent VTE. Oral anticoagulants are teratogenic and should be avoided by patients who are pregnant; unfractionated heparin or LMWH are safe alternatives. Unfractionated heparin, LMWH, and oral anticoagulants can be safely administered to nursing mothers.

Entities:  

Year:  1999        PMID: 11096468     DOI: 10.1007/s11936-999-0006-8

Source DB:  PubMed          Journal:  Curr Treat Options Cardiovasc Med        ISSN: 1092-8464


  46 in total

Review 1.  Heparin-induced thrombocytopenia: towards consensus.

Authors:  T E Warkentin; B H Chong; A Greinacher
Journal:  Thromb Haemost       Date:  1998-01       Impact factor: 5.249

2.  A prospective study of the value of monitoring heparin treatment with the activated partial thromboplastin time.

Authors:  D Basu; A Gallus; J Hirsh; J Cade
Journal:  N Engl J Med       Date:  1972-08-17       Impact factor: 91.245

Review 3.  Hemorrhagic complications of thrombolytic therapy in the treatment of myocardial infarction and venous thromboembolism.

Authors:  M N Levine; S Z Goldhaber; J M Gore; J Hirsh; R M Califf
Journal:  Chest       Date:  1995-10       Impact factor: 9.410

4.  Guide to anticoagulant therapy. Part 2: Oral anticoagulants. American Heart Association.

Authors:  J Hirsh; V Fuster
Journal:  Circulation       Date:  1994-03       Impact factor: 29.690

5.  Feasibility study of catheter-directed thrombolysis with recombinant staphylokinase in deep venous thrombosis.

Authors:  S Heymans; R Verhaeghe; L Stockx; D Collen
Journal:  Thromb Haemost       Date:  1998-03       Impact factor: 5.249

Review 6.  Pharmacology of the low-molecular-weight heparins.

Authors:  A G Turpie
Journal:  Am Heart J       Date:  1998-06       Impact factor: 4.749

7.  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

8.  Use of recombinant hirudin as antithrombotic treatment in patients with heparin-induced thrombocytopenia.

Authors:  F Schiele; A Vuillemenot; P Kramarz; Y Kieffer; T Anguenot; Y Bernard; J P Bassand
Journal:  Am J Hematol       Date:  1995-09       Impact factor: 10.047

9.  Trial of different intensities of anticoagulation in patients with prosthetic heart valves.

Authors:  J N Saour; J O Sieck; L A Mamo; A S Gallus
Journal:  N Engl J Med       Date:  1990-02-15       Impact factor: 91.245

10.  Protamine neutralization of intravenous and subcutaneous low-molecular-weight heparin (tinzaparin, Logiparin). An experimental investigation in healthy volunteers.

Authors:  J Holst; B Lindblad; D Bergqvist; K Garre; H Nielsen; U Hedner; P B Ostergaard
Journal:  Blood Coagul Fibrinolysis       Date:  1994-10       Impact factor: 1.276

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