[A new treatment of deep venous thrombosis: low molecular weight heparin fractions. Randomized study]. 1988

R Faivre, and Y Neuhart, and Y Kieffer, and F Apfel, and D Magnin, and D Didier, and F Toulemonde, and J P Bassand, and J P Maurat
Service de Cardiologie, CHU St-Jacques, Besançon.

Sixty-eight patients with acute deep vein thrombosis were allocated at random to two treatment groups. One group (n = 33) received a fixed dose of 750 anti-Xa units of a low molecular weight heparin (CY 222 Choay Institute); the other group (n = 35) received standard heparin in doses of 500 IU/kg/24 h. Both treatments were given for 10 days in two daily subcutaneous injections. A second phlebography was performed on the last day of treatment. No haemorrhagic complication was observed in the group treated with CY 222, as opposed to three cases of haemorrhage in the group treated with standard heparin. The initial phlebographic score and the location of deep vein thrombotic lesions were the same in both groups. Angiographic improvement, with more than 30% thrombolysis, was obtained at the end of treatment in 64% of patients in the CY 222 group and in 65% of patients in the standard heparin group (NS). In 2 patients treated with standard heparin the second phlebography showed extension of the thrombosis. The initial score remained unchanged in 1/3 of patients in both groups. The activated partial thromboplastin time was prolonged (2 or 3 fold the normal value) in the standard heparin group and unchanged in the CY 222 group. Anti-Xa activity was significantly higher in the CY 222 group than in the standard heparin group. It is concluded that CY 222 and standard heparin were equally effective in patients with deep vein thrombosis. However, haemorrhagic complications were more frequent with standard heparin that with CY 222.

UI MeSH Term Description Entries
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D008970 Molecular Weight The sum of the weight of all the atoms in a molecule. Molecular Weights,Weight, Molecular,Weights, Molecular
D010690 Phlebography Radiographic visualization or recording of a vein after the injection of contrast medium. Venography,Phlebographies,Venographies
D011655 Pulmonary Embolism Blocking of the PULMONARY ARTERY or one of its branches by an EMBOLUS. Pulmonary Thromboembolism,Thromboembolism, Pulmonary,Embolism, Pulmonary,Embolisms, Pulmonary,Pulmonary Embolisms,Pulmonary Thromboembolisms,Thromboembolisms, Pulmonary
D011897 Random Allocation A process involving chance used in therapeutic trials or other research endeavor for allocating experimental subjects, human or animal, between treatment and control groups, or among treatment groups. It may also apply to experiments on inanimate objects. Randomization,Allocation, Random
D004341 Drug Evaluation Any process by which toxicity, metabolism, absorption, elimination, preferred route of administration, safe dosage range, etc., for a drug or group of drugs is determined through clinical assessment in humans or veterinary animals. Evaluation Studies, Drug,Drug Evaluation Studies,Drug Evaluation Study,Drug Evaluations,Evaluation Study, Drug,Evaluation, Drug,Evaluations, Drug,Studies, Drug Evaluation,Study, Drug Evaluation
D005260 Female Females
D005342 Fibrinolysis The natural enzymatic dissolution of FIBRIN. Fibrinolyses
D006493 Heparin A highly acidic mucopolysaccharide formed of equal parts of sulfated D-glucosamine and D-glucuronic acid with sulfaminic bridges. The molecular weight ranges from six to twenty thousand. Heparin occurs in and is obtained from liver, lung, mast cells, etc., of vertebrates. Its function is unknown, but it is used to prevent blood clotting in vivo and vitro, in the form of many different salts. Heparinic Acid,alpha-Heparin,Heparin Sodium,Liquaemin,Sodium Heparin,Unfractionated Heparin,Heparin, Sodium,Heparin, Unfractionated,alpha Heparin

Related Publications

R Faivre, and Y Neuhart, and Y Kieffer, and F Apfel, and D Magnin, and D Didier, and F Toulemonde, and J P Bassand, and J P Maurat
May 1988, Therapie,
R Faivre, and Y Neuhart, and Y Kieffer, and F Apfel, and D Magnin, and D Didier, and F Toulemonde, and J P Bassand, and J P Maurat
September 1999, The Journal of family practice,
R Faivre, and Y Neuhart, and Y Kieffer, and F Apfel, and D Magnin, and D Didier, and F Toulemonde, and J P Bassand, and J P Maurat
October 1998, The Western journal of medicine,
R Faivre, and Y Neuhart, and Y Kieffer, and F Apfel, and D Magnin, and D Didier, and F Toulemonde, and J P Bassand, and J P Maurat
November 1991, Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke,
R Faivre, and Y Neuhart, and Y Kieffer, and F Apfel, and D Magnin, and D Didier, and F Toulemonde, and J P Bassand, and J P Maurat
January 1995, Revue medicale de Bruxelles,
R Faivre, and Y Neuhart, and Y Kieffer, and F Apfel, and D Magnin, and D Didier, and F Toulemonde, and J P Bassand, and J P Maurat
November 1988, Lancet (London, England),
R Faivre, and Y Neuhart, and Y Kieffer, and F Apfel, and D Magnin, and D Didier, and F Toulemonde, and J P Bassand, and J P Maurat
April 2002, Thrombosis research,
R Faivre, and Y Neuhart, and Y Kieffer, and F Apfel, and D Magnin, and D Didier, and F Toulemonde, and J P Bassand, and J P Maurat
August 1996, The New England journal of medicine,
R Faivre, and Y Neuhart, and Y Kieffer, and F Apfel, and D Magnin, and D Didier, and F Toulemonde, and J P Bassand, and J P Maurat
August 1996, The New England journal of medicine,
R Faivre, and Y Neuhart, and Y Kieffer, and F Apfel, and D Magnin, and D Didier, and F Toulemonde, and J P Bassand, and J P Maurat
December 1999, Managed care (Langhorne, Pa.),
Copied contents to your clipboard!