Circulation, Vol 85, 1380-1389, Copyright © 1992 by American Heart Association
C Thery, G Simonneau, G Meyer, O Helenon, F Bridey, C Armagnac, P d'Azemar and JP Coquart
BACKGROUND. We compared the efficacy and safety of different dosages of a
low-molecular-weight heparin, CY 216 D (Fraxiparine), in the treatment of
submassive pulmonary embolism with unfractionated heparin in a prospective,
randomized, dose-finding study. METHODS AND RESULTS. The primary outcome
was the evolution of pulmonary vascular obstruction. We enrolled 101
patients. Four patient groups were formed: standard heparin by continuous
intravenous infusion (group 1) and Fraxiparine subcutaneously 400, 600, and
900 anti-Xa Institute Choay units/kg, respectively (groups 2, 3, and 4).
Inclusions were stopped prematurely in groups 3 and 4 because of the
incidence of major bleedings. At day 8, the improvement of the pulmonary
vascular obstruction and the major bleedings were similar in groups 1 and
2. CONCLUSIONS. The Fraxiparine dosage of 400 anti-Xa Institute Choay
units/kg is as effective and safe as unfractionated heparin in the
treatment of submassive pulmonary embolism.
ARTICLES
Randomized trial of subcutaneous low-molecular-weight heparin CY 216 (Fraxiparine) compared with intravenous unfractionated heparin in the curative treatment of submassive pulmonary embolism. A dose-ranging study
Hopital Cardiologique, Lille, France.
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