SummaryIn a prospective multicenter trial, 149 consecutive patients with phlebographically proven proximal and/or distal deep vein thrombosis of the leg were randomly allocated to receive subcutaneously for 10 days either low molecular weight heparin CY 216 (Fraxiparine) in a fixed dose or unfractionated heparin (UFH) in doses adjusted according to the activated partial thromboplastin time. Pre- and post-treatment phlebograms were assessed blindly using the Arnesen’s score system in 134 patients available for analysis of the treatment efficacy. The mean phlebographic score after 10 days of treatment was significantly decreased in both groups (p <0.001) in comparison with the baseline score but the difference in score changes between the two groups was not statistically significant. There was an improvement in 45/ 68 patients (66%) in the Fraxiparine group and in 32/66 patients (48%) in the UFH group, and an increase in the thrombus size in 10/68 (15%) and 12/66 (18%), respectively. One symptomatic non-fatal pulmonary embolism and one major bleeding episode were observed in the UFH group. During a follow-up period of 3 months, two rethromboses had occurred in the UFH group and none in the Fraxiparine group. It is concluded that subcutaneous fixed dose Fraxiparine is safe and at least as effective as subcutaneous adjusted UFH in the treatment of deep vein thrombosis.

varicose veins, especially those complicated with superficial thrombophlebitis revealed increased free radical generation. Its sources might be neutrophils, and in vv complicated with superficial thrombophlebitis-xanthine oxidase.

The walls of human abdominal aortas and atherosclerosis-induced aneurysms contain similar amounts of collagen. The quantitative ratio between collagens of various types of this protein does not differ significantly either, whereas solubility of the collagen in aneurysmal wall and its susceptibility to the action of EDTA are distinctly decreased. In contrast with collagen, the amount of elastin in aneurysms is significantly lower. Total amount of glycosaminoglycans slightly decreased as compared with that of normal tissue, but the ratio of particular compounds varies. The percentage of chondroitin sulphate is increased and that of heparan sulphate significantly decreased. The significance of these changes in pathogenesis of aneurysms is discussed.

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Varicose saphenous vein segments, segments of those veins with thrombophlebitis, and segments of normal veins obtained during operation on 23 patients were studied to define the pattern of pro-oxidative and antioxidative systems in these tissues. In segments of varicose veins (VV) the activity of superoxide dismutase (SOD) was significantly decreased as compared with normal veins: 7.8 ±2.9 vs 13.5 ±4.3 U/mg of protein (P < 0.05), but it was almost unchanged in the segments of W with thrombophlebitis. The activity of glutathione reductase (GSH-R) in all studied segments was similar and amounted to about 12.0 IU. The content of free sulfhydryl (SH) groups, the concentration of ascorbic acid, and thiobarbituric acid-reactive substances (TBA-RS) in segments of VV were significantly decreased by 40%, 48%, and 47%, respectively (P < 0.05) as compared with segments of normal veins. The values of ascorbic acid and TBA-RS in the segments of W with thrombophlebitis were increased by 13% and 16%, respectively, as compared with segments of normal veins. Decreased activities of SOD and reduced levels of free SH-groups and of ascorbic acid concentration in W may indicate impaired antioxidant mechanisms in this tissue.