Thromb Haemost 1985; 54(04): 813-817
DOI: 10.1055/s-0038-1660139
Original Article
Schattauer GmbH Stuttgart

A Comparison Between Low Molecular Weight Heparin (KABI 2165) and Standard Heparin in the Intravenous Treatment of Deep Venous Thrombosis

Göran Bratt
The Department of Medicine, Huddinge University Hospital, Huddinge, Sweden
,
Eva Törnebohm
The Department of Medicine, Huddinge University Hospital, Huddinge, Sweden
,
Staffan Granqvist
The Department of Medicine, Huddinge University Hospital, Huddinge, Sweden
,
Wiveca Åberg
The Department of Medicine, Huddinge University Hospital, Huddinge, Sweden
,
Dieter Lockner
The Department of Medicine, Huddinge University Hospital, Huddinge, Sweden
› Author Affiliations
Further Information

Publication History

Received 17 May 1985

Accepted 17 September 1985

Publication Date:
19 July 2018 (online)

Summary

In order to study whether a low molecular weight heparin (LMWH) of mw 4000 D is effective in the treatment of deep venous thrombosis (DVT), patients with DVT verified by phlebography were randomized to treatment by continuous intravenous infusion of either unfractionated heparin (UFH) or LMWH. The initial dose was 240 U (anti F Xa)/kg/12 h. TTiis study (study I) was stopped because of major bleeding in 2 newly operated patients in the LMWH group after 27 patients had been treated. The heparin activity measured as F Xa inhibition assayed in retrospect, was found to be much higher in the LMWH group (mean 1.6-2.0 anti F Xa U/ml) than in the UFH group (mean 0.5-0.8 anti F Xa U/ml).

A second study was therefore initiated in which the DVT patients were randomly given UFH (240 U/kg/12 h) or LMWH only 120 U (anti F Xa)/kg/12 h, as initial doses (study II). In this study 27 patients could be evaluated, the mean heparin activity still being higher in the LMWH group (0.9-1.2 anti F Xa U/ml) than in the UFH group (0.5-0.7 anti F Xa U/ml).

A second phlebographic investigation showed progression of thrombus size in 3 (11%) of the UFH patients of studies I and II (n = 29) and improvement in 14 (48%). There was no progression in any LMWH patient, 6 (50%) had improved in study I and 10 (77%) in study II. The mean decrease of thrombus size score (according to Marder) during treatment did not differ between the 3 groups.

Antithrombin III decreased significantly in the UFH group but not in the LMWH groups. Aminotransferases increased in all 3 groups. There was no difference in mean capillary bleeding time between the 3 treatment groups.

Although this material is relatively small, our findings suggest that LMWH seems to be of similar effectivity as UFH.

 
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