scholarly journals Tissue plasminogen activator (rt-PA) vs heparin in deep vein thrombosis: results of a randomized trial

1991 ◽  
Vol 13 (5) ◽  
pp. 775-776
Author(s):  
Bruce S. Cutler
CHEST Journal ◽  
1990 ◽  
Vol 97 (4) ◽  
pp. 172S-175 ◽  
Author(s):  
A. G. Turpie ◽  
M. N. Levine ◽  
J. Hirsh ◽  
J. S. Ginsberg ◽  
M. Cruickshank ◽  
...  

CHEST Journal ◽  
1990 ◽  
Vol 97 (4) ◽  
pp. 172S-175S ◽  
Author(s):  
Alexander G.G. Turpie ◽  
Mark N. Levine ◽  
Jack Hirsh ◽  
Jeffrey S. Ginsberg ◽  
Moira Cruickshank ◽  
...  

1990 ◽  
Vol 60 (3) ◽  
pp. 247-251 ◽  
Author(s):  
Jens V. Sørensen ◽  
Michael R. Lassen ◽  
Lars C. Borris ◽  
Peter S. Jørgensen ◽  
Peter Schøtt ◽  
...  

1991 ◽  
Vol 66 (04) ◽  
pp. 426-429 ◽  
Author(s):  
Marcel Levi ◽  
Anthonie W A Lensing ◽  
Harry R Büller ◽  
Paolo Prandoni ◽  
Gerard Dooijewaard ◽  
...  

SummaryIn the present study 57 consecutive patients with a first episode of venographically proven deep vein thrombosis were investigated to evaluate the release of tissue-type plasminogen activator (t-PA) and of urokinase-type plasminogen activator (u-PA) in response to DDAVP stimulation as well as the resting plasminogen activator inhibitor (PAI) concentration, comparing this to the results obtained in 66 similar patients with a clinical suspicion of thrombosis but with a normal venogram. All assays were performed without knowledge of the patient's status.Four patients in the deep vein thrombosis-group (7%) had an absent u-PA antigen response upon DDAVP infusion, while a normal response was observed in all control subjects. Patients and controls showed similar increases in t-PA antigen level upon DDAVP. High resting PAI antigen levels were encountered in 5 patients in the deep vein thrombosis-group (9%) and in 6 subjects in the control group (9%).The results from this controlled study indicate that a defective release of u-PA may occur in patients with deep vein thrombosis and may have pathogenetic significance. Furthermore it is concluded that elevation of PAI levels cannot be considered as a specific risk factor for venous thrombosis.


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