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Thrombolysis in Myocardial Infarction (TIMI) Trial--phase I: hemorrhagic manifestations and changes in plasma fibrinogen and the fibrinolytic system in patients treated with recombinant tissue plasminogen activator and streptokinase
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Authors
Rao, A. KonetiPratt, Craig
Berke, Andrew
Jaffe, Allan
Ockene, Ira S.
Schreiber, Theodore L.
Bell, William R.
Knatterud, Genell L.
Robertson, Thomas L.
Terrin, Michael L.
UMass Chan Affiliations
Department of Medicine, Division of Cardiovascular MedicineDocument Type
Journal ArticlePublication Date
1988-01-01Keywords
Clinical Trials as TopicFibrinogen
*Fibrinolysis
Hemorrhage
Humans
Myocardial Infarction
Random Allocation
Recombinant Proteins
Streptokinase
Thrombocytopenia
Tissue Plasminogen Activator
Amino Acids, Peptides, and Proteins
Cardiology
Cardiovascular Diseases
Enzymes and Coenzymes
Therapeutics
Tissues
Metadata
Show full item recordAbstract
Two hundred ninety patients with acute myocardial infarction were treated according to random assignment with an intravenous infusion of either 80 mg of recombinant tissue plasminogen activator (rt-PA) over 3 h or 1.5 million units of streptokinase over 1 h. Patients received an intravenous bolus of heparin (5,000 U [USP]) before pretreatment coronary angiography and a continuous infusion (1,000 U/h) starting 3 h later. The frequency of major and minor hemorrhagic events (33% rt-PA, 31% streptokinase) and associated transfusions (22% rt-PA, 20% streptokinase) were comparable in both groups. More than 70% of bleeding episodes in each group occurred at catheterization or vascular puncture sites. Precipitable fibrinogen levels, measured in plasma samples collected in the presence of a protease inhibitor (aprotinin), declined in rt-PA and streptokinase groups by averages of 26 and 57% at 3 h and by 33 and 58% at 5 h, respectively (rt-PA versus streptokinase, p less than 0.001). At 5 h the plasma plasminogen declined by 57% (rt-PA) and 82% (streptokinase) (p less than 0.001); plasma fibrin(ogen) degradation products were higher in streptokinase-treated patients (244 +/- 12 micrograms/ml, mean +/- SE) than in rt-PA-treated patients (97 +/- 9 micrograms/ml, p less than 0.001). At 27 h, plasma fibrinogen and plasminogen levels were lower and fibrin(ogen) degradation products higher than pretreatment levels in both groups. The frequency of hemorrhagic events was higher in patients with greater changes in plasma factors at 5 h; within treatment groups the levels of fibrin(ogen) degradation products correlated with bleeding complications (p less than 0.005). Thus, in the doses administered, rt-PA induces systemic fibrinogenolysis that is substantially less intense than that induced by streptokinase. The high frequency of bleeding encountered is related to the protocol used, including vigorous anticoagulation, arterial punctures and thrombolytic therapy. These findings emphasize the need for avoidance of invasive procedures and for meticulous care in the selection and management of patients subjected to thrombolytic therapy.Source
J Am Coll Cardiol. 1988 Jan;11(1):1-11.
DOI
10.1016/0735-1097(88)90158-1Permanent Link to this Item
http://hdl.handle.net/20.500.14038/26348PubMed ID
3121710Related Resources
ae974a485f413a2113503eed53cd6c53
10.1016/0735-1097(88)90158-1