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Alteplase. A Reappraisal of Its Pharmacology and Therapeutic Use in Vascular Disorders Other Than Acute Myocardial Infarction

Overview
Journal Drugs
Specialty Pharmacology
Date 1995 Aug 1
PMID 8521760
Citations 2
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Abstract

Alteplase is the product of recombinant DNA technology and is chemically identical to endogenous tissue-type plasminogen activator: Plasminogen is converted to plasmin by alteplase, and fibrinolysis of blood thrombi is subsequently stimulated. Alteplase is now firmly established as a treatment of choice in the management of acute myocardial infarction. The efficacy of intravenous alteplase in the treatment of pulmonary thromboembolism has also been established and appears to be similar to that of streptokinase and urokinase in this indication and in arterial thrombotic occlusion. However, its use in this latter indication and in other vascular disorders has not been as extensively documented. Although trials demonstrating the efficacy of intravenous alteplase in patients with deep vein thrombosis and intra-arterial alteplase in patients with arterial thrombotic occlusion exist, reliable data on the efficacy of the fibrinolytic in ischaemic stroke and intracranial haemorrhage are scarce. Little clinical benefit is apparent in patients with unstable angina, although careful use may be warranted in those with definite pretreatment coronary thrombi. Of concern, there is a suggestion that general use of alteplase in patients with unstable angina may be associated with increased incidence of myocardial infarction. The incidence of major haemorrhage associated with alteplase therapy increases with increasing dose and appears to be similar to that seen with other fibrinolytic agents. Thus, further well-designed studies of the use of alteplase in ischaemic stroke and cerebral haemorrhage are required. However, a small subset of patients with unstable angina and definite pretreatment coronary thrombi may benefit from alteplase therapy. Further, preliminary data suggest efficacy in the therapy of deep vein thrombosis and arterial thrombotic occlusion, and alteplase has a proven place in the fibrinolytic treatment of pulmonary thromboembolism.

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References
1.
. Early effects of tissue-type plasminogen activator added to conventional therapy on the culprit coronary lesion in patients presenting with ischemic cardiac pain at rest. Results of the Thrombolysis in Myocardial Ischemia (TIMI IIIA) Trial. Circulation. 1993; 87(1):38-52. DOI: 10.1161/01.cir.87.1.38. View

2.
Meyerovitz M, Goldhaber S, Reagan K, Polak J, Kandarpa K, Grassi C . Recombinant tissue-type plasminogen activator versus urokinase in peripheral arterial and graft occlusions: a randomized trial. Radiology. 1990; 175(1):75-8. DOI: 10.1148/radiology.175.1.2107563. View

3.
KRAUSE F, Endsin O . [Local catheter-mediated lysis of the femoral artery: rt-PA versus urokinase]. Rofo. 1993; 158(1):46-8. DOI: 10.1055/s-2008-1032599. View

4.
NERI SERNERI G, Gensini G, Poggesi L, Trotta F, Modesti P, Boddi M . Effect of heparin, aspirin, or alteplase in reduction of myocardial ischaemia in refractory unstable angina. Lancet. 1990; 335(8690):615-8. DOI: 10.1016/0140-6736(90)90407-v. View

5.
Folk J, HERSHEY J, Rivers M . Lack of effectiveness of tissue plasminogen activator 20 or more days after vitrectomy. Arch Ophthalmol. 1991; 109(5):614. DOI: 10.1001/archopht.1991.01080050020010. View