Literature DB >> 7775709

Current issues concerning thrombolytic therapy for acute myocardial infarction.

C H Hennekens1, C J O'Donnell, P M Ridker, V J Marder.   

Abstract

Data are now available from three large-scale randomized trials that directly compare the risks and benefits of thrombolytic agents in acute myocardial infarction. In the interpretation of results from the Gruppo Italiano per lo Studio della Sopravvivenza nell'Infarto Miocardico (GISSI-2) trial and its International Extension, the Third International Study of Infarct Survival (ISIS-3), and the Global Utilization of Streptokinase and Tissue Plasminogen Activator for Occluded Coronary Arteries (GUSTO-1) trial, there are areas of both agreement and controversy. It is generally agreed that the agents most commonly used in the United States--tissue-type plasminogen activator (t-PA), streptokinase and anisoylated plasminogen streptokinase activator complex (APSAC)--all reduce mortality when given to patients with acute evolving myocardial infarction. Further, it is clear that thrombolytic therapy given to such patients presenting up to 12 h after onset of symptoms reduces the mortality rate by approximately 20%, that aspirin therapy for patients presenting up to 24 h reduces the mortality rate by approximately 23% and that the benefits of thrombolytic therapy and aspirin are additive. Finally, and of most importance, the earlier administration as well as the more widespread use of thrombolytic therapy and aspirin would save many more lives. The totality of evidence clearly indicates that streptokinase produces significantly fewer strokes and cerebral hemorrhages than either t-PA or APSAC. Whether or not accelerated t-PA has a small advantage for mortality is less conclusive.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1995        PMID: 7775709     DOI: 10.1016/0735-1097(95)00107-f

Source DB:  PubMed          Journal:  J Am Coll Cardiol        ISSN: 0735-1097            Impact factor:   24.094


  6 in total

Review 1.  New thrombolytic strategy: bolus administration of tPA and urokinase-fibrinogen conjugate.

Authors:  A V Maksimenko; E G Tischenko
Journal:  J Thromb Thrombolysis       Date:  1999-06       Impact factor: 2.300

Review 2.  Alteplase: a pharmacoeconomic evaluation of its use in the management of myocardial infarction.

Authors:  L B Barradell; K L Goa
Journal:  Pharmacoeconomics       Date:  1995-11       Impact factor: 4.981

3.  Engineering of plasmin-resistant forms of streptokinase and their production in Bacillus subtilis: streptokinase with longer functional half-life.

Authors:  X C Wu; R Ye; Y Duan; S L Wong
Journal:  Appl Environ Microbiol       Date:  1998-03       Impact factor: 4.792

4.  Locally activity-released bifunctional fusion protein enhances antithrombosis and alleviates bleeding risk.

Authors:  Bingxing Shi; Aiping Yu; Yuying Liu; Jingchuan Li; Jide Jin; Chunna Dong; Chutse Wu
Journal:  J Thromb Thrombolysis       Date:  2007-05-09       Impact factor: 2.300

5.  Gene therapy to promote thromboresistance: local overexpression of tissue plasminogen activator to prevent arterial thrombosis in an in vivo rabbit model.

Authors:  J M Waugh; M Kattash; J Li; E Yuksel; M D Kuo; M Lussier; A B Weinfeld; R Saxena; E D Rabinovsky; S Thung; S L Woo; S M Shenaq
Journal:  Proc Natl Acad Sci U S A       Date:  1999-02-02       Impact factor: 11.205

6.  A successfully thrombolysed acute inferior myocardial infarction due to type A aortic dissection with lethal consequences: the importance of early cardiac echocardiography.

Authors:  Grigorios Tsigkas; Georgios Kasimis; Konstantinos Theodoropoulos; Konstantinos Chouchoulis; Nikolaos G Baikoussis; Efstratios Apostolakis; Eleni Bousoula; Athanasios Moulias; Dimitrios Alexopoulos
Journal:  J Cardiothorac Surg       Date:  2011-08-24       Impact factor: 1.637

  6 in total

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