Literature DB >> 7579782

Does the potential for development of streptokinase antibodies change the risk-benefit ratio in older patients?

J Brügemann1, P A de Graeff, J van der Meer, K I Lie.   

Abstract

In patients with acute myocardial infarction (MI), quick initiation of thrombolytic therapy is the best strategy for improvement of survival and reduction of morbidity. Streptokinase, a purified product of haemolytic streptococci, is the most commonly administered agent. The compound anistreplase (a complex of streptokinase to plasminogen), is available but currently not often used. The non-antigenic competitor for these two compounds for the indication of MI is alteplase (recombinant tissue plasminogen activator, rt-PA). Due to former use of streptokinase or its derivative anistreplase, patients may develop specific antibodies to the foreign protein, whereas cross-reacting antibodies may be due to streptococcal infections. These antibodies may neutralise streptokinase or its derivative in case of (re)administration and may mediate adverse events, sometimes serious. Since advanced age by itself is certainly not a contraindication to thrombolytic therapy, and because reinfarction occurs frequently, the benefit-risk ratio of re-exposure to streptokinase or its derivative is decreased in the elderly who present with reinfarction. In the framework of tailored thrombolytic therapy, alteplase or urokinase appear to be the drugs of choice in these patients.

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Year:  1995        PMID: 7579782     DOI: 10.2165/00002512-199507020-00005

Source DB:  PubMed          Journal:  Drugs Aging        ISSN: 1170-229X            Impact factor:   3.923


  30 in total

Review 1.  Is the development of antibodies to streptokinase clinically relevant?

Authors:  M B Buchalter
Journal:  Drugs       Date:  1994-08       Impact factor: 9.546

2.  Allergic reactions to streptokinase consistent with anaphylactic or antigen-antibody complex-mediated damage.

Authors:  K G McGrath; B Zeffren; J Alexander; K Kaplan; R Patterson
Journal:  J Allergy Clin Immunol       Date:  1985-09       Impact factor: 10.793

3.  Thrombolytic therapy for acute myocardial infarction in a 110-year-old man.

Authors:  A Katz; G Cohn; A Mashal; N Cristal
Journal:  Am J Cardiol       Date:  1993-05-01       Impact factor: 2.778

4.  Anti-streptokinase antibodies inhibit fibrinolytic effects of anistreplase in acute myocardial infarction.

Authors:  J Brügemann; J van der Meer; V J Bom; W van der Schaaf; P A de Graeff; K I Lie
Journal:  Am J Cardiol       Date:  1993-08-15       Impact factor: 2.778

5.  Lack of influence of pretreatment antistreptokinase antibody on efficacy in a multicenter patency comparison of intravenous streptokinase and anistreplase in acute myocardial infarction.

Authors:  R Fears; J Hearn; R Standring; J L Anderson; V J Marder
Journal:  Am Heart J       Date:  1992-08       Impact factor: 4.749

6.  Overt and subclinical reactions to streptokinase in acute myocardial infarction.

Authors:  M Lynch; B L Pentecost; W A Littler; R A Stockley
Journal:  Am J Cardiol       Date:  1994-11-01       Impact factor: 2.778

Review 7.  Tailored thrombolytic therapy. A perspective.

Authors:  M L Simoons; A E Arnold
Journal:  Circulation       Date:  1993-12       Impact factor: 29.690

8.  Effect of "fast track" admission for acute myocardial infarction on delay to thrombolysis.

Authors:  A C Pell; H C Miller; C E Robertson; K A Fox
Journal:  BMJ       Date:  1992-01-11

9.  Comparison of effects of thrombolytic therapy on left ventricular function in patients over with those under 60 years of age.

Authors:  H White; D Cross; M Scott; R Norris
Journal:  Am J Cardiol       Date:  1991-05-01       Impact factor: 2.778

Review 10.  Streptokinase. A review of its pharmacology and therapeutic efficacy in acute myocardial infarction in older patients.

Authors:  P E Battershill; P Benfield; K L Goa
Journal:  Drugs Aging       Date:  1994-01       Impact factor: 3.923

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