Key result
Intravenous recombinant tissue plasminogen activator resulted in a similar infarct-related artery patency rate (75%) compared to streptokinase (76%) in patients with a first myocardial infarction.
Why the study?
Does recombinant tissue plasminogen activator (rt-PA) improve left ventricular function or patency compared to streptokinase in patients with a first myocardial infarction?
Does recombinant tissue plasminogen activator (rt-PA) improve left ventricular function or patency compared to streptokinase in patients with a first myocardial infarction?
Absolute Event Rate: 75% vs 76%
In patients with a first myocardial infarction, intravenous rt-PA and streptokinase resulted in similar left ventricular ejection fraction, infarct-related artery patency, and mortality at three weeks.
IN this issue of the Journal, White and his colleagues1 report on a clinical trial in which 270 patients presenting with a first myocardial infarction were randomly assigned to receive intravenously either 1.5 million units of streptokinase or 100 mg of recombinant tissue plasminogen activator (rt-PA). Left ventricular function was evaluated by contrast ventriculography and revealed no difference in the global ejection fraction three weeks after the infarction. The patency rate of the infarct-related artery was 76 percent in the group receiving streptokinase and 75 percent in the group receiving rt-PA. No significant difference in mortality was observed.It . . .
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E Rapaport (1989) conducted an editorial in first myocardial infarction (n=270). recombinant tissue plasminogen activator (rt-PA) vs. streptokinase (1.5 million units intravenously) was evaluated on patency rate of the infarct-related artery. Intravenous recombinant tissue plasminogen activator resulted in a similar infarct-related artery patency rate (75%) compared to streptokinase (76%) in patients with a first myocardial infarction.
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