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Myocardial Infarction and Functional Outcome Assessment in Pigs
Published on: April 25, 2014
Left ventricular function as an end-point of thrombolytic therapy
1Coronary Care Unit, Green Land Hospital, Auckland, New Zealand.
European Heart Journal
|August 1, 1990
Summary
This study found no significant difference in left ventricular (LV) function between streptokinase and tissue plasminogen activator for myocardial infarction recovery. Both thrombolytic drugs equally improved LV ejection fraction three weeks post-infarction.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Medicine
Background:
- Left ventricular (LV) function, assessed by ejection fraction (EF) or end-systolic volume (ESV), is crucial for clinical prognosis after myocardial infarction (MI).
- Deterioration of LV function post-MI is a significant adverse prognostic factor, highlighting the importance of agents that improve cardiac function for long-term survival.
Purpose of the Study:
- To compare the efficacy of two thrombolytic drugs, streptokinase (SK) and tissue plasminogen activator (tPA), in preserving LV function after acute myocardial infarction.
- To investigate whether early administration of SK or tPA leads to differential effects on LV ejection fraction and infarct-related artery patency.
Main Methods:
- A double-blind comparison of streptokinase (SK) versus tissue plasminogen activator (tPA) administered early (2.5 +/- 0.6 hours) after myocardial infarction onset.
- Assessment of LV ejection fraction (EF) at 3 weeks post-infarction and infarct-related artery patency rates at 3 weeks in patients treated with either SK or tPA.
Main Results:
- No significant difference in LV ejection fraction (EF) was observed at 3 weeks between the SK group (58 +/- 12%, n=116) and the tPA group (58 +/- 12%, n=124).
- Infarct-related artery patency rates at 3 weeks were similar for both drugs: 75% for SK and 76% for tPA.
- The study suggests that while tPA may offer more rapid reperfusion, later reperfusion with SK might prevent infarct expansion, potentially explaining the similar LV function outcomes.
Conclusions:
- Early administration of both streptokinase and tissue plasminogen activator equally improves left ventricular function three weeks after myocardial infarction.
- There is currently no evidence to suggest one thrombolytic drug is superior to the other for preserving LV function post-MI.
- Further research into the mechanisms of infarct healing and LV remodeling is warranted to fully understand the long-term implications of different reperfusion strategies.

