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Prehospital Thrombolysis: A Manual from Berlin
Published on: November 27, 2013
Lessons we have learned from the GUSTO trial. Global Utilization of Streptokinase and Tissue Plasminogen Activator
D R Holmes1, R M Califf, E J Topol
1Division of Cardiovascular Diseases, Mayo Clinic, Rochester, Minnesota 55905, USA.
Insights
Accelerated tissue-type plasminogen activator (t-PA) significantly reduced mortality in acute myocardial infarction patients compared to streptokinase. This improved outcome, despite a slight increase in stroke risk, highlights t-PA
Area of Science:
- Cardiology
- Pharmacology
- Clinical Trials
Background:
- Thrombolytic therapy is crucial for acute myocardial infarction (AMI).
- Controversies exist regarding optimal drug choice, heparin use, and timing.
- The Global Utilization of Streptokinase and Tissue Plasminogen Activator for Occluded Coronary Arteries (GUSTO) trial aimed to resolve these issues.
Purpose of the Study:
- To compare the efficacy and safety of accelerated tissue-type plasminogen activator (t-PA) versus streptokinase in AMI treatment.
- To investigate the impact of reperfusion on cardiac function and mortality.
Main Methods:
- A large-scale clinical trial (GUSTO) involving 41,021 patients.
- Comparison of accelerated t-PA monotherapy with streptokinase monotherapy strategies.
- Analysis of subgroup outcomes, including age, infarction location, and comorbidities.
- Angiographic substudy to evaluate reperfusion mechanisms and Thrombolysis in Myocardial Infarction (TIMI) flow grades.
Main Results:
- Accelerated t-PA demonstrated a 15% reduction in all-cause mortality compared to streptokinase (p = 0.001).
- This benefit was consistent across various patient subgroups.
- A small but significant increase in hemorrhagic stroke (0.2%) was observed with t-PA (p = 0.03).
- The combined endpoint of death or disabling stroke was significantly lower with t-PA (p = 0.006).
Conclusions:
- Accelerated t-PA is superior to streptokinase in reducing mortality for acute myocardial infarction.
- Improved TIMI grade 3 flow and left ventricular function contribute to better outcomes.
- Risk-benefit analysis favors accelerated t-PA, despite a slight increase in hemorrhagic stroke risk.
Abstract:
Thrombolytic therapy remains a mainstay for the treatment of patients with acute myocardial infarction. This therapy has been the subject of intense investigation and multiple studies as well as substantial controversy. Controversial issues include, among others, the specific drug, need for heparin, the relation between time to treatment and outcome and risk/benefit considerations. The Global Utilization of Streptokinase and Tissue Plasminogen Activator for Occluded Coronary Arteries (GUSTO) trial of 41,021 patients addressed many of these issues. The results of the main trial were conclusive--treatment with accelerated tissue-type plasminogen activator (t-PA) resulted in a decreased mortality rate with a 15% reduction (95% confidence interval 5.9 to 21.3) compared with the two streptokinase monotherapy strategies (p = 0.001). Virtually all subgroup analyses, including age, nonanterior infarction location, patients undergoing bypass graft surgery and hypertensive patients, showed remarkable consistency with improved outcome with accelerated t-PA. This reduction in all-cause mortality with accelerated t-PA was associated with a small (absolute 0.2%) but significant increase in hemorrhagic stroke (p = 0.03). A combined end point of death or disabling stroke, or both, was still decreased in the accelerated t-PA group compared with the streptokinase group (p = 0.006). The angiographic substudy evaluated the mechanism of improved outcome and documented that reperfusion therapy works by restoring Thrombolysis in Myocardial Infarction (TIMI) grade 3 flow early, improving left ventricular function and improving mortality. The most favorable outcome seen with t-PA was related to the finding that it resulted in improved TIMI grade 3 flow compared with that for streptokinase.
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