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Tissue plasminogen activator and acute pulmonary embolism
S Z Goldhaber1, C M Kessler, J Heit
1Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts 02115.
Journal of Cellular Biochemistry
|December 1, 1988
Summary
Peripheral intravenous recombinant human tissue-type plasminogen activator (rt-PA) effectively treats pulmonary embolism (PE), rapidly dissolving clots and improving pulmonary hypertension and right ventricular function.
Area of Science:
- Cardiology
- Pulmonology
- Pharmacology
Background:
- Pulmonary embolism (PE) is a significant cause of morbidity and mortality.
- Effective treatment strategies for PE are crucial for improving patient outcomes.
- Recombinant human tissue-type plasminogen activator (rt-PA) is a thrombolytic agent with potential for PE treatment.
Purpose of the Study:
- To assess the efficacy and safety of peripheral intravenous rt-PA in patients with PE.
- To evaluate the impact of rt-PA on pulmonary artery pressure, lung perfusion, and right ventricular function.
- To investigate the effects of rt-PA on fibrinogen levels and fibrinolysis.
Main Methods:
- A study involving 47 patients with angiographically documented PE.
- Administration of peripheral intravenous rt-PA (50 mg/2 h, with an optional additional 40 mg/4 h).
- Assessment of angiographic clot lysis, pulmonary artery pressure, lung scan perfusion defects, and right ventricular function pre- and post-treatment.
Main Results:
- 94% of patients showed angiographic evidence of clot lysis within 6 hours.
- Significant reduction in pulmonary artery pressure (P < 0.0001) and lung perfusion defects (P < 0.01).
- Improvement in right ventricular function and diameter, with normalization or improvement in wall movement.
Conclusions:
- Peripheral intravenous rt-PA is effective in achieving rapid clot lysis in PE.
- rt-PA treatment leads to significant improvements in pulmonary hemodynamics and right ventricular function.
- The study highlights the potential of rt-PA as a therapeutic option for selected PE patients.