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Tissue plasminogen activator in acute pulmonary embolism
1Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston 12005.
Chest
|May 1, 1989
Summary
Recombinant human tissue-type plasminogen activator (rtPA) shows high efficacy and safety for acute pulmonary embolism (PE) treatment. Further trials are comparing rtPA with urokinase and heparin, aiming for large-scale studies on mortality and recurrent PE.
Area of Science:
- Cardiology
- Pulmonary Medicine
- Pharmacology
Background:
- Thrombolytic therapy for acute myocardial infarction (AMI) has renewed interest in its use for acute pulmonary embolism (PE).
- Investigating recombinant human tissue-type plasminogen activator (rtPA) for acute PE treatment is crucial.
Purpose of the Study:
- To evaluate the efficacy and safety of rtPA in patients with acute PE.
- To compare rtPA with urokinase (UK) and heparin in managing PE.
- To assess the impact of rtPA on right ventricular function in PE patients.
Main Methods:
- An open-label study assessed rtPA's efficacy and safety.
- A comparative trial evaluated rtPA against an FDA-approved dose of urokinase (UK).
- Ongoing trials compare rtPA with a novel UK regimen and heparin, using echocardiography to assess right ventricular function.
Main Results:
- The open-label study demonstrated over 90% efficacy and safety for rtPA.
- rtPA showed more rapid and safer outcomes compared to UK in a prior trial.
- Ongoing trials are collecting data on rtPA's comparative effectiveness.
Conclusions:
- rtPA is a promising therapeutic agent for acute PE, demonstrating high efficacy and safety.
- Comparative studies are essential to establish optimal thrombolytic strategies for PE.
- Large-scale trials are needed to confirm the benefits of thrombolysis over heparin in reducing PE-related mortality and recurrence.