Tissue plasminogen activator in acute pulmonary embolism

Chest. 1989 May;95(5 Suppl):282S-289S. doi: 10.1378/chest.95.5_supplement.282s.

Abstract

The use of thrombolytic therapy to treat AMI has reawakened interest in thrombolysis for acute pulmonary embolism (PE). We have investigated the use of recombinant human tissue-type plasminogen activator (rtPA) in patients with acute PE. In an open label study, rtPA achieved more than 90% efficacy and safety. In a trial comparing rtPA with an FDA-approved dose of urokinase (UK), rtPA appeared more rapid and safer. We are now conducting a comparative trial of rtPA with a novel dosing regimen of UK. In addition, a concurrent trial is comparing rtPA vs heparin for improvement in right ventricular function, assessed by echocardiography, among PE patients. However, the greatest challenge in PE research is to undertake a large-scale trial that compares thrombolysis and heparin for reduction of clinically relevant end points such as mortality and recurrent PE.

Publication types

  • Clinical Trial
  • Comparative Study
  • Controlled Clinical Trial

MeSH terms

  • Clinical Trials as Topic
  • Humans
  • Pulmonary Embolism / drug therapy*
  • Recombinant Proteins / therapeutic use
  • Tissue Plasminogen Activator / therapeutic use*
  • Urokinase-Type Plasminogen Activator / therapeutic use

Substances

  • Recombinant Proteins
  • Tissue Plasminogen Activator
  • Urokinase-Type Plasminogen Activator