Randomized, controlled trial of ultrasound-assisted catheter-directed thrombolysis for acute intermediate-risk pulmonary embolism

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Nils Kucher - , University of Bern (Author)
  • Peter Boekstegers - , Helios Hospital Siegburg (Author)
  • Oliver J. Müller - , Heidelberg University  (Author)
  • Christian Kupatt - , Ludwig Maximilian University of Munich (Author)
  • Jan Beyer-Westendorf - , Department of Internal Medicine I, University Hospital Carl Gustav Carus Dresden (Author)
  • Thomas Heitzer - , Klinikum Dortmund gGmbH (Author)
  • Ulrich Tebbe - , Hospital Lippe (Author)
  • Jan Horstkotte - , Helios Hospital Siegburg (Author)
  • Ralf Müller - , Helios Hospital Siegburg (Author)
  • Erwin Blessing - , Heidelberg University  (Author)
  • Martin Greif - , Ludwig Maximilian University of Munich (Author)
  • Philipp Lange - , Ludwig Maximilian University of Munich (Author)
  • Ralf Thorsten Hoffmann - , Institute and Polyclinic of Diagnostic and Interventional Radiology, University Hospital Carl Gustav Carus Dresden (Author)
  • Sebastian Werth - , Department of Internal Medicine III, University Hospital Carl Gustav Carus Dresden (Author)
  • Achim Barmeyer - , Klinikum Dortmund gGmbH (Author)
  • Dirk Härtel - , Hospital Lippe (Author)
  • Henriette Grünwald - , University of Greifswald (Author)
  • Klaus Empen - , University of Greifswald (Author)
  • Iris Baumgartner - , University of Bern (Author)

Abstract

BACKGROUND - : In patients with acute pulmonary embolism, systemic thrombolysis improves right ventricular (RV) dilatation, is associated with major bleeding, and is withheld in many patients at risk. This multicenter randomized, controlled trial investigated whether ultrasound-assisted catheter-directed thrombolysis (USAT) is superior to anticoagulation alone in the reversal of RV dilatation in intermediate-risk patients. METHODS AND RESULTS - : Fifty-nine patients (63±14 years) with acute main or lower lobe pulmonary embolism and echocardiographic RV to left ventricular dimension (RV/LV) ratio ≥1.0 were randomized to receive unfractionated heparin and an USAT regimen of 10 to 20 mg recombinant tissue plasminogen activator over 15 hours (n=30; USAT group) or unfractionated heparin alone (n=29; heparin group). Primary outcome was the difference in the RV/LV ratio from baseline to 24 hours. Safety outcomes included death, major and minor bleeding, and recurrent venous thromboembolism at 90 days. In the USAT group, the mean RV/LV ratio was reduced from 1.28±0.19 at baseline to 0.99±0.17 at 24 hours (P<0.001); in the heparin group, mean RV/LV ratios were 1.20±0.14 and 1.17±0.20, respectively (P=0.31). The mean decrease in RV/LV ratio from baseline to 24 hours was 0.30±0.20 versus 0.03±0.16 (P<0.001), respectively. At 90 days, there was 1 death (in the heparin group), no major bleeding, 4 minor bleeding episodes (3 in the USAT group and 1 in the heparin group; P=0.61), and no recurrent venous thromboembolism. CONCLUSIONS - : In patients with pulmonary embolism at intermediate risk, a standardized USAT regimen was superior to anticoagulation with heparin alone in reversing RV dilatation at 24 hours, without an increase in bleeding complications.

Details

Original languageEnglish
Pages (from-to)479-486
Number of pages8
JournalCirculation
Volume129
Issue number4
Publication statusPublished - 28 Jan 2014
Peer-reviewedYes

External IDs

PubMed 24226805

Keywords

Keywords

  • Pulmonary embolism