Treatment of severe venous thrombo-embolism with intravenous Hirudin (HBW 023): an open pilot study

Thromb Haemost. 1993 Sep 1;70(3):386-8.

Abstract

Recombinant Hirudin (rH) is an anticoagulant agent with a specific antithrombin activity independent of antithrombin III. We report the results of the first open pilot study on the curative treatment of acute venous thrombo-embolism (VTE) with rH (HBW 023) in ten patients. The dose of rH tested was 0.07 mg/kg (i.v. bolus) followed by 0.05 mg kg-1 h-1 (i.v. infusion) for 5 days, without activated partial thromboplastin time (APTT) adjustment. Within the trial, no death, VTE recurrence or major bleeding was observed; lung scan pulmonary vascular obstruction improved from 44 to 37%, whereas the venographic Marder score was unchanged; APTT ratio ranged between 1.2 and 2.8. The dose of rH assessed in this study seems to be safe and efficient in the treatment of acute VTE.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Female
  • Follow-Up Studies
  • Hirudin Therapy*
  • Humans
  • Injections, Intravenous
  • Male
  • Middle Aged
  • Pilot Projects
  • Recombinant Proteins / therapeutic use
  • Thromboembolism / drug therapy*
  • Thromboembolism / etiology
  • Thrombophlebitis / complications

Substances

  • Recombinant Proteins