Thromb Haemost 1993; 70(03): 386-388
DOI: 10.1055/s-0038-1649590
Original Article
Clinical Studies
Schattauer GmbH Stuttgart

Treatment of Severe Venous Thrombo-Embolism with Intravenous Hirudin (HBW 023): An Open Pilot Study

Authors

  • Florence Parent

    1   The Department of Pneumology, Université Paris-Sud, Clamart, France
  • Françoise Bridey

    2   The Department of Haematology, Université Paris-Sud, Clamart, France
  • Marie Dreyfus

    2   The Department of Haematology, Université Paris-Sud, Clamart, France
  • Dominique Musset

    3   The Department of Radiology, Université Paris-Sud, Clamart, France
  • Gilles Grimon

    4   Department of Nuclear Medicine, Hôpital Antoine Béclère, Université Paris-Sud, Clamart, France
  • Pierre Duroux

    1   The Department of Pneumology, Université Paris-Sud, Clamart, France
  • Dominique Meyer

    2   The Department of Haematology, Université Paris-Sud, Clamart, France
  • Gérald Simonneau

    1   The Department of Pneumology, Université Paris-Sud, Clamart, France
Further Information

Publication History

Received 23 November 1992

Accepted after revision 05 April 1993

Publication Date:
05 July 2018 (online)

Preview

Summary

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.