Low molecular heparin (Enoxaparin) as an alterantive treatment of acute deep venous thrombosis in gynecologic oncology patients

A. Fishman*, M. Altaras, Z. Klein, R. Aviram, Y. Beyth

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

While heparin has been the standard treatment in established deep vein thrombosis (DVT), it carries associated potential hazards of hemorrhage and induction of thrombocytopenia. Enoxaparin (Rhone-Poulenc Rorer Pharm. Inc., France) is a low molecular weight heparin which has antithrombotic properties, and has been demonstrated effective in prophylaxis of DVT, apparently without severe treatment related bleeding complications. Six patients with genital malignancies, presenting with Doppler sonography confirmed deep venous thrombosis, were treated with Enoxaparin. A uniform dosage of 2 mg/kg/day in two divided doses was administered subcutaneously for 10 days during hospitalization and then continued on an out-patient basis. The clinical symptoms of venous thromboses diminished in all six patients. Enoxaparin represents an effective treatment of DVT, with the potential advantage of a lessening hemorrhagic complications. With administration of low molecular heparin, the activated partial thromboplastin time (aPTT) is not dramatically altered, making laboratory monitoring unnecessary. Our clinical findings demonstrate an easily applied therapy for gynecologic oncology patients, which is potentially safer to use, less costly, and less dependent on laboratory monitoring than the normal regimen.

Original languageEnglish
Pages (from-to)365-367
Number of pages3
JournalEuropean Journal of Gynaecological Oncology
Volume17
Issue number5
StatePublished - 1996
Externally publishedYes

Keywords

  • Deep venous thrombosis
  • Gynecologic-oncology patients
  • Low-molecular heparin

Fingerprint

Dive into the research topics of 'Low molecular heparin (Enoxaparin) as an alterantive treatment of acute deep venous thrombosis in gynecologic oncology patients'. Together they form a unique fingerprint.

Cite this