Plasma levels of D-dimer and circulating endothelial adhesion molecules in veno-occlusive disease of the liver following allogeneic bone marrow transplantation

Eur J Haematol. 1998 Feb;60(2):106-11. doi: 10.1111/j.1600-0609.1998.tb01006.x.

Abstract

Veno-occlusive disease (VOD) of the liver is a frequent and life-threatening complication of BMT. Recently, successful treatment by t-PA has been reported but has been compromised by fatal bleeding events. Therefore, t-PA application should be restricted to patients with severe VOD. However, moderate and severe forms of VOD are difficult to distinguish in early stages. We analyzed plasma levels of cross-linked fibrin degradation products (D-dimer) and soluble endothelial adhesion molecules such as sE-selectin, sVCAM-1 and sICAM-1 in 10 consecutive patients undergoing allogeneic BMT to evaluate their use in identifying severe forms of VOD. During the observation period, 4 episodes of VOD occurred, 2 of which were fatal due to early onset of multiorgan failure. Concentrations of D-dimer generally increased after transplantation. However, there was an additional significant increase in D-dimer levels during severe VOD. Thus, D-dimer levels above 1000 microg/l were only found in 2 cases with severe VOD and fatal outcome. When compared with bilirubin concentrations substantial increases of D-dimers appeared earlier during the course of severe VOD. In contrast, VOD episodes were not accompanied by significant increases in sE-selectin, sVCAM-1 and sICAM-1 levels. It is concluded that measurement of D-dimer concentrations may aid accuracy to the early diagnosis of severe VOD.

MeSH terms

  • Adult
  • Aged
  • Bone Marrow Transplantation / adverse effects*
  • Cell Adhesion Molecules / blood*
  • Female
  • Fibrin Fibrinogen Degradation Products / metabolism*
  • Hepatic Veno-Occlusive Disease / blood*
  • Hepatic Veno-Occlusive Disease / etiology
  • Humans
  • Male
  • Middle Aged
  • Prospective Studies
  • Transplantation, Homologous

Substances

  • Cell Adhesion Molecules
  • Fibrin Fibrinogen Degradation Products
  • fibrin fragment D