Is veno-occlusive disease a specific syndrome or the exacerbation of physiopathologic hemostatic changes in hematopoietic stem cell transplantation (HSCT)?
L. Villalon et al., Is veno-occlusive disease a specific syndrome or the exacerbation of physiopathologic hemostatic changes in hematopoietic stem cell transplantation (HSCT)?, THROMB RES, 99(5), 2000, pp. 439-446
The objective of the present study was to analyze whether veno-occlusive di
sease (VOD) is based on specific findings or whether this syndrome is the e
xacerbation of changes in hemostatic parameters that develop following hema
topoietic stem cell transplantation (HSCT), 40 patients undergoing HSCT wer
e enrolled (6 allogeneic bone marrow transplantation and 34 peripheral stem
cell rescue-2 allogeneic, 32 autologous). Measurements of hemostatic param
eters (endothelial, hypercoagulability and fibrinolytic markers) were obtai
ned prior to chemotherapy and weekly thereafter for 3 weeks. The incidence
of VOD was 15%. HSCT showed a state of moderate hypercoagulability (increas
e of thrombin-antithrombin complex and fibrinogen, and decrease of Factor V
II, Protein C, and antithombin-III), probably as a consequence of marked en
dothelial damage (increase of von Willebrand Factor and tissue plasminogen
activator), All these alterations create a potentially prothrombotic state,
more pronounced in VOD. The decreasing incidence of VOD and the moderate d
isease in all patients suggest that increasing improvements in transplant s
trategies have reduced the risk and severity of a syndrome that at the begi
nning of the transplantation era was a leading cause of morbidity/mortality
, (C) 2000 Elsevier Science Ltd. All rights reserved.