L. Kessler et al., POSSIBLE INVOLVEMENT OF VON-WILLEBRAND-FACTOR IN PANCREATIC GRAFT THROMBOSIS AFTER KIDNEY-PANCREAS TRANSPLANTATION - A RETROSPECTIVE STUDY, Clinical transplantation, 12(1), 1998, pp. 35-42
Early postoperative graft thrombosis remains the second cause of failu
re in pancreas transplantation. Thus, the aim of this study was to com
pare retrospectively coagulation and fibrinolysis in type I diabetic r
ecipients of simultaneous kidney-pancreas transplants having or not ex
perienced thrombosis of their pancreatic graft. From December 1990 to
August 1996, 30 simultaneous kidney-pancreas transplants were performe
d in 30 uremic type I diabetic patients. Acute thrombosis of the pancr
eatic graft was observed among 6 patients (group A), whereas 24 did no
t develop thrombosis (group B) although 4 died from other causes. The
control groups were composed of kidney transplant (group C) or haemodi
alysed (group D) non-diabetic patients, type I diabetics with HbA1C <
8% (group E) or greater than or equal to 8% (group F) who were not in
end-stage renal failure and kidney. transplant type I diabetic patient
s (group G). Beginning at least 6 months after transplantation, we ana
lysed hemostatic factors (fibrinogen, thrombin, and prothrombin times)
, coagulation inhibitors (proteins C and S), fibrinolysis (plasminogen
activator inhibitor) and endothelial cell abnormalities (Von Willebra
nd factor: VWf). Micro and macrovascular complications were evaluated
on a score ranging from 0 to 12. Hemostatic factors, coagulation inhib
itors and fibrinolysis were similar in groups A and B whereas VWf diff
ered significantly in group A (3.49 +/- 0.93 IU/ml) as compared to gro
up B (2.04 +/- 0.92 IU/ml) (p < 0.05). VWf was also significantly incr
eased in group A relative to the control groups C, D, E, F, and G. The
score of vascular complications was increased in groups A and B and s
ignificantly higher in group A (9 +/- 0.81 vs. 6.07 +/- 1.75) (p < 0.0
1), while a correlation (r = 0.812, p > 0.05) was observed between VWf
levels and the severity of vascular complications. These results poin
t out the possible involvement of VWf in the pathogenesis of pancreati
c vein thrombosis in kidney-pancreas transplantation.