Summary
Study Objective
Cytokines increase endothelial tissue factor (TF) and tissue plasminogen activator
inhibitor type -1 (PAI-1) expression in vitro. Tissue factor interacts with factor VII to facilitate thrombosis and PAI-1 inhibits
fibrinolysis by endogenous plasminogen activators.
Because cytokine release is increased in children with sepsisinduced multiple organ
failure (MOF), we hypothesized a cytokine associated increase in circulating TF and
PAI-1 antigen release, and systemic activity in these patients.
Study Design
One hundred and seven consecutive children, who met the criteria for sepsis, and 10
critically ill children without sepsis, were enrolled in the study. Plasma TF and
PAI-1 antigen and activity levels, Interleukin-6 antigen levels (IL-6), nitrite +
nitrate levels (marker of nitric oxide production) and number of organs failing were
measured on days 1-3 of sepsis.
Results
Increased TF and PAI-1 antigen, and PAI-1 activity levels were associated with increasing
IL-6 and nitrite + nitrate levels (p <0.05), the development of MOF (p <0.05), and
mortality (p <0.05). Increased systemic PAI-1 activity was associated with cardiovascular,
renal, and hepatic failure (p <0.05). Increased systemic TF activity was associated
with the development of coagulopathy (p <0.05) and tended to be associated with mortality
(p =0.06, power .77)
Conclusions
A shift to an anti-fibrinolytic endothelium phenotype characterizes children who develop
sepsis-induced MOF and mortality. Children with coagulopathy have a shift to a pro-coagulant
phenotype. These findings support potential therapeutic roles for PAI-1 and TF pathway
inhibitors in reversal of this devastating pathophysiologic process.
Keywords
Thrombosis - fibrinolysis - nitric oxide - cytokines - sepsis - interleukin-6