Several therapeutic approaches to sepsis and disseminated intravascular coa
gulation (DIC) have shown promising results in animal models. Large control
led trials in humans, however, have failed to show a clearly beneficial eff
ect of a single drug or substance on outcome and survival so that treatment
remains uncertain. As one researcher stated: "... sepsis is a classical ex
ample of a disease greater than the sum of its parts; it is a complex proce
ss in which intervention in one area might have only a modest effect on the
final outcome." We believe that the complex pathophysiological setting of
septic shock will undoubtedly require a multifaceted approach. Consequently
, we attempt to arrest DIC and restore adequate tissue perfusion by interve
ntion with heparin, AT and if possible protein C (PC) in the earliest stage
of the disease, with the aim of blocking ongoing microthrombus formation a
nd to support fibrinolysis.
Growing understanding of the basic underlying mechanisms teaches us how to
successfully stabilise the individual decompensated sub-systems like coagul
ation in septic patients. We should learn to accept these steps to reach th
e goal of a better outcome in terms of survival in this devastating illness
.