Inflammatory "one hit" and "two hit" models have recently been proposed to
account for the development of multiple organ failure (MOF) in trauma and c
ritically ill surgical patients when no source of infection can be found. I
n the "one hit" model, the initial insult is so massive that a systemic inf
lammatory response syndrome is triggered and leads rapidly to MOF. In the "
two hit" scenario, less severely injured patients develop MOF as a result o
f a reactivation of their inflammatory response caused by an adverse and of
ten minor intercurrent event. At first sight, the theory is attractive beca
use it seems to fit commonly observed clinical patterns. Indeed, injured pa
tients often respond to initial resuscitation but, after an insult of some
sort, develop organ dysfunction and die. The "two hit" model is furthermore
mirrored at the cellular level. Inflammatory cells are indeed susceptible
of being primed by an initial stimulus and reactivated subsequently by a re
latively innocuous insult. However, in the absence of clinical and biologic
al corroboration based on cytokine secretion patterns, these models should
not be accepted uncritically.