Progress in the care of the critically ill patient with life-threateni
ng infection has been hampered by inconsistent, often confusing termin
ology. The clinical syndrome of sepsis-familiar to all yet definable b
y none-describes a highly heterogeneous group of disorders with differ
ent causes and differing prognoses. The imminent availability of media
tor-directed therapy has created a sense of urgency to develop better
methods for delineating discrete clinical syndromes and to modulate th
e host response, which may bring both benefit and harm, depending on t
he clinical circumstances. The term systemic inflammatory response syn
drome (SIRS) nas introduced several gears ago to describe the familiar
clinical syndrome of sepsis, independent of its cause, SIRS can resul
t from trauma, pancreatitis, drug reactions, autoimmune disease, and a
host of other disorders; when it arises in response to infection, sep
sis is said to be present. SIPS describes a dynamic process that has a
daptive survival value for the host. The maladaptive consequence of th
is process in the critically ill patient is the development of progres
sive hut potentially reversible remote organ dysfunction-the multiple
organ dysfunction syndrome, The development of cogent conceptual frame
works for classification of the septic response in critically ill pati
ents is more than a question of linguistic pedantry, Optimal therapy p
resupposes identification of an homogeneous patient population with a
characteristic disease process and a predictable response to an interv
ention. Although progress has been made in identifying such groups of
critically ill patients, the disappointing results of clinical trials
of agents that so clearly demonstrate efficacy in animal models indica
tes that considerable work remains.