Multiple organ failure remains the leading cause of death in the inten
sive care unit. Increasing numbers of investigators have focused their
attention on the role of gastrointestinal tract in the pathogenesis o
f this syndrome. Their data indicate that inadequate gut perfusion rea
ds to a measurable imbalance between oxygen delivery and the needs of
the tissues, i.e., ischaemia. Gut ischaemia of sufficient duration imp
airs gastrointestinal tract barrier function, facilitating the passage
of enteric bacterial endotoxin into the circulation. It has been hypo
thesized that production of tumor necrosis factor alpha, and other bio
logic mediators by endotoxin-stimulated macrophages, triggers a genera
lized and uncontrolled inflammatory response that ultimately leads to
multiple organ failure. Preliminary evidence suggests that survival ca
n be improved significantly if gut ischaemia is promptly identifed and
aggressively treated by administration of fluids and inotropic drugs,
using gastric intramucosal pH as the therapeutic endpoint. Future stu
dies are needed to determine whether additional treatment modalities c
an improve outcome once the inflammatory response has fully developed.