The characteristics of two types of intraperitoneal (i.p.) soilage sep
sis models, autologous fecal inoculum (FEC) and a pure culture of Esch
erichia coli (EC), were studied in 26 male Yucatan minipigs (20-30 kg)
. Early (1-4 h) and late (24-72 h) changes were different between the
two groups. The EC group was characterized early by hypotension, low c
ardiac output, and increased systemic and pulmonary vascular resistanc
es, along with leukopenia, hypoglycemia, lactacidemia, and elevated bl
ood urea nitrogen. Of the pigs in the EC group that survived the early
effects, there were few significant differences in physiological para
meters, compared to control pigs, that would indicate ongoing patholog
ical processes. In contrast, the FEC group pigs demonstrated early hyp
otension, but with increased cardiac output and reduced systemic vascu
lar resistance. Other parameter changes were similar to those seen in
the EC pigs, but to a lesser degree, with the exception of elevations
in serum lactate dehydrogenase. Also in contrast to the EC group, most
of the changes in the FEC group persisted in later days, and FEC pigs
demonstrated leukocytosis. There were also greater elevations in circ
ulating lipopolysaccharide (LPS) concentrations in the EC group that r
eturned later to baseline levels. In the FEC group, there were persist
ently elevated LPS concentrations over 72 h. These observations sugges
t that pigs challenged with intraperitoneal E. coli demonstrated an in
itial acute peritonitis and damaging physiologic effects of high level
s of circulating LPS. Survivors in this group improved and were physio
logically stable after 24 h. Pigs that received i.p. autologous feces
developed an early acute peritonitis phase with lower levels of circul
ating LPS, and later developed pronounced peritoneal reaction as demon
strated by multiple abdominal abscesses, pyogenic granuloma formation,
and adhesions with physiological evidence of developing sepsis over 7
2 h. These observations indicate that i.p. EC models evoke a systemic
response not unlike intravenous administration of LPS or EC, however,
the FEC model produced a systemic response akin to a slower developing
septic process.