Background. The use of radiographic contrast media in the setting of possib
le bowel ischemia and potential perforation is known to carry a risk of mor
bidity and mortality. However, studies of the effect of available contrast
media on host immunological defense mechanisms are lacking. We have examine
d the effect of barium and of two water-soluble contrast agents of differin
g iodine concentration and osmolality, Conray 30 and Cysto Conray II, on le
ukocyte phagocytosis.
Materials and methods. Blood samples were incubated with the contrast media
alone (termed the "resting state"), and in combination with a standard pha
gocytic challenge (Zymosan polysaccharide extract) and with Staphylococcus
epidermidis, Streptococcus faecalis and Escherichia coli, to determine the
effect of contrast media upon leukocyte phagocytic response. Incubation wit
h saline was used as control. In the case of barium, the "resting state" an
d standard challenge experiments were repeated at nine dilutions, ranging f
rom 1:1 to 1:1000. The leukocyte phagocytic response was measured in two wa
ys: CO2 generation (an index of metabolic activity) and chemiluminescence (
an index of generation of reactive oxygen species and bacterial killing).
Results. Barium, at clinical dilutions, causes a significant increase of ba
se-line "resting state" phagocytic activity, which in turn leads to signifi
cant blunting of subsequent response to phagocytic challenge and adversely
affects the response to all bacteria tested. There is no baseline activatio
n of leukocytes by the water-soluble media, although there was some inhibit
ion (rather than activation) of leukocyte metabolic activity. The effect of
the water-soluble media on bacteria was more complex (although inhibition
is minor compared to barium).
Conclusions. Our data demonstrate that barium is a significant activator of
phagocytic cells, which results in deactivation of phagocytic response whe
n challenged; these data serve to explain the enhanced adverse effect of ba
rium in cases of fecal peritonitis.