The objective of the study was to investigate possible changes in vanc
omycin serum levels induced by cardio-pulmonary bypass (CPB). Ten card
iac patients (seven males, three females, aged between 56 and 81), who
underwent cardiac surgery requiring CPB, took part in the study. Vanc
omycin (15 mg kg(-1)) was intravenously infused over 60 min before ana
esthesia and blood samples were taken at appropriate times after drug
administration (0, 0.5, 1, 6, 8 h), after starting CPB (0, 5, 30 and 6
0 min) and after aortic unclamping (0, 5, 30, 60, 120 min). Drug serum
concentrations were determined by means of a fluorescence polarizatio
n immunoassay. The area under the concentration-time curve (AUC) measu
red during CPB were compared with the AUC extrapolated in the same int
erval by fitting a two-compartment pharmacokinetic model to drug conce
ntrations obtained before and after CPB. Five minutes after starting C
PB vancomycin serum levels decreased, on average, by 40.9% and remaine
d steadily lower than the expected values over the next 60 min. In the
same interval, the measured AUC was 31.7% lower than the expected AUC
. In no instance did serum levels fall below the MIC for most common p
athogens (1-2 mg l(-1)). At aortic unclamping serum levels slightly re
bounded but tended to remain lower than the expected concentrations ov
er the next 120 min. In conclusion, during CPB vancomycin serum levels
invariably decreased but, at the dose employed (15 mg kg(-1)), remain
ed in a potentially effective range for antimicrobial prophylaxis. (C)
1998 The Italian Pharmacological Society.