We have evaluated the disposition of milrinone in seven patients with
low cardiac output after elective cardiac surgery involving cardiopulm
onary bypass. Patients received a loading dose of milrinone 50 mu g kg
(-1) given over 10 min followed immediately by an infusion of 0.5 mu g
kg(-1) min(-1), continued for a minimum of 5 h. Plasma concentrations
of milrinone were measured at designated intervals during the infusio
n and for 6 h after its termination, by high pressure liquid chromatog
raphy. Concentrations greater than 100 ng ml(-1) were produced in all
patients within 2 min of starting the loading dose and were maintained
for the duration of the infusion. Volume of distribution, clearance a
nd terminal half-life were similar to those found in patients with chr
onic cardiac failure.