M. Hynynen et al., CONTINUOUS-INFUSION OF NIMODIPINE DURING CORONARY-ARTERY SURGERY - HEMODYNAMIC AND PHARMACOKINETIC STUDY, British Journal of Anaesthesia, 74(5), 1995, pp. 526-533
A continuous infusion of nimodipine 15 or 30 mu g kg(-1) h(-1) was adm
inistered from the evening before operation to the second morning afte
r operation to 14 patients undergoing elective coronary artery bypass
grafting (CABG) surgery. Nimodipine was tolerated well by all seven pa
tients who received the lower dose. However, of the seven patients who
received the higher dose, in two patients the infusion had to be disc
ontinued after induction of anaesthesia and immediately after surgery,
respectively, because of excessive vasodilatation and hypotension. At
steady state before cardiopulmonary bypass (CPB),total plasma nimodip
ine concentration was higher than expected on the basis of previous re
ports in non-surgical subjects. Similarly, mean clearance of nimodipin
e was lower than predicted, that is 0.53 (range 0.40-0.72) litre kg(-1
) h(-1). Initiation of CPB decreased total plasma nimodipine concentra
tion, but the unbound plasma concentration did not decrease because of
the increase observed in the free fraction of nimodipine in plasma. A
s evaluated in a separate closed extracorporeal circuit, nimodipine wa
s sequestered into the circuit. Addition of stored whole blood to the
priming solution attenuated this sequestration. It is concluded that c
learance of nimodipine, as assessed before CPB at steady state, was re
duced in patients undergoing CABG and receiving a continuous infusion
of nimodipine. Using this finding of decreased clearance in designing
infusion schemes of nimodipine for cardiac surgical patients, it shoul
d be possible to predict more accurately the desired plasma nimodipine
concentration and therefore reduce the possibility of unexpected haem
odynamic responses.