CONTINUOUS-INFUSION OF NIMODIPINE DURING CORONARY-ARTERY SURGERY - HEMODYNAMIC AND PHARMACOKINETIC STUDY

Citation
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
Citations number
33
Categorie Soggetti
Anesthesiology
ISSN journal
00070912
Volume
74
Issue
5
Year of publication
1995
Pages
526 - 533
Database
ISI
SICI code
0007-0912(1995)74:5<526:CONDCS>2.0.ZU;2-M
Abstract
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.