Flezzani P, Alvis M J, Jacobs J R, Schilling M M, Bai S, Reves J G
Department of Anesthesiology, Duke University Medical Center, Durham, NC 27710.
Can J Anaesth. 1987 Nov;34(6):566-9. doi: 10.1007/BF03010512.
In order to investigate the ability of a computer-assisted continuous infusion (CACI) system to maintain constant plasma levels of sufentanil during cardiopulmonary bypass (CPB) using pharmacokinetic data derived from healthy surgical patients to determine the infusion rate, ten patients were anaesthetized with diazepam, enflurane and oxygen until ten minutes prior to the expected time of initiation of CPB. At that point, an infusion of sufentanil, aimed to reach a central compartment concentration of 5 ng.ml-1, was started via CACI. Plasma concentrations of sufentanil, haematocrit, total protein and albumin concentrations, and nasopharyngeal and CPB inflow temperatures were obtained at predetermined intervals before and up to 90 min after the initiation of CPB. Plasma concentrations of sufentanil reached 3.8 +/- 0.4 ng.ml-1 before CPB and approached the 5.0 ng.ml-1 set point (4.7 +/- 0.4 ng.ml-1) over the 90 min of CPB. In conclusion, our results show that it is possible to obtain stable plasma levels of sufentanil on CPB using a pharmacokinetically driven infusion scheme; however, our data suggest that use of such a system may lead to accumulation of drug during CPB.
为了研究计算机辅助持续输注(CACI)系统在体外循环(CPB)期间维持舒芬太尼血浆浓度恒定的能力,利用来自健康手术患者的药代动力学数据确定输注速率,对10例患者使用地西泮、恩氟烷和氧气进行麻醉,直至预期开始CPB前10分钟。此时,通过CACI开始输注舒芬太尼,目标是使中央室浓度达到5 ng.ml-1。在CPB开始前及开始后90分钟内的预定时间点获取舒芬太尼的血浆浓度、血细胞比容、总蛋白和白蛋白浓度,以及鼻咽部和CPB流入温度。CPB前舒芬太尼的血浆浓度达到3.8±0.4 ng.ml-1,并在CPB的90分钟内接近5.0 ng.ml-1的设定值(4.7±0.4 ng.ml-1)。总之,我们的结果表明,使用药代动力学驱动的输注方案在CPB期间有可能获得稳定的舒芬太尼血浆浓度;然而,我们的数据表明,使用这样的系统可能会导致CPB期间药物蓄积。