Crankshaw D P, Morgan D J, Beemer G H, Karasawa F
Department of Anaesthesia, Royal Melbourne Hospital, Victoria, Australia.
Anesth Analg. 1993 Mar;76(3):556-61. doi: 10.1213/00000539-199303000-00019.
A variable rate infusion regimen, designed to rapidly achieve and maintain a target arterial concentration (CT) of 100 micrograms.L-1 of alfentanil, was developed using the method of Plasma Drug Efflux. This method uses a series of clearance values (Ep), calculated as the ratio of instantaneous infusion rate/arterial plasma drug concentration normalized to lean body mass (LBM), at various sampling times during a suboptimal infusion regimen. Values of Ep are used to calculate an infusion rate versus time profile to achieve CT, and the process is repeated in consecutive small groups of subjects to yield an optimal result, i.e., it is an iterative process. Thirty-three adult surgical patients were given alfentanil during anesthesia for approximately 1 h before cardiopulmonary bypass. In an initial group of four patients, who received a simple two-stage infusion, plasma alfentanil concentration was measured at frequent intervals and Ep(L.min-1.kg LBM-1) was estimated at each sampling time. The calculated infusion-rate-versus-time profile to produce CT was obtained from the product Ep x CT for each time point and was transferred to the read-only memory of a computerized infusion pump. This new variable infusion profile was used in four patients, and the process was repeated in three further groups of 5, 8, and 12 patients using infusion profiles calculated from the previous group. Each set of concentration data was assessed by calculating the performance error (PE), the median performance error (MDPE), i.e., bias, and the median absolute value of PE (MDAPE), i.e., inaccuracy.(ABSTRACT TRUNCATED AT 250 WORDS)
采用血浆药物外排法制定了一种可变速率输注方案,旨在快速达到并维持阿芬太尼动脉血药浓度(CT)为100微克·升⁻¹。该方法在次优输注方案的不同采样时间使用一系列清除率值(Ep),Ep计算为瞬时输注速率与按瘦体重(LBM)标准化的动脉血浆药物浓度之比。Ep值用于计算达到CT的输注速率与时间曲线,然后在连续的小群受试者中重复该过程以获得最佳结果,即这是一个迭代过程。33名成年外科手术患者在体外循环前麻醉期间给予阿芬太尼约1小时。在最初的4名患者组中,他们接受简单的两阶段输注,频繁测量血浆阿芬太尼浓度,并在每个采样时间估计Ep(升·分钟⁻¹·千克LBM⁻¹)。通过每个时间点的Ep×CT乘积获得产生CT的计算出的输注速率与时间曲线,并将其传输到计算机化输注泵的只读存储器中。这种新的可变输注曲线用于4名患者,并在前一组计算出的输注曲线基础上,在另外三组分别为5名、8名和12名患者中重复该过程。通过计算性能误差(PE)、中位性能误差(MDPE)即偏差以及PE的中位绝对值(MDAPE)即不准确性来评估每组浓度数据。(摘要截断于250字)