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Population pharmacokinetics of remifentanil in infants and children undergoing cardiac surgery

机译:瑞芬太尼在接受心脏手术的婴幼儿中的群体药代动力学

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Background The aim of this study was to provide a model-based analysis of the pharmacokinetics of remifentanil in infants and children undergoing cardiac surgery with cardiopulmonary bypass (CPB). Methods We studied nine patients aged 0.5 to 4 years who received a continuous remifentanil infusion via a computer-controlled infusion pump during cardiac surgery with mildly hypothermic CPB were studied. Arterial blood samples taken prior to, during and after CPB were analyzed for remifentanil concentrations using a validated gas-chromatographic mass-spectrophotometric assay. We used population mixed-effects modeling to characterize remifentanil pharmacokinetics. The final model was evaluated by its predictive performance. Results The pharmacokinetics of remifentanil was described by a 1-compartment model with adjustments for CPB. Population mean parameter estimates were 1.41 L for volume of distribution (V) and 0.244 L/min for clearance. V was increased during CPB and post-CPB to 2.41 times the pre-CPB value. The median prediction error and the median of individual median absolute prediction error were 2.44% and 21.6%, respectively. Conclusion Remifentanil dosage adjustments are required during and after CPB due to marked changes in the V of the drug. Simulations indicate that a targeted blood concentration of 14 ng/mL is achieved and maintained in 50% of typical patients by administration of an initial dose of 18 μg remifentanil followed by an infusion of 3.7 μg/min before, during and post-CPB, supplemented with a bolus dose of 25 μg given at the start of CPB.
机译:背景技术这项研究的目的是对瑞芬太尼在接受心肺转流术(CPB)进行心脏手术的婴儿和儿童中的药代动力学进行基于模型的分析。方法我们研究了9位0.5至4岁的患者,这些患者在心脏手术期间使用轻度低温CPB通过计算机控制的输液泵连续接受瑞芬太尼输注。使用经过验证的气相色谱质谱法分析CPB之前,期间和之后采集的动脉血样品中瑞芬太尼的浓度。我们使用人群混合效应模型来表征瑞芬太尼的药代动力学。最终模型通过其预测性能进行评估。结果瑞芬太尼的药代动力学由1室模型描述,并调整了CPB。总体平均参数估计值为分配体积(V)为1.41 L,清除率为0.244 L / min。在CPB期间和CPB之后,V增加到CPB之前值的2.41倍。中位数预测误差和单个中位数绝对预测误差的中位数分别为2.44%和21.6%。结论由于药物V的明显变化,在CPB期间和之后需要调整瑞芬太尼的剂量。模拟表明,通过在补充CPB之前,期间和之后注射初始剂量为18μg瑞芬太尼,然后输注3.7μg/ min,在50%的典型患者中达到并维持了14 ng / mL的目标血药浓度在CPB开始时给予25μg的推注剂量。

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