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Predictive performance of the 'Minto' remifentanil pharmacokinetic parameter set in morbidly obese patients ensuing from a new method for calculating lean body mass.

机译:通过一种计算瘦体重的新方法,“ Minto”瑞芬太尼药代动力学参数组在病态肥胖患者中的预测性能。

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BACKGROUND AND OBJECTIVES: In a previous article, we showed that the pharmacokinetic set of remifentanil used for target-controlled infusion (TCI) might be biased in obese patients because it incorporates flawed equations for the calculation of lean body mass (LBM), which is a covariate of several pharmacokinetic parameters in this set. The objectives of this study were to determine the predictive performance of the original pharmacokinetic set, which incorporates the James equation for LBM calculation, and to determine the predictive performance of the pharmacokinetic set when a new method to calculate LBM was used (the Janmahasatian equations). METHODS: This was an observational study with intraoperative observations and no follow-up. Fifteen morbidly obese inpatients scheduled for bariatric surgery were included in the study. The intervention included manually controlled continuous infusion of remifentanil during the surgery and analysis of arterial blood samples to determine the arterial remifentanil concentration, to be compared with concentrations predicted by either the unadjusted or the adjusted pharmacokinetic set. The statistical analysis included parametric and non-parametric tests on continuous variables and determination of the median performance error (MDPE), median absolute performance error (MDAPE), divergence and wobble. RESULTS: The median values (interquartile ranges) of the MDPE, MDAPE, divergence and wobble for the James equations during maintenance were -53.4% (-58.7% to -49.2%), 53.4% (49.0-58.7%), 3.3% (2.9-4.7%) and 1.4% h(-1) (1.1-2.5% h(-1)), respectively. The respective values for the Janmahasatian equations were -18.9% (-24.2% to -10.4%), 20.5% (13.3-24.8%), 2.6% (-0.7% to 4.5%) and 1.9% h(-1) (1.4-3.0% h(-1)). The performance (in terms of the MDPE and MDAPE) of the corrected pharmacokinetic set was better than that of the uncorrected one. The predictive performance of the original pharmacokinetic set is not clinically acceptable. Use of a corrected LBM value in morbidly obese patients corrects this pharmacokinetic set and allows its use in obese patients. The 'fictitious height' can be a valid alternative for use of TCI infusion of remifentanil in morbidly obese patients until commercially available infusion pumps and research software are updated and new LBM equations are implemented in their algorithms.
机译:背景和目的:在上一篇文章中,我们表明用于肥胖症患者的瑞芬太尼用于靶控输注(TCI)的药代动力学组可能存在偏差,因为它结合了有缺陷的方程式来计算瘦体重(LBM),即该组中几个药代动力学参数的协变量。这项研究的目的是确定结合了James方程进行LBM计算的原始药代动力学组的预测性能,以及使用新的计算LBM的方法(Janmahasatian方程)确定药代动力学组的预测性能。 。方法:这是一项观察性研究,没有术中观察,也没有随访。计划进行肥胖治疗的15名病态肥胖住院患者被纳入研究。干预措施包括在手术过程中手动控制的瑞芬太尼的连续输注和动脉血样的分析以确定动脉瑞芬太尼的浓度,并与未经调整或调整后的药代动力学组预测的浓度进行比较。统计分析包括对连续变量的参数和非参数检验,并确定中位数性能误差(MDPE),中位数绝对性能误差(MDAPE),发散和摆动。结果:维护期间James方程的MDPE,MDAPE,散度和摆动的中值(四分位数范围)分别为-53.4%(-58.7%至-49.2%),53.4%(49.0-58.7%),3.3%(分别为2.9-4.7%和1.4%h(-1)(1.1-2.5%h(-1))。 Janmahasatian方程的相应值分别为-18.9%(-24.2%至-10.4%),20.5%(13.3-24.8%),2.6%(-0.7%至4.5%)和1.9%h(-1)(1.4 -3.0%h(-1))。校正后的药代动力学组的性能(就MDPE和MDAPE而言)要优于未校正的药代动力学组。原始药代动力学组的预测性能在临床上不可接受。在病态肥胖患者中使用校正后的LBM值可纠正此药代动力学设置,并允许其在肥胖患者中使用。 “假想身高”可能是在病态肥胖患者中使用TCI输注瑞芬太尼的有效选择,直到更新了市售输液泵和研究软件并在其算法中实现了新的LBM方程式。

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