接受心肺旁路手术的韩国成年患者体内舒芬太尼的群体药代动力学模型。

IF 3.1 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Vipada Khaowroongrueng, Kuk Hui Son, Sang-Min Lee, JiYeon Lee, Chun-Gon Park, Seok In Lee, Dongseong Shin, Kwang-Hee Shin
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引用次数: 0

摘要

舒芬太尼因其心血管安全性和良好的药代动力学特性而经常被用作心脏手术的麻醉剂。然而,人们对舒芬太尼在接受心肺旁路(CPB)手术的患者中的药代动力学特征仍然知之甚少,而这对于达到理想的麻醉水平和减少手术并发症至关重要。因此,本研究旨在建立心肺旁路手术患者舒芬太尼的群体药代动力学模型,并阐明影响其药代动力学特征的临床因素。研究对象为接受 CPB 心脏手术并使用舒芬太尼进行麻醉的成人患者。采集动脉血样本以量化舒芬太尼的血浆浓度和临床实验室参数,包括炎症细胞因子。采用非线性混合效应模型建立了群体药代动力学模型。使用最终模型的药代动力学参数进行了模拟。共有 20 名患者被纳入最终分析。舒芬太尼药代动力学模型采用双室模型,考虑了 CPB 的影响。舒芬太尼清除率在 CPB 和暖宫阶段增加了 2.80 倍,而中心室容积在 CPB 期间增加了 2.74 倍。CPB 是影响药物清除率和分布容积的重要协变量。尽管 CPB 期间 IL-6、IL-8 和 TNF-α 等炎性细胞因子水平升高,但未发现其他重要的协变量。模拟结果显示,目标控制输注的负荷剂量为 30 微克,维持输注剂量为 40 微克/小时。此外,还在 CPB 开始时添加了 60 μg 的栓塞剂量,以调整此阶段的暴露变化。考虑到舒芬太尼的目标浓度,采用统一的给药方案可实现有效镇痛。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Population pharmacokinetic modeling of sufentanil in adult Korean patients undergoing cardiopulmonary bypass surgery

Population pharmacokinetic modeling of sufentanil in adult Korean patients undergoing cardiopulmonary bypass surgery

Sufentanil is frequently used as an anesthetic agent in cardiac surgery owing to its cardiovascular safety and favorable pharmacokinetics. However, the pharmacokinetics profiles of sufentanil in patients undergoing cardiopulmonary bypass (CPB) surgery remain less understood, which is crucial for achieving the desired level of anesthesia and mitigating surgical complications. Therefore, this study aimed to develop a population pharmacokinetic model of sufentanil in patients undergoing CPB surgery and elucidate the clinical factors affecting its pharmacokinetic profile. Adult patients who underwent cardiac surgery with CPB and were administered sufentanil for anesthesia were enrolled. Arterial blood samples were collected to quantify plasma concentrations of sufentanil and clinical laboratory parameters, including inflammatory cytokines. A population pharmacokinetic model was established using nonlinear mixed-effects modeling. Simulations were performed using the pharmacokinetic parameters of the final model. Overall, 20 patients were included in the final analysis. Sufentanil pharmacokinetics were modeled using a two-compartment model, accounting for CPB effects. Sufentanil clearance increased 2.80-fold during CPB and warming phases, while the central compartment volume increased 2.74-fold during CPB. CPB was a significant covariate affecting drug clearance and distribution volume. No other significant covariates were identified despite increased levels of the inflammatory cytokines, including IL-6, IL-8, and TNF-α during CPB. The simulation indicated a 30 μg loading dose and 40 μg/h maintenance infusion for target-controlled infusion. Additionally, a bolus dose of 60 μg was added at CPB initiation to adjust for exposure changes during this phase. Considering the target sufentanil concentrations, a uniform dosing regimen was acceptable for effective analgesia.

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来源期刊
CiteScore
5.00
自引率
11.40%
发文量
146
审稿时长
8 weeks
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