首页> 外文期刊>BMC Anesthesiology >Population pharmacokinetic-pharmacodynamic model of propofol in adolescents undergoing scoliosis surgery with intraoperative wake-up test: a study using Bispectral index and composite auditory evoked potentials as pharmacodynamic endpoints
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Population pharmacokinetic-pharmacodynamic model of propofol in adolescents undergoing scoliosis surgery with intraoperative wake-up test: a study using Bispectral index and composite auditory evoked potentials as pharmacodynamic endpoints

机译:丙泊酚在接受脊柱侧弯手术的青少年的术中唤醒试验中的群体药代动力学模型:使用双光谱指数和复合听觉诱发电位作为药效学终点的研究

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In adolescents limited data are available on the pharmacokinetics (PK) and pharmacodynamics (PD) of propofol. In this study we derived a PK-PD model for propofol in adolescents undergoing idiopathic scoliosis surgery with an intraoperative wake-up test with reinduction of anesthesia using both Bispectral Index (BIS) and composite A-line ARX index (cAAI) as endpoints. Fourteen adolescents (9.8–20.1?years) were evaluated during standardized propofol-remifentanil anesthesia for idiopathic scoliosis surgery with an intraoperative wake-up test with reinduction of anesthesia. BIS and cAAI were continuously measured and blood samples collected. A propofol PKPD model was developed using NONMEM. The time courses of propofol concentrations, BIS and cAAI values during anesthesia, intra-operative wakeup and reduction of anesthesia were best described by a two-compartment PK model linked to an inhibitory sigmoidal Emax PD model. For the sigmoidal Emax model, the propofol concentration at half maximum effect (EC50) was 3.51 and 2.14?mg/L and Hill coefficient 1.43 and 6.85 for BIS and cAAI, respectively. The delay in PD effect in relation to plasma concentration was best described by a two compartment effect-site model with a keo of 0.102?min??1, ke12 of 0.121?min??1 and ke21 of 0.172?min??1. A population PKPD model for propofol in adolescents was developed that successfully described the time course of propofol concentration, BIS and cAAI in individuals upon undergoing scoliosis surgery with intraoperative wake-up test and reinduction of anesthesia. Large differences were demonstrated between both monitors. This may imply that BIS and cAAI measure fundamentally different endpoints in the brain.
机译:在青少年中,关于异丙酚的药代动力学(PK)和药效学(PD)的数据有限。在这项研究中,我们使用双频谱指数(BIS)和复合A线ARX指数(cAAI)作为终点,通过接受术中唤醒试验并麻醉性降低的特发性脊柱侧凸手术的青少年,得出了异丙酚的PK-PD模型。在标准丙泊酚-瑞芬太尼麻醉期间对14例青少年(9.8–20.1岁)进行了特发性脊柱侧凸手术,并在术中进行了麻醉诱导的唤醒测试,以评估他们的状态。持续测量BIS和cAAI,并收集血液样本。使用NONMEM开发了异丙酚PKPD模型。麻醉,手术中苏醒和麻醉减少期间丙泊酚浓度,BIS和cAAI值的时程最好通过与抑制性乙状结肠Emax PD模型相关的两室PK模型来描述。对于S型Emax模型,BIS和cAAI的半最大效应(EC50)的异丙酚浓度分别为3.51和2.14?mg / L,希尔系数为1.43和6.85。 PD效应相对于血浆浓度的延迟最好用两室效应部位模型描述,其keo为0.102Ω·min-1,ke12为0.121Ω·min-1,ke21为0.172Ω·min-1。建立了青少年异丙酚的人群PKPD模型,该模型成功描述了接受脊柱侧弯手术并进行术中唤醒测试和麻醉诱导的个体中异丙酚浓度,BIS和cAAI的时间过程。两个监视器之间显示出很大的差异。这可能意味着BIS和cAAI测量的是大脑中根本不同的端点。

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