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COVID-19 药物治疗在体外膜肺氧合回路中易被隔离:一项体外膜肺氧合研究。

COVID-19 Drug Treatments Are Prone to Sequestration in Extracorporeal Membrane Oxygenation Circuits: An Ex Vivo Extracorporeal Membrane Oxygenation Study.

机构信息

From the University of Queensland Centre for Clinical Research, Faculty of Medicine, The University of Queensland, Australia.

Department of Intensive Care Medicine, Royal Brisbane and Women's Hospital, Herston, Queensland, Australia.

出版信息

ASAIO J. 2024 Jun 1;70(6):546-552. doi: 10.1097/MAT.0000000000002120. Epub 2023 Dec 21.

Abstract

Drug treatments for coronavirus disease 2019 (COVID-19) dramatically improve patient outcomes, and although extracorporeal membrane oxygenation (ECMO) has significant use in these patients, it is unknown whether ECMO affects drug dosing. We used an ex vivo adult ECMO model to measure ECMO circuit effects on concentrations of specific COVID-19 drug treatments. Three identical ECMO circuits used in adult patients were set up. Circuits were primed with fresh human blood (temperature and pH maintained within normal limits). Three polystyrene jars with 75 ml fresh human blood were used as controls. Remdesivir, GS-441524, nafamostat, and tocilizumab were injected in the circuit and control jars at therapeutic concentrations. Samples were taken from circuit and control jars at predefined time points over 6 h and drug concentrations were measured using validated assays. Relative to baseline, mean (± standard deviation [SD]) study drug recoveries in both controls and circuits at 6 h were significantly lower for remdesivir (32.2% [±2.7] and 12.4% [±2.1], p < 0.001), nafamostat (21.4% [±5.0] and 0.0% [±0.0], p = 0.018). Reduced concentrations of COVID-19 drug treatments in ECMO circuits is a clinical concern. Remdesivir and nafamostat may need dose adjustments. Clinical pharmacokinetic studies are suggested to guide optimized COVID-19 drug treatment dosing during ECMO.

摘要

药物治疗 2019 年冠状病毒病(COVID-19)可显著改善患者的预后,虽然体外膜肺氧合(ECMO)在这些患者中有重要的应用,但尚不清楚 ECMO 是否会影响药物剂量。我们使用体外成人 ECMO 模型来测量 ECMO 回路对特定 COVID-19 药物治疗浓度的影响。使用 3 个相同的 ECMO 回路来建立模型,回路用新鲜的人体血液进行预充(温度和 pH 值保持在正常范围内)。使用 3 个装有 75ml 新鲜人体血液的聚苯乙烯瓶作为对照。以治疗浓度将瑞德西韦、GS-441524、那屈肝素和托珠单抗注射到回路和对照瓶中。在 6 小时内的预定时间点从回路和对照瓶中取样,并使用验证后的检测方法测量药物浓度。与基线相比,瑞德西韦(32.2%[±2.7]和 12.4%[±2.1],p<0.001)和那屈肝素(21.4%[±5.0]和 0.0%[±0.0],p=0.018)在 6 小时时,无论是在对照瓶还是回路中,研究药物的平均回收率(±标准偏差[SD])均显著降低。ECMO 回路中 COVID-19 药物治疗浓度降低是一个临床问题。瑞德西韦和那屈肝素可能需要调整剂量。建议进行临床药代动力学研究,以指导 ECMO 期间 COVID-19 药物治疗的优化剂量。

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