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首页> 外文期刊>Therapeutic Drug Monitoring >Pharmacokinetic profile of voriconazole in a critically Ill patient on therapeutic plasma exchange
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Pharmacokinetic profile of voriconazole in a critically Ill patient on therapeutic plasma exchange

机译:伏立康唑在重症患者血浆置换治疗中的药代动力学

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BACKGROUND: Extracorporeal removal of drugs during therapeutic plasma exchange (TPE) can lead to decreased efficacy, as shown in several reports discussing altered pharmacokinetics (PKs) of antibiotics during TPE. In particular, drugs with a low volume of distribution or a high protein binding are susceptible to extracorporeal removal, as these drugs remain substantially within the intravascular space. No information is known about antifungal drug removal during TPE. We report the PKs of voriconazole in a critically ill patient undergoing TPE. METHODS: A 61-year-old man, presenting with catastrophic antiphospholipid syndrome for which TPE was started, developed probable pulmonary invasive aspergillosis. Intravenous voriconazole was started. Blood samples were taken under steady state conditions to calculate PK parameters of voriconazole, both with and without TPE. RESULTS: PK parameters (area under the curve, Cl, Vd, and t1/2) were equivalent on both days. Voriconazole has a distribution volume of 4.5 L/kg and a protein binding of 58%, suggesting that drug removal during TPE would not be clinically significant. Our data support this assumption. CONCLUSION: Based on our findings, it seems that TPE does not alter the PK behavior of voriconazole. Voriconazole dosages should not be adjusted during TPE.
机译:背景:在治疗性血浆置换(TPE)期间体外清除药物会导致功效降低,如讨论TPE期间抗生素药代动力学(PKs)改变的几份报告所述。特别地,具有低分布体积或高蛋白结合的药物易于被体外去除,因为这些药物基本上保留在血管内空间内。没有关于TPE期间抗真菌药物去除的信息。我们报告伏立康唑在接受TPE的重症患者中的PKs。方法:一名61岁男性,患有开始使用TPE的灾难性抗磷脂综合征,发展为可能的肺部侵袭性曲霉病。开始静脉内伏立康唑。在稳态条件下采集血样以计算伏立康唑在有无TPE时的PK参数。结果:PK参数(曲线下的面积,Cl,Vd和t1 / 2)在两天内均相等。伏立康唑的分布体积为4.5 L / kg,蛋白质结合率为58%,这表明TPE期间的药物去除在临床上并不重要。我们的数据支持这一假设。结论:根据我们的发现,看来TPE不会改变伏立康唑的PK行为。在TPE期间不应调整伏立康唑的剂量。

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