首页> 外文期刊>American Journal of Kidney Diseases: The official journal of the National Kidney Foundation >Pharmacokinetic modeling and simulation of procainamide and n-acetylprocainamide in a patient receiving continuous renal replacement therapy: A novel approach to guide renal dose adjustments
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Pharmacokinetic modeling and simulation of procainamide and n-acetylprocainamide in a patient receiving continuous renal replacement therapy: A novel approach to guide renal dose adjustments

机译:接受连续性肾脏替代治疗的患者中普鲁卡因胺和正乙酰普鲁卡因胺的药代动力学建模和模拟:一种指导调整肾脏剂量的新方法

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摘要

To the Editor: Procainamide and its major metabolite, N-acetylprocainamide (NAPA), prolong the QTc interval and can promote torsades de pointes, particularly at high concentrations (>30 mg/L combined procainamide/NAPA). Excretion of procainamide and NAPA is reduced in patients with CKD; their elimination in patients undergoing continuous renal replacement therapy (CRRT) has not been evaluated. Therefore, appropriate dose adjustments in this population are unknown. This report describes the pharmacokinetics (PK) of procainamide and NAPA in a CKD stage 5 patient undergoing CRRT. PK simulations of drug exposure following several dosing regimens were performed to help guide dosing in patients undergoing CRRT.
机译:致编者:普鲁卡因酰胺及其主要代谢物N-乙酰基普鲁卡因酰胺(NAPA)延长QTc间隔,并能促进尖端扭转型室速,特别是在高浓度(> 30 mg / L普鲁卡因酰胺/ NAPA的情况下)。 CKD患者的普鲁卡因胺和NAPA排泄减少;尚未评估接受持续肾脏替代疗法(CRRT)的患者对它们的消除作用。因此,在该人群中适当的剂量调整是未知的。该报告描述了接受CRRT的CKD 5期患者中普鲁卡因酰胺和NAPA的药代动力学(PK)。在几种给药方案后进行了药物暴露的PK模拟,以帮助指导接受CRRT的患者给药。

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