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咪达唑仑在危重症儿科患者中的药代动力学

Pharmacokinetics of midazolam in critically ill pediatric patients.

作者信息

Nahara M C, McMorrow J, Jones P R, Anglin D, Rosenberg R

机构信息

Colleges of Pharmacy and Medicine, Ohio State University and Children's Research Institute, Children's Hospital Columbus, Ohio, USA.

出版信息

Eur J Drug Metab Pharmacokinet. 2000 Jul-Dec;25(3-4):219-21. doi: 10.1007/BF03192317.

Abstract

Midazolam is frequently used to produce sedation in critically ill pediatric patients. We studied the pharmacokinetics of midazolam in 22 patients (age 8 days to 16 years). The intravenous infusion rate to produce sedation ranged from 49-385 mcg/kg/hr. The blood samples were obtained at steady-state and midazolam was measured by gas chromatography with electron capture. The steady-state plasma concentrations of midazolam ranged from 49-385 ng/mL. The total clearance, apparent volume of distribution, and elimination half-life ranged from 0.1-3.1 L/kg/hr, 0.2-3.5 L/kg, and 0.3-10.9 hours, respectively. The marked interpatient variability in pharmacokinetics explains in part, the substantial variation in dosage requirements of midazolam to produce sedation in critically ill pediatric patients.

摘要

咪达唑仑常用于为危重症儿科患者实施镇静。我们研究了22例患者(年龄8天至16岁)体内咪达唑仑的药代动力学。产生镇静作用的静脉输注速率为49 - 385微克/千克/小时。在稳态时采集血样,采用电子捕获气相色谱法测定咪达唑仑。咪达唑仑的稳态血浆浓度为49 - 385纳克/毫升。总清除率、表观分布容积和消除半衰期分别为0.1 - 3.1升/千克/小时、0.2 - 3.5升/千克和0.3 - 10.9小时。患者间药代动力学的显著差异部分解释了在危重症儿科患者中使用咪达唑仑产生镇静作用时剂量需求的大幅变化。

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