极低出生体重儿单次静脉给药地塞米松的药代动力学。

B Charles, P Schild, P Steer, D Cartwright, T Donovan
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引用次数: 33

摘要

研究了7例平均(+/- SD)胎龄25.6 +/- 0.5周、支气管肺发育不良的极低出生体重儿的单剂量地塞米松药代动力学。静脉注射地塞米松磷酸钠(0.369 +/- 0.04 mg/kg地塞米松)后,地塞米松浓度平均峰值为250.5 +/- 70.7 ng/ml。采用高效液相色谱法测定血浆地塞米松浓度。平均清除率(0.143 +/- 0.028升/公斤/小时)约为先前儿童和成人报告的一半,而半衰期(9.26 +/- 3.34小时)比这些患者长2- 3倍。分布体积(1.9 +/- 0.483升/kg)比先前一项成人研究报告的大,但与另一项研究中儿科和成人患者的分布体积相似。
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Pharmacokinetics of dexamethasone following single-dose intravenous administration to extremely low birth weight infants.

The single-dose pharmacokinetics of dexamethasone were studied in 7 extremely low birth weight infants of mean (+/- SD) gestational age 25.6 +/- 0.5 weeks suffering bronchopulmonary dysplasia. A mean peak dexamethasone concentration of 250.5 +/- 70.7 ng/ml was obtained following an intravenous bolus dose (0.369 +/- 0.04 mg/kg dexamethasone) of dexamethasone sodium phosphate. Dexamethasone was measured in plasma by HPLC. Mean clearance (0.143 +/- 0.028 litres/kg/h) was approximately half that reported previously in children and adults, while the half-life (9.26 +/- 3.34 h) was 2- to 3-fold longer than in these patients. The volume of distribution (1.9 +/- 0.483 litres/kg) was larger than reported in a previous study in adults, but was similar to that determined in pediatric and adult patients in another study.

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