新生儿静脉注射克林霉素的药代动力学。

G Koren, Y Zarfin, D Maresky, T E Spiro, S M MacLeod
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引用次数: 0

摘要

我们研究了12名新生儿(胎龄26-39周[平均+/- SD, 30.6 +/- 4.7];出生体重640-2700克,[平均1,322±688];出生后1-24天[平均,9.6 +/- 8.5]),因怀疑或证实为坏死性小肠结肠炎(10例)或怀疑为厌氧败血症(2例)接受克林霉素磷酸治疗,剂量为每6小时3.2- 11mg /kg。克林霉素稳定状态下的平均血清浓度范围为12.7 ~ 40微克/毫升(治疗范围为2 ~ 10微克/毫升)。高浓度可归因于消除T1/2(6.3 +/- 2.1小时)比大龄儿童或成人长100%。克林霉素清除率(61.6 +/- 31.6 hr ml/kg/hr)低于大龄儿童或成人。由于观察到T1/2的延长和相应较低的清除率,新生儿静脉注射克林霉素的剂量应减少到15- 20mg /kg/天,分4次每日给药。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacokinetics of intravenous clindamycin in newborn infants.

We studied 12 newborn infants (gestational ages 26-39 wk [mean +/- SD, 30.6 +/- 4.7]; birth weight 640-2700 g, [mean, 1,322 +/- 688]; postnatal age 1-24 days [mean, 9.6 +/- 8.5]) who received clindamycin phosphate for suspected or proven necrotizing enterocolitis (ten patients) or suspected anaerobic septicemia (two patients) in doses of 3.2-11 mg/kg every six hours. Range of mean serum concentration of clindamycin at steady state was between 12.7 and 40 micrograms/ml (therapeutic range = 2-10 micrograms/ml). High concentrations could be attributed to elimination T1/2 (6.3 +/- 2.1 hr) 100% longer than in older children or adults. Clindamycin clearance (61.6 +/- 31.6 hr ml/kg/hr) was lower than in older children or adults. Because of the observed prolongation in T1/2 and correspondingly lower clearance, the IV dose of clindamycin in newborn infants should be reduced to 15-20 mg/kg/day given in four daily doses.

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