[Kinetics of multiple-dose amikacin in the newborn infant].

A Olivesi, J Camboulives, C Charrel, D Unal
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Abstract

A pharmacokinetic study of amikacin was carried out in 12 neonates hospitalized in the intensive care unit. Serum amikacin levels were measured using a bacteriological method after one of several intramuscular injections of 7.5 micrograms/kg. Serum levels were greater than 10 micrograms/ml during the first three hours in 11 cases with values greater than or equal to 30 micrograms/ml. during the first two hours in five cases. The half life was measured in five patients and varied between three and eight hours. The plasma clearance was between 8.9 and 14 mil per minute per 1.73 m2. There is an unpredictable accumulation of this antibiotic especially in premature babies aged less than five days with a birth weight less than two kg. This accumulation is transitory when the clinical evolution of the case is favorable but it can be prolonged in unfavorable cases. The elimination of amikacin depends mainly on a patient's renal function. So, because of the risk of ototoxicity, the dosage should be reduced to 10 mg per kg-1 per 24 h-1, with measurements of the serum peak level and the level just before the following injection.

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[新生儿多剂量阿米卡星动力学]。
对重症监护病房12例新生儿阿米卡星进行了药代动力学研究。在肌肉注射7.5微克/千克后,用细菌学方法测定血清阿米卡星水平。11例前3小时血清浓度大于10微克/毫升,大于或等于30微克/毫升。五个病例的头两个小时。对5名患者的半衰期进行了测量,从3小时到8小时不等。血浆清除率在每分钟每1.73 m2 8.9 - 14mil之间。这种抗生素的积累是不可预测的,特别是在出生不足5天、出生体重不足2公斤的早产儿中。当病例的临床进展有利时,这种积累是短暂的,但在不利的情况下,它可以延长。阿米卡星的消除主要取决于患者的肾功能。因此,由于有耳毒性的风险,剂量应减少到每kg-1每24 h-1 10mg,并测量血清峰值水平和下一次注射前的水平。
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