Yogev R, Kolling W M
Antimicrob Agents Chemother. 1981 Nov;20(5):583-6. doi: 10.1128/AAC.20.5.583.
Serum and ventricular fluid pharmacokinetic data for amikacin were evaluated prospectively in 10 hydrocephalic children with suspected ventriculitis. After the fourth or fifth intravenous 7.5-mg/kg dose of amikacin given every 8 h, mean peak serum levels were 24.3 +/- 3.2 microgram/ml (achieved at 0.5 h) with a calculated half-life of 2.2 +/- 1.1 h. Mean peak ventricular fluid levels in five patients with bacterial infection were 6.1 +/- 2.0 microgram/ml (achieved at 3 h). In the remaining five patients without bacterial ventriculitis, very low levels (less than or equal to 0.7 microgram/ml) of amikacin were detected. Ventricular fluid pleocytosis was directly correlated and glucose levels were inversely correlated with penetration of amikacin. Systemic therapy with amikacin may be the treatment of choice for children with ventriculitis meningitis caused by bacteria which are highly susceptible to this drug, thereby permitting the avoidance of the potentially hazardous intraventricular route of administration.
对10名疑似脑室炎的脑积水患儿进行了前瞻性评估,以获取阿米卡星的血清和脑室液药代动力学数据。每8小时静脉注射7.5mg/kg剂量的阿米卡星,在第四次或第五次给药后,血清平均峰值水平为24.3±3.2微克/毫升(在0.5小时达到),计算得出的半衰期为2.2±1.1小时。5例细菌感染患者的脑室液平均峰值水平为6.1±2.0微克/毫升(在3小时达到)。在其余5例无细菌性脑室炎的患者中,检测到的阿米卡星水平非常低(≤0.7微克/毫升)。脑室液中细胞增多与阿米卡星的渗透呈正相关,葡萄糖水平与阿米卡星的渗透呈负相关。对于对该药物高度敏感的细菌引起的脑室炎脑膜炎患儿,阿米卡星全身治疗可能是首选治疗方法,从而避免了潜在危险的脑室内给药途径。