Ahmed A, París M M, Trujillo M, Hickey S M, Wubbel L, Shelton S L, McCracken G H
Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas 75235-9063, USA.
Antimicrob Agents Chemother. 1997 Jan;41(1):49-53. doi: 10.1128/AAC.41.1.49.
In vitro and in vivo studies have demonstrated that the bacteriologic efficacy of once-daily aminoglycoside therapy is equivalent to that achieved with conventional multiple daily dosing. The impact of once-daily dosing for meningitis has not been studied. Using the well-characterized rabbit meningitis model, we compared two regimens of the same daily dosage of gentamicin given either once or in three divided doses for 24 or 72 h. The initial 1 h mean cerebrospinal fluid (CSF) gentamicin concentration for animals receiving a single dose (2.9 +/- 1.7 micrograms/ml) was threefold higher than that for the animals receiving multiple doses. The rate of bacterial killing in the first 8 h of treatment was significantly greater for the animals with higher concentrations in their CSF (-0.21 +/- 0.19 versus -0.03 +/- 0.22 log10 CFU/ml/h), suggesting concentration-dependent killing. By 24h, the mean reduction in bacterial titers was similar for the two regimens. In animals treated for 72 h, no differences in bactericidal activity was noted for 24, 48, or 72 h. Gentamicin at two different dosages was administered intracisternally to a separate set of animals to achieve considerably higher CSF gentamicin concentrations. In these animals, the rate of bacterial clearance in the first 8 h (0.52 +/- 0.15 and 0.58 +/- 0.15 log10 CFU/ml/h for the lower and higher dosages, respectively) was significantly greater than that in animals treated intravenously. In conclusion, there is evidence of concentration-dependent killing with gentamicin early in treatment for experimental E. coli meningitis, and once-daily dosing therapy appears to be at least as effective as multiple-dose therapy in reducing bacterial counts in CSF.
体外和体内研究均已表明,每日一次氨基糖苷类药物治疗的细菌学疗效等同于传统的每日多次给药疗法。每日一次给药对脑膜炎的影响尚未得到研究。我们使用特征明确的兔脑膜炎模型,比较了相同每日剂量庆大霉素的两种给药方案,一种为单次给药,另一种为分三次给药,给药时间分别为24小时或72小时。接受单次给药的动物,其最初1小时脑脊液(CSF)中庆大霉素的平均浓度(2.9±1.7微克/毫升)是接受多次给药动物的三倍。治疗开始后8小时内,脑脊液中药物浓度较高的动物细菌杀灭率显著更高(-0.21±0.19对-0.03±0.22 log10 CFU/毫升/小时),提示存在浓度依赖性杀菌作用。到24小时时,两种给药方案的细菌滴度平均降低情况相似。在接受72小时治疗的动物中,24小时、48小时或72小时时杀菌活性均无差异。向另一组动物脑池内注射两种不同剂量的庆大霉素,以使脑脊液中庆大霉素浓度显著更高。在这些动物中,最初8小时的细菌清除率(较低剂量和较高剂量分别为0.52±0.15和0.58±0.15 log10 CFU/毫升/小时)显著高于静脉给药治疗的动物。总之,有证据表明在实验性大肠杆菌脑膜炎治疗早期,庆大霉素存在浓度依赖性杀菌作用,且每日一次给药疗法在降低脑脊液中细菌数量方面似乎至少与多次给药疗法同样有效。