Bertrand Y, Bréant V, Vray C, Nakache C, Barbé G, Dürr F, Aulagner G
Service d'hématologie-immunologie pédiatrique et de transplantation de moelle osseuse, Institut Pasteur, France.
Arch Pediatr. 1996 Sep;3(9):854-60. doi: 10.1016/0929-693x(96)87572-5.
The efficacy of single daily dose of amikacin has been recently demonstrated in neutropenic children with fever.
Eighteen children aged 1 to 15 years were included in the study. All patients were febrile and granulocytopenic and had indwelling intravenous catheter. Amikacin was administered as a 30-minute intravenous infusion once daily (20 mg/kg on day 1, then 15 mg/kg) for 3 to 30 days; the patients received amikacin in combination with piperacillin and vancomycin. Serum levels of amikacin were measured on days 1, 3, 6 and 10, and 30 min, 60 min and 180 min after the end of the infusion.
All patients responded favourably to the antibiotic therapy. Sixty-two kinetics were performed: peak amikacin concentrations measured (30 min after 30-min infusion) on day 1 averaged 43.7 micrograms/mL (+/- 13.8). A significant increase in peak serum concentrations was observed during the treatment (day 3 vs day 10) without change in the trough serum concentrations. The volumes of distribution were considerably important in these granulocytopenic children and there was a large inter and intra-patient variability; the elimination half-life of the amikacin was short (1.45 h). There was no significant nephrotoxicity in any patient.
The use of single daily dose amikacin in combination with a broad spectrum beta-lactam antibiotic and vancomycin was efficient and safe in febrile granulocytopenic children. The simulation of the amikacin behaviour in the deep compartment should be evaluated; in fact, it might reflect better accumulation of the drug than serum concentrations.
近期已证实每日单次剂量的阿米卡星对发热的中性粒细胞减少儿童有效。
18名年龄在1至15岁的儿童纳入本研究。所有患者均发热且粒细胞减少,并有留置静脉导管。阿米卡星通过静脉输注30分钟,每日一次给药(第1天20mg/kg,之后15mg/kg),持续3至30天;患者接受阿米卡星联合哌拉西林和万古霉素治疗。在第1、3、6和10天以及输注结束后30分钟、60分钟和180分钟测量血清阿米卡星水平。
所有患者对抗生素治疗反应良好。共进行了62次药代动力学研究:第1天测量的阿米卡星峰值浓度(30分钟输注结束后30分钟)平均为43.7微克/毫升(±13.8)。治疗期间观察到峰值血清浓度显著增加(第3天与第10天相比),而谷值血清浓度无变化。这些粒细胞减少儿童的分布容积相当大,患者间和患者内存在较大变异性;阿米卡星的消除半衰期较短(1.45小时)。所有患者均未出现明显肾毒性。
每日单次剂量的阿米卡星联合广谱β-内酰胺抗生素和万古霉素在发热的粒细胞减少儿童中使用有效且安全。应评估阿米卡星在深部腔室中的行为模拟;实际上,它可能比血清浓度更好地反映药物的蓄积情况。