Tod M, Lortholary O, Seytre D, Semaoun R, Uzzan B, Guillevin L, Casassus P, Petitjean O
Hôpital Avicenne, and Centre de Recherche en Pathologie Infectieuse et Tropicale 93, UFR de Médecine Paris-Nord, Bobigny, France.
Antimicrob Agents Chemother. 1998 Apr;42(4):849-56. doi: 10.1128/AAC.42.4.849.
Once-daily (o.d.) administration of 20 mg of amikacin per kg of body weight to neutropenic patients has been validated by clinical studies, but amikacin pharmacokinetics have been documented only for the 7.5-mg/kg twice-daily (b.i.d.) regimen in this population. In order to determine in neutropenic patients (i) the influence of the dosing regimen on the kinetics of amikacin, (ii) the linearity of kinetics of amikacin in the range of 7.5 to 20 mg/kg, and (iii) the influence of patient characteristics on the disposition of amikacin and (iv) to provide a rationale for dosing recommendations, we evaluated the population pharmacokinetics of amikacin administered to 57 febrile neutropenic adults (neutrophil count, <500/mm3) being treated for a hematological disorder and receiving amikacin at 7.5 mg/kg b.i.d. (n = 29) or 20 mg/kg o.d. (n = 28) and administered intravenously over 0.5 h. A total of 278 blood samples were obtained (1 to 14 samples per patient) during one or several administration intervals (1 to 47). Serum amikacin levels were measured by the enzyme-multiplied immunoassay technique. A mixed-effect modeling approach was used to fit a bicompartmental model to the data (NONMEM software). The influences of the dosing regimen and the demographic and biological indices on the pharmacokinetic parameters of amikacin were evaluated by the maximum-likelihood ratio test on the population model. The dosing regimen had no influence on amikacin pharmacokinetic parameters, i.e., the kinetics of amikacin were linear over the range of 7.5 to 20 mg/kg. Amikacin elimination clearance (CL) was only correlated with creatinine clearance or its covariates, namely, sex, age, body weight, and serum creatinine level. The interindividual variability of CL was 21%, while those of the central volume of distribution, the distribution clearance, and the tissue volume of distribution were 15, 30, and 25%, respectively. On the basis of the expected distribution of amikacin concentrations in this population, dosing recommendations as a function of creatinine clearance (CL[CR]) are proposed: for patients with normal renal function (CL[CR] of 80 to 130 ml/min), 20 mg/kg o.d. is recommended, whereas for patients with severe renal impairment (CL[CR], 10 to 20 ml/min), a dosage of 17 mg/kg every 48 h is recommended.
临床研究已证实,对中性粒细胞减少患者每日一次(o.d.)给予每千克体重20毫克阿米卡星是有效的,但在该人群中,仅记录了每日两次(b.i.d.)、每次7.5毫克/千克给药方案下的阿米卡星药代动力学情况。为了确定在中性粒细胞减少患者中:(i)给药方案对阿米卡星动力学的影响;(ii)7.5至20毫克/千克剂量范围内阿米卡星动力学的线性关系;(iii)患者特征对阿米卡星处置的影响;以及(iv)为给药建议提供依据,我们评估了57名发热性中性粒细胞减少成人(中性粒细胞计数<500/mm³)的阿米卡星群体药代动力学,这些患者因血液系统疾病接受治疗,接受7.5毫克/千克b.i.d.(n = 29)或20毫克/千克o.d.(n = 28)的阿米卡星静脉滴注,滴注时间为0.5小时。在一个或多个给药间隔(1至47个)期间共采集了278份血样(每位患者1至14份)。采用酶放大免疫分析技术测定血清阿米卡星水平。使用混合效应建模方法将二室模型拟合到数据(NONMEM软件)。通过对群体模型的最大似然比检验评估给药方案以及人口统计学和生物学指标对阿米卡星药代动力学参数的影响。给药方案对阿米卡星药代动力学参数没有影响,即阿米卡星在7.5至20毫克/千克剂量范围内的动力学呈线性。阿米卡星清除率(CL)仅与肌酐清除率或其协变量相关,即性别、年龄、体重和血清肌酐水平。CL的个体间变异性为21%,而中央分布容积、分布清除率和组织分布容积的个体间变异性分别为15%、30%和25%。根据该人群中阿米卡星浓度的预期分布,提出了根据肌酐清除率(CL[CR])制定的给药建议:对于肾功能正常(CL[CR]为80至130毫升/分钟)的患者,建议每日一次给予20毫克/千克;而对于严重肾功能损害(CL[CR]为10至20毫升/分钟)患者,建议每48小时给予17毫克/千克的剂量。