Dvorchik Barry, Damphousse David
Barry Dvorchik and Associates, Inc, 5809 Piney Lane Drive, Suite 105, Tampa, FL 33625, USA.
J Clin Pharmacol. 2004 Jun;44(6):612-20. doi: 10.1177/0091270004265646.
Daptomycin is a novel lipoprotein antibiotic that was recently approved for the treatment of complicated skin and skin structure infections caused by aerobic gram-positive bacteria. The pharmacokinetics of daptomycin was evaluated after a single 0.5-hour intravenous infusion of 4 mg/kg to groups of young adult (18-30 years) and geriatric (>or= 75 years) volunteers. Daptomycin was safe and well tolerated. No adverse events related to the infusion were reported. With increased age, there were increases in the area under the plasma concentration-time curve extrapolated to infinity (AUC( infinity )) and the terminal elimination half-life. Systemic (CL) and renal clearance (CL(R)) both decreased with increasing age. The observed changes seen in CL between the two cohorts were most likely a result of changes in renal function, as estimated by creatinine clearance. No statistically significant differences were observed between the two groups in the maximum plasma concentration (C(max)) and volume of distribution at steady state (Vd(ss)). The confidence intervals for the arithmetic mean ratios of the fraction of the dose excreted in the urine as daptomycin (%Fe) (geriatric subjects over younger subjects) were 60% to 101%, indicating that %Fe(dose) was lower in geriatric subjects. These results demonstrate that changes in the pharmacokinetics of daptomycin in the elderly are attributable to changes in renal function, whereas age per se is not a significant factor.
达托霉素是一种新型脂蛋白抗生素,最近被批准用于治疗由需氧革兰氏阳性菌引起的复杂性皮肤及皮肤结构感染。对年轻成人(18 - 30岁)和老年(≥75岁)志愿者组单次静脉输注0.5小时、剂量为4mg/kg的达托霉素后,评估了其药代动力学。达托霉素安全且耐受性良好。未报告与输注相关的不良事件。随着年龄增长,血浆浓度-时间曲线外推至无穷大的面积(AUC(∞))和终末消除半衰期增加。全身清除率(CL)和肾脏清除率(CL(R))均随年龄增长而降低。两个队列中观察到的CL变化很可能是肾功能变化的结果,通过肌酐清除率估算。两组在最大血浆浓度(C(max))和稳态分布容积(Vd(ss))方面未观察到统计学显著差异。尿液中以达托霉素形式排泄的剂量分数(%Fe)(老年受试者与年轻受试者相比)的算术平均比值的置信区间为60%至101%,表明老年受试者的%Fe(剂量)较低。这些结果表明,老年人中达托霉素药代动力学的变化归因于肾功能的变化,而年龄本身不是一个重要因素。