Koo J, Tight R, Rajkumar V, Hawa Z
Department of Pharmacy, VA Medical Center, Fargo, North Dakota 58102, USA.
Am J Med. 1996 Aug;101(2):177-83. doi: 10.1016/s0002-9343(96)80074-x.
Once-daily dosing has been suggested as an alternative method of dosing aminoglycosides that would reduce their toxicity while maintaining efficacy. There have been no studies published to date comparing once-daily dosing and pharmacokinetic dosing of aminoglycosides. We conducted a randomized controlled trial comparing the safety and effectiveness of 4 mg/kg IV once-daily dosing of gentamicin or tobramycin with a pharmacokinetic dosing method using an initial dose of 2 mg/kg IV every 12 hours.
Ninety-six patients were randomly assigned to either the once-daily dosing group (4 mg/kg) or the pharmacokinetic dosing group (initial dose of 2 mg/kg every 12 hours). In the once-daily dosing group, the dosing interval was extended by 12 to 24 hours to maintain a serum trough concentration < 1.5 mg/L regardless of the peak concentration. Dosing in the other group was adjusted based on the individual pharmacokinetic data to achieve a serum peak concentration of 6 to 10 mg/L and a trough concentration below 1.5 mg/L. The patients studied were predominantly elderly males (mean age 69 years). All patients were assessed for treatment efficacy and nephrotoxicity.
There was no significant difference between the two groups with regard to clinical and bacteriologic efficacy. Incidence of nephrotoxicity was 24% in the once-daily group and 14% in the pharmacokinetic dosing group but the difference was not statistically significant (P = 0.13). Unlike previous studies, we found a correlation between high serum peak concentration and incidence of nephrotoxicity in the once-daily dosing group. Nephrotoxicity developed in six out of 10 patients (60%) with an initial serum peak concentration greater than 12.0 mg/L compared to two out of 24 patients (8.3%) with an initial peak concentration less than 12.0 mg/L (P < 0.001) in the once-daily group. Serum peak concentrations in the pharmacokinetic dosing group were not correlated with nephrotoxicity.
Once-daily dosing and pharmacokinetic dosing of aminoglycosides appear to have equal efficacy and toxicity. However, in the elderly population, high serum peak concentrations that occur with once-daily aminoglycoside dosing may increase the risk of nephrotoxicity.
每日一次给药被认为是氨基糖苷类药物给药的一种替代方法,该方法在维持疗效的同时可降低其毒性。迄今为止,尚无已发表的研究比较氨基糖苷类药物的每日一次给药和药代动力学给药。我们进行了一项随机对照试验,比较庆大霉素或妥布霉素每日一次静脉注射4mg/kg与采用每12小时静脉注射2mg/kg初始剂量的药代动力学给药方法的安全性和有效性。
96例患者被随机分配至每日一次给药组(4mg/kg)或药代动力学给药组(每12小时初始剂量2mg/kg)。在每日一次给药组中,给药间隔延长12至24小时,以维持血清谷浓度<1.5mg/L,而不考虑峰浓度。另一组的给药根据个体药代动力学数据进行调整,以达到血清峰浓度6至10mg/L且谷浓度低于1.5mg/L。所研究的患者主要为老年男性(平均年龄69岁)。所有患者均评估治疗效果和肾毒性。
两组在临床和细菌学疗效方面无显著差异。每日一次给药组的肾毒性发生率为24%,药代动力学给药组为14%,但差异无统计学意义(P=0.13)。与既往研究不同,我们发现每日一次给药组中高血清峰浓度与肾毒性发生率之间存在相关性。在每日一次给药组中,初始血清峰浓度大于12.0mg/L的10例患者中有6例(60%)发生肾毒性,而初始峰浓度小于12.0mg/L的24例患者中有2例(8.3%)发生肾毒性(P<0.001)。药代动力学给药组的血清峰浓度与肾毒性无相关性。
氨基糖苷类药物的每日一次给药和药代动力学给药似乎具有相同的疗效和毒性。然而,在老年人群中,每日一次氨基糖苷类药物给药时出现的高血清峰浓度可能会增加肾毒性风险。