Thibault Céline, Kassir Nastya, Théorêt Yves, Varin France, Litalien Catherine, Autmizguine Julie
Clinical Pharmacology Unit, CHU Sainte-Justine, Montreal, QC, Canada.
Department of Pediatrics, CHU Sainte-Justine, Montreal, QC, Canada.
J Popul Ther Clin Pharmacol. 2017 Aug 21;24(3):e33-344. doi: 10.22374/1710-6222.24.1.3.3.
Extended piperacillin-tazobactam (TZP) infusions have been associated with favourable outcomes. There are currently no pediatric dosing recommendations.
To determine appropriate TZP dosing strategies in children 2 months - 6 years according to age and different minimal inhibitory concentrations (MICs).
Age and weight were simulated for 1000 children. pharmacokinetic parameter estimates were generated using published clearance and volume of distribution data. For different dosing regimens, we estimated the probability of target attainment (PTA) over a range of MICs from 4 to 128 mg/L. The pharmacodynamic (PD) target was defined as free piperacillin concentrations above the MIC for ≥ 50% of the dosing interval. A PTA ≥ 90% was defined as optimal.
PTA decreased as MIC and age increased. In all age groups, standard dosing regimens (240-300 mg/kg/day, 0.5h infusions) failed to reach PTAs ≥ 90% at MICs ≥ 16 mg/L. Standard 0.5h infusions reached PTAs ≥ 90% at MICs up to 8 mg/L in infants > 2 to 6m. No 0.5h infusion reached PTAs ≥ 90% for MICs ≥ 4 mg/L in children > 6m. While none of the tested regimens were optimal at MICs > 16 mg/L in children > 6m, 100 mg/kg/dose every 6h as a 3h infusion reached PD target at MICs of 32 mg/L in infants > 2 to 6m.
Up to MICs of 16 mg/L, 90 mg/kg/dose every 8h as a 2h infusion in infants > 2 to 6m and 100 mg/kg/dose every 8h as a 4h infusion in children > 6m-6y achieved PTAs ≥ 90%.
延长哌拉西林-他唑巴坦(TZP)输注时间与良好的治疗效果相关。目前尚无儿童用药剂量推荐。
根据年龄和不同的最低抑菌浓度(MIC)确定2个月至6岁儿童合适的TZP给药策略。
模拟1000名儿童的年龄和体重。使用已发表的清除率和分布容积数据生成药代动力学参数估计值。对于不同的给药方案,我们估计了在4至128mg/L的一系列MIC范围内达到目标的概率(PTA)。药效学(PD)目标定义为游离哌拉西林浓度在给药间隔的≥50%时间内高于MIC。PTA≥90%被定义为最佳。
PTA随着MIC和年龄的增加而降低。在所有年龄组中,标准给药方案(240 - 300mg/kg/天,0.5小时输注)在MIC≥16mg/L时未能达到PTA≥90%。在2至6个月以上的婴儿中,标准的0.5小时输注在MIC高达8mg/L时达到PTA≥90%。在6个月以上的儿童中,没有0.5小时输注在MIC≥4mg/L时达到PTA≥90%。虽然在6个月以上的儿童中,当MIC>16mg/L时,没有一种测试方案是最佳的,但在2至6个月以上的婴儿中,每6小时100mg/kg/剂量作为3小时输注在MIC为32mg/L时达到了PD目标。
在MIC高达16mg/L时,2至6个月以上的婴儿每8小时90mg/kg/剂量作为2小时输注以及6个月至6岁儿童每8小时100mg/kg/剂量作为4小时输注可使PTA≥90%。