Department of Pharmacy, Division of Pharmacotherapy, NYU Langone Medical Center, 550 First Avenue, GBH-SC2-097, New York, NY 10016, USA.
Ther Drug Monit. 2013 Apr;35(2):217-22. doi: 10.1097/FTD.0b013e3182834335.
To identify whether therapeutic hypothermia in newborns with hypoxic ischemic encephalopathy affects gentamicin pharmacokinetics.
Retrospective case-control study consisting of 16 neonates who underwent therapeutic hypothermia and received gentamicin with interpretable peak and trough serum levels obtained during the period of cooling and at steady state; comparator group consisting of 7 neonates met the criteria but did not undergo therapeutic hypothermia.
Significant differences in gentamicin pharmacokinetics were noted between the therapeutic hypothermia group and the comparator group in elimination rate constant (0.08/h versus 0.11/h; P < 0.01), elimination half-life (9.16 hours versus 6.56 hours; P < 0.01), and clearance (0.04 L/kg.h(-1) versus 0.05 L/kg.h(-1); P < 0.01), respectively. Higher gentamicin trough serum concentrations were seen with the therapeutic hypothermia group (1.68 mcg/mL versus 0.77 mcg/mL; P < 0.01).
Therapeutic hypothermia is associated with alterations in gentamicin pharmacokinetics, reducing gentamicin clearance by 25.5% in neonates with hypoxic ischemic encephalopathy, which may result in increased trough serum concentrations.
确定新生儿缺氧缺血性脑病接受治疗性低温后,是否会影响庆大霉素的药代动力学。
回顾性病例对照研究,纳入了 16 名接受治疗性低温并在冷却期和稳态期间获得可解释的庆大霉素峰和谷血清水平的新生儿;对照组由 7 名符合标准但未接受治疗性低温的新生儿组成。
与对照组相比,治疗性低温组的庆大霉素药代动力学有显著差异,消除率常数(0.08/h 与 0.11/h;P<0.01)、消除半衰期(9.16 小时与 6.56 小时;P<0.01)和清除率(0.04 L/kg.h(-1) 与 0.05 L/kg.h(-1);P<0.01)。治疗性低温组的庆大霉素谷浓度更高(1.68 mcg/mL 与 0.77 mcg/mL;P<0.01)。
治疗性低温与庆大霉素药代动力学的改变有关,使缺氧缺血性脑病新生儿的庆大霉素清除率降低 25.5%,可能导致谷浓度升高。