Hahn Andrea, Jensen Caroline, Fanous Hani, Chaney Hollis, Sami Iman, Perez Geovanny F, Louie Stan, Koumbourlis Anastassios C, Bost James E, van den Anker John N
J Pediatr Pharmacol Ther. 2018 Sep-Oct;23(5):379-389. doi: 10.5863/1551-6776-23.5.379.
To determine the frequency of subtherapeutic exposure to intravenously administered β-lactam antibiotics in a cohort of cystic fibrosis (CF) patients who were treated for a pulmonary exacerbation, and its impact on pulmonary function.
Nineteen CF patients between the ages of 5 and 21 years treated at Children's National Health System for a pulmonary exacerbation were followed between March 2015 and August 2016 in a prospective, longitudinal study. Pharmacokinetic modeling and minimum inhibitory concentrations (MICs) of the involved pathogens were used to determine therapeutic or subtherapeutic β-lactam antibiotic exposure based on the time the antibiotic concentration was above the MIC. Clinical outcomes were measured by spirometry values.
The 19 participants were treated with a total of 29 courses of antibiotics. The most common β-lactam antibiotics used in a treatment course were ceftazidime (62%) and meropenem (45%). There was no difference in age, CF genotype, or creatinine clearance between the 9 participants (47%) who reached therapeutic concentrations versus the 10 (53%) who did not. Those who achieved sufficiently high antibiotic exposure had more significant improvement of their pulmonary function tests.
We found that sufficient antibiotic exposure during treatment of CF pulmonary exacerbations was associated with improved pulmonary function. Moreover, it was impossible to predict, solely from the dosing regimen used, which patients were going to reach therapeutic β-lactam antibiotic serum concentrations. This suggests that CF patients may benefit from closer monitoring of their β-lactam exposure and bacterial MIC for optimal clinical outcomes.
确定在一组因肺部病情加重而接受治疗的囊性纤维化(CF)患者中,静脉注射β-内酰胺类抗生素治疗浓度不足的发生率及其对肺功能的影响。
在2015年3月至2016年8月期间,对在儿童国家卫生系统接受治疗的19名年龄在5至21岁之间因肺部病情加重的CF患者进行了一项前瞻性纵向研究。根据抗生素浓度高于最低抑菌浓度(MIC)的时间,使用药代动力学模型和所涉及病原体的MIC来确定β-内酰胺类抗生素的治疗性或亚治疗性暴露。通过肺活量测定值来衡量临床结果。
19名参与者共接受了29个疗程的抗生素治疗。一个治疗疗程中最常用的β-内酰胺类抗生素是头孢他啶(62%)和美罗培南(45%)。在达到治疗浓度的9名参与者(47%)与未达到治疗浓度的10名参与者(53%)之间,年龄、CF基因型或肌酐清除率没有差异。那些抗生素暴露量足够高的参与者,其肺功能测试有更显著的改善。
我们发现,在CF肺部病情加重治疗期间,足够的抗生素暴露与肺功能改善有关。此外,仅根据所用的给药方案,无法预测哪些患者将达到β-内酰胺类抗生素的治疗性血清浓度。这表明,CF患者可能受益于对其β-内酰胺类抗生素暴露和细菌MIC进行更密切的监测,以获得最佳临床结果。