Ceftriaxone Pharmacokinetics and Pharmacodynamic Target Attainment for Three Pediatric Patients Receiving Continuous Kidney Replacement Therapy.

Q2 Medicine
H Rhodes Hambrick, Francisco Cervantes, Min Dong, Peter Tang, Trent Arbough, Alexander A Vinks, Tomoyuki Mizuno, Stuart L Goldstein, Jennifer Kaplan, Sonya Tang Girdwood
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引用次数: 0

Abstract

Ceftriaxone is used commonly for sepsis, including in children requiring continuous kidney replacement therapy (CKRT). No reports exist of pharmacokinetic (PK) parameters for children receiving ceftriaxone on CKRT. We enrolled children admitted to our pediatric intensive care unit (PICU) who received CKRT for >24 hours and received >1 dose of ceftriaxone while on and off CKRT. We measured free ceftriaxone -concentrations from residual blood samples then used Bayesian estimation with PK modeling software to generate concentration-time profiles and determine PK parameters and the percentage of time free ceftriaxone concentrations were above 1× or 4× MIC (% fT >MIC). Three patients aged 2 to 17 years were included; all were anuric at CKRT initiation and received 50 mg/kg (max 2000 mg) ceftriaxone every 12 to 24 hours. Total ceftriaxone clearance (CL) was 0.50 to 3.67 L/hr while receiving CKRT and 0.29 to 2.71 L/hr while off, indicating CKRT provided 25% to 42% of total ceftriaxone CL. All achieved 100% fT >1× and 4× MIC using an estimated MIC (1 mg/L) for patients 1 to 2 (no culture data) and a measured MIC (0.016 mg/L) for patient 3. Therefore, CKRT contributed significantly to total ceftriaxone clearance in 3 children though the dosing strategies used in each patient attained PD targets.

三名接受持续肾脏替代疗法的儿科患者的头孢曲松药代动力学和药效学目标达成情况。
头孢曲松常用于治疗败血症,包括需要持续肾脏替代疗法(CKRT)的儿童。目前还没有关于接受头孢曲松持续肾脏替代疗法(CKRT)的儿童药代动力学(PK)参数的报告。我们招募了入住儿科重症监护室(PICU)、接受 CKRT 超过 24 小时且在接受和停止 CKRT 期间接受过超过 1 次头孢曲松治疗的患儿。我们测量了残留血样中游离头孢曲松的浓度,然后使用贝叶斯估计和 PK 建模软件生成浓度-时间曲线,确定 PK 参数和游离头孢曲松浓度高于 1 倍或 4 倍 MIC 的时间百分比(% fT >MIC)。该研究共纳入了 3 名年龄在 2 到 17 岁之间的患者;他们在开始接受 CKRT 时均无尿,每 12 到 24 小时接受 50 毫克/千克(最大 2000 毫克)头孢曲松的治疗。接受 CKRT 治疗时,头孢曲松总清除率(CL)为 0.50 至 3.67 升/小时,停药时为 0.29 至 2.71 升/小时,这表明 CKRT 提供了头孢曲松总清除率的 25% 至 42%。1 号和 2 号患者使用估计的 MIC(1 毫克/升)(无培养数据),3 号患者使用测量的 MIC(0.016 毫克/升),所有患者都达到了 100% fT >1 倍和 4 倍 MIC。因此,尽管每位患者使用的给药策略都达到了 PD 目标,但 CKRT 对 3 名儿童的头孢曲松总清除率有显著影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Pediatric Pharmacology and Therapeutics
Journal of Pediatric Pharmacology and Therapeutics Medicine-Pediatrics, Perinatology and Child Health
CiteScore
2.40
自引率
0.00%
发文量
90
期刊介绍: The Journal of Pediatric Pharmacology and Therapeutics is the official journal of the Pediatric Pharmacy Advocacy Group. JPPT is a peer-reviewed multi disciplinary journal that is devoted to promoting the safe and effective use of medications in infants and children. To this end, the journal publishes practical information for all practitioners who provide care to pediatric patients. Each issue includes review articles, original clinical investigations, case reports, editorials, and other information relevant to pediatric medication therapy. The Journal focuses all work on issues related to the practice of pediatric pharmacology and therapeutics. The scope of content includes pharmacotherapy, extemporaneous compounding, dosing, methods of medication administration, medication error prevention, and legislative issues. The Journal will contain original research, review articles, short subjects, case reports, clinical investigations, editorials, and news from such organizations as the Pediatric Pharmacy Advocacy Group, the FDA, the American Academy of Pediatrics, the American Society of Health-System Pharmacists, and so on.
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