在 PEDI-CEFI 2 期研究中,使用标准抗生素治疗的三个月至十八岁以下住院儿科感染患者服用单剂量或多剂量头孢哌酮的药代动力学、安全性和耐受性。

IF 2.9 4区 医学 Q3 IMMUNOLOGY Pediatric Infectious Disease Journal Pub Date : 2024-09-04 DOI:10.1097/INF.0000000000004529
John S Bradley, Elaine Orchiston, Simon Portsmouth, Mari Ariyasu, Takamichi Baba, Takayuki Katsube, Oluwaseun Makinde
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引用次数: 0

摘要

背景:在全球范围内,新生儿和婴幼儿耐多药革兰氏阴性菌感染日益增多,而抗生素的选择却很有限:在全球范围内,新生儿、婴儿和儿童耐多药革兰氏阴性菌感染日益增多,而抗生素的选择却很有限:这项国际性、多中心、开放标签的 2 期研究调查了单剂量和多剂量头孢妥喏的药代动力学、安全性和耐受性[3 小时输注(每 8 小时一次),体重≥34 千克者剂量为 2000 毫克,体重≥60 千克者剂量为 60 毫克/千克]:共有 53 名患者(中位年龄:73.5 个月)接受了治疗。在肾功能正常或轻度肾功能损害的患者中,无论年龄和体重如何,单剂量(24 人)和多剂量(29 人)头孢哌酮的血浆浓度分布相似。单剂量头孢羟氨苄在输注结束时的几何平均浓度为 72.7 至 97.1 μg/mL,多剂量头孢羟氨苄在输注结束时的几何平均浓度为 88.8 至 106.0 μg/mL。8 小时后,单剂量头孢羟氨苄的相应谷浓度在 7.86 至 10.8 μg/mL 之间,多剂量头孢羟氨苄的相应谷浓度在 9.64 至 18.1 μg/mL 之间。无死亡病例,无与头孢羟氨苄相关的严重不良事件,无明显的实验室异常或停药:多剂量头孢羟氨苄根据体重连续给药5-14天,可达到稳态血浆浓度,在整个给药期间均高于革兰氏阴性菌的药敏断点。头孢羟氨苄的耐受性良好。
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Pharmacokinetics, Safety and Tolerability of Single-dose or Multiple-dose Cefiderocol in Hospitalized Pediatric Patients Three Months to Less Than Eighteen Years Old With Infections Treated With Standard-of-care Antibiotics in the PEDI-CEFI Phase 2 Study.

Background: Multidrug-resistant Gram-negative bacterial infections are increasing globally in neonates, infants and children; antibiotic options are limited.

Methods: This international, multicenter, open-label phase 2 study, investigated the pharmacokinetics, safety and tolerability of single-dose and multiple-dose cefiderocol [as a 3-hour infusion (every 8 hours) dosed at 2000 mg for body weight ≥34 kg and at 60 mg/kg for body weight <34 kg], over a range of renal function, in hospitalized pediatric patients with aerobic Gram-negative bacterial infection; multiple-dose patients required standard-of-care systemic antibiotics for 5-14 days. Four cohorts of pediatric patients were enrolled (cohort 1: 12 to <18 years, cohort 2: 6 to <12 years, cohort 3: 2 to <6 years and cohort 4: 3 months to <2 years).

Results: A total of 53 patients (median age: 73.5 months) were enrolled. Plasma concentration profiles were similar with single-dose (n = 24) and multiple-dose (n = 29) cefiderocol, irrespective of age and body weight in those with normal renal function or mild renal impairment. Geometric mean concentrations at the end of infusion ranged between 72.7 and 97.1 μg/mL for single-dose cefiderocol and between 88.8 and 106.0 μg/mL after multiple doses. At 8 hours, corresponding trough concentrations ranged from 7.86 to 10.8 μg/mL with single-dose cefiderocol and from 9.64 to 18.1 μg/mL with multiple doses. There were no deaths, no cefiderocol-related serious adverse events, significant related laboratory abnormalities or discontinuations.

Conclusions: Multiple-dose cefiderocol, administered for 5-14 days and according to body weight, achieved steady-state plasma concentrations that remained above the susceptibility breakpoints of Gram-negative bacteria throughout the dosing period. Cefiderocol was well tolerated.

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来源期刊
CiteScore
6.30
自引率
2.80%
发文量
566
审稿时长
2-4 weeks
期刊介绍: ​​The Pediatric Infectious Disease Journal® (PIDJ) is a complete, up-to-the-minute resource on infectious diseases in children. Through a mix of original studies, informative review articles, and unique case reports, PIDJ delivers the latest insights on combating disease in children — from state-of-the-art diagnostic techniques to the most effective drug therapies and other treatment protocols. It is a resource that can improve patient care and stimulate your personal research.
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