Association of Vancomycin Trough Concentration and Clearance With Febrile Neutropenia in Pediatric Patients

万古霉素 医学 中性粒细胞减少症 发热性中性粒细胞减少症 内科学 低谷(经济学) 儿科 重症监护医学 化疗 金黄色葡萄球菌 遗传学 生物 宏观经济学 经济 细菌
作者
Erino Amano,Ryota Tanaka,Hiroyuki Ono,Ryosuke Tatsuta,Takehiro Hashimoto,Kazufumi Hiramatsu,Hiroki Itoh
出处
期刊:Therapeutic Drug Monitoring [Lippincott Williams & Wilkins]
卷期号:44 (4): 543-551 被引量:4
标识
DOI:10.1097/ftd.0000000000000978
摘要

Background: Febrile neutropenia promotes renal drug excretion. Adult and pediatric patients with febrile neutropenia exhibit a lower vancomycin concentration/dose (relative to bodyweight) ratio than those with other infections. In pediatric patients, renal function relative to bodyweight varies depending on age, and vancomycin clearance is age dependent. This study aimed to analyze the effects of febrile neutropenia on the pharmacokinetics of vancomycin in age-stratified pediatric patients. Methods: This retrospective, single-center, observational cohort study analyzed 112 hospitalized pediatric patients who met the selection criteria and intravenously received vancomycin at the Department of Pediatrics of the Oita University Hospital between April 2011 and October 2019. Results: The febrile neutropenia (n = 46) cohort exhibited a significantly higher estimated glomerular filtration rate than the nonfebrile neutropenia (n = 66) cohort. Compared with those in the nonfebrile neutropenia cohort, the daily vancomycin dose relative to bodyweight and vancomycin clearance were significantly higher, and the vancomycin trough concentration and vancomycin concentration/dose ratio were significantly lower in the febrile neutropenia cohort. In the age groups of 1–6 and 7–12 years, compared with those in the nonfebrile neutropenia cohort, the vancomycin concentration/dose ratio was significantly lower, and vancomycin clearance was significantly higher in the febrile neutropenia cohort. Univariate and multivariate analyses identified febrile neutropenia as the independent factor influencing vancomycin concentration/dose ratio and clearance only in pediatric patients aged 1–6 years. Conclusions: Increased initial dosage and therapeutic drug monitoring-guided dose optimization are critical for the therapeutic efficacy of vancomycin in pediatric patients with febrile neutropenia, especially in those aged 1–6 years.

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