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与儿科患者伏立康唑浓度相关的因素

Factors Associated With Voriconazole Concentration in Pediatric Patients.

作者信息

Kang Suyeon, Yee Jeong, Kim Jae Youn, Han Hye Won, Kang Sang Oh, Lee Kyung Eun, Gwak Hye Sun

机构信息

Graduate School of Converging Clinical & Public Health, Ewha Womans University.

Department of Pharmacy, Asan Medical Center.

出版信息

Ther Drug Monit. 2020 Dec;42(6):866-871. doi: 10.1097/FTD.0000000000000804.

Abstract

BACKGROUND

Serum concentrations of voriconazole are difficult to predict, especially in pediatric patients, because of its complex pharmacokinetic characteristics. This study aimed to identify the factors associated with the concentration of voriconazole in pediatric patients.

METHODS

This cohort study was based on retrospective data collection and involved the administration of voriconazole to pediatric patients younger than 18 years, between January 2010 and August 2017. Electronic medical records of the patients were reviewed to collect demographic characteristics, voriconazole treatment regimen, and factors that could potentially influence voriconazole trough concentrations. A voriconazole trough serum concentration of less than 1.0 mcg/mL or greater than 5.5 mcg/mL was defined as outside the therapeutic range and was set as the outcome of this study.

RESULTS

Among the 114 patients enrolled, 61 patients were included in the analysis. Oral administration of a maintenance dose of voriconazole and C-reactive protein (CRP) level were significantly and independently associated with a low initial trough concentration of voriconazole (<1.0 mcg/mL). Alanine aminotransferase levels were a significant factor associated with a high initial trough concentration of voriconazole (>5.5 mcg/mL) after adjusting for sex, age, weight, and serum creatinine (odds ratio 5.42; 95% confidence interval 1.34-21.97).

CONCLUSIONS

Considering the variability of voriconazole concentrations in pediatric patients, monitoring certain parameters and considering the route of administration could help determine the therapeutic range of voriconazole and subsequently avoid unwanted effects.

摘要

背景

伏立康唑的血清浓度难以预测,尤其是在儿科患者中,因为其药代动力学特征复杂。本研究旨在确定与儿科患者伏立康唑浓度相关的因素。

方法

本队列研究基于回顾性数据收集,纳入了2010年1月至2017年8月期间接受伏立康唑治疗的18岁以下儿科患者。查阅患者的电子病历以收集人口统计学特征、伏立康唑治疗方案以及可能影响伏立康唑谷浓度的因素。伏立康唑谷血清浓度低于1.0 mcg/mL或高于5.5 mcg/mL被定义为超出治疗范围,并被设定为本研究的结局。

结果

在纳入的114例患者中,61例患者纳入分析。口服维持剂量的伏立康唑和C反应蛋白(CRP)水平与伏立康唑低初始谷浓度(<1.0 mcg/mL)显著且独立相关。在调整性别、年龄、体重和血清肌酐后,丙氨酸转氨酶水平是与伏立康唑高初始谷浓度(>5.5 mcg/mL)相关的显著因素(比值比5.42;95%置信区间1.34 - 21.97)。

结论

考虑到儿科患者伏立康唑浓度的变异性,监测某些参数并考虑给药途径有助于确定伏立康唑的治疗范围,从而避免不良影响。

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