Therapeutic Drug Monitoring of Voriconazole: Unbound Concentration With Clinical Efficacy and Adverse Events.

IF 2.3 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Tiantian Zhang, Zhicong Qiu, Wenhao Chu, Wenli Li, Xikun Wu, Yuxin Wang, Yishuo Zhai, Wei Zhang, Zhiqing Zhang
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引用次数: 0

Abstract

Background: Voriconazole is widely used for patients with fungal infections, but the correlations between the unbound concentration (Cfree) of voriconazole in plasma and clinical outcomes remains unclear.

Objective: The aim of this study was to analyze the correlation between Cfree and clinical outcomes.

Methods: A retrospective analysis was conducted at the Second Hospital of Hebei Medical University from February 2021 to March 2024 (Shijiazhuang, China). Patients who received voriconazole with at least one measured concentration in our center were enrolled. Based on determined the Cfree of voriconazole, factors that might affect Cfree were analyzed in conjunction with patient characteristics, and the correlations between voriconazole Cfree and the clinical efficacy as well as AEs in patients were investigated.

Results: A total of 60 blood samples were collected from 56 patients. Voriconazole Cfree was positive correlation with creatinine, while negative correlation with creatinine clearance. The Cfree of patients in the clinical effective group was significantly higher than that in the clinical ineffective group, and the Cfree of patients in the group with AEs was significantly higher than that in the group without AEs (P = 0.006, 0.025). Voriconazole Cfree (odds ratio [OR] = 2.617, 95% confidence interval [CI]:1.142-6.000, P = 0.023) and albumin level (OR = 1.085, 95% CI: 1.000-1.177, P = 0.050) were independent influencing factors of clinical efficacy, the receiver operating characteristic (ROC) cut off for Cfree and efficacy was 0.8 μg·mL-1. Voriconazole Cfree (OR = 1.979, 95% CI: 1.008-3.888, P = 0.048) was an independent risk factor for AEs, the ROC cut off for Cfree and AEs was 1.2 μg·mL-1.

Conclusions and relevance: Voriconazole Cfree was positively correlated with clinical efficacy and the incidence of AEs in patients.

伏立康唑治疗药物监测:非结合浓度与临床疗效及不良事件。
背景:伏立康唑广泛用于真菌感染患者,但血浆中伏立康唑的游离浓度(Cfree)与临床结局的相关性尚不清楚。目的:本研究的目的是分析Cfree与临床预后的相关性。方法:回顾性分析河北医科大学第二医院2021年2月至2024年3月(中国石家庄)的病例。在本中心接受伏立康唑至少一种测量浓度的患者入组。在测定伏立康唑Cfree的基础上,结合患者特点分析可能影响Cfree的因素,探讨伏立康唑Cfree与患者临床疗效及不良反应的相关性。结果:共采集56例患者60份血样。伏立康唑Cfree与肌酐正相关,与肌酐清除率负相关。临床有效组患者Cfree显著高于临床无效组,发生不良事件组患者Cfree显著高于无不良事件组(P = 0.006, 0.025)。伏立康唑Cfree(比值比[OR] = 2.617, 95%可信区间[CI]:1.142 ~ 6.000, P = 0.023)和白蛋白水平(OR = 1.085, 95% CI: 1.000 ~ 1.177, P = 0.050)是临床疗效的独立影响因素,Cfree和疗效的受试者工作特征(ROC)截止值为0.8 μg·mL-1。伏立康唑Cfree (OR = 1.979, 95% CI: 1.008 ~ 3.888, P = 0.048)是ae的独立危险因素,Cfree和ae的ROC cut (ROC cut off)为1.2 μg·mL-1。结论及相关性:Voriconazole Cfree与患者临床疗效及不良事件发生率呈正相关。
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
CiteScore
5.70
自引率
0.00%
发文量
166
审稿时长
3-8 weeks
期刊介绍: Annals of Pharmacotherapy (AOP) is a peer-reviewed journal that advances pharmacotherapy throughout the world by publishing high-quality research and review articles to achieve the most desired health outcomes.The articles provide cutting-edge information about the most efficient, safe and cost-effective pharmacotherapy for the treatment and prevention of various illnesses. This journal is a member of the Committee on Publication Ethics (COPE). Average time from submission to first decision: 14 days
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