Pharmacokinetic Variability and Target Attainment of Fluconazole in Critically Ill Patients

被引:9
|
作者
Van Daele, Ruth [1 ,2 ]
Wauters, Joost [3 ,4 ]
Lagrou, Katrien [5 ,6 ,7 ]
Denooz, Raphael [8 ]
Hayette, Marie-Pierre [9 ]
Gijsen, Matthias [1 ,2 ]
Brueggemann, Roger J. [10 ,11 ]
Debaveye, Yves [12 ,13 ]
Spriet, Isabel [1 ,2 ]
机构
[1] Katholieke Univ Leuven, Clin Pharmacol & Pharmacotherapy, Dept Pharmaceut & Pharmacol Sci, B-3000 Leuven, Belgium
[2] Univ Hosp Leuven, Pharm Dept, B-3000 Leuven, Belgium
[3] Katholieke Univ Leuven, Lab Clin Infect & Inflammatory Disorders, Dept Microbiol Immunol & Transplantat, B-3000 Leuven, Belgium
[4] Univ Hosp Leuven, Med Intens Care Unit, B-3000 Leuven, Belgium
[5] Univ Hosp Leuven, Dept Clin Lab Med, Excellence Ctr Med Mycol ECMM, B-3000 Leuven, Belgium
[6] Univ Hosp Leuven, Natl Reference Ctr Mycosis, Excellence Ctr Med Mycol ECMM, B-3000 Leuven, Belgium
[7] Katholieke Univ Leuven, Dept Microbiol Immunol & Transplantat, B-3000 Leuven, Belgium
[8] Univ Liege, Lab Clin Forens Environm & Ind Toxicol, CHU Sart Tilman, B-4000 Liege, Belgium
[9] Univ Liege, Lab Clin Microbiol, CIRM, B-4000 Liege, Belgium
[10] Radboud Univ Nijmegen Med Ctr, Radboud Inst Hlth Sci, Dept Pharm, NL-6525 GA Nijmegen, Netherlands
[11] Radboud Univ Nijmegen Med Ctr, Ctr Expertise Mycol Radboudumc CWZ, NL-6525 GA Nijmegen, Netherlands
[12] Katholieke Univ Leuven, Lab Intens Care Med, Dept Cellular & Mol Med, B-3000 Leuven, Belgium
[13] Univ Hosp Leuven, Intens Care Unit, B-3000 Leuven, Belgium
关键词
fluconazole; critically ill patients; pharmacokinetics; target attainment; variability; exposure; POPULATION PHARMACOKINETICS; SERUM; EPIDEMIOLOGY; CANDIDAEMIA; CANDIDIASIS; MANAGEMENT; GUIDELINE; DIAGNOSIS; EXPOSURE; NEED;
D O I
10.3390/microorganisms9102068
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Fluconazole is one of the oldest antifungal drugs. Previous studies have raised concerns considering variability in exposure and inadequate target attainment in critically ill patients. The current study aims to define variability and target attainment for fluconazole exposure in a large group of critically ill patients. Methods: In this pharmacokinetic study, daily plasma trough samples and, if possible, 24 h urine samples were collected to determine fluconazole concentration. A minimum target trough concentration of 10-15 mg/L was selected, corresponding to a free area under the concentration-time curve above the minimum inhibitory concentration (fAUC/MIC) of at least 100 for an MIC of 4 mg/L. Covariates that significantly influenced fluconazole exposure were identified. Results: In total, 288 plasma samples from 43 patients, with a median age of 66 years, were included. The median fluconazole trough concentration was 22.9 mg/L. A notable component of the measured concentrations was below the target trough concentrations (13% < 10 mg/L and 27% < 15 mg/L). The intra- and intersubject variability were 28.3% and 50.5%, respectively. The main covariates determining fluconazole exposure were the administered dose (mg/kg), augmented renal clearance, and renal replacement therapy. Conclusions: Fluconazole trough concentrations are variable in critically ill patients and a considerable number of these concentrations was below the predefined target trough concentrations.</p>
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页数:12
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